Fluorocarbon- organosilicon copolymers and coatings prepared by hot-filament chemical vapor deposition

[0001] This application claims the benefit of priority to U.S. Provisional Patent Application Serial No. 60/340,911, filed Oct. 30, 2001.

[0003] Fluorocarbon and organosilicon thin films produced by chemical vapor deposition have a wide variety of applications, ranging from biocompatible coatings for medical implants, to low K dielectrics in integrated circuits. Noort, R. V, Black, M. M. Biocompatibility of Clinical Implant Materials; Williams, D. F. Ed.; CRC Press: Boca Raton, 1981; Vol. 2, p 79-98; Chawla, A. S. Artif. Organs 1979, 3, 92; Chawla, A. S. Biomaterials 1981, 2, 83; Ocumpaugh, D. E., Lee, H. L., Biomedical Polymers; Rembaum, A., Shen, M., Eds.; Marcel Dekker: New York, 1971; p 101; Thomson, L. A., Law, F. C., James, K. H., Rushton, N. Biomaterials 1991, 12, 781; Guidoin, R., Chakfe, N., Maurel, S., How, T., Batt, M., Marois, M., Gosselin, C. Biomaterials 1993, 14, 678; and Lau, K. K. S., Gleason, K. K. Mater. Res. Soc. Symp. Proc. 1999, 544, 209; Rosenmayer, T., Huey, W. Mater. Res. Soc. Symp. Proc. 1996, 427, 463; Peters, L. Semicond. Int. 2000, 23, 108; Loboda, M. J. Microelect. Eng. 2000, 50, 15; and Grill, A., Patel, V. J. Appl. Phys. 1999, 85, 3314. Fluorocarbon films have been found to be biocompatible and have low dielectric constants. However, they also have a high degree of roughness and do not adhere well to silicon substrates. Silicone films are biocompatible and offer the additional advantages of excellent adhesion to silicon substrates and superior thermal stability. But the dielectric constant of these films is higher than that of the fluorocarbon films. A fluorocarbon-organosilicon copolymer film therefore has the potential to incorporate the desirable attributes of each class of material into a single film.

[0004] The addition of fluorine to organosilicon films is anticipated to lower the dielectric constant, increase electrical resistivity, reduce surface energy, increase hydophobicity, and reduce permeability to water. All of these trends are favorable for biopassivation applications. The copolymer films can also retain the desirable adhesion characteristics and mechanical properties of the organosilicon homopolymer. Flexible copolymer films could also be used as biopassivation coatings on biomedical device components.

[0005] Transparent, tough, hard, scratch resistant films having extreme hydrophobicity would make excellent protective and dirt resistant coatings on window glass, windshields, and eyewear. Since the substrate remains at low temperature during the process, temperature sensitive materials such as plastics and fabrics can also be coated. Potential applications include anti-fouling coatings on marine vessels and equipment, coatings for food containers, and biological and chemical laboratory equipment. The hybrid copolymer can also serve as an intermediate transition layer for graded coatings such as the stack substrate-organosilicon-copolymer-fluoropolymer. Such an arrangement can produce an adherent interface with a hydrophobic surface, or even a film in which one surface is hydrophobic and the other hydrophilic.

[0006] Organosilicon or fluorocarbon homopolymers can be coated onto surfaces by a number of techniques such as spin-on coating, casting or chemical vapor deposition. An important advantage of chemical vapor deposition (CVD) is the ability to create copolymers that are difficult to synthesize by bulk or solution techniques, such as fluorocarbon-organosilicon copolymers. Fluorocarbon polymers are normally synthesized by free radical polymerization, whereas polysiloxanes are made by ionic polymerization techniques. Synthesis of a copolymer would thus require a transformation from ionic polymerization to free radical polymerization (or vice versa). Although several transformation techniques have been reported in the literature, to our knowledge, none of these methods have been applied to the synthesis of fluorocarbon-organosilicon copolymers. Serhatli, I. E., Galli, G., Yagci, Y., Chiellini, E. Polym. Bull. 1995, 34, 539; Cunliffe, A. V., Hayes, G. F., Richards, D. H. J. Polym. Sci. (B) 1976, 14, 483; Souel, T., Schue, F., Abadie, M., and Richards, D. H. Polymer 1977, 18, 1292.

[0007] Among the different CVD techniques available, hot-filament CVD (HFCVD, also known as pyrolytic or hot-wire CVD) is unique in several respects. In HFCVD, a precursor gas is thermally decomposed by a resistively heated filament. The resulting pyrolysis products adsorb onto a substrate maintained at around room temperature and react to form a film. HFCVD does not require the generation of a plasma, thereby avoiding defects in the growing film produced by UV irradiation and ion bombardment. In addition, films produced by HFCVD have a better-defined chemical structure because there are fewer reaction pathways than in the less selective plasma-enhanced CVD method. HFCVD provides films with a substantially lower density of dangling bonds, i.e. unpaired electrons. Further, HFCVD has been shown to produce films that have a low degree of crosslinking. Limb, S. J., Lau, K. K. S., Edell, D. J., Gleason, E. F., Gleason, K. K. Plasmas and Polymers 1999, 4, 21.

[0008] HFCVD has been used to deposit fluorocarbon films that are spectroscopically similar to poly(tetrafluoroethylene) (PTFE) as well as organosilicon films that consist of linear and cyclic siloxane repeat units. Limb, S. J., Lau, K. K. S., Edell, D. J., Gleason, E. F., Gleason, K. K. Plasmas and Polymers 1999, 4, 21. Few attempts have been made to create fluorocarbon-organosilicon copolymers by CVD, and these have been limited to plasma-enhanced CVD (PECVD). Sakata, J., Yamamoto, M., Tajima, I. J. Polym. Sci. (A) 1988, 26, 1721; Kim, D. S., Lee, Y. H., Park, N. Appl. Phys. Lett 1996, 69, 2776; Shirafuji, T., Miyazaki, Y., Nakagami, Y., Hayashi, Y., Nishino, S. Jpn. J. Appl. Phys. 1999, 38 Pt. 1 No. 7B, 4520; H. Kotoh, M. Muroyama, M. Sasaki, M. Iwasawa, Jpn. J. Appl. Phys. 1996, 35 Pt. 1, No. 2B, 1464; and P. Favia, G. Caporiccio, R. d'Agostino, J. Polym. Sci. Part A: Polym. Chem. 1994, 32, 121-130. Sakata et al. obtained thin films using hexamethyldisiloxane (HMDSO) and tetrafluoromethane (CF₄) by plasma-enhanced CVD. Sakata, J., Yamamoto, M., Tajima, I. J. Polym. Sci. (A) 1988, 26, 1721. The structure of the films was found to be different from a simple blend of fluorocarbon and organosilicon polymers. In other words, the polymer film did not consist of simple block or random copolymers. The authors observed the presence of SiF bonds, and the data presented indicates that most of the fluorine in the films was bonded to silicon.

[0009] Similar results were obtained by Kim et al. with HMDSO and perfluorobenzene (C₆F₆). Kim, D. S., Lee, Y. H., Park, N. Appl. Phys. Lett 1996, 69, 2776. This investigation also included dielectric constant measurements and adhesion tests. The dielectric constants of the copolymer films were found to lie between those of the respective homopolymeric films, between 2 (pure fluorocarbon) and 4 (pure organosilicon). Annealing the films brought about a slight decrease in the dielectric constant. Adhesion of these films to silicon substrates was measured using the ASTM tape test and was determined to be better than that of pure fluorocarbon films.

[0010] Favia et al. investigated the plasma-enhanced CVD of a cyclic fluorinated siloxane, (3,3,3-trifluoropropyl)methylcyclotrisiloxane. P. Favia, G. Caporiccio, R. d'Agostino, J. Polym. Sci. Part A: Polym. Chem. 1994, 32, 121-130. The authors examined the effects of varying substrate temperature and substrate bias on the deposition rate and chemical composition of the films. Films deposited with substrate temperatures below 200 C. were determined to be structurally similar to the precursor. The carbon and hydrogen content of the films was found to decrease at higher substrate temperatures along with the deposition rate. Increasing the substrate bias resulted in greater crosslinking and higher deposition rate. The authors emphasize the absence of SiF, SiH and OH bonds in their films.

[0011] There still exists a need for a reliable method of depositing fluorocarbon-organosilicon copolymer thin films with well-resolved bonding environments. We describe herein HFCVD methods for forming fluorocarbon-organosilicon films without the complex structures and undefined spectroscopic features associated with PECVD methods. Extensive spectroscopic characterization confirms the presence of covalent bonds between CF₂ groups and siloxane-based polymeric units in the film.

[0012] The invention overcomes limitations of prior deposition processes to enable production of copolymer thin films with well defined bonding environments, and addresses the many biomedical and microfabrication applications for such a film. Accordingly, in one aspect, the invention provides a method for forming a copolymer thin film on the surface of a structure. Preferably, the copolymer is a fluorocarbon-organosilicon copolymer. This is accomplished by exposing the monomer gasses of a fluorocarbon precursor and organosilicon precursor to a source of heat having a temperature sufficient to pyrolyze the monomer gasses and produce a source of reactive CF₂ and siloxane species in the vicinity of the structure surface. The structure surface is maintained at a substantially lower temperature than that of the heat source to induce deposition and polymerization of the CF₂ and siloxane species on the structure surface.

[0013] Preferably, the gas mixture comprises hexafluoropropylene oxide and hexamethylcyclotrisiloxane, and the heat source preferably is a resistively-heated conducting filament suspended over the structure surface or a heated plate having a pyrolysis surface that faces the structure. The heat source temperature is preferably greater than about 400K and the structure surface is preferably maintained at a temperature less than about 300K.

[0014] The structure on which surface the film is formed can be, for example only, a length of wire, a substrate, a neural probe, a razor blade, a ribbon cable, or a microstructure having multiple surfaces all maintained at a temperature substantially lower than that of the heat source.

[0015] In another aspect, the invention provides a method for coating a non planar and flexible structure with a flexible fluorocarbon-organosilicon copolymer film. The coating is accomplished by exposing the structure to an environment in which monomer gasses are pyrolyzed to produce reactive CF₂ and organosilicon species.

[0016] The invention also provides a method for substantially encapsulating a length of wire in a flexible fluorocarbon-organosilicon copolymer thin film. In the method, the wire length is supported on a wire holder such that surfaces of the wire length are substantially unmasked and portions of the wire length are out of contact with each other. The encapsulation process includes the step of exposing the monomer fluorocarbon and organosilicon gasses to a heat source to pyrolyze the monomer gasses and produce a source of reactive CF₂ and organosilicon species in the vicinity of the wire length, which is, e.g., between about 10 microns and 100 microns in diameter. The wire length is maintained at a temperature substantially lower than that of the heat source to induce deposition and polymerization of the CF₂ and organosilicon species on the wire length.

