Synthesis poly thiophene

Linear Polymer with Chiral Units 9.4.2.1 Synthesis of Poly (thiophene) 11724a... 

Thin polymer films have been prepared by surface catalysis in ultrahigh vacuum and electrochemical deposition from solution. These two routes of synthesis result in poly(thiophene), poly(aniline) and poly(3,5-lutidine) films that have similar infrared spectra. These polymer films are highly orientationally ordered the rings are perpendicular to the surface in poly(thiophene) and poly(3,5-lutidine) films, and the phenyl rings are parallel to the surface in poly(aniline). 

In this paper we describe the preparation of thin polymer films by surface catalysis and anodic deposition. The results indicate that both synthesis routes produce orientationally ordered films that have similar infrared spectra. It is also shown that thin ordered films of poly(thiophene) have different electrochemical behavior than the fibrous films that are electrically conducting. 

J. Roncali, Conjugated poly(thiophenes) synthesis, functionalization, and applications, Chem. Rev., 92 711-738, 1992. 

Another approach to CPL is the synthesis of conjugated polymers with intrinsic chiro-optical properties. A variety of polymers with CPPL have been synthesized so far. Most of them are based upon well-known conjugated polymers such as poly(thiophene)s [4,111], polyphenylene vinylene)s [123], poly(thienylene vinylene)s [124], ladder polymers [125], PPPs [126], polyphenylene ethynylene)s, [127] and poly(fluorenes) [128]. All of them have been modified with chiral side-chains, which induce the chiro-optical properties. 

The synthesis of well-defined LCB polymers have progressed considerably beyond the original star polymers prepared by anionic polymerization between 1970 and 1980. Characterization of these new polymers has often been limited to NMR and SEC analysis. The physical properties of these polymers in dilute solution and in the bulk merit attention, especially in the case of completely new architectures such as the dendritic polymers. Many other branched polymers have been prepared, e.g. rigid polymers like nylon [123], polyimide [124] poly(aspartite) [125] and branched poly(thiophene) [126], There seems to be ample room for further development via the use of dendrimers and hyperbran-... 

We have presented evidence to prove the structure of electrochemical ly generally poly(thiophene) from dithiophene both by independent synthesis and spectroscopy. Diodes and photodiodes were fabricated from lightly doped chemically and electrochemically synthesized PT. 

Shi et al. [70] were the first to demonstrate the use of an air and moisture stable ionic liquid, [C4mim][PF,s], for the electrochemical synthesis of poly(thiophene), grown onto a platinum working electrode by potentiodynamic, constant potential or constant current techniques. The use of growth potentials between 1.7 and 1.9 V (vs. Ag/AgCl) reportedly gave smooth, blue-green electroactive films, whereas potentials above 2 V resulted in film destruction by overoxidation. 

The synthesis and characterization of polyacetylene (PA) provided new incentive for understanding 7r-electronic spectra, electron-phonon interactions and electronic correlations[l, 2, 14]. The electrical conductivity of chemically doped PA rivals that of metals. Families in Fig. 2 such as polydiacetylenes (PDAs), poly thiophenes (PTs), cr-conjugated polysilane (PSs) and polyparaphenylene vinylene (PPVs), among... 

Synthesis, functionalization, and uses of conjugated poly(thiophenes) 92CRV711. 

Summaries on the synthesis, properties, and uses of polythiophenes are included in two general reviews on poly thiophenes [259,260]. A synopsis of important aspects of polythiophenes are also included in several reviews on various aspects of conducting polymers [221-226], Cation radicals are the propagating species in both electrochemical and chemical oxidative polymerizations of thiophene and its derivatives. The polymer obtained by this method is linked primarily by a,a-linkages. However, other types of linkages (a,f3 and /3,/3) are present in varying amounts (Fig. 59). Substituted thiophene derivatives can couple in a head-to-tail or head-to-head manner. 

Several mechanisms have been proposed for both electrochemical and chemical oxidative synthesis of poly thiophenes. The proposed mechanisms are similar to those proposed for polypyrrole formation. The first step of the polymerization is the oxidation of the thiophene monomer to a cation radical. The subsequent steps are controversial. There are several possibilities. The cation radical can couple with another cation radical or with a neutral species. Alternatively, the cation radical can deprotonate to form a neutral radical. This radical can then couple with another radical or with a neutral species. Several of these possibilities are discussed below. 

Because poly thiophene itself is prone to overoxidation during polymerization, most practical work has been carried out using alkylated thiophenes, which have higher overoxidation potentials. Synthesis of functionalized thiophenes (such as alkylated monomers) is much easier to achieve than that of its pyrrole counterpart. The decreased activity of the sulfur group compared to that of the -NH group means that the laborious steps involved in protecting the heteroatom during synthesis are not required for thiophene. 

Heterocycle-based electroconductive polymers , Berlin, A., Plastic Eng. (N.Y.) (Electrical and Optical Polymer Systems), 1998, 45, 47 Heterocycle-based electric conductors , Pagani, G. A., Heterocycles, 1994, 37, 2069 Conjugated poly(thiophenes) synthesis, functionalisation and applications , Roncali, J., Chem. Rev., 1992, 92, 711. 

For the electrosynthesis of PEDOT and PPy, water was the preferred electrolyte solvent. Although some reports suggest that under special experimental conditions the aqueous electropolymerization of poly(thiophene) derivatives is possible, all attempts conducted in this study failed, including deposition at low pH values and using bithiophene which exhibits a lower oxidation potential than thiophene as the monomeric species [43, 44], Typically, boron trifluoride diethyl etherate and (fairly) anhydrous acetonitrile were used instead [34]. Although both solvents were successfully used to prepare poly(thiophene) inverse opals via the templated synthesis using poly(styrene) microsphere arrays, they tended to destroy the styrenic DG-structured scaffold [2 ]. 

Roncali, J. [1992], Conjugated poly[thiophenes) Synthesis, functionalization, and appiications, Chem. Rev., 92, pp. 711-738. Gadgii, B., Damlin, R, Aaritaio, T, Kankare, ]., and Kvarnstrdm, C. (2013). Electrosynthesis and characterization of viologen cross linked thiophene copolymer, Electrochim. Acta, 97, pp. 378-385. Nalwa, H. S. (2001). Advanced Functional Molecules and Polymers Electronic and Photonic Properties, 3 (Gordon and Breach Science Publishers, Amsterdam, The Netherlands]. 

J. Roncah, Conjugated Poly(Thiophenes) Synthesis, Functionalization, and Apphcations. Chem. Rev. 1992,92,711-738. 

---