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Journal ArticleDOI

Studies on 3-(2-ethylhexyl)thiophene polymers

TLDR
In this article, the thermal stability of the polymers was improved due to the addition of thiophene rings with (2-ethylhexyl)thiophene, even though the absorption wavelength was red-shifted, there was no characteristic change in photoemission for the latter polymer.
Abstract
The regio-regularity and properties of the poly[3-(2-ethylhexyl)thiophene] were studied, and compared with the poly[3′-(2-ethylhexyl)-2,2′,5′,2′′-terthiophene]. The thermal stability of the polymers was improved due to the addition of thiophene rings with (2-ethylhexyl)thiophene. Due to the additional thiophenes at the 2,5 position of ethylhexylthiophene, even though the absorption wavelength was red-shifted, there is no characteristic change in photoemission for the latter polymer. Addition of thiophene rings to the 3-(2-ethylhexyl)thiophene improves the thermal properties without loosing the 3-(2-ethylhexyl)thiophene characteristics.

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Journal ArticleDOI

Thiophene-Based Trimers and Their Bioapplications: An Overview.

TL;DR: In this paper, a review of the state of the art for terthiophenes and their derivatives is presented, along with an in-depth presentation of their numerous bio-applications.
Journal ArticleDOI

Solution processible statistical poly(3-methoxythiophene)-co-poly(3-hexylthiophene) copolymer

TL;DR: In this paper, the synthesis of a thiophene monomer, 3-methoxythiophene, and its polymerization, poly(3-mETHoxyntiophene)) (PMoT), and statistical copolymerization with 3-hexylthiophene (P3HT), using Grignard Metathesis polymerization in place of more traditional electropolymerisation of alkoxy thiophenes.
Journal ArticleDOI

Synthesis, structures, and density functional theory computational study of thiophene‐containing and fluorodecorated imine‐linked polymers

TL;DR: In this paper, a series of extended-conjugated and thermally stable thiophene-containing imine-linked polymers were synthesized via a Schiff-base condensation reaction between aryl aldehydes and 2,6-diaminopyridine building blocks.
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