Literature DB >> 14737336

The role of borole in a fully conjugated electron-rich system.

Sanghoon Kim1, Kee-Hyung Song, Sang Ook Kang, Jaejung Ko.   

Abstract

The reaction of the 3,3[prime or minute]-dilithiobithieno complex with TipB(OMe)(2) affords a borole with an extended conjugated electron-rich [small pi]-electron system; the electronic perturbation by the introduction of push-pull substituents is described.

Entities:  

Year:  2003        PMID: 14737336     DOI: 10.1039/b312028g

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


  2 in total

1.  Rational design of organoboron derivatives as chemosensors for fluoride and cyanide anions and charge transport and luminescent materials for organic light-emitting diodes.

Authors:  Ruifa Jin; Shanshan Tang; Dongmei Luo
Journal:  J Mol Model       Date:  2014-03-05       Impact factor: 1.810

2.  Taming the beast: fluoromesityl groups induce a dramatic stability enhancement in boroles.

Authors:  Zuolun Zhang; Robert M Edkins; Martin Haehnel; Marius Wehner; Antonius Eichhorn; Lisa Mailänder; Michael Meier; Johannes Brand; Franziska Brede; Klaus Müller-Buschbaum; Holger Braunschweig; Todd B Marder
Journal:  Chem Sci       Date:  2015-07-13       Impact factor: 9.825

  2 in total

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