Literature DB >> 23318646

Methods to produce B-C, B-P, B-N and B-S bonds in boron clusters.

David Olid1, Rosario Núñez, Clara Viñas, Francesc Teixidor.   

Abstract

Boranes, heteroboranes and metallacarboranes, all named as boron clusters, offer an alternative to typical organic molecules or organic molecular materials. Carbon and boron share the important property of self-catenation thus these elements can produce individually large and sophisticated molecules. Boron clusters and organic molecules display electronic, physical, chemical and geometrical characteristics manifestly different. These differences highlight the complementarity of organic molecules and boron clusters, and therefore the feasibility or necessity to produce hybrid molecules incorporating both types of fragments. To join these two types of fragments, or alternatively these two types of molecular compounds, tools are needed. In this review the current methods of producing boron clusters with carbon, B-C, nitrogen, B-N, phosphorus, B-P and sulphur bonds, B-S, are indicated. As there are many existing borane clusters of different sizes, heteroboranes and metallacarboranes, the revision of methods to generate the B-C, B-P, B-S, and B-N bonds has been restricted to the most widely used boron clusters; [B12H12](2-), dianionic and an example of a borane, 1,2-C2B10H12, neutral and an example of a heteroborane, and [Co(C2B9H11)2](-), monoanionic and an example of a metallacarborane.

Entities:  

Year:  2013        PMID: 23318646     DOI: 10.1039/c2cs35441a

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  19 in total

1.  Oxidative Generation of Boron-Centered Radicals in Carboranes.

Authors:  Harrison A Mills; Joshua L Martin; Arnold L Rheingold; Alexander M Spokoyny
Journal:  J Am Chem Soc       Date:  2020-03-03       Impact factor: 15.419

2.  Synthesis and Applications of Perfunctionalized Boron Clusters.

Authors:  Jonathan C Axtell; Liban M A Saleh; Elaine A Qian; Alