Literature DB >> 24470351

α-Oligofurans: an emerging class of conjugated oligomers for organic electronics.

Ori Gidron1, Michael Bendikov.   

Abstract

While the field of organic electronics has developed extensively in recent years, it remains limited by number of materials available. Further expansion requires the innovation of new types of π-conjugated backbones, but suitable candidates are discovered only very rarely. The recent introduction of a new class of conjugated materials, long α-oligofurans, was therefore greeted with considerable interest. α-Oligofurans possess many of the properties required to excel in applications as organic electronic materials, can be manufactured from renewable resources, and are expected to be biodegradable. This Minireview provides an account of long oligofurans from the perspectives of their synthesis, molecular properties, chemical reactivity, and use in electronic devices.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  conjugation; fluorescence; heterocycles; oligomerization; organic electronics

Year:  2014        PMID: 24470351     DOI: 10.1002/anie.201308216

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


  9 in total

1.  Effect of donor strength of extended alkyl auxiliary groups on optoelectronic and charge transport properties of novel naphtha[2,1-b:6,5-b']difuran derivatives: simple yet effective strategy.

Authors:  Aijaz Rasool Chaudhry; R Ahmed; Ahmad Irfan; A Shaari; Ahmad Radzi Mat Isa; Shabbir Muhammad; Abdullah G Al-Sehemi
Journal:  J Mol Model       Date:  2015-07-16       Impact factor: 1.810

2.  Solid-State Emission Enhancement via Molecular Engineering of Benzofuran Derivatives.

Authors:  Jérémie Grolleau; Ravil Petrov; Magali Allain; William G Skene; Pierre Frère
Journal:  ACS Omega       Date:  2018-12-27

3.  Four-coordinate triarylborane synthesis via cascade B-Cl/C-B cross-metathesis and C-H bond borylation.

Authors:  Kai Yang; Guan Zhang; Qiuling Song
Journal:  Chem Sci       Date:  2018-08-13       Impact factor: 9.825

4.  Optical Spectra of Oligofurans: A Theoretical Approach to the Transition Energies, Reorganization Energies, and the Vibronic Activity.

Authors:  Karolina Filipowska; Marek T Pawlikowski; Marcin Andrzejak
Journal:  Molecules       Date:  2021-11-26       Impact factor: 4.411

5.  New fused conjugated molecules with fused thiophene and pyran units for organic electronic materials.

Authors:  Daoliang Chen; Danlei Zhu; Gaobo Lin; Mingxu Du; Dandan Shi; Qian Peng; Lang Jiang; Zitong Liu; Guanxin Zhang; Deqing Zhang
Journal:  RSC Adv       Date:  2020-03-26       Impact factor: 4.036

6.  Furan Is Superior to Thiophene: A Furan-Cored AIEgen with Remarkable Chromism and OLED Performance.

Authors:  Zheng Zhao; Han Nie; Congwu Ge; Yuanjing Cai; Yu Xiong; Ji Qi; Wenting Wu; Ryan T K Kwok; Xike Gao; Anjun Qin; Jacky W Y Lam; Ben Zhong Tang
Journal:  Adv Sci (Weinh)       Date:  2017-02-27       Impact factor: 16.806

7.  Fused electron deficient semiconducting polymers for air stable electron transport.

Authors:  Ada Onwubiko; Wan Yue; Cameron Jellett; Mingfei Xiao; Hung-Yang Chen; Mahesh Kumar Ravva; David A Hanifi; Astrid-Caroline Knall; Balaji Purushothaman; Mark Nikolka; Jean-Charles Flores; Alberto Salleo; Jean-Luc Bredas; Henning Sirringhaus; Pascal Hayoz; Iain McCulloch
Journal:  Nat Commun       Date:  2018-01-29       Impact factor: 14.919

8.  Highly Planarized Naphthalene Diimide-Bifuran Copolymers with Unexpected Charge Transport Performance.

Authors:  Rukiya Matsidik; Alessandro Luzio; Özge Askin; Daniele Fazzi; Alessandro Sepe; Ullrich Steiner; Hartmut Komber; Mario Caironi; Michael Sommer
Journal:  Chem Mater       Date:  2017-06-13       Impact factor: 9.811

9.  A macrocyclic oligofuran: synthesis, solid state structure and electronic properties.

Authors:  Sandip V Mulay; Or Dishi; Yuan Fang; Muhammad R Niazi; Linda J W Shimon; Dmitrii F Perepichka; Ori Gidron
Journal:  Chem Sci       Date:  2019-08-19       Impact factor: 9.825

  9 in total

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