Literature DB >> 18729480

Advances in molecular design and synthesis of regioregular polythiophenes.

Itaru Osaka1, Richard D McCullough.   

Abstract

Regioregular poly(3-alkylthiophene)s (rrP3ATs) are an important class of pi-conjugated polymers that can be used in plastic electronic devices such as solar cells and field-effect transistors. rrP3ATs can be ordered in three dimensions: conformational ordering along the backbone, pi-stacking of flat polymer chains, and lamellar stacking between chains. All of these features lead to the excellent electrical properties of these materials. Creative molecular design and advanced synthesis are critical in controlling the properties of the materials as well as their device performance. This Account reports the advances in molecular design of new functional polythiophenes as well as the associated polymerization methods. Many functionalized regioregular polythiophenes have been designed and synthesized and show fascinating properties such as high conductivity, mobility, chemosensitivity, liquid crystallinity, or chirality. The methods for the synthesis of rrP3ATs are also applicable to other functional side chains. Di- and triblock copolymers consisting of rrP3AT and polyacrylate or polystyrene have also been successfully synthesized, which can facilitate the assembly of the polythiophene segments. The synthesis of rrP3ATs has evolved into a simple and economical system in which the synthesis can be carried out quickly at room temperature and is thus suitable for large-scale manufacturing. Intensive study has revealed that the regioregular polymerization of 3-alkylthiophenes proceeds by a chain-growth mechanism and can be made into a living system. This feature enables precise control of the molecular weight and facile end-group functionalization of the polymer chains, leading to tailor-made regioregular polythiophenes for specific applications. In addition, researchers have recently designed and synthesized regiosymmetric polythiophenesthese are regioregular but not coupled in a head-to-tail fashionby various methods. These reports indicate that these regiosymmetric polymers show very high mobilities when used in field-effect transistors due to their highly ordered structure. The remarkable performance of regioregular polythiophenes in recent years has allowed for the rapid development in printable electronics and seems destined to lead to further advances in this field.

Entities:  

Year:  2008        PMID: 18729480     DOI: 10.1021/ar800130s

Source DB:  PubMed          Journal:  Acc Chem Res        ISSN: 0001-4842            Impact factor:   22.384


  29 in total

1.  Design strategies for organic semiconductors beyond the molecular formula.

Authors:  Zachary B Henson; Klaus Müllen; Guillermo C Bazan
Journal:  Nat Chem       Date:  2012-09       Impact factor: 24.427

2.  Polymerization of tellurophene derivatives by microwave-assisted palladium-catalyzed ipso-arylative polymerization.

Authors:  Young S Park; Qin Wu; Chang-Yong Nam; Robert B Grubbs
Journal:  Angew Chem Int Ed Engl       Date:  2014-08-21       Impact factor: 15.336

3.  Photochemistry of furyl- and thienyldiazomethanes: spectroscopic characterization of triplet 3-thienylcarbene.

Authors:  Caroline R Pharr; Laura A Kopff; Brian Bennett; Scott A Reid; Robert J McMahon
Journal:  J Am Chem Soc       Date:  2012-03-30       Impact factor: 15.419

Review 4.  Recent developments in the synthesis of regioregular thiophene-based conjugated polymers for electronic and optoelectronic applications using nickel and palladium-based catalytic systems.

Authors:  Bibi Amna; Humaira Masood Siddiqi; Abbas Hassan; Turan Ozturk
Journal:  RSC Adv       Date:  2020-01-27       Impact factor: 4.036

5.  Fluorescent oligo and poly-thiophenes and their utilization for recording biological events of diverse origin-when organic chemistry meets biology.

Authors:  Andreas Aslund; K Peter R Nilsson; Peter Konradsson
Journal:  J Chem Biol       Date:  2009-08-02

6.  Modular Synthesis of Polymers Containing 2,5-di(thiophenyl)-N-arylpyrrole.

Authors:  Tran N B Truong; Suchol Savagatrup; Intak Jeon; Timothy M Swager
Journal:  J Polym Sci A Polym Chem       Date:  2018-03-22       Impact factor: 2.702

7.  Synthesis and Study the Effect of Donor-Acceptor Substituent on Fluorescence Behavior of Thieno[3, 2-c]pyridine Derivatives.

Authors:  Raghunath B Toche; Sunil N Chavan
Journal:  J Fluoresc       Date:  2013-10-27       Impact factor: 2.217

8.  (E)-3-(2,3,4,5,6-Penta-fluoro-styr-yl)thio-phene.

Authors:  Sébastien Clément; Olivier Coulembier; Franck Meyer; Matthias Zeller; Christophe M L Vande Velde
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-03-24

9.  Polymer semiconductors incorporating head-to-head linked 4-alkoxy-5-(3-alkylthiophen-2-yl)thiazole.

Authors:  Xin Zhou; Peng Chen; Chang Woo Koh; Sheng Chen; Jianwei Yu; Xianhe Zhang; Yumin Tang; Luca Bianchi; Han Guo; Han Young Woo; Xugang Guo
Journal:  RSC Adv       Date:  2018-10-18       Impact factor: 3.361

10.  Functionalized Poly(3-hexylthiophene)s via Lithium-Bromine Exchange.

Authors:  Byungjin Koo; Ellen M Sletten; Timothy M Swager
Journal:  Macromolecules       Date:  2014-12-31       Impact factor: 5.985

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