[0017] In another aspect of the invention, there is provided a method for casting a flexile structure in a desired configuration. This is accomplished by deforming the structure into the desired configuration and exposing the deformed structure to an environment in which monomer gasses of a fluorocarbon and organosilicon are pyrolyzed at high temperatures to form reactive monomeric species. Exposure of the deformed structure to the reactive monomeric species is maintained for a duration sufficient to produce on the deformed structure a fluorocarbon-organosilicon copolymer film having a thickness of more than about 5 microns.

[0018] The invention also provides a length of twisted wire that includes a plurality of entwined wires and a flexible fluorocarbon-organosilicon copolymer thin film encapsulating the entwined wire plurality along at least a portion of the twisted wire length. Also provided by the invention is a length of tubing that includes a thin-walled, flexible polymeric cylinder and flexible fluorocarbon-organosilicon copolymer thin film on an outer surface of the cylinder along at least a portion of the tubing length.

[0019] In another aspect, there is provided by the invention a neural probe. The neural probe includes a substantially cylindrical shaft portion having a diameter less than about 100 microns and a tip portion connected to the shaft portion by a tapered shaft portion. The tip has a diameter less than about 15 microns. A flexible fluorocarbon-organosilicon copolymer film encapsulates the tapered shaft portion and cylindrical shaft portion of the probe.

[0020] The invention additionally provides a substrate having a fluorocarbon-organosilicon copolymer thin film of less than 20 microns in thickness thereon; and further provides a microfabricated electronic circuit including at least one conducting layer having a fluorocarbon-organosilicon copolymer thin film of less than about 20 microns in thickness thereon.

[0021] In exemplary embodiments, the polymer thin film on the substrate or conducting layer has a dangling bond density of less than about 10¹⁸ spins/cm³.

[0022] The invention is also drawn to a fluorocarbon-organosilicon copolymer coating prepared by HFCVD methods where monomeric fluorocarbon and organosilicon gasses are pyrolyzed to form reactive CF₂ and organosilicon species which copolymerize at ambient temperatures.

[0023] The invention is also drawn to an apparatus for carrying out HFCVD of two or more monomeric gasses to form a copolymer film on a structure surface.

[0024] The various methods of forming fluorocarbon-organosilicon copolymer thin films provided by the invention, and the resulting films, address a wide range of thin film applications, including biomedical and microfabrication applications, as well as numerous mechanical configurations in which a thin coating possessing the combined properties of fluorocarbon and organosilicon films is desired. Other features and advantages of the invention will be apparent from the claims, and from the following detailed description.

[0025] FIG. 1 depicts deposition rates of HFCVD films deposited from V₃D₃ and PFOSF as a function of filament temperature (T_f). Data points marked with circles are for films deposited from V₃D₃ and PFOSF. The data point marked with a square represents a film deposited from V₃D₃ alone.

[0026] FIG. 2 depicts TGA analysis of the HFCVD films deposited from V₃D₃ and PFOSF at three different filament temperatures.

[0027] FIG. 3 depicts environmental scanning electron micrographs of HFCVD wire coatings on 50 m diameter platinum wires deposited from V₃D₃ and PFOSF at filament temperatures of (a) 540 C., (b) 440 C., and (c) 370 C.

[0028] FIG. 4 depicts FTIR spectra of (a) copolymer film, (b) silicone film and (c) fluorocarbon film, all deposited by HFCVD under the same conditions. The fluorocarbon precursor is HFPO and the silicone precursor is D₃.

[0029] FIG. 5 depicts the low wavenumber region from an FTIR spectrum of the fluorocarbon-organosilicon copolymer deposited from D₃ and HFPO.

[0030] FIG. 6 depicts FTIR spectrum of the HFCVD film deposited from V₃D₃ and PFOSF at a filament temperature of 370 C.

[0031] FIG. 7 depicts a carbon (Is) high-resolution x-ray photoelectron spectroscopic scan of the HFCVD copolymer film deposited from D₃ and HFPO, showing CF₂ and CH₃ peaks.

[0032] FIG. 8 depicts solid-state ¹⁹F NMR spectrum of the HFCVD copolymer film deposited from D₃ and HFPO. The feature at 72 ppm is a spectrometer artifact.

[0033] FIG. 9 depicts solid-state ¹³C NMR spectra of the HFCVD copolymer film deposited from D₃ and HFPO, obtained with (a) ¹H and (b) ¹⁹F decoupling.

[0034] FIG. 10 depicts solid-state ²⁹Si NMR spectra of the HFCVD copolymer film deposited from D₃ and HFPO, obtained with (a) ¹H and (b) ¹⁹F cross-polarization and decoupling.

[0035] FIG. 11 depicts a solid-state ¹⁹F NMR spectrum of the HFCVD film deposited from V₃D₃ and PFOSF at a filament temperature of 370 C. The feature at 72 ppm is a spectrometer artifact.

[0036] FIG. 12 depicts solid-state ¹³C NMR spectra of the HFCVD film deposited from V₃D₃ and PFOSF at a filament temperature of 370 C. obtained with (a) ¹⁹F decoupling and (b) ¹H decoupling.

[0037] FIG. 13 depicts ¹³C NMR spectra of the HFCVD films deposited from V₃D₃ and PFOSF at filament temperatures of (a) 370 C., (b) 440 C., and (c) 540 C.

[0038] FIG. 14 depicts ²⁹Si NMR spectra of the HFCVD films deposited from V₃D₃ and PFOSF at filament temperatures of (a) 370 C., (b) 440 C., and (c) 540 C.

[0039] FIG. 15 depicts the basic structure of an exemplary neural probe that bears a coating of the present invention.

[0040] FIG. 16 depicts the stud-pull adhesion test used to quantify strength of the adhesion to a surface of a fluorocarbon-organosilicon copolymer film of the present invention.

[0041] FIG. 17 depicts a CVD reactor and a hot filament array used to deposit the copolymer films of the present invention on a surface.

[0042] Definitions

[0043] For convenience, certain terms employed in the specification, examples, and appended claims are collected here.

[0044] The term copolymer as used herein means a polymer of two or more different monomers.

[0045] The term fluorocarbon as used herein means a halocarbon compound in which fluorine replaces some or all hydrogen atoms.

[0046] The term organosilicon as used herein means a compound containing at least one SiC bond.

[0047] The term chemical vapor deposition as used herein means a process which transforms gaseous molecules or radicals into solid material in the form of thin film or powder on the surface of a substrate.

[0048] The term carbene as used herein means a reactive intermediate that has the general formula R₂C:, in which carbon has only a sextet of electrons.

[0049] The abbreviation HFPO as used herein means hexafluoropropylene oxide, an epoxide of the formula CF₃CF(O)CF₂ and presented below.

[0050] The term D units as used herein means a chemical unit of formula OSi(CH₃)₂.

[0051] The term D₃ as used herein means hexamethylcyclotrisiloxane, a cyclic compound of the formula (OSi(CH₃)₂)₃ and presented below.

[0052] The term D₄ as used herein means octamethylcyclotetrasiloxane, a cyclic compound of the formula (OSi(CH₃)₂)₄ and presented below.

[0053] The term V₃D₃ as used herein means 1,3,5-trivinyl-1,3,5-trimethylcyclotrisiloxane, a cyclic compound of the formula (OSi(CH₃)(CHCH₂))₃ and presented below.

[0054] The term PFOSF as used herein means perfluorooctane sulfonyl fluoride.

[0055] The term biopassivation as used herein means the property of a structure surface that renders the structure impervious to its biological environment.

[0056] For purposes of this invention, the chemical elements are identified in accordance with the Periodic Table of the Elements, CAS version, Handbook of Chemistry and Physics, 67th Ed., 1986-87, inside cover.

[0057] Fluorocarbon and Organosilicon Film Structure

[0058] The repeat units in the copolymer film consist of fluorocarbon units, siloxane units, and linkages between them. Spectroscopic data indicates that the fluorocarbon content of the films is almost entirely in the form of CF₂ and that siloxane D units are present in both linear and cyclic form. There are four distinct types of copolymer linkages. The SiCF₂Si linkage can be present between siloxane rings or between rings and linear siloxane groups. The (CH₃)₂Si(CF₂)(O) link is linear, and could act as a junction between linear siloxane segments and fluorocarbon units. (O)₂Si(CF₂)₂ units are branch points, and can be present in siloxane rings or in linear chains. The (O)₃Si(CF₂) unit, which is present in low concentration, is a crosslinking group.

[0059] All of the siloxane rings in the film have some degree of CF₂ substitution, and hence these can also be considered as crosslinking groups and branch points. Since there is no evidence of tertiary carbon, crosslinking and branching occur entirely via these siloxane moieties.

[0060] Chain termination takes place primarily with siloxane rings (SiSi bonding between the repeat unit and the terminating ring). Termination could also occur by means of CF₃CF₂Si or CF₃CF₂CF₂, but the concentration of these linkages is small.

[0061] Notably, and in contrast to films deposited by PECVD, films deposited via hot-filament CVD (HFCVD) have well-defined compositions. For example, PECVD-deposited fluorocarbon films comprise a variety of CF groups (e.g., CF₃, tertiary C, and CF, in addition to CF₂), while HFCVD-deposited fluorocarbon films consist almost entirely of CF₂, along with a small amount of CF₃ moieties. Further, the initiating and terminating groups in HFCVD are well-defined; whereas the precursors in PECVD processes undergo much greater fragmentation (these films have SiF bonds, for instance, that result from total fragmentation of the fluorocarbon precursors). A consequence of the nature of the HFCVD process is that only the most thermally stable groups (e.g., CF₂ and siloxane rings) appear in the film, resulting in more thermally stable films.

[0062] One of the most important specific chemical differences between hot-filament CVD and plasma-enhanced CVD is the occurrence of ion-bombardment and ultraviolet-irradiation in the latter technique. Due to this difference, HFCVD films do not contain defects seen in PECVD films. For example, HFCVD films do not have dangling bonds, which are always produced in PECVD processes. Dangling bonds are unpaired electrons left behind in the film. If such bonds are present, the film will undergo reactions with components of the ambient atmosphere (such as water, for instance, resulting in a large number of hydroxyl groups). Therefore, PECVD films are more susceptible to atmospheric ageing, and degradation of their optical, electrical and chemical properties. Moreover, films produced by HFCVD processes are less dense than those produced by plasma-enhanced CVD processes. Due to the differences between the nucleation and growth mechanisms the two processes, it is possible to make porous films using HFCVD, but not using PECVD. Porosity is an important property for semiconductor applications because it allows further lowering of the dielectric constant of existing low- materials by virtue of the low dielectric constant of air.

