Polypyrrole monomer

The Teixidor team further improved upon this chemistry by covalently linking units of 109 to the polypyrrole monomer prior to electropolymerization.139 A [3,3 -Co(C2B<)H11)2] anion was covalently bound to a pyrrole via a spacer through one of its boron atoms by the reaction of the species [3,3 -Co(8-C4H802-l,2-C2B9H10)(r,2 -(C2B9H11)2] with potassium pyrrole, as functionalization through... 

Functionalized conducting monomers can be deposited on electrode surfaces aiming for covalent attachment or entrapment of sensor components. Electrically conductive polymers (qv), eg, polypyrrole, polyaniline [25233-30-17, and polythiophene/23 2JJ-J4-j5y, can be formed at the anode by electrochemical polymerization. For integration of bioselective compounds or redox polymers into conductive polymers, functionalization of conductive polymer films, whether before or after polymerization, is essential. In Figure 7, a schematic representation of an amperomethc biosensor where the enzyme is covalendy bound to a functionalized conductive polymer, eg, P-amino (polypyrrole) or poly[A/-(4-aminophenyl)-2,2 -dithienyl]pyrrole, is shown. Entrapment of ferrocene-modified GOD within polypyrrole is shown in Figure 7. 

Polypyrroles. Highly stable, flexible films of polypyrrole ate obtained by electrolytic oxidation of the appropriate pyrrole monomers (46). The films are not affected by air and can be heated to 250°C with Htde effect. It is beheved that the pyrrole units remain intact and that linking is by the a-carbons. Copolymerization of pyrrole with /V-methy1pyrro1e yields compositions of varying electrical conductivity, depending on the monomer ratio. Conductivities as high as 10 /(n-m) have been reported (47) (see Electrically conductive polymers). 

Significant variations in the properties of polypyrrole [30604-81-0] ate controlled by the electrolyte used in the polymerization. Monoanionic, multianionic, and polyelectrolyte dopants have been studied extensively (61—67). Properties can also be controlled by polymerization of substituted pyrrole monomers, with substitution being at either the 3 position (5) (68—71) or on the nitrogen (6) (72—75). An interesting approach has been to substitute the monomer with a group terminated by an ion, which can then act as the dopant in the oxidized form of the polymer forming a so-called self-doped system such as the one shown in (7) (76—80). 

Figure 13. (a) Substituted polypyrrole, (b) self-doped polypyrrole, (c) heteroaromatic polymer showing the monomer unit, (d) composite polypyrrole-polyelectrolyte, and (e) hybrid material. (Polyaniline macroion photo supplied by Gomez-Romero and M. Lira.)... 

Polypyrrole hybrids [Fig. 13(e)], electrogenerated from solutions containing the monomer and a salt of an inorganic macroion or a polyoxide.90-92... 

The stoichiometry of the redox reactions of conducting polymers (n and m in reactions 1 and 2) is quite variable. Under the most widely used conditions, polypyrroles and polythiophenes can be reversibly oxidized to a level of one hole per ca. 3 monomer units (i.e., a degree of oxidation, n, of ca. 0.3).7 However, this limit is dictated by the stability of the oxidized film under the conditions employed (Section V). With particularly dry and unreactive solvents, degrees of oxidation of 0.5 can be reversibly attained,37 and for poly-(4,4 -dimethoxybithiophene), a value of n = 1 has been reported.38 Although much fewer data are available for n-doping, it appears to involve similar stoichiometries [i.e., m in Eq. (2) is typically ca. 0.3].34,39"41 Polyanilines can in principle be reversibly p-doped to one... 

A number of approaches are available to improve the morphology and homogeneity of electrochemically deposited conducting polymer films. Priming of the electrode surface with a monolayer of adsorbed or covalently bonded monomer leads to more compact deposits of polyaniline,87,88 poly thiophene,80 and polypyrrole.89,90 Electrode rotation has been shown to inhibit the deposition of powdery overlayers during poly(3-methylthiophene) deposition.81... 

