Literature DB >> 21604707

Four-coordinate organoboron compounds with a π-conjugated chelate ligand for optoelectronic applications.

Ying-Li Rao1, Suning Wang.   

Abstract

Four-coordinate organoboron compounds with a π-conjugated chelate backbone have emerged recently as highly attractive materials for a number of applications including use as emitters and electron-transport materials for organic light-emitting diodes (OLEDs) or organic field transistors, photoresponsive materials, and sensory and imaging materials. Many applications of this class of boron compounds stem from the electronic properties of the π-conjugated chelate backbone. Charge-transfer transitions from an aromatic substituent attached to the boron center of the π-conjugated chelate backbone and steric congestion have also been found to play important roles in the luminescent and photochromic properties of the four-coordinate boron compounds. This article provides an update-to-date account on the application aspects of this important class of compounds in materials science with the emphasis on OLED applications and photochromic switching.
© 2011 American Chemical Society

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Year:  2011        PMID: 21604707     DOI: 10.1021/ic200658v

Source DB:  PubMed          Journal:  Inorg Chem        ISSN: 0020-1669            Impact factor:   5.165


  13 in total

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2.  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

3.  Blue Thermally Activated Delayed Fluorescence from a Biphenyl Difluoroboron β-Diketonate.

Authors:  Margaret L Daly; Christopher A DeRosa; Caroline Kerr; William A Morris; Cassandra L Fraser
Journal:  RSC Adv       Date:  2016-08-30       Impact factor: 3.361

4.  syn-1,2-carboboration of alkynes with borenium cations.

Authors:  Ian A Cade; Michael J Ingleson
Journal:  Chemistry       Date:  2014-08-19       Impact factor: 5.236

5.  A Three-Component Assembly Promoted by Boronic Acids Delivers a Modular Fluorophore Platform (BASHY Dyes).

Authors:  Fábio M F Santos; João N Rosa; Nuno R Candeias; Cátia Parente Carvalho; Ana I Matos; Ana E Ventura; Helena F Florindo; Liana C Silva; Uwe Pischel; Pedro M P Gois
Journal:  Chemistry       Date:  2015-12-22       Impact factor: 5.236

6.  Enhancing electron affinity and tuning band gap in donor-acceptor organic semiconductors by benzothiadiazole directed C-H borylation.

Authors:  D L Crossley; I A Cade; E R Clark; A Escande; M J Humphries; S M King; I Vitorica-Yrezabal; M J Ingleson; M L Turner
Journal:  Chem Sci       Date:  2015-06-12       Impact factor: 9.825

7.  C-H Borylation/Cross-Coupling Forms Twisted Donor-Acceptor Compounds Exhibiting Donor-Dependent Delayed Emission.

Authors:  Daniel L Crossley; Pakapol Kulapichitr; James E Radcliffe; Jay J Dunsford; Inigo Vitorica-Yrezabal; Rachel J Kahan; Adam W Woodward; Michael L Turner; Joseph J W McDouall; Michael J Ingleson
Journal:  Chemistry       Date:  2018-06-25       Impact factor: 5.236

8.  Boron(iii) β-diketonate-based small molecules for functional non-fullerene polymer solar cells and organic resistive memory devices.

Authors:  Panpan Li; Quanbin Liang; Eugene Yau-Hin Hong; Chin-Yiu Chan; Yat-Hin Cheng; Ming-Yi Leung; Mei-Yee Chan; Kam-Hung Low; Hongbin Wu; Vivian Wing-Wah Yam
Journal:  Chem Sci       Date:  2020-10-08       Impact factor: 9.825

9.  Facile Arylation of Four-Coordinate Boron Halides by Borenium Cation Mediated Boro-desilylation and -destannylation.

Authors:  Daniel L Crossley; Jessica Cid; Liam D Curless; Michael L Turner; Michael J Ingleson
Journal:  Organometallics       Date:  2015-12-08       Impact factor: 3.876

Review 10.  Boron: Its Role in Energy-Related Processes and Applications.

Authors:  Zhenguo Huang; Suning Wang; Rian D Dewhurst; Nikolai V Ignat'ev; Maik Finze; Holger Braunschweig
Journal:  Angew Chem Int Ed Engl       Date:  2020-04-06       Impact factor: 15.336

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