[0063] Initiation of Cyclic Vinylmethylsiloxane Polymerization

[0064] The role of an initiator (perfluorooctane sulfonyl fluoride, PFOSF) in the polymerization of 1,3,5-trivinyl-1,3,5-trimethylcyclotrisiloxane (V₃D₃) by hot-filament chemical vapor deposition (HFCVD) has been demonstrated. Use of the initiator allows rapid deposition of films at significantly lower filament temperatures. Polymerization is initiated when radical species produced by the pyrolysis of PFOSF react with V₃D₃. Chain propagation occurs along the vinyl bonds of V₃D₃, resulting in chains with hydrocarbon backbones and siloxane rings as pendant groups. Chains are terminated by fluorocarbon radicals, sulfonyl fluoride radicals or other propagating chains.

[0065] The use of an initiator in HFCVD allows films to be deposited at significantly higher rates and provides greater control over chemical composition and morphology. This was demonstrated by Pryce Lewis et al. for fluorocarbon films deposited from hexafluoropropylene oxide (HFPO) using perfluorooctane sulfonyl fluoride (PFOSF) as an initiator. Pryce Lewis, H. G.; Caulfield, J. A.; Gleason, K. K. Langmuir 2001, 17, 7652. In the mechanism proposed for film growth, the generation of free radicals from the pyrolysis of PFOSF is the initiation step:

[0066] The fluorocarbon radical subsequently combines with the propagating species, difluorocarbene (CF₂), which is generated by the pyrolysis of HFPO. The use of PFOSF resulted in higher deposition rates, more efficient utilization of HFPO, and endcapping by CF₃ groups.

[0067] PFOSF can be used as an initiator in the HFCVD of polymeric films from a cyclic vinylmethylsiloxane, 1,3,5-trivinyl-1,3,5-trimethylcyclotrisiloxane (V₃D₃). As in the case of fluorocarbon films, use of PFOSF allows rapid deposition of films at relatively low filament temperatures. Spectroscopic characterization shows that chain propagation occurs by polymerization across the vinyl bonds of V₃D₃. This HFCVD process thus resembles classical free radical polymerization of vinyl monomers driven by an initiator. Odian, G. Principles of Polymerization, Wiley-Interscience: New York, 1991. The synthetic approach described in this work can be applied to other vinyl monomers. In addition, the combination of PFOSF with V₃D₃ results in a fluorocarbon-organosilicon copolymer with unique chemical properties compared to those produced in past HFCVD work or by conventional synthesis. Murthy, S. K.; Gleason, K. K. Macromolecules 2002, 35, 1967; Doeff, M. M.; Lindner, E. Macromolecules 1989, 22, 2951; Chen, G. J.; Tamborski, C. J. Organomet. Chem. 1985, 293, 313; Owen, M. J. In Block Copolymers Science and Technology; Meier, D. J., Ed.; MMI Press: Midland, 1983; Vol. 3, p 129; and Owen, M. J.; Kobayashi, H. Macromol Symp. 1994, 82, 115.

[0068] Deposition Rate

[0069] The synthesis of organosilicon films from V₃D₃ by HFCVD using a Nichrome filament with no initiator requires filament temperatures greater than 530 C. Under these conditions, the deposition rate is relatively low (around 100 /min), and deteriorates as filament age increases. Introducing PFOSF into the reaction chamber results in much higher film growth rates and allows deposition at lower filament temperatures, as indicated in FIG. 1. Further, there is significantly less change in deposition rate over time during individual experiments.

[0070] Plots such as FIG. 1 have been used in the vapor deposition literature to obtain activation energies by using Arrhenius equations to fit the data. Pryce Lewis, H. G.; Caulfield, J. A.; Gleason, K. K. Langmuir 2001, 17, 7652; Kubono, A.; Okui, N. Prog. Polym. Sci. 1994, 19, 389; and Pierson, H. O. Handbook of Chemical Vapor Deposition, 2nd ed.; Noyes Publications: Norwich, N.Y., 1999. However, such a calculation is not justified in this instance because the deposition rate is not zero order in PFOSF in the range of filament temperatures being considered. Changing the PFOSF/V₃D₃ flow ratio does result in changes in deposition rate, indicating that the deposition rate is dependent on the concentration of PFOSF. Nevertheless, FIG. 1 shows that there are two distinct regimes of film growth. In the region between 350 C. and 420 C., the deposition rate is strongly influenced by filament temperature. Since films from V₃D₃ alone cannot be deposited in this filament temperature range, this suggests that film growth is initiator-limited between 350 C. and 420 C. Above 420 C., the increase in deposition rate is less rapid, and it is postulated that film growth is limited by mass-transfer effects. For fluorocarbon films deposited from HFPO and PFOSF, similar behavior was observed, with the transition point at 460 C. The difference in transition temperatures is most likely due to differences in reaction kinetics.

[0071] No enhancement in deposition rate was observed when similar experiments were performed using hexamethylcyclotrisiloxane (D₃) and PFOSF as precursors. Since the only difference between the two siloxane precursors, D₃ and V₃D₃, is the presence of vinyl groups in the latter, these results indicate that vinyl groups play a critical role in initiation and subsequent film growth.

[0072] Film Structure

[0073] The polymerization of V₃D₃ in this HFCVD process is initiated by reactions between fluorocarbon radicals and vinyl groups in the V₃D₃ molecules. Radical species generated by these reactions can react with other V₃D₃ molecules to propagate chains along vinyl bonds. These chains consist of hydrocarbon backbones with siloxane rings as pendant groups. Cross-linking between chains occurs if more than one vinyl group on any V₃D₃ molecule undergoes initiation and propagation reactions. Chain termination occurs when these propagating chains react with fluorocarbon radicals, sulfonyl fluoride radicals or with other propagating chains. As the filament temperature is increased, vinyl abstraction from the silicon atoms becomes more prevalent, as does breakdown of the siloxane rings to vinylmethylsilanone. As a result, the concentration of siloxane rings decreases and the films consist of polymer chains with siloxane backbones. Furthermore, these siloxane chains have a high degree of crosslinking via T groups.

[0074] Thermal Analysis

[0075] FIG. 2 shows the TGA results for films deposited at 370 C., 440 C., and 540 C. The six-membered cyclic siloxane, hexamethylcyclotrisiloxane, is known to be more thermally stable than linear poly(dimethylsiloxane) (PDMS). M. J. Michalczyk, W. E. Fameth, A. J. Vega Chem. Mater. 5, 1687 (1993). It is also known that cross-linking siloxane rings into network structures improves thermal stability. M. J. Michalczyk, W. E. Fameth, A. J. Vega Chem. Mater. 5, 1687 (1993). In this arrangement, the siloxane rings are the repeat units, and the structure takes advantage of the superior thermal stability of the siloxane rings relative to linear PDMS. The HFCVD film deposited using a filament temperature of 370 C. is similar to this type of architecture since the structure consists of carbon backbone chains with siloxane ring pendant groups. Individual siloxane rings can be connected to more than one carbon chain since more than one vinyl group on a ring can undergo polymerization. The HFCVD film deposited at 540 C., on the other hand, is almost completely devoid of ring structures, and would therefore have lower thermal stability relative to the 370 C. film.

[0076] As expected, the onset of thermal decomposition of the 370 C. film occurs at a higher temperature compared to the 540 C. film (FIG. 2). The film deposited at 440 C. lies in-between, consistent with a mixture of rings and linear units in the film structure.

[0077] The chemical structure of fluorocarbon-organosilicon films synthesized from V₃D₃ and PFOSF by HFCVD is dependent on filament temperature. At low filament temperature, the films are comprised of carbon-backbone polymer chains with siloxane rings as pendant groups, whereas at higher filament temperatures the films consist of linear siloxane chains crosslinked via T groups. The retention of the siloxane ring structure confers greater thermal stability on the low filament temperature films. The high concentration of T groups in the high filament temperature films is manifest in the form of brittleness observed in wire coatings. Overall, the 370 C. film appears to be the best candidate for biomedical applications based on its flexibility and thermal stability.

[0078] Wire Coatings

[0079] FIG. 3 shows micrographs of wire coatings made from V₃D₃ and PFOSF at the same set of filament temperatures. The wires were tied into loops to examine the flexibility of the copolymer coating. The difference in chemical composition manifests itself in the form of brittleness, which increases as filament temperature is increased. The film deposited with a filament temperature of 540 C. cracks extensively when the wire is bent and peels off almost completely. The 440 C. coating is marginally better, and the 370 C. coating shows no apparent cracking. This trend is consistent with the brittleness observed with increasing T group concentration in organosilicon films deposited by plasma CVD by Cech et al. and also with the higher rigidity of ladder-like siloxane polymers (comprised almost entirely of T groups) relative to linear polysiloxanes. V. Cech, P. Horvath, M. Trchova, J. Zemek, J. Matejkova J. Appl. Polym. Sci. 82, 2106 (2001); and T. V. Timofeeva, I. L. Dubchak, V. G. Dashevsky, Y. T. Struchkov Polyhedron 3, 1109 (1984).

[0080] This test demonstrates a qualitative similarity between these coatings and fluorocarbon coatings deposited from hexafluoropropylene oxide by Limb et al. S. J. Limb, K. K. Gleason, D. J. Edell, E. F. Gleason J. Vac. Sci. Technol. A 15, 1814 (1997). Fluorocarbon coatings with a high degree of crosslinking were found to be more brittle than those comprised of mostly linear chains.

[0081] Spectroscopic Results

[0082] The instrumentation and methods for measuring the spectroscopic data discussed below are disclosed under the Exemplification section.

[0083] Fourier Transform Infrared (FTIR) Spectroscopy

[0084] FIG. 4 shows the FTIR spectrum of a copolymer film compared with the spectra of homopolymeric fluorocarbon and silicone films obtained from HFPO and D₃ respectively. Table 1 gives the absorption band assignments from the literature. All of the bands associated with the pure fluorocarbon and the pure silicone film appear in the hybrid film, although slight shifts in position occur in some of the bands. Limb, S. J., Lau, K. K. S., Edell, D. J., Gleason, E. F., Gleason, K. K. Plasmas and Polymers 1999, 4, 21.

