Literature DB >> 30353633

A New Perspective on Borane Chemistry: The Nucleophilicity of the B-H Bonding Pair Electrons.

Qianyi Zhao1, Rian D Dewhurst2, Holger Braunschweig2, Xuenian Chen1,3.   

Abstract

A number of recently discovered nucleophilic boron compounds, such as boryl anions and borylenes, are breaking the rules regarding boron and boron-containing compounds and their reputation as Lewis acids/electrophiles. In a similar fashion, the B-H bonding pair electrons in boranes also show nucleophilicity which is ascribed to the lower electronegativity of boron relative to that of hydrogen. However, this nucleophilicity of the B-H bond has received far less attention. Explorations of the nucleophilicity of the B-H bonding pair electrons have led to the formation of B-H-B bonded units and B-H⋅⋅⋅H-Y dihydrogen bonds, based on which new chemistry has been uncovered, including the elucidation of the mechanism of formation of aminodiborane (ADB), the diammoniate of diborane (DADB), and lithium or sodium salts of octahydrotriborates (B3 H8 - ), as well as the development of more convenient and straightforward synthetic routes to these reagents. Moreover, the recognition of the nucleophilic properties of the B-H bonding pair electrons will also help to more deeply understand the different mechanisms operating in hydroboration reactions.
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Lewis acid/base; borane; nucleophilicity

Year:  2019        PMID: 30353633     DOI: 10.1002/anie.201809733

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  8 in total

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2.  Synthesis and structures of anionic rhenium polyhydride complexes of boron-hydride ligands and their application in catalysis.

Authors:  Liam J Donnelly; Simon Parsons; Carole A Morrison; Stephen P Thomas; Jason B Love
Journal:  Chem Sci       Date:  2020-09-09       Impact factor: 9.825

3.  B-B vs. B-H Bond Activation in a (μ-Hydrido)diborane(4) Anion upon Cycloaddition with CO2 , Isocyanates, or Carbodiimides.

Authors:  Timo Trageser; Dariusz Bebej; Michael Bolte; Hans-Wolfram Lerner; Matthias Wagner
Journal:  Angew Chem Int Ed Engl       Date:  2021-05-07       Impact factor: 15.336

4.  B-B Bond Nucleophilicity in a Tetraaryl μ-Hydridodiborane(4) Anion.

Authors:  Timo Trageser; Michael Bolte; Hans-Wolfram Lerner; Matthias Wagner
Journal:  Angew Chem Int Ed Engl       Date:  2020-03-19       Impact factor: 15.336

5.  Catalyst-free reductive cyclization of bis(2-aminophenyl) disulfide with CO2 in the presence of BH3NH3 to synthesize 2-unsubstituted benzothiazole derivatives.

Authors:  Xiao Li; Zhenbao Liu; Hailong Hong; Limin Han; Ning Zhu
Journal:  RSC Adv       Date:  2022-06-20       Impact factor: 4.036

6.  Unraveling hydridic-to-protonic dihydrogen bond predominance in monohydrated dodecaborate clusters.

Authors:  Yanrong Jiang; Qinqin Yuan; Wenjin Cao; Zhubin Hu; Yan Yang; Cheng Zhong; Tao Yang; Haitao Sun; Xue-Bin Wang; Zhenrong Sun
Journal:  Chem Sci       Date:  2022-08-12       Impact factor: 9.969

7.  Ambiphilic boryl groups in a neutral Ni(ii) complex: a new activation mode of H2.

Authors:  Pablo Ríos; Javier Borge; Francisco Fernández de Córdova; Giuseppe Sciortino; Agustí Lledós; Amor Rodríguez
Journal:  Chem Sci       Date:  2020-12-22       Impact factor: 9.825

Review 8.  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

  8 in total

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