Literature DB >> 29214697

Incorporation of 2,6-Connected Azulene Units into the Backbone of Conjugated Polymers: Towards High-Performance Organic Optoelectronic Materials.

Hanshen Xin1, Congwu Ge1, Xuechen Jiao2, Xiaodi Yang3, Kira Rundel2, Christopher R McNeill2, Xike Gao1.   

Abstract

Azulene is a promising candidate for constructing optoelectronic materials. An effective strategy is presented to obtain high-performance conjugated polymers by incorporating 2,6-connected azulene units into the polymeric backbone, and two conjugated copolymers P(TBAzDI-TPD) and P(TBAzDI-TFB) were designed and synthesized based on this strategy. They are the first two examples for 2,6-connected azulene-based conjugated polymers and exhibit unipolar n-type transistor performance with an electron mobility of up to 0.42 cm2  V-1  s-1 , which is among the highest values for n-type polymeric semiconductors in bottom-gate top-contact organic field-effect transistors. Preliminary all-polymer solar cell devices with P(TBAzDI-TPD) as the electron acceptor and PTB7-Th as the electron donor display a power conversion efficiency of 1.82 %.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  all-polymer solar cells; azulenes; conjugation; organic field-effect transistor; polymers

Year:  2017        PMID: 29214697     DOI: 10.1002/anie.201711802

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  5 in total

Review 1.  Development of Heterocycle-Substituted and Fused Azulenes in the Last Decade (2010-2020).

Authors:  Taku Shoji; Tetsuo Okujima; Shunji Ito
Journal:  Int J Mol Sci       Date:  2020-09-25       Impact factor: 5.923

Review 2.  In vitro and in vivo biological activities of azulene derivatives with potential applications in medicine.

Authors:  Paweł Bakun; Beata Czarczynska-Goslinska; Tomasz Goslinski; Sebastian Lijewski
Journal:  Med Chem Res       Date:  2021-01-30       Impact factor: 1.965

3.  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

4.  A Colorimetric Chemosensor Based on a Nozoe Azulene That Detects Fluoride in Aqueous/Alcoholic Media.

Authors:  Lloyd C Murfin; Kirstie Chiang; George T Williams; Catherine L Lyall; A Toby A Jenkins; Jannis Wenk; Tony D James; Simon E Lewis
Journal:  Front Chem       Date:  2020-01-29       Impact factor: 5.221

5.  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

  5 in total

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