TABLE 1
Absorption Band Assignments for FTIR Spectra
	Copolymer	Literature
ASSIGNMENT	cm1	cm1	Reference
CF2 rocking	514	516-520	a, b
CF2 wagging	610	650	c
SiC stretching, CH3 rocking in	808	805	d
SiMe2
SiC stretching, CH3 rocking in	848	845	d
SiMe3
SiC stretching, CH3 rocking in	899	N/A	N/A
Si(Me)2(CF2)
SiOSi asymmetric stretching	1043; 1107	1050	d
CF2 symmetric stretching	1155	1160	c
CF2 asymmetric stretching	1223	1220	c
CH3 symmetric bending in	1265	1260	d
SiMex
CH symmetric stretching in sp3	2913	2900	d
CH3
CH asymmetric stretching in sp3	2967	2960	d
CH3
a. Moynihan, R. E. J. Am. Chem. Soc. 1959, 81, 1045;
b. Liang, C. Y.; Krimm, S. J. Chem. Phys. 1956, 25, 563;
c. d'Agostino, R.; Cramarossa, F.; Fracassi, F.; Illuzzi, F. In Plasma Deposition, Treatment, and Etching of Polymers; d'Agostino, R., Ed.; Academic Press: San Diego, 1990; p 95-162;
d. Rau, C.; Kulisch, W. Thin Solid Films 1994, 249, 28.

[0085] The FTIR bands in all three HFCVD films in FIG. 4 are relatively narrow (FWHM of 60 cm¹ or less), aiding in the resolution of specific chemical environments. For example, the symmetric (1155 cm¹) and asymmetric (1223 cm¹) CF₂ stretches can be clearly resolved in FIG. 4(c). In plasma deposited films, there is typically only one broad band in the 1100-1500 cm¹ region resulting from overlap of several types of CF bonding environments. Limb, S. J.; Lau, K. K. S.; Edell, D. J.; Gleason, E. F.; Gleason, K. K. Plasmas and Polymers 1999, 4, 21. The narrowness of the FTIR bands thus indicates the structural simplicity of the HFCVD copolymer films.

[0086] The asymmetric stretching mode (ASM) of the siloxane (SiOSi) group is also easily resolvable. The region around these bands in the copolymer spectrum is expanded for detail in FIG. 5. The ASM appears as a doublet, as in the case of polydimethylsiloxane chains with three or more siloxane units, or ring structures of more than eight siloxane units. Richards, R. E.; Thompson, H. W. J. Chem. Soc. 1949, 124; and Wright, N.; Hunter, M. J. J. Am. Chem. Soc. 1947, 69, 803. Both peaks of this doublet in the copolymer film (1043 and 1107 cm¹) are shifted towards higher wavenumbers relative to the pure silicone film (1020 and 1068 cm¹). No shift would be expected if the fluorocarbon and organosilicon moieties were simply depositing together as two independent phases. Also, it is known that electronegative substituents on the silicon atom increase the SiO stretching frequency. Lin-Vien, D.; Colthup, N.; Fatteley, W. G.; Grasselli, J. G. The Handbook of Infrared and Raman Characteristic Frequencies of Organic Molecules; Academic Press: San Diego, 1991; p 258. Hence, the shift of the ASM is consistent with copolymerization, where bonds are formed between silicon atoms and CF₂ groups.

[0087] Two other modes (rocking and wagging) of the CF₂ groups appear at 514 and 610 cm¹ in the copolymer spectrum. The band at 610 cm¹ is shifted relative to its position in the pure fluorocarbon spectrum (620 cm¹). This shift towards lower wavenumbers is consistent with the shift of the ASM in the opposite direction, an effect of the redistribution of electron density caused by copolymerization.

[0088] In the pure silicone film, SiC stretching bands appear at 808 and 848 cm¹. The copolymer spectrum contains both of these bands and a third band at 899 cm¹. The SiC stretching mode is dependent on the vibrations of the substituents on the silicon atom. Matsurra, H., Ohno, K., Sato, T., Murata, H. J. Mol. Struct. 1979, 52, 13. Hence it is likely that the band at 899 cm¹ is due to the SiC stretching mode of a siloxane moiety that has both methyl and CF₂ substituents bonded to silicon.

[0089] The bands at 2913 and 2967 cm¹ represent the symmetric and asymmetric stretching modes of the CH bond in sp³ CH₃ respectively. The absence of sp³ CH₂ bands indicates that there is no crosslinking through methylene bridges.

[0090] FIG. 6 shows the FTIR spectrum of the film deposited from V₃D₃ and PFOSF at a filament temperature of 370 C. The asymmetric stretching mode (ASM) of the siloxane (SiOSi) group appears as a doublet with the low wavenumber band more intense than the high wavenumber band. In their investigation of organosilicon films deposited from D₃ by HFCVD, Pryce Lewis et al observed a similar trend in the ASM when the films had a greater proportion of siloxane rings relative to linear chains comprised of dimethylsiloxane groups. Pryce Lewis, H. G.; Casserly, T. B.; Gleason, K. K. J. Electrochem. Soc. 2001, 148(12), F212. The trend in the ASM therefore indicates that the siloxane ring structure of V₃D₃ molecules is substantially preserved.

[0091] Bands associated with vinyl groups appear at 3060, 3020, 1599 and 614 cm¹. The intensity of these bands is small in the FTIR spectrum. In fluorocarbon films deposited by HFCVD, two stretching modes of CF₂ groups are observed at around 1160 cm¹ and 1220 cm¹. d'Agostino, R.; Cramarossa, F.; Fracassi, F.; Illuzzi, F. In Plasma Deposition, Treatment, and Etching ofPolymers; d'Agostino, R., Ed.; Academic Press: New York, 1990, p 95. These peaks appear to be shifted towards lower wavenumbers in the spectra shown in FIG. 6, with the former band being masked by the left-hand peak of the ASM. This shift could be caused by bonding with CH₂ groups. The conversion of vinyl groups and the shift in peak position are both consistent with Reactions 2-4.

[0092] The peak at 1409 cm¹ is in the region of the CH₂ scissor mode, but its intensity and width suggest that it may be comprised of more than one band. This is also the region where the symmetric SO₂ stretching mode in CH₃SO₂F appears. Lin-Vien, D.; Colthup, N.; Fatteley, W. G.; Grasselli, J. G. The Handbook of Infrared and Raman Characteristic Frequencies of Organic Molecules, Academic Press: New York, 1991. It is therefore postulated that the second band in this region may be due to this mode in a related moiety, the CH(Si)SO₂F group.

[0093] X-ray Photoelectron Spectroscopy

[0094] Table 2 summarizes atomic composition data obtained from a survey scan. The Si:O ratio is approximately 1:1.13.

TABLE 2
XPS Survey Scan Data
Binding Energy		Atomic Concentration
eV	ELEMENT	%
101	Si	(2p)	13.55
283	C	(1s)	30.70
531	O	(1s)	15.33
576	Cr	(2p)	0.48
687	F	(1s)	38.42
859	Ni	(2p)	1.53

[0095] The high-resolution Si (2p) scan (not shown) contains a single peak with no apparent shoulders. The line width of this peak is slightly larger than that obtained from a film deposited under the same conditions using D₃ only. Hence, while the Si:O ratio suggests that the silicon atoms in the copolymer film are almost entirely in the 2 oxidation state, the line width of the Si (2p) peak indicates the possibility of a small concentration of different oxidation states.

[0096] A C 1s high-resolution scan (FIG. 7) indicates the presence of only two types of carbon moieties, CF₂ and CH₃. The respective assignments at 290.0 eV and 282.8 eV were made using data obtained from a pure fluorocarbon and a pure silicone film. The assumption that most of carbon present is either in the form of CF₂ or CH₃ will greatly simplify the process of making peak assignments in the NMR spectra.

[0097] The XPS survey scan also detected small amounts of nickel and chromium in the film (>1.5 atomic %). Since the same pyrolytic deposition could not be performed using a tantalum filament of equivalent diameter, this observation suggests that nichrome plays a catalytic role in the process.

[0098] Solid-State Nuclear Magnetic Resonance Spectroscopy

[0099] The ¹⁹F NMR spectrum of the copolymer film is shown in FIG. 8, with spinning side bands labeled by asterisks. The remaining seven peaks represent resolved isotropic chemical shifts for fluorine. Chemical shift assignments are listed in Table 3.

TABLE 3
Chemical shift assignments for the 19F NMR spectrum
	Chemical Shift
	ppm	STRUCTURE	% Area	Reference
	83.6	CF3*CF2	1.65	f, g, h, i, j, k, l
	104.5	CF2*O	2.97	m
	123.4	CF2CF2*CF2	70.30	f, g, h, i, j, k, l
	128.0	CF3CF2*CF2	0.08	f, g, h, i, j, k, l
	131.1	CF2CF2*Si	6.27	e
	135.3	CF3CF2*Si	1.10	e
	144.4	SiCF2*Si	17.63	e
	e. Sharp, K. G.; Li, S., Johannesen, R. B. Inorg. Chem. 1976, 15, 2295;
	f. Emsley, J. W., Phillips, L. Prog. NMR Spectrosc. 1971, 7, 1;
	g. Dec, S. F., Wind, R. A., Maciel, G. E. Macromolecules 1987, 20, 2754;
	h. English, A. D.' Garza, O. T. Macromolecules 1979, 12, 351;
	i. Harris, R. K., Jackson, P. Chem. Rev. 1991, 91, 1427;
	j. Kitoh, H., Muroyama, M., Sasaki, M., Iwasawa, M. Jpn. J. Appl. Phys. 1996, 35 Pt. 1, No. 2B, 1464;
	k. Tonelli, C., Tortelli, V. J. Fluorine Chem. 1994, 67, 125;
	l. Tortelli, V.; Tonelli, C.; Corvaja, C. J. Fluorine Chem. 1993, 60, 165;
	m. Banks, R. E., Fluorocarbons and their Derivatives, 2nd ed.; MacDonald Technical and Scientific: London, 1970; p. 237.

[0100] ¹⁹F NMR spectra of homopolymeric fluorocarbon films deposited by the same technique show three peaks: CF₂CF₂*CF₂ at 123 ppm, CF₃CF₂*CF₂ at 128 ppm, and CF₃CF₂ around 84 ppm. Limb, S. J.; Lau, K. K. S.; Edell, D. J.; Gleason, E. F.; Gleason, K. K. Plasmas and Polymers 1999, 4, 21. All three of these peaks are present in FIG. 8.

[0101] The assignments for the peaks at 131.1, 135.3 and 144.4 ppm are based on chemical shifts reported for various SiCF₂ environments in perfluoro(alkylsilanes) by Sharp et al. Sharp, K. G.; Li, S.; Johannesen, R. B. Inorg. Chem. 1976, 15, 2295. It is postulated that these peaks correspond to CF₂CF₂*Si, CF₃CF₂Si, and SiCF₂*Si respectively. The side bands that appear at 46 and 243 ppm are associated with the SiCF₂*Si peak, indicating a broad chemical shift tensor and a lack of mobility of the fluorine atoms in this environment. The ¹⁹F spectrum also indicates the presence of a small number of CF₂O linkages (104.5 ppm). These could form as a result of copolymerization of CF₂ units and linear siloxane chains.

