Literature DB >> 23624944

Study of a bifuran vs. bithiophene unit for the rational design of π-conjugated systems. What have we learned?

Ori Gidron1, Neta Varsano, Linda J W Shimon, Gregory Leitus, Michael Bendikov.   

Abstract

A comparative study of two structural isomers highlights the advantages of bifuran vs. bithiophene units in conjugated systems, such as higher fluorescence, solubility, and increased stability of the oxidized species. Importantly, we have found that the small bifuran unit bestows the advantages found in longer oligofurans, and should be considered in the rational design of π-conjugated systems.

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Year:  2013        PMID: 23624944     DOI: 10.1039/c3cc41795f

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  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

2.  Conducting polyfurans by electropolymerization of oligofurans.

Authors:  Dennis Sheberla; Snehangshu Patra; Yair H Wijsboom; Sagar Sharma; Yana Sheynin; Abd-Elrazek Haj-Yahia; Adva Hayoun Barak; Ori Gidron; Michael Bendikov
Journal:  Chem Sci       Date:  2014-10-17       Impact factor: 9.825

  2 in total

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