2015
DOI: 10.1039/c5py00480b
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Electroactive and bioactive films of random copolymers containing terthiophene, carboxyl and Schiff base functionalities in the main chain

Abstract: A new bis-thienyl type monomer with preformed azomethine linkages (AzbT) was chemically synthesized and, subsequently, electro-copolymerized with 2,2′:5′,2′′-terthiophene (Th 3 ). AzbT:Th 3 mixtures with different molar ratios (i.e. 50:50, 60:40 and 80:20) were considered, the resulting thin films being made of random insoluble copolymers, P(AzbT-co-Th 3 )s. The content of AzbT in P(AzbT-co-Th 3 )s was found to increase with the AzbT:Th 3 molar ratio in the electropolymerization medium. Furthermore, charact… Show more

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Cited by 10 publications
(5 citation statements)
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“…The oligo--caprolactone contains in its structural units electron-withdrawing ester groups, while the chain end shows a reactive hydroxyl function. As it was previously noticed, 69 such structural peculiarities could hinder electrochemical polymerization by a high oxidation potential. The ester group is a well-known moiety for increasing of oxidation potential.…”
Section: Synthesis and Characterization Of Pth-g-pcl Copolymersmentioning
confidence: 72%
“…The oligo--caprolactone contains in its structural units electron-withdrawing ester groups, while the chain end shows a reactive hydroxyl function. As it was previously noticed, 69 such structural peculiarities could hinder electrochemical polymerization by a high oxidation potential. The ester group is a well-known moiety for increasing of oxidation potential.…”
Section: Synthesis and Characterization Of Pth-g-pcl Copolymersmentioning
confidence: 72%
“…Table 3 summarized the atomic percent composition (C 1s, S 2p, Cl 2p, and Fe 2p). The Cl/S ratios obtained correspond to doping level and the number of positive charges per thiophene ring . The Cl/S (0.02, 0.21, 0.27, and 0.32) ratios showed an increasing trend with the increase of doping time, which results in the increase of electrical conductivities (10 −6 , 10 −5 , 10 −4 , and 10 −2 S cm −1 ).…”
Section: Resultsmentioning
confidence: 93%
“…As it can be seen, the optical properties of the PTh backbone, were considerably affected by the presence of caprolactone oligomer side chains. In Figure 3a, a clear, sharp absorption band which is usually find in polythiophenes around 400 nm, attributable to conjugated main chain, 42 is missing and only three small shoulders are distinguishable at 370, 400 and 470 nm (inset). This means that in the investigated acetone solution (dispersion) at least three types of chromophores exist, that most probable could be polythiophene chains with different conjugation chain length.…”
Section: The Optoelectronic and Electrochemical Properties Of Pth-g-(mentioning
confidence: 95%