[0102] The presence of SiCF₃ linkages was ruled out on the basis of ¹⁹F and ¹⁹Si NMR performed on a model compound CF₃Si(CH₃)₃. The observed ¹⁹F and ²⁹Si shifts for this compound were 27.8 ppm and 36.2 ppm respectively.

[0103] FIG. 9 shows the ¹³C NMR spectra obtained with ¹H and ¹⁹F decoupling. Chemical shift assignments for these spectra are summarized in Table 4. Assignments for peaks (i)-(iii) are taken from the literature. Ovenall, D. W., Chang, J. J. J. Magn. Reson. 1977, 25, 361; Kaplan, S., Dilks, A. J. Appl. Polym. Sci.: Appl. Polym. Symp. 1984, 38, 105; Mallouk, T., Hawkins, B. L., Conrad, M. P., Zilm, K., Maciel, G. E., Bartlett, N. Phil Trans. R. Soc. Lond. A 1985, 314, 179; Schwerk, U., Engelke, F., Kleber, R., Michel, D. Thin Solid Films 1993, 230, 102; and Hagaman, E. W., Murray, D. K., Cul, G. D. D. Energy Fuels 1998, 12, 399.

TABLE 4
Chemical shift assignments for the 13C NMR spectrum
	Chemical Shift
Peak	ppm	STRUCTURE	% Area
(i)	0	CH3	62.0
(ii)	112	CF2	29.4
(iii)	119	CF3	1.1
(iv)	131	SiCF2Si	7.5

[0104] In these spectra, the CH₃ and CF₂ peaks are the most intense; hence the NMR analysis of the bulk film is in qualitative agreement with the surface analysis by C (1s) high-resolution XPS (FIG. 7). As expected, the CH₃ peak is narrowest in the proton-decoupled spectrum, while the CF₂ and CF₃ peaks are narrowest in the fluorine-decoupled spectrum. There is a small amount of CF₃, evidenced by the presence of a shoulder on the peak at 118.6 ppm.

[0105] Given the appreciable content of SiCF₂*Si in the ¹⁹F spectrum, it seems likely that this moiety would also appear in the ¹³C spectra. The peak at 131 ppm narrows considerably under fluorine decoupling and is therefore postulated to represent the SiCF₂Si moiety. This hypothesis was tested by performing the following calculation.

[0106] In the ¹⁹F spectrum, the contribution of fluorine atoms in SiCF₂Si (peak area/2) was divided by the sum of contributions from all of the fluorine atoms (sum of all CF₂ peak areas)/2CF₃ peak area/3. From the ¹³C spectrum, the peak area of SiCF₂Si was divided by the total area occupied by fluorocarbon groups peaks (ii) through (iv). The resulting values are in agreement (within 10%), supporting the respective assignments in the ¹⁹F and ¹³C spectra. These assignments are further substantiated by the ¹⁹F and ¹³C NMR data reported for a related molecule (FMe₂SiCF₂SiMe₂F) by Fritz and Bauer. Fritz, G., Bauer, H. Angew. Chem. Int. Ed. Engl. 1983, 22, 730. The identification of the SiCF₂Si linkage shows conclusively that the film is indeed a copolymer.

[0107] ²⁹Si NMR spectra obtained with ¹H and ¹⁹F cross-polarization and dipolar decoupling (CP/DD) are shown in FIG. 10, with peak assignments listed in Table 5.

TABLE 5
Chemical shift assignments for the 29Si NMR spectrum
	Chemical Shift
	ppm	STRUCTURE
	0	(CH3)2Si(O)(CF2)
	6.4	o-R3
	15.5	(O)2Si*(CH3)2
	92.0	(O)2Si*(CF2)2
	112.0	(O)3Si(CF2)

[0108] While the CP/DD method increases sensitivity, the peak areas do not yield quantitative concentrations. This is in contrast to the ¹⁹F and ¹³C NMR spectra, which were obtained by direct polarization. The limited amount of film available precluded the use of direct polarization for ²⁹Si NMR.

[0109] The narrowing effect of ¹H decoupling is greatest for the peaks at 0, 6.4 and 15.5 ppm, indicating that these silicon environments are in the vicinity of hydrogen. The most intense of these peaks (15.5 ppm) is assigned to the D unit (O)₂Si*(CH₃)₂) assuming a small shift relative to its 19 ppm position in spectra of films deposited from pure D₃. This downfield shift is attributed to the effect of electronegative CF₂ groups bonded to neighboring siloxane groups, and is consistent with the shifts observed in the FTIR spectrum of the copolymer FIG. 4(a). Assuming a similar downfield shift, the peak at 6.4 ppm is assigned to the o-R₃ environment in the copolymer film.

[0110] The o-R₃ represents a ring structure of three siloxane units that is bound to the film structure by SiSi bonds. The presence of these groups is attributed to a reaction pathway involving abstraction of one or more methyl groups in D₃ with retention of the ring structure. The absence of peaks at 9 and 19 ppm suggests that all of the siloxane ring structures have some degree of fluorocarbon substitution.

[0111] The peak at 0 ppm is assigned to linear siloxane units with two methyl groups and one CF₂ unit bonded to each silicon atom. The proposed bonding to CF₂ is consistent with the 0 ppm peak being the most prominent of the three peaks in this portion of the ¹⁹F cross-polarized and decoupled spectrum FIG. 10 (b). Also, since the CF₂ group is less electronegative than oxygen, this moiety must lie between the M group (Me₃Si*O, typically observed at 6 ppm) and the D group (15.5 ppm). Marsmann, H. In NMR: Oxygen-17 and Silicon-29; Diehl, P., Fluck, E., Kosfeld, R., Eds.; Springer-Verlag: New York, 1981; p 65. The combination of one CF₂ group and one oxygen atom would, however, cause the silicon atom to appear as Si2 in the XPS. The FTIR band at 899 cm¹ is probably due to the SiC stretching mode in this moiety.

[0112] The peak at 92.0 ppm is most enhanced by ¹⁹F cross polarization and decoupling, indicating CF₂ and silicon in close proximity. This peak is assigned to the (O)₂Si*(CF₂)₂ moiety, since the large number of fluorine atoms would cause such an enhancement. The assignment is supported by the reported position of the (SiO)₄Si* (commonly known as Q) moiety in the literature (105 to 110 ppm). Marsmann, H. In NMR: Oxygen-17 and Silicon-29; Diehl, P., Fluck, E., Kosfeld, R., Eds.; Springer-Verlag: New York, 1981; p 65. Replacing two of the oxygen atoms with less electronegative CF₂ groups would cause a downfield shift. The peak at 112.0 ppm is believed to be due to the (O)₃Si*(CF₂) moiety, which bears a closer resemblance to the Q group. The peak is sharper in the ⁹F cross-polarized spectrum, indicating that it must be proximate to a fluorocarbon group. The oxidation state of silicon in (O)₃Si*(CF₂) is 3, and the intensity of the peak indicates that only a very small amount is present. This is probably why it is not easily resolvable in the Si(2p) high-resolution scan.

[0113] FIG. 11 shows the ¹⁹F NMR spectrum of a film deposited from V₃D₃ and PFOSF at a filament temperature of 370 C. Chemical shift assignments are given in Table 6. The peaks in this spectrum can be divided into three groups. The peaks between 140 and 100 ppm are due to fluorine atoms in CF₂ groups. The peaks between 100 and 50 ppm are due to fluorine atoms in CF₃ groups. The single peak at 55.6 ppm is due to fluorine atoms in SO₂F groups.

TABLE 6
Chemical Shift Assignments for the 19F Spectrum.
	Chemical		Area
Peak	Shift (ppm)	Structure	(arbitrary units)	Ref
(i)	55.6	CH(Si) SO2F*	25.86	17
(ii)	66.3	CF3*CH2	19.50	18
(iii)	82.1	CF3*CF2CF2	100.00	19, 20
(iv)	86.3	CF3*CF2CH2	21.63	18
(v)	112.0	CF3CF2*CH2	13.55	18
(vi)	115.5	CH2CF2*CF2	39.88	21
(vii)	123.5	CF2CF2*CF2	52.84	20
(viii)	127.0	CF3CF2*CF2	76.66	20
(17) Hollitzer, E.; Sartori, P. J. Fluor. Chem. 1987, 35, 329.
(18) Tanuma, T.; Irisawa, J. J. Fluor. Chem. 1999, 99, 157.
(19) Katoh, E.; Sugimoto, H.; Kita, Y.; Ando, I. J. Mol. Struct. 1995, 355, 21.
(20) Harris, R. K.; Jackson, P. Chem. Rev. 1991, 91, 1427.
(21) Itoh, T.; Maeda, K.; Shibata, H.; Tasaka, S.; Hashimoto, M. J. Phys. Soc. Jpn. 1998, 67, 23.

[0114] The pyrolysis of PFOSF results in the scission of the CS bond, producing perfluorooctane radicals and sulfonyl fluoride radicals, as shown in Equation 1. The presence of CH₂CF₂*CF₂ (115.5 ppm) in the ¹⁹F NMR spectrum suggests that the fluorocarbon radicals formed in this pyrolysis reaction react with the vinyl groups of V₃D₃, as indicated in Equation 2. This reaction pathway offers an explanation as to why PFOSF acts an initiator on V₃D₃ but not on D₃.

[0115] The greater width of the 115.5 ppm peak relative to the two other CF₂* peaks is attributed to the location of a second peak, the CF₃CF₂*CH₂ group, at 112.0 ppm. Tanuma, T.; Irisawa, J. J. Fluor. Chem. 1999, 99, 157. The accompanying CF₃*CF₂CH₂ shift is observed at 86.3 ppm. The validity of these assignments was verified using the integrated peak areas listed in Table 6. For internal consistency, the contribution of fluorine atoms to peak iv (peak area/3) was compared with the contribution to peak v (peak area/2). An additional calculation was performed to check the consistency of peaks associated with CF₃ groups directly bonded to CF₂ groups. The fluorine contribution to peaks iii and iv (sum of peak areas/3) was compared to the contribution to peaks v and viii (sum of peak areas/2). In both calculations the values under comparison were in agreement to within 10%, supporting the respective assignments.

