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Functionalization of spiro[fluorene-9,9′-xanthene] with diketopyrrolopyrrole to generate a promising, three-dimensional non-fullerene acceptor
Materials Chemistry Frontiers ( IF 6.0 ) Pub Date : 2020-09-15 , DOI: 10.1039/d0qm00515k
Amanpreet Kaur Hundal 1, 2, 3, 4, 5 , Salman Ali 5, 6, 7, 8, 9 , Mohammed Jameel 5, 6, 7, 8, 9 , Lathe Jones 1, 2, 3, 4, 5 , Navneet Kaur 10, 11, 12, 13 , Richard A. Evans 14, 15, 16, 17 , Jing-Liang Li 17, 18, 19 , Steven J. Langford 5, 6, 7, 8, 9 , Akhil Gupta 5, 6, 7, 8, 9
Affiliation  

A spiro[fluorene-9,9′-xanthene], often described as a “low-cost spiro,” has been functionalized with terminal diketopyrrolopyrrole units to generate a promising, three-dimensional non-fullerene acceptor. The new acceptor, coded as SFX1, was readily synthesized using the Suzuki cross-coupling reaction and was sufficiently soluble in a variety of commonly used, film-processing solvents such as chlorobenzene and o-dichlorobenzene. SFX1 displayed promising optoelectronic properties and the HOMO/LUMO energy levels complementary to the commercially available and commonly used donor polymers P3HT and PTB7. The joining of two high-potential building blocks – the spiro[fluorene-9,9′-xanthene] and diketopyrrolopyrrole – demonstrates a new strategy where the device performance [D : A 1 : 1.2 = 9.42% (D = PTB7)] validates its use as a potential, three-dimensional non-fullerene acceptor.

中文翻译:

用二酮基吡咯并吡咯官能化螺[芴-9,9'-an吨]以生成有前途的三维非富勒烯受体

螺环[芴-9,9'-x吨](通常被称为“低成本螺环”)已通过末端二酮吡咯并吡咯单元进行功能化,以产生有希望的三维非富勒烯受体。使用Suzuki交叉偶联反应可以轻松合成编码为SFX1的新受体,并且该受体应充分溶于各种常用的膜加工溶剂,例如氯苯和邻二氯苯。SFX1显示出有希望的光电性能和HOMO / LUMO能级与可商购和常用的供体聚合物P3HT和PTB7互补。结合使用两个高潜力的构建基–螺[芴-9,9'-x吨]和二酮基吡咯并吡咯–展示了一种新的策略,可以验证设备的性能[D:A 1:1.2 = 9.42%(D = PTB7)]用作潜在的三维非富勒烯受体。
更新日期:2020-09-20
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