Literature DB >> 26392327

Highly emissive organic solids with remarkably broad color tunability based on N,C-chelate, four-coordinate organoborons.

Aslam C Shaikh1, Dnyanesh S Ranade2, Shridhar Thorat3, Arunava Maity1, Prasad P Kulkarni2, Rajesh G Gonnade3, Parthapratim Munshi4, Nitin T Patil1.   

Abstract

Molecular fluorophores based on N,C-chelate, four-coordinate organoborons exhibit tunable solid-state emission colors that cover the whole visible region from blue to red. The emission color can be tuned through the substituents on either quinolines or the boron center.

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Year:  2015        PMID： 26392327     DOI： 10.1039/c5cc06351e

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


  9 in total

Review 1.  A comprehensive overview of directing groups applied in metal-catalysed C-H functionalisation chemistry.

Authors:  Carlo Sambiagio; David Schönbauer; Remi Blieck; Toan Dao-Huy; Gerit Pototschnig; Patricia Schaaf; Thomas Wiesinger; Muhammad Farooq Zia; Joanna Wencel-Delord; Tatiana Besset; Bert U W Maes; Michael Schnürch
Journal:  Chem Soc Rev       Date:  2018-08-28       Impact factor: 54.564

2.  Organic solid fluorophores regulated by subtle structure modification: color-tunable and aggregation-induced emission.

Authors:  Jing Nan Zhang; Hui Kang; Nan Li; Shi Ming Zhou; Hua Ming Sun; Shi Wei Yin; Na Zhao; Ben Zhong Tang
Journal:  Chem Sci       Date:  2016-08-30       Impact factor: 9.825

3.  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

4.  An arch-bridge-type fluorophore for bridging the gap between aggregation-caused quenching (ACQ) and aggregation-induced emission (AIE).

Authors:  Manna Huang; Ruina Yu; Ke Xu; Shuxian Ye; Shi Kuang; Xinhai Zhu; Yiqian Wan
Journal:  Chem Sci       Date:  2016-03-29       Impact factor: 9.825

5.  Arylisoquinoline-derived organoboron dyes with a triaryl skeleton show dual fluorescence.

Authors:  Vânia F Pais; Tristan Neumann; Ignacio Vayá; M Consuelo Jiménez; Abel Ros; Uwe Pischel
Journal:  Beilstein J Org Chem       Date:  2019-11-04       Impact factor: 2.883

6.  Synthesis of Conjugated Polymers Containing B←N Bonds with Strong Electron Affinity and Extended Absorption.

Authors:  Bo Pang; Zhonghai Tang; Yongchun Li; Huifeng Meng; Ying Xiang; Yuqing Li; Jianhua Huang
Journal:  Polymers (Basel)       Date:  2019-10-09       Impact factor: 4.329

7.  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 8.  Recent Advances in π-Conjugated N^C-Chelate Organoboron Materials.

Authors:  Ashanul Haque; Rayya A Al-Balushi; Paul R Raithby; Muhammad S Khan
Journal:  Molecules       Date:  2020-06-06       Impact factor: 4.411

9.  Highly Emissive Far Red/Near-IR Fluorophores Based on Borylated Fluorene-Benzothiadiazole Donor-Acceptor Materials.

Authors:  Daniel L Crossley; Inigo Vitorica-Yrezabal; Martin J Humphries; Michael L Turner; Michael J Ingleson
Journal:  Chemistry       Date:  2016-07-27       Impact factor: 5.236
  9 in total

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