Literature DB >> 30560667

Dibora[10]annulenes: Construction, Properties, and Their Ring-Opening Reactions.

Weidong Zhang1, Demei Yu1, Zhijun Wang1, Bingjie Zhang1, Letian Xu1, Guoping Li1, Ni Yan2, Eric Rivard3, Gang He1.   

Abstract

The selective construction of various dibora[10]annulenes through mild boron-tin exchange reactions is reported. Dibora[10]annulenes exhibit optical and electrochemical properties of value for future sensing applications. Controlled addition of the Lewis base pyridine to dibora[10]annulenes instigates a selective ring-opening reaction. This work explores a new area of boron chemistry that represents the first step in the potential formation of dibora[10]annulene-derived polymers.

Entities:  

Year:  2018        PMID: 30560667     DOI: 10.1021/acs.orglett.8b03538

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


  3 in total

1.  Synthesis of 9-borafluorene analogues featuring a three-dimensional 1,1'-bis(o-carborane) backbone.

Authors:  Sam Yruegas; Jonathan C Axtell; Kent O Kirlikovali; Alexander M Spokoyny; Caleb D Martin
Journal:  Chem Commun (Camb)       Date:  2019-03-05       Impact factor: 6.222

2.  Diboramacrocycles: reversible borole dimerisation-dissociation systems.

Authors:  Sonja Fuchs; Arumugam Jayaraman; Ivo Krummenacher; Laura Haley; Marta Baštovanović; Maximilian Fest; Krzysztof Radacki; Holger Helten; Holger Braunschweig
Journal:  Chem Sci       Date:  2022-02-04       Impact factor: 9.825

3.  Alkene insertion reactivity of a o-carboranyl-substituted 9-borafluorene.

Authors:  Tobias Bischof; Xueying Guo; Ivo Krummenacher; Lukas Beßler; Zhenyang Lin; Maik Finze; Holger Braunschweig
Journal:  Chem Sci       Date:  2022-06-02       Impact factor: 9.969

  3 in total

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