US 4,640,749 AGrant
Electrically Conductive Pyrrole Copolymers and Their Preparation
Issue Date:1987-02-03
•19 Claims
Abstract
Highly electrically conductive copolymers of pyrroles and alkynes and/or aromatics, which possess good mechanical properties coupled with a well-balanced spectrum of properties, are prepared by anodic polymerization of the pyrroles and alkynes and/or aromatics in a polar solvent in the presence of a suitable conductive salt.
Metadata
Assignee
- BASF Aktiengesellschaft
Inventors
- Herbert Naarmann
- Gernot Koehler
- Johannes Schlag
Application Information
Application Number:US 7314582
Filing Date:1985-05-07
Priority Date:1982-06-24
Art Unit:112
Classifications
IPC:
C25C 100
Field of Search:
20452652859 R;72258;259392;423
Patent Drawings
This patent does not have any drawings.
Description
In the Examples which follow, and illustrate the invention, parts and percentages are by weight, unless stated otherwise.
EXAMPLE 1
120 ml of acetonitrile, 0.48 g of pyrrole and 0.39 g of tributylammonium m-nitrobenzenesulfonate were initially taken in a glass vessel., two platinum electrodes, each having an area of 14 cm.sup.2 were introduced into the solution at a distance of 4 cm apart, and electrolysis was carried out using a current of 140 amp.sec, while stirring. During electrolysis, a black polypyrrole film was deposited on the anode. 0.5 g of terphenyl was then introduced into the electrolyte, and was polymerized anodically onto the polypyrrole film, under the above conditions. The coated anode was washed with acetonitrile and dried at 60.degree. C., after which the copolymer film formed could be detached from the platinum. The 78 .mu.m thick film had a tensile strength of 51 N/mm.sup.2 and an electrical conductivity of 80 Ohm.sup.-1 cm.sup.-1.
A similar polymer was obtained in a shorter time when the terphenyl was replaced by terphenyl m-nitrobenzenesulfonate, the procedure being otherwise identical.
EXAMPLE 2
Electrolysis was carried out in the apparatus described in Example 1 and under the conditions stated in that Example, except that in this case 0.5 g of pyrrole, 0.2 g of terphenyl and, as the conductive salt, 0.6 g of tributylammonium perchlorate were initially taken, and the monomer mixture was copolymerized. The resulting 58 .mu.m thick film had a tensile strength of 60N/mm.sup.2 and an electrical conductivity of 43 Ohm.sup.-1 cm.sup.-1.
EXAMPLE 3
120 ml of acetonitrile, 0.48 g of pyrrole and, as the conductive salt, 1.4 g of 2-nitrophenol and 1.85 g of tributylamine were initially taken in an electrolysis vessel as described in Example 1, and the mixture was stirred. Electrolysis was carried out using a current of 140 amp.sec, while 0.6 g of acetylene was metered in at the same time. The resulting 60 .mu.m thick copolymer film had a tensile strength of 41N/mm.sup.2 and an electrical conductivity of 21 Ohm.sup.-1 cm.sup.-1.
EXAMPLE 4
120 ml of acetonitrile, 0.48 g of pyrrole, 0.2 g of phenalene, 1.5 g of tributylammonium sulfate, 0.2 g of 1,6-heptadiyne and 0.93 g of tributylamine were stirred in an electrolysis apparatus as described in Example 1, and electrolysis was carried out using a current of 140 amp.sec. The resulting 57 .mu.m thick copolymer film had a tensile strength of 35N/mm.sup.2 and an electrical conductivity of 33 Ohm.sup.-1 cm.sup.-1.
EXAMPLE 5
120 ml of acetonitrile, 0.5 g of tetracene, 0.56 g of N-methylpyrrole and 0.39 g of tributylammonium perchlorate were initially taken, under argon, in an electrolysis apparatus as described in Example 1, and the mixture was stirred. The anode used was a polypyrrole film, and electrolysis was carried out using a current of 80 amp.sec. The resulting 60 .mu.m thick film had a tensile strength of 19N/mm.sup.2 and an electrical conductivity of 16 Ohm.sup.-1 cm.sup.-1.
EXAMPLE 6
120 ml of acetonitrile, 0.61 g of 3,4-dimethylpyrrole and 0.45 g of tributylammonium hexafluorophosphate were initially taken, under argon, in an electrolysis apparatus as described in Example 1, and the mixture was stirred. The anode used was a p-conductive polyacetylene film doped with 10% of PF.sub.6.sup.-, and electrolysis was carried out using a current of 140 amp.sec. The resulting 65 .mu.m thick film had a tensile strength of 20N/mm.sup.2 and an electrical conductivity of 14 Ohm.sup.-1 cm.sup.-1.
