2016
DOI: 10.1002/app.43641
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α‐Thiophene end‐capped styrene copolymer containing fullerene pendant moieties: Synthesis, characterization, and gas sensing properties

Abstract: We report the synthesis, characterization, and gas sensing properties of a styrene copolymer bearing α‐thiophene end group and fullerene (C60) pendant moieties P(S‐co‐CMS‐C60). First, the copolymer of styrene (S) and chloromethylstyrene (CMS) monomers was prepared in bulk via a bimolecular nitroxide‐mediated radical polymerization (NMP) technique using benzoyl peroxide (BPO) as the radical initiator and nitroxy‐functional thiophene compound (Thi‐TEMPO) as the co‐radical and this gave α‐thiophene end‐capped cop… Show more

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Cited by 5 publications
(4 citation statements)
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“…Therefore, they have been frequently studied for sensing, especially for fluorescence sensing . For the development of chemiresistors, oligothiophenes with well‐defined structures are preferred as candidates for the sensory materials because they possess at least the following two advantages: 1) high polarizability of sulfur electrons may provide a variety of intra‐ and intermolecular interactions, which are favorable for charge transport; and 2) easy modulation of chemical and physical properties through convenient structural modification . However, oligothiophenes are photochemically and thermally unstable, which adds a limitation to their applications in optical sensing …”
Section: Introductionsupporting
confidence: 56%
“…Therefore, they have been frequently studied for sensing, especially for fluorescence sensing . For the development of chemiresistors, oligothiophenes with well‐defined structures are preferred as candidates for the sensory materials because they possess at least the following two advantages: 1) high polarizability of sulfur electrons may provide a variety of intra‐ and intermolecular interactions, which are favorable for charge transport; and 2) easy modulation of chemical and physical properties through convenient structural modification . However, oligothiophenes are photochemically and thermally unstable, which adds a limitation to their applications in optical sensing …”
Section: Introductionsupporting
confidence: 56%
“…In the literature, many studies are devoted to examining the formation of polymeric materials based on polythiophenes or polythiophene derivatives and fullerenes or fullerene derivatives. [43][44][45][46][139][140][141][142][143][144][145][146][147][148][149][150][151][152] Because the oligo-and polythiophenes possess advantageous electronic properties, these materials show promise for use in applications mainly in organic electronics [45,138,139,147,148] and photoelectronics. [43,44,46,137,[141][142][143][144][145][146][147] In these "double cable" systems, the polythiophene backbone and fullerene pedant moiety independently retain their ground state properties.…”
Section: Polythiophene-based Side-chain C 60 Polymersmentioning
confidence: 99%
“…[163] Despite of intense electrochemical studies of the side-chain fullerene polymers, a little attention was paid to investigation of their conducting properties. Recently, Sennik and co-workers [140] investigated conducting properties of α-thiophene end capped styrene copolymer bearing C 60 side groups. They reported the conductivity of this material depends exponentially on the temperature.…”
Section: Wwwadvancedsciencenewscom © 2020 Wiley-vch Gmbhmentioning
confidence: 99%
“…Extensive studies of stable nitroxide free radicals have established the value of these unique compounds in applications such as spin labels , co‐oxidants , building blocks for magnetic materials , synthesis of paramagnetic biomolecules , and mediators of polymerization . These diverse applications were possible after M.B.…”
Section: Introductionmentioning
confidence: 99%