[0116] The appearance of the CF₃CF₂CH₂ group and the CF₃CH₂ group suggest that some of the perfluorooctane radicals generated by the pyrolysis of PFOSF are capable of further breakdown as shown in Equation 3. These reactions could proceed by separation of CF₂ units from the perfluorooctane chains in the form of difluorocarbene. Alternatively, the CF₂ units could leave the chains in pairs, as tetrafluoroethylene. The radicals generated in these reactions could then react with V₃D₃ molecules by pathways analogous to Equation 2. $\begin{array}{cc}{{\mathrm{CF}}_3\left({\mathrm{CF}}_2\right)}_7^{*}->\begin{array}{c}{{\mathrm{CF}}_3\left({\mathrm{CF}}_2\right)}_n^{*}\\ {\mathrm{CF}}_3^{*}\end{array}\mathrm{where}n<7& \left(3\right)\end{array}$

[0117] The chemical shift of fluorine atoms in SO₂F groups is between 40 and 70 ppm and depends on the nature of atoms bonded to the sulfur atom. Banks, R. E. Fluorocarbons and their Derivatives, 2nd ed.; MacDonald Technical and Scientific: London, 1970; p 237. For instance, the chemical shift of CF₂SO₂F* is around 45 ppm, and that of CH₂SO₂F* is approximately 53 ppm. Hollitzer, E.; Sartori, P. J. Fluor. Chem. 1987, 35, 329. The peak at 55.6 ppm is assigned to a moiety similar to the latter, CH(Si)SO₂F*. Moieties of this type would result from reactions between the free radicals generated per Equation 2 and SO₂F radicals. Since no sulfur-containing groups were observed in fluorocarbon films deposited from HFPO and PFOSF, the presence of SO₂F groups in these films suggests that the CS bond is stronger when the substituents on the carbon atom are not electronegative. Pryce Lewis, H. G.; Caulfield, J. A.; Gleason, K. K. Langmuir 2001, 17, 7652.

[0118] FIG. 12 shows the ¹³C NMR of the same film obtained with¹H and ¹⁹F decoupling. Chemical shift assignments for these spectra are given in Table 7.

TABLE 7
Chemical Shift Assignments for the 13C NMR Spectra
	Chemical		Area
	Shift (ppm)	Structure	(arbitrary units)	Ref
	2 to 0	CH3	281.30	23
	12-41	CH2 and CH(Si)	150.64	24
	51.1	CH(Si)SO2F	12.23	17
	109	CF2	100.00	25
	117	CF3	47.88	25
	135	Vinyl group	88.38
	(17) Hollitzer, E.; Sartori, P. J. Fluor. Chem. 1987, 35, 329.
	(23) Taylor, R. B.; Parbhoo, B.; Fillmore, D. M. In The Analytical Chemistry of Silicones; Smith, A. L., Ed.; Wiley-Interscience: New York, 1991, p 347.
	(24) Pretsch, E.; Bhlmann, P.; Affolter, C. Structure Determination of Organic Compounds, 3rd ed.; Springer-Verlag: New York, 2000.
	(25) Lau, K. K. S.; Gleason, K. K. J. Electrochem. Soc. 1999, 146, 2652.

[0119] In the absence of Equation 3, all of the perfluorooctane radicals produced by Equation 1 would contain 7 CF₂ groups for every CF₃ group. The ¹³C NMR spectra indicate that the ratio of CF₂ groups to CF₃ groups is much smaller (approximately 2:1), providing support for further breakdown of these chains as given by Equation 3. The CF₂/CF₃ ratio calculated from the ¹³C spectra is in quantitative agreement with that calculated from the ¹⁹F spectrum. The latter ratio is given by (sum of all CF₂* peak areas/2)/(sum of all CF₃* peak areas/3). This calculation indicates that the ¹³C spectra are consistent with the ¹⁹F spectrum.

[0120] The broad peak between 12 and 41 ppm observed in the ¹H-decoupled ¹³C spectrum is absent in the ¹⁹F-decoupled spectrum, consistent with a hydrocarbon moiety with no fluorine atoms bonded to carbon. This peak lies in the region associated with CH₂ groups (5-45 ppm) as well as CH groups (25-60 ppm). Pretsch, E.; Bhlmann, P.; Affolter, C. Structure Determination of Organic Compounds, 3rd ed.; Springer-Verlag: New York, 2000. The presence of these groups suggests that the free radical species produced by the reaction between fluorocarbon radicals and V₃D₃ (Reaction 2) can react further with V₃D₃ molecules in a chain propagation step, as indicated in Equation 4. Here, I represents any initiator fragment produced per Equation 3.

[0121] The chemical shifts of CH₂ groups and CH groups can vary significantly with position on a carbon backbone. In p-pentane, for instance, the chemical shifts of the first CH₂ group (CH₃CH₂CH₂CH₂CH₃) and the second CH₂ group (CH₃CH₂CH₂CH₂CH₃) are 22.8 ppm and 34.8 ppm respectively. Pretsch, E.; Bhlmann, P.; Affolter, C. Structure Determination of Organic Compounds, 3rd ed.; Springer-Verlag: New York, 2000. The width of the 12-41 ppm peak is thus consistent with carbon-backbone polymer chains of varying lengths.

[0122] The peak at 51.1 ppm is assigned to the CH(Si)SO₂F moiety based on the reported shift for {umlaut over (C)}H₂SO₂F (47.95 ppm by Hollitzer and Sartori). Hollitzer, E.; Sartori, P. J. Fluor. Chem. 1987, 35, 329. The presence of this peak in the ¹³C NMR spectra is further evidence of reactions between the propagating radicals (produced per Equations 3 and 4) and O₂F radicals. These reactions would act as termination steps. Termination reactions could also occur by reactions between any fluorocarbon radicals and the propagating chains, or reactions between two propagating chains. The termination step is illustrated in Equation 5.

[0123] FIG. 13 shows the ¹³C NMR spectra of the V₃D₃ films produced at three different filament temperatures. Chemical shift assignments for these spectra are given in Table 7. In our prior investigation of the chemical structure of films deposited at a filament temperature of 370 C.,⁹ the peak between 12 and 41 ppm was shown to be evidence of carbon-backbone chains formed by polymerization across the vinyl bonds of V₃D₃ (Equation 4). Here, I represents a fluorocarbon initiator fragment produced by the thermal decomposition of PFOSF. S. K. Murthy, B. D. Olsen, K. K. Gleason Langmuir 18, 6424 (2002).

[0124] This peak decreases in intensity as the filament temperature is increased. The same trend is followed by the peak at 135 ppm, which corresponds to unreacted vinyl groups. If the vinyl groups in V₃D₃ were simply undergoing polymerization reactions per Equation 4, the decrease in intensity of the 135 ppm peak should be accompanied by an increase in the 12-41 ppm peak. Since this is not the case, the ¹³C NMR spectra indicate the possibility of vinyl group abstraction at higher filament temperatures.

[0125] FIG. 14 shows ²⁹Si NMR spectra of the same set of films, with peak assignments listed in Table 8.

TABLE 8
Chemical Shift Assignments for the 29Si NMR Spectra.
	Peak	Chemical Shift (ppm)	Structure
	i	10.9
	ii	16.4
	iii	21.9
	iv	31.0 to 33.7	(CH3)(O)2Si*-CHCH2
			(linear)
	v	63.7 to 69.2
	vi	108.4 to 114.0

[0126] The most significant effect of increasing filament temperature is the increase in intensity of the peak located between 64 and 69 ppm. This peak is assigned to the (O)₃Si(CH₃) (commonly known as T) group. Pryce Lewis, H. G.; Casserly, T. B.; Gleason, K. K. J. Electrochem. Soc. 2001, 148(12), F212. The formation of this moiety would require the abstraction of vinyl groups from the siloxane groups in V₃D₃, and is therefore consistent with the trend seen in the ¹³C NMR spectra. Abstraction of vinyl groups could proceed with the generation of ethylene, as shown in Equation 5.

[0127] Another requirement for T group formation is the creation of a third SiO bond. For this to occur, the six-membered siloxane rings would either have to open or break down. It is known that scission of the SiO bond in cyclic siloxanes to produce diradicals of the form Si(CH₃)₂(OSiCH₃₂)_nO is unlikely. L. E. Guselnikov, N. S. Nametkin Chem. Rev. 79, 529 (1979); and M. G. Voronkov J. Organomet. Chem. 557, 143 (1998). It is therefore postulated that the first step in T group formation is the breakdown of the six-membered ring to yield a dimer and monomer as illustrated in Equation 6.

[0128] This postulate is made on the basis of generalized thermal decomposition pathways described for peralkylcyclosiloxanes by Voronkov. M. G. Voronkov J. Organomet. Chem. 557, 143 (1998). In the scheme proposed for hexamethylcyclotrisiloxane, the six-membered ring decomposes into a dimer and monomer, and the highly unstable dimer subsequently breaks down into two monomer units. In the case of V₃D₃, such a pathway would yield a total of three vinylmethylsilanone molecules.

[0129] The second step in the formation of T groups would then be reaction of vinylmethylsilanone with a vinyl-abstracted siloxane group, as shown in Equation 7.

[0130] The radical species produced by this reaction could undergo propagation reactions with other dimethylsilanone molecules, or termination reactions with fluorocarbon radicals. The ²⁹Si NMR spectrum of the precursor V₃D₃ contains only one peak at 22 ppm. This peak appears in the spectrum of the film deposited at the lowest filament temperature (FIG. 14a), and is assigned to the vinylmethylsiloxane group in a ring structure of three siloxane units. Also present in FIG. 14a is a peak at 10.9 ppm, which is assigned to the siloxane group in a pendant ring that is directly bonded to a carbon-backbone chain (peak i in Table 8; see reaction 4). Since both of the carbon atoms attached to the silicon atom of interest in this moiety are sp3 hybridized, its chemical shift is close to the 10 ppm shift reported for the dimethylsiloxane groups in hexamethylcyclotrisiloxane. Pryce Lewis, H. G.; Casserly, T. B.; Gleason, K. K. J. Electrochem. Soc. 2001, 148(12), F212. As the filament temperature is increased, these two peaks are replaced by a single peak at 16.4 ppm. This peak is assigned to the linear-siloxane chain version of the (CH₂)CHSi(O)₂(CH₃) group. Similarly, peak iv represents the vinylmethylsiloxane group in a linear chain. T. Zundel, J. M. Yu, L. Lestel, D. Teyssie, S. Boileau Macromol. Symp. 88, 177 (1994). The concentration of vinyl groups is highest in FIG. 14a (as evidenced by the presence of the 22 ppm peak and the intensity of the 33.7 ppm peak), a result that is consistent with the ¹³C NMR data.

[0131] The peaks between 10 and 34 ppm indicate that the siloxane groups in the films are primarily in the form of rings when the filament temperature is low. At higher filament temperatures, these groups are mainly in linear chains. The proposed mechanism for the conversion of six-membered siloxane rings into linear chains is via equation 6 and subsequent reaction of the vinylmethylsilanone molecules to form linear siloxane chains as shown in Equation 8. These chains could also undergo vinyl-abstraction reactions and form cross-links via T groups in pathways analogous to Equations 5 and 7.