EXAMPLE 7
120 ml of acetonitrile, 0.84 ml of water, 0.48 g of pyrrole and 0.8 g of tetramethylammonium tetrafluoroborate were initially taken in an electrolysis apparatus as described in Example 1, and the mixture was stirred. The anode used in this case was a p-conductive polyacetylene film doped with 15% of BF.sub.4.sup.-, and electrolysis was carried out using a current of 100 amp.sec. The resulting 55 .mu.m thick co-polymer film had a tensile strength of 30N/mm.sup.2 and an electrical conductivity of 15 Ohm.sup.-1 cm.sup.-1.
EXAMPLE 8
The procedure was carried out as described in Example 7, except that in this case the anode employed was a p-conductive polyphenylene doped with 23% of AsF.sub.6.sup.-. After the pyrrole had been polymerized onto the polyphenylene, the conductivity of the film was 150 Ohm.sup.-1 cm.sup.-1.
EXAMPLE 9
120 ml of acetonitrile, 0.84 ml of water, 0.48 g of pyrrole, 0.5 g of tetracene, 0.3 g of phenylacetylene and 1.18 g of concentrated sulfuric acid were initially taken in an electrolysis apparatus as described in Example 1, and the mixture was stirred. Electrolysis was carried out using a current of 100 amp.sec. The resulting 20 .mu.m thick film had a tensile strength of 15N/mm.sup.2 and an electrical conductivity of 7 Ohm.sup.-1 cm.sup.-1.
EXAMPLE 10 120 ml of acetonitrile, 0.84 ml of water, 0.48 g of pyrrole, 0.5 g of acenaphthene, 0.5 g of 1,6-heptadiyne and 1.15 g of K(AsF.sub.6) were initially taken in an electrolysis vessel as described in Example 1, and the mixture was stirred. Electrolysis was carried out using a current of 100 amp.sec. The resulting 32 .mu.m thick copolymer film had a tensile strength of 18N/mm.sup.2 and an electrical conductivity of 50 Ohm.sup.-1 cm.sup.-1.
EXAMPLE 11
120 ml of acetonitrile, 0.48 g of pyrrole, 0.5 g of azulene and 0.39 g of tributylammonium m-nitrobenzenesulfonate were initially taken in a glass vessel, two platinum electrodes, each having an area of 14 cm.sup.2, were introduced into the solution at a distance of 4 cm apart, and electrolysis was carried out using a current of 140 amp.sec., while stirring. During electrolysis, a black, smooth film was deposited on the anode. The coated anode was washed with acetonitrile and dried at 60.degree. C. under a pressure of 10 mm Hg for 5 hours, after which the copolymer film formed could be detached from the platinum. The 40 .mu.m thick film had a tensile strength of 15N/mm.sup.2 and an electrical conductivity of 45 Ohm.sup.-1 cm.sup.-1.
A similar polymer was obtained when 0.4 g of potassium naphthalenedisulfonate was used as the conductive salt, the procedure being otherwise identical.
EXAMPLE 12
Electrolysis was carried out in an apparatus as described in Example 11 and under the conditions stated in that Example, except that in this case 0.5 g of pyrrole, 0.8 g of indene and, as the conductive salt, 0.6 g of triethylammonium perchlorate were initially taken and the monomer mixture was copolymerized. The resulting 42 .mu.m thick film had a tensile strength of 40N/mm.sup.2 and an electrical conductivity of 41 Ohm.sup.-1 cm.sup.-1.
EXAMPLE 13
120 ml of acetonitrile, 0.48 g of pyrrole and, as the conductive salt, 1.4 g of trinitrophenol and 1.85 g of tributylamine were initially taken in an electrolysis vessel as described in Example 11, and the mixture was stirred. Electrolysis was carried out using a current of 140 amp.sec. while 0.52 g of indene was metered in at the same time. The resulting 44 .mu.m thick copolymer film had a tensile strength of 39N/mm.sup.2 and an electrical conductivity of 62 Ohm.sup.-1 cm.sup.-1.
EXAMPLE 14
120 ml of acetonitrile, 0.48 g of pyrrole, 0.2 g of indene, 0.3 g of cyclopentadiene, 1.5 g of benzenesulfonic acid and 0.93 g of tributylamine were stirred in an electrolysis apparatus as described in Example 11, and electrolysis was carried out using a current of 140 amp.sec. The resulting 45 .mu.m thick copolymer film had a tensile strength of 40N/mm.sup.2 and an electrical conductivity of 64 Ohm.sup.-1 cm.sup.-1.
EXAMPLE 15
120 ml of acetonitrile, 0.61 g of 3,4-dimethylpyrrole, 0.39 g of indene and 0.45 g of tributylammonium hexafluorophosphate were initially taken in an electrolysis apparatus as described in Example 11, and the mixture was stirred. The anode used was a p-conductive polyacetylene film doped with 10% of PF.sub.6.sup.-, and electrolysis was carried out using a current of 150 amp.sec. The resulting 50 .mu.m thick film had a tensile strength of 35N/mm.sup.2 and an electrical conductivity of 35 Ohm.sup.-1 cm.sup.-1.
