Literature DB >> 25054235

Azulene methacrylate polymers: synthesis, electronic properties, and solar cell fabrication.

Egle Puodziukynaite1, Hsin-Wei Wang, Jimmy Lawrence, Adam J Wise, Thomas P Russell, Michael D Barnes, Todd Emrick.   

Abstract

We report the synthesis of novel azulene-substituted methacrylate polymers by free radical polymerization, in which the azulene moieties represent hydrophobic dipoles strung pendant to the polymer backbone and impart unique electronic properties to the polymers. Tunable optoelectronic properties were realized by adjusting the azulene density, ranging from homopolymers (having one azulene group per repeat unit) to copolymers in which the azulene density was diluted with other pendant groups. Treating these polymers with organic acids revealed optical and excitonic behavior that depended critically on the azulene density along the polymer chain. Copolymers of azulene with zwitterionic methacrylates proved useful as cathode modification layers in bulk-heterojunction solar cells, where the relative azulene content affected the device metrics and the power conversion efficiency reached 7.9%.

Entities:  

Year:  2014        PMID: 25054235     DOI: 10.1021/ja504670k

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  7 in total

1.  Calculation of conductive polymer-based SO2 and SO3 gas sensor mechanisms by using the DFT method.

Authors:  Hacer Azak; Resul Gorgul; Burak Tekin; Murat Yildiz
Journal:  J Mol Model       Date:  2019-11-28       Impact factor: 1.810

2.  Crystal structure of 1,3-bis-{[4-(acetyl-sulfanyl)phenyl]ethynyl}azulene.

Authors:  Sebastian Förster; Wilhelm Seichter; Edwin Weber
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2015-12-31

3.  Protonation tuning of quantum interference in azulene-type single-molecule junctions.

Authors:  Guogang Yang; Sara Sangtarash; Zitong Liu; Xiaohui Li; Hatef Sadeghi; Zhibing Tan; Ruihao Li; Jueting Zheng; Xiaobiao Dong; Junyang Liu; Yang Yang; Jia Shi; Zongyuan Xiao; Guanxin Zhang; Colin Lambert; Wenjing Hong; Deqing Zhang
Journal:  Chem Sci       Date:  2017-09-07       Impact factor: 9.825

4.  Biazulene diimides: a new building block for organic electronic materials.

Authors:  Hanshen Xin; Congwu Ge; Xiaodi Yang; Honglei Gao; Xiaochun Yang; Xike Gao
Journal:  Chem Sci       Date:  2016-07-19       Impact factor: 9.825

5.  Three-component reaction of azulene, aryl glyoxal and 1,3-dicarbonyl compound for the synthesis of various azulene derivatives.

Authors:  Jing Gong; Anatoly A Peshkov; Jiafeng Yu; Sagadat Amandykova; Aidana Gimnkhan; Jianjun Huang; Stepan Kashtanov; Olga P Pereshivko; Vsevolod A Peshkov
Journal:  RSC Adv       Date:  2020-03-10       Impact factor: 4.036

6.  Azulenesulfonium Salts: Accessible, Stable, and Versatile Reagents for Cross-Coupling.

Authors:  Paul Cowper; Yu Jin; Michael D Turton; Gabriele Kociok-Köhn; Simon E Lewis
Journal:  Angew Chem Int Ed Engl       Date:  2016-01-14       Impact factor: 15.336

7.  Azulene Functionalization by Iron-Mediated Addition to a Cyclohexadiene Scaffold.

Authors:  Petter Dunås; Lloyd C Murfin; Oscar J Nilsson; Nicolas Jame; Simon E Lewis; Nina Kann
Journal:  J Org Chem       Date:  2020-10-21       Impact factor: 4.354

  7 in total

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