In 1979, Diaz et al. produced the first flexible, stable polypyrrole (PPy) film with high conductivity (1(X) Scm ). The substance was polymerized on a Pt-electrode by anodic oxidation in acetonitrile. The then known chemical methods of synthesis " usually produced low conductivity powders from the monomers. By contrast, electropolymerization in organic solvents formed smooth and manageable films of good conductivity. Thus, this technique soon gained general currency, stimulating further electropolymerization experiments with other monomers. In 1982, Tourillon... 

There are large numbers of naturally occurring representatives, especially of pyrrole that include the important polypyrroles (porphyrins and corrins), and the nitropyrrole antibiotics such as pyr-rolomycins and pyrroxamycin. Derivatives of furan have been used as fungicides and A-vinylpyr-rolidone is an important monomer for the production of blood plasma extenders and for cosmetic applications. On account of the similarity in the pathways for the aerobic degradation of monocyclic furan, thiophene, and pyrrole, all of them are considered here. Anaerobic degradation of furans is discussed in Part 2 of this chapter. 

Elemental analysis shows that the polymer generally contains four monomer units per dopant ion [20], and that there is also more hydrogen than would be expected (cf. polypyrrole) [20, 395], although this may vary depending on the starting material [409,410,414], Even in the neutral form, the polymer contains a small quantity of anions (0.5-1%) [19], although Waltman et al. [400] found that the extent to which the counter ion is incorporated into the polymer on polymerisation depends strongly on the nature of the /J-substituent (if present). 

Figure 40 The pyrrole monomer, l-(jV-but-4-yl-pyrrol)-l,2-bis(diphenylphosphinoborane) (62), used for electropolymerization to yield polypyrroles with diphosphine ligands protected from oxidation by borane groups. (Adapted from ref. 86.)...

A typical example of such a polymer is polypyrrole. The exact mechanism by which the electropolymerisation of pyrrole occurs remains a source of controversy however, by assuming 100% growth efficiency, then it can be calculated that 2.25 electrons are removed per monomer unit. Only two electrons are required to polymerise the monomer however, the film is formed in a highly oxidised state, corresponding to one electron per four units, see Figure 2.20. 

Figure 3.76 (a) Plot of the log of the polypyrrole film conductivity polymer potential, , fora 10mV potential difference applied across a 13.9pm-thick film in 0.1 M tetraethylammonium tetrafluoroborate/CH3CN. (b) Plot of polypyrrole conductivity vs. fractional charge per pyrrole monomer subunit (qimm) in 0.1 M tetraethylammonium tetrafluorobnrate/CH3CN From Feldman et at. (1985). Copyright 1985 American Chemical Society. 

This means that for a given polypyrrole chain if a unit cell (chosen as 6 monomer units on the basis of the observed maximum doping level of 2 charges per 6 monomer units) already has a polaron on it and a second charge is injected onto the same chain, it is more favourable to form a second polaron on another vacant unit cell than to force spin pairing to give a bipolaron. If, however, all the other unit cells are already occupied, then a bipolaron will be formed in the unit cell, rather than two polarons. 

Fig. 5.17 Schematic of electropolymerization of CNT-polypyrrole hybrid via (a) ester linkage and (b) noncovalent pyrene linkage of pyrrole monomer with schematic of hybrid and SEM. Scale 200 nm. Reproduced with permission from [222], (2008) Elsevier.

An alternate method to produce templated electrodes is the use of chemical reduction of the monomer in the presence of a track-etched or alumina membrane. Parthasarathy et al. [46] have produced enzyme-loaded nanotubules by a combination of both electrochemical and chemical deposition. Initially, the alumina membrane was sealed at one end with a thick Au film (Figure 1.9a), after which the membrane was placed into a mixture of pyrrole and Et4NBF4. The pyrrole was then electropolymerized to form a small plug of polypyrrole at the closed end of the alumina membrane (Figure 1.9b). Subsequently, the membrane was placed into a... 

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