[0132] Film Properties

[0133] Biopassivation

[0134] Biopassivating coatings, i.e., coatings that insulate an article and render it impervious to its biological environment, are generating an increased amount of attention as many biomedical and other applications are not optimally addressed by available coatings in the art such as polytetrafluoroethylene, also known as PTFE, (CF₂)_n, and Teflon, for example. Biologically-implantable devices such as neural probes, catheter inserts, implantable tubing, and other such devices, all of which are becoming increasingly complicated in geometry, are preferably encapsulated with a film to render the devices impervious to a biological environment, rather than being housed in a bulky PTFE package structure. Such implantable devices typically require of an encapsulating film not only the desired biological compatibility, but due to complex topology and connections to lead wires and associated circuitry, also inherently require an encapsulating film to be conformal and thin, as well as electrically insulating, tough, and flexible. Such a film should further be a good permeation barrier against the implantation environment. The fluorocarbon-organosilicon copolymer coatings of the present invention show improved biopassivation properties over the organosilicon polymers alone in saline soaking tests. Additionally, the fluorocarbon-organosilicon copolymer coatings have lower dielectric constants and increased hydrophobicity relative to organosilicon coatings alone. All of which favors increased biopassivation.

[0135] Rigidity/Flexibility as a Factor of Crosslinking

[0136] The flexibility of the copolymer coatings of the present invention makes them ideally suited for the many applications listed below. For instance it would not be desirable to have coated wires in biomedical applications that are brittle and flake under strain. In this area, organosilicon coatings have been lacking, but fluorocarbon coatings have performed well. By copolymerizing the organosilicon and fluorocarbon active species, the coatings of the present invention improve upon the flexibility of organosilicon coatings alone.

[0137] Coating rigidity/flexibility is a function of the amount of crosslinking between the polymer chains. HFCVD is advantageous over plasma enhanced chemical vapor deposition (PECVD) in this regard as fewer number of side reactive species capable of forming crosslinking bonds are formed during HFCVD. Further, lower filament temperature results in less crosslinking and therefore less rigidity and brittleness. The present invention, therefore, offers a way of tuning the degree of flexibility according to the application by adjusting the filament temperature.

[0138] Various techniques may be used to quantify the degree of crosslinking in a coating of the present invention. For example, peak area calculations using ²⁹Si NMR data may be used. However, the ²⁹Si NMR spectra must have been acquired without cross-polarization in order for the data to useful for quantification of crosslinking. Nevertheless, even if the spectral data was acquired with cross-polarization, a qualitative assessment of crosslinking can be made by comparing peak areas within a spectrum. For example, if a film has a large number of crosslinking groups, e.g., (O)₃Si(CF₂), relative to other groups, then significant crosslinking can be inferred.

[0139] The flexibility of the coatings of the present invention may be quantified using the technique of nano-indentation. This technique enables the measurement of the modulus and toughness of thin films.

[0140] Adhesion

[0141] A useful film has to have good adherence to the surface upon which it is coated. In this regard organosilicon films have performed well but fluorocarbon films have been lacking. It is therefore expected that a copolymer film between fluorocarbons and organosilicons will improve adherence over fluorocarbon films alone. Indeed, this is what is observed. In adhesion tests using a stud-pull tester to measure adhesion, 2 micron films were deposited on silicon wafers via HFCVD. Copolymer films of two compositions were analyzed: fluorocarbon-rich and organosilicon-rich. The results are presented in Table 9 below.

TABLE 9
Adhesion values for various polymers and copolymers.
	Fluorocarbon-Organosilicon
	Copolymer Film
	Fluorocarbon	Fluorocarbon	Organosilicon	Organosilicon
	Film	Rich	Rich	Film
Adhesion	0.00	0.30	0.74	0.53
( 1000
psi)

[0142] As expected, bonding of the organosilicon film is better than the fluorocarbon film, and the copolymer film shows improved adhesion over the fluorocarbon film. Additionally, the organosilicon-rich copolymer film showed improved adhesion over the organosilicon film. Variation with composition suggests that adhesion can be tuned to a desired level by adjusting composition feed into the HFCVD reactor.

[0143] Supercritical CO₂ Solubility

[0144] Processing used in microelectronics is increasingly designed with environmental impact in mind. As technologies change, new process insertion points occur. The role of copolymers in microelectronics has traditionally been confined to photoresist materials, but is expanding to include low dielectric constant (low-) materials. By merging the role of resist and dielectric materials, the fluorocarbon-organosilicon copolymer films can be used as directly patterned low- dielectric films. Super critical carbon dioxide (SCF CO₂) is a promising development medium for fluorocarbon-organosilicon copolymer resists. Similar to other fluorine-containing materials, the fluorocarbon-organosilicon copolymers are insoluble in aqueous developers. Performance enhancement is possible with SCF CO₂ due to the unique properties of the supercritical phase, including low viscosity, negligible surface tension, high diffusivity relative to the gas phase, and a density similar to that of the liquid phase. The solvating capability of SCF CO₂ towards the fluorocarbon-organosilicon copolymer films can be fine-tuned by temperature and pressure control. We have found SCF CO₂ suitable as a developer for HFCVD fluorocarbon-organosilicon system, as well as for fluorinated resists patterned with small and high aspect ratio features that may otherwise experience pattern collapse due to surface tension from aqueous developers. Combined, HFCVD film formation and dry development present a unique processing combination with impressive environmental and safety advantages over current solvent-based spin-on coating and aqueous development. Solvent -based technologies typically generate large quantities of liquid waste that is hazardous and costly to dispose of. HFCVD techniques generate only gaseous effluent and CVD chemistries can be designed to minimize the toxicity of this effluent. CO₂ is non-toxic, non-flammable, recyclable material that is typically collected from waste-streams of other synthetic processes and is available at a low cost with no waste generation.

[0145] Multilayer Approach

[0146] The advantage of HFCVD deposition of a fluorocarbon and organosilicon to form a fluorocarbon-organosilicon copolymer upon a structure surface is that the fluorocarbon-organosilicon copolymer combines the desirable properties of the fluorocarbon with the desirable properties of the organosilicon. In the case of fluorocarbons, those properties include low dielectric constants, high resistivity, low surface energy, high hydrophobicity, and flexibility. In the case of organosilicons, the desirable properties include superior thermal stability, better adhesion to silicon substrates, smooth films, and they are suitable for implantations. However, both individual coatings also possess undesirable properties. Fluorocarbons have high degrees of roughness and poor adhesion to silicon substrates. Organosilicons have lower resistivity and higher dielectric constants.

[0147] A multilayer approach would not only be able to exploit the advantageous properties of both types of coatings more effectively, but is also particularly well suited to CVD techniques. In a multilayer approach, only one gaseous monomer would initially be fed into the HFCVD chamber depositing a first layer upon a structure surface. In one embodiment a pure organosilicon layer would be deposited upon a surface to take advantage of its superior adhesion properties. Next, the composition of the feed gas would be varied to include a fluorocarbon so that the next layer is a fluorocarbon-organosilicon copolymer. The composition of the feed gas would then be varied again resulting in an outer layer of just the fluorocarbon polymer to take advantage of its high resistivity, low surface energy, and high hydrophobicity. In the multilayer method the hybrid interlayer is for compatibility between the outer organosilicon and fluorocarbon layers. Compositional changes can be made by varying the feed gas and process conditions in real time offering the potential for a wide range of coating properties.

[0148] Exemplary Organosilicon and Halocarbon Monomers

[0149] An organosilicon monomer used in a method of the present invention may be selected from the group of suitable organosilicons. For example, the organosilicon monomer used may be hexamethylcyclotrisiloxane, octamethylcyclotetrasiloxane, 1,3,5-trivinyl-1,3,5-trimethylcyclotrisiloxane, 1,3,5,7-tetravinyl-1,3,5,7-tetramethylcyclotrisiloxane, 3-(N-allylamino)propyltrimethoxysilane, allyldichlorosilane, allyldimethoxysilane, allyldimethylsilane, allyltrichlorosilane, allyltrimethoxysilane, allyltrimethylsilane, bis(dimethylamino)vinylmethylsilane, para-(t-butyldimethylsiloxy)styrene, decamethylcyclopentasiloxane, diethylsilane, dimethylethoxysilane, dimethylsilane, divinyldimethylsilane, divinyltetramethyldisilane, 1,3-divinyltetramethyldisiloxane, ethyltrimethoxysilane, hexamethyldisiloxane, 1,1,3,3,5,5-hexamethyltrisiloxane, hexavinyldisiloxane, methyltriethoxysilane, methyltrimethoxysilane, methylsilane, tetraethoxysilane, tetraethylcyclotetrasiloxane, tetraethylsilane, tetramethoxysilane, 1,1,3,3-tetramethyldisiloxane, tetramethylsilane, tetravinylsilane, trimethylsilane, vinyldimethylsilane, vinylmethylbis(trimethylsiloxy)-silane 3-vinylheptamethyltrisiloxane, vinylmethyldiethoxysilane, vinyloxytrimethylsilane, vinylpentamethyldisiloxane, vinyltetramethyldisiloxane, vinyltrimethoxysilane, or vinyltrimethylsilane.

[0150] A halocarbon monomer used in a method of the present invention may be selected from the group of suitable halocarbons. For example, the halocarbon monomer used may be hexafluoropropylene oxide, tetrafluoroethylene, hexafluorocyclopropane, octafluorocyclobutane, perfluorooctanesulfonyl fluoride, octafluoropropane, trifluoromethane, difluoromethane, difluorodichloromethane, difluorodibromomethane, difluorobromomethane, difluorochloromethane, trifluorochloromethane, tetrafluorocyclopropane, tetrachlorodifluorocyclopropane, trichlorotrifluoroethane, or dichlorotetrafluorocyclopropane.

[0151] Film Applications

[0152] The film properties discussed above and the method of preparing the thin fluorocarbon-organosilicon copolymer films on a structure surface lend themselves to varied array of applications. The unique properties of the fluorocarbon-organosilicon copolymer film and the ambient temperature at which the structure is coated allow for applications ranging from biomedical devices to clothing. Below is a table listing selected applications of the thin copolymer films of the invention.

TABLE 10
Selected applications of the current invention
General Category
Application
Biomedical
Filters/Membranes, DNA Microarrays, BioChips, Functional Membranes,
96-Well Trays, Centrifuges
Optics
Optical Waveguides and Communication, Optical Filters, Optic Fibers
Medical
Medical Blades, Surgical Sutures, Syringes, Fine Wires-Pacemakers,
Neural Probes, Inhalers, Stents, Needles, Filters/membranes, Forceps,
Endoscopic Tools
Kitchenware
Roasters, Quiche Pans, Pressure Pots, Poultry Cookers, Pots, Pizza Pans,
Microwave Browning Trays, Breadmaker Pans, Bakeware, Egg Rings,
Knives, Ladles Ice Trays, Sandwhich Makers, Shot Glasses, Spatulas,
Spoons, Stock Pots, Stovetops, Waffle Irons, Utensils, Beaters
Cutting Edges (Reduced Force)
Razor Blades, Knives, Scissors, Pruners
Microfluid Delivery
Microcontact Printing, Ink-jet Printer Parts
Government Projects
Ferroelectrics, NASA Specifications
Hydrophobic Self Cleaning and Waterproofing Surfaces
Stain-proof Fabrics, Sleeping Bags, Tents, Waterproof Clothing,
Condensers-for drop-wise condensation, Shoes, Hats, Swim Suits,
Eye-glasses, Windows-home, Car Windshield, Plane Windows, Watch
Parts, Display Glass/Plastic, Coatings for Tiles/Metals, Rugs/Carpets
Reduced Fiction/Drag Reduction Applications
Underside of Ships, Waterslides, Skies/Snowboards, Ice-skates/Sleds,
Propellers, Golf Balls, Swimming Caps, Lubrication of Motors, Dental
Floss, Bearing Housings, Bearings, Agitators, Pistons, Saw Blades, Fan
Blades, Hinge Pins, Knuckle Joints, Chutes, Toggle Joints
Non-Stick Surfaces and Containers
Molds/Casts, Low Temp Cookware, High Temp Cookware, Catheters,
Antigraffiti Surfaces, Reactor Coatings, Reactor Windows, Bottles, Drip
Pans, Glue Pans, Ink Pans, Ink Trays, Oil Pans
Corrosion Resistant
Screws, Nails, Bolts, Nuts, Rivets, Clamps, Gears, Gaskets, Dry Vents,
Exhaust Systems, Springs, Water Valves, Wire Cloth, Wire Goods
Anti-fog
Goggles, Mirrors, Windows
Anti-fouling
Heat Exchangers/Air Conditioners/Refrigerators, Coatings on the Inside of
Tubes and Pipes, Seals-Valves, O Rings
Protective Coating
Coating on the Outside of Wires/Fibers/Cables, Sensors, Protective
Coating on Art, Toys, Microelectronics, Particles and Fibers for
Composite/Reinforced Materials, Antistiction/Seals MEMS, X-ray Tubes,
Zippers, Insulators, Lavatory Bowls
Generalized Mechanical Systems
Jet Engine Components, Turbo Pump Components, Chemical Processing
Equipment, Dairy Process Equipment, Marine Components, Power Tool
Components, Photocopier Parts, Printing Equipment Pump Components,
Web Press Parts, Automotive Components

[0153] The invention now being generally described, it will be more readily understood by reference to the following examples, which are included merely for purposes of illustration of certain aspects and embodiments of the present invention, and are not intended to limit the invention.

[0154] General Spectroscopic Methods

[0155] Fourier-transform infrared (FTIR) spectroscopy was performed on the deposited films using a Nicolet Magna 860 spectrometer or a Nicolet nexus 870 spectrometer in transmission mode. The spectra were baseline corrected and normalized to a thickness of approximately 7000 . X-ray photoelectron spectroscopy (XPS) was carried out on a Kratos Axis Ultra spectrometer using a monochlromatized aluminum K- source.

[0156] Solid-state NMR spectroscopy was performed on a homebuilt spectrometer comprising a 6.338 T Oxford superconducting magnet and a 3.2 mm Chemagnetics magic angle sample spinning (MAS) probe. For this analysis, approximately 14 mg of film was scraped off wafers from nine 30-min depositions, and packed into a zirconia rotor of 11 mm³ internal volume. Sample spinning at the magic angle of 54.7 was performed in order to mitigate spectral broadening due to strong homonuclear dipolar and anisotropic chemical shift effects. The sample spinning speeds were 5 kHz, 25 kHz and 10 kHz for ²⁹Si, ¹⁹F and ¹³C respectively.

[0157] ²⁹Si NMR was performed with proton cross-polarization (CP) and proton decoupling to enhance the signal and resolution from the low natural abundance ²⁹Si nuclei. The ¹H-²⁹Si CP time was 5 ms and the 90 pulse width was 1.3 s. ²⁹Si spectra were also obtained with fluorine cross-polarization and fluorine decoupling. The purpose of this was to determine which silicon atoms were in close proximity (<10 ) to fluorine-containing moieties. Contact time experiments indicated that a CP time of 5 ms was sufficient to maximize signal intensity. The 90 pulse width for these measurements was 1.2 s. ²⁹Si chemical shifts were externally referenced to tetramethylsilane.

[0158] ¹⁹F NMR spectra were obtained by direct polarization with a 90 pulse width of 1.2 s. Chemical shifts were externally referenced to trichlorofluoromethane. ¹³C spectra were obtained by direct polarization with proton decoupling as well as direct polarization with fluorine decoupling. The 90 pulse width was 1.8 s for both types of spectra. ¹³C chemical shifts were externally referenced to tetramethylsilane.

[0159] Deposition Methods

[0160] Start Up Procedure

[0161] Prior to each experiment, the interior of the deposition chamber was cleaned thoroughly with paper towels and Scotch Brite soaked in acetone or isopropanol. The filament wire was then strung onto the holder, and the holder was placed inside the reactor and connected to the power supply. The chamber was then evacuated.

[0162] The filament voltage was then raised to 86.5V over a 5 min span. HFPO was then flowed into the chamber at a rate of 30 sccm with the chamber pressure maintained at 1 Torr for 20 min. The chamber was then evacuated, and the filament power was turned down over a 5 min span.

[0163] After turning off the power the filament completely, the chamber was pumped up to atmospheric pressure. The filament holder was removed, and the interior of the chamber was cleaned as described above.

[0164] The substrate and filament holder were then placed on the stage. The filament holder was then connected to the power supply and the chamber was pumped down to vacuum. Filament power was raised to 86.5V over a 5 min span. The valve on the D3 line was opened to the appropriate setting, followed by the valve on the HFPO line. The chamber pressure was then set to 1 Torr.

[0165] Depositing the Copolymer Film

[0166] Depositions were performed in a custom-built vacuum chamber on to silicon wafer substrates. Pressure within the chamber was controlled by a butterfly valve connected to a PI coontroller. Substrates were placed on a stage maintained at a low temperature (155 C.) by the circulation of chilled water through internal coils. Precursor breakdown was achieved by means of a resistively heated nichrome (80% nickel, 20% chromium; Omega Engineering) wire 0.038 cm in diameter. The frame holding the filament wire was equipped with springs to compensate for thermal expansion of the wire upon heating. The distance between the filament wire and the substrate was 1.4 cm. Filament temperature was measured by a 2.2 m infrared pyrometer. The spectral emissivity was estimated to be 0.85 based on direct contact thermocouple experiments.

[0167] Fluorocarbon and D₃ Copolymer

[0168] The flow of fluorocarbon precursor, hexafluoropropylene oxide gas (HFPO), into the chamber was controlled by an MKS Model 1295C Mass Flow Controller (MFC). The silicone precursor, hexamethylcyclotrisiloxane (D₃) was vaporized in a stainless steel vessel that was heated to 905 C. The lines leading from the vessel to the vacuum chamber were maintained at 1305 C. Flow of vapor from the vessel into the chamber was regulated by a needle valve.

[0169] Depositions were performed at a filament temperature of 620 C. and a chamber pressure of 1 Torr. Precursor flow rates were 20 sccm for HFPO and 28 scem for D₃. The duration of these depositions ranged between 10 min and 30 min. The deposition rate, determined by profilometry, was approximately 250 /min.

[0170] PFOSF Initiated V₃D₃ Polymerization

[0171] Film depositions were carried out in a custom-built vacuum chamber described previously. Precursor breakdown was achieved by use of a resistively heated 0.038-cm-diameter Nichrome wire (80% nickel, 20% chromium; Omega Engineering). The filament temperature was measured using a 2.2 m infrared pyrometer with a spectral emissivity of 0.85. V₃D₃ (Gelest) was vaporized in a stainless steel vessel that was heated to 1105 C. and fed to the reactor through a line maintained at 1405 C. PFOSF (Aldrich) was vaporized in a glass container held at 605 C. and fed through a line held at 905 C. The flow of both V₃D₃ and PFOSF into the reactor was regulated by needle valves. Depositions were carried out at a range of filament temperatures between 350 and 540 C. with a chamber pressure of 0.5 Torr. For all depositions, the flow rates of V₃D₃ and PFOSF were 23 sccm and 12 sccm respectively. The stage supporting the substrate was maintained at 252 C. Film thickness was measured by profilometry, using a Tencor P-10 Surface Profiler.

[0172] For thermogravimetric analysis (TGA), films were deposited on silicon wafers at filament temperatures of 370, 440, and 540 C. For chemical characterization by solid-state nuclear magnetic resonance (NMR) spectroscopy and thermal stability studies by thermogravimetric analysis (TGA), longer duration depositions (approximately 60 minutes long) were carried out to prepare 14-16 mg samples for each of the three filament temperatures. Sample preparation for TGA was done by scraping films off wafers and loading into a platinum pan covered with aluminum foil. TGA was performed on a Perkin Elmer TGA 7 analyzer using nitrogen as the purge gas with a flow rate of 20 ml/min. Samples were held at 40 C. for 3 min and then heated to approximately 450 C. at a rate of 10 C./min.

[0173] Films were also deposited on 50-m-diameter platinum wires (A-M Systems). These wires were mounted on an aluminum ring with posts, and the distance between the wires and the reactor stage was 0.5 cm. The distance between the substrate wires and the Nichrome filament was 1.8 cm. The structure of the coatings was observed using a FEI/Philips XL30 environmental scanning microscope (ESEM).

[0174] Shut Down Procedure

[0175] The filament power was turned down rapidly (in less than 10 sec) with the precursors still flowing. The D3 valve was then closed, then the HFPO valve. Chamber was then evacuated to base pressure, and then pumped up to atmospheric pressure.

[0176] Adhesion Testing

[0177] The instrument used is a Sebastian I Adherence Tester made by Quad Group, and the procedure is as follows. The samples being analyzed were typically cut into 2 cm² pieces. 2.7 mm epoxy coated aluminum pull studs (also supplied by Quad Group) were secured onto the test surface by means of clips. The sample was then placed in an oven to cure the epoxy at a temperature of 150 degrees C. for about 1 hour. The sample was then allowed to cool to room temperature. The sample was then mounted onto the adherence tester. The device clamped the stud and pulled it with a measured force until the stud was pulled off the sample surface.

[0178] Incorporation by Reference

[0179] All of the patents and publications cited herein are hereby incorporated by reference.

[0180] Equivalents

[0181] Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. Such equivalents are intended to be encompassed by the following claims.