EXAMPLE 16
120 ml of acetonitrile, 0.84 ml of water, 0.48 g of pyrrole, 0.8 g of azulene, 0.2 g of indene and 1.0 g of tetramethylammonium tetrafluoroborate were initially taken in an electrolysis apparatus as described in Example 11, and the mixture was stirred. The anode used in this case was a p-conductive polyacetylene film doped with 15% of SO.sub.4.sup.2-, and electrolysis was carried out using a current of 100 amp.sec. The resulting 50 .mu.m thick copolymer film had a tensile strength of 60N/mm.sup.2 and an electrical conductivity of 45 Ohm.sup.-1 cm.sup.-1.
EXAMPLE 17
Electrolysis was carried out as described in Example 16, except that in this case the anode used was a p-conductive polyphenylene doped with 23% of AsF.sub.6.sup.-. After the mixture of pyrrole, azulene and indene had been polymerized onto the polyphenylene, the conductivity of the film was 15 Ohm.sup.-1 cm.sup.-1.
EXAMPLE 18
120 ml of dioxane, 0.84 ml of water, 0.48 g of pyrrole, 0.5 g of indene, 0.3 g of cyclopentadiene and 1.18 g of concentrated sulfuric acid were initially taken in an electrolysis apparatus as described in Example 11, and the mixture was stirred. Electrolysis was carried out using a current of 100 amp.sec. The resulting 30 .mu.m thick film had a tensile strength of 30N/mm.sup.2 and an electrical conductivity of 10 Ohm.sup.-1 cm.sup.-1.
EXAMPLE 19
120 ml of acetonitrile, 0.84 ml of water, 0.48 g of pyrrole, 0.5 g of indene, 0.5 g of azulene and 1.15 g of K(AsF.sub.6) were initially taken in an electrolysis vessel as described in Example 11, and the mixture was stirred. Electrolysis was carried out using a current of 100 amp.sec. The resulting 40 .mu.m thick copolymer film had a tensile strength of 28N/mm.sup.2 and an electrical conductivity of 10 Ohm.sup.-1 cm.sup.-1.
Claims
We claim:
1. An electrically conductive copolymer characterized by a capability for being converted from a p-conductive to an n-conductive system, and wherein said copolymer is obtained by the anodic oxidation of a pyrrole monomer and one or more comonomers selected from the group consisting of an alkyne and an aromatic, with the weight ratio of pyrrole units to comonomer units being in the range of from 20:80 to 90:10.
2. A copolymer as defined in claim 1, wherein the pyrrole units are essentially based on unsubstituted pyrrole.
3. A copolymer as defined in claim 1, which contains acetylene as copolymerized units.
4. A copolymer as defined in claim 1, which contains oligophenylenes or polynuclear fused aromatic ring systems as copolymerized units.
5. A copolymer as claimed in claim 1, which, contains 5-membered non-benzoid aromatic hydrocarbon ring systems as copolymerized units.
6. A copolymer as claimed in claim 1, which contains azulene or indene as copolymerized units.
7. A copolymer as defined in claim 1, wherein the comonomers are randomly distributed.
8. A process for the preparation of an electrically conductive copolymer which comprises: copolymerizing a pyrrole and an alkyne, a pyrrole and an aromatic or a pyrrole, an alkyne and an aromatic by anodic oxidation in a polar solvent and in the presence of a suitable conductive salt.
9. The process of claim 8, wherein the components of the copolymer are polymerized together.
10. The process of claim 8, wherein the components of the copolymer are polymerized in succession to form the copolymer.
11. The process of claim 8, wherein the pyrrole is first polymerized alone and an alkyne is then polymerized onto the resulting polypyrrole film.
12. The process of claim 8, wherein the pyrrole is first polymerized alone and an aromatic is then polymerized onto the resulting polypyrrole film.
13. The process of claim 8, wherein the pyrrole is first polymerized alone and both an alkyne and aromatic are then polymerized onto the resulting polypyrrole film.
14. The process of claim 8, wherein the anode used is an electrically conductive polyalkyne.
15. The process of claim 8, wherein the anode used is an electrically conductive polyaromatic.
16. The process of claim 8, wherein the anode used is a polypyrrole.
17. The process of claim 8, wherein pyrroles are polymerized by anodic oxidation in a polar solvent and in the presence of a suitable conductive salt, and an electrically conductive polyalkyne or an electrically conductive polyaromatic is used as the anode.
18. The process of claim 8, wherein the conductive salt used is an ionic or ionizable compound possessing an anion from the group consisting of BF.sub.4.sup.-, AsF.sub.4.sup.-, AsF.sub.6.sup.-, SbF.sub.6.sup.-, SbCl.sub.6.sup.-, PF.sub.6.sup.-, ClO.sub.4.sup.-, HSO.sub.4.sup.-, CH.sub.3 SO.sub.4.sup.- and SO.sub.4.sup.-2.
19. The process of claim 8, wherein the conductive salt used is a salt of an aromatic possessing acidic groups.