Literature DB >> 34080878

Sterically Protected and Conformation-Restricted BOBHY Dyes with Bright Near-Infrared Fluorescence: N2O-type Expanded BOPHY Dyes Derived from Boronic Acids.

Jun Wang1,2, Xingbao Fang1, Xing Guo1, Qinghua Wu1, Qingbao Gong1, Changjiang Yu1, Erhong Hao1, Lijuan Jiao1.   

Abstract

A new family of N2O-type hydrazine-containing bipyrrole boron complexes has been developed via a one-pot condensation of formylisoindole, hydrazine, and various organoboronic acids. Because of the conformation-restricted coplanar structure and the axial-substituted aryl groups, these novel dyes show deep-red absorption, bright near-infrared (NIR) fluorescence in both solution and solid states, and good solubility in organic solvents. The derivative with pyridinium ions also has been synthesized as an NIR mitochondrially targetable fluorescent probe.

Entities:  

Year:  2021        PMID: 34080878     DOI: 10.1021/acs.orglett.1c01515

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  The Stability of Unsubstituted BOPHY in Various Media.

Authors:  Erol Tunca; Efdal Teknikel
Journal:  J Fluoresc       Date:  2022-03-23       Impact factor: 2.217

2.  Access to tetracoordinate boron-doped polycyclic aromatic hydrocarbons with delayed fluorescence and aggregation-induced emission under mild conditions.

Authors:  Long Jiang; Yu Wang; Dehui Tan; Xiaobin Chen; Tinghao Ma; Baoliang Zhang; Deng-Tao Yang
Journal:  Chem Sci       Date:  2022-04-29       Impact factor: 9.969

  2 in total

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