Literature DB >> 24865374

Direct arylation as a versatile tool towards thiazolo[5,4-d]thiazole-based semiconducting materials.

Julija Kudrjasova1, Roald Herckens, Huguette Penxten, Peter Adriaensens, Laurence Lutsen, Dirk Vanderzande, Wouter Maes.   

Abstract

A series of thiazolo[5,4-d]thiazole-based small molecule organic optoelectronic materials is synthesized via a straightforward microwave-activated Pd-catalyzed C-H arylation protocol. The procedure allows us to obtain extended 2,5-dithienylthiazolo[5,4-d]thiazole chromophores with tailor-made energy levels and absorption patterns, depending on the introduced (het)aryl moieties and the molecular (a)symmetry, by shortened sequences without organometallic intermediates. The synthesized materials can be applied as either electron donor or electron acceptor light-harvesting materials in molecular bulk heterojunction organic solar cells.

Entities:  

Year:  2014        PMID: 24865374     DOI: 10.1039/c4ob00360h

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  Facile synthesis and biological assays of novel 2,4-disubstituted hydrazinyl-thiazoles analogs.

Authors:  Fateme Ghanbari Pirbasti; Nosrat O Mahmoodi
Journal:  Mol Divers       Date:  2016-01-11       Impact factor: 2.943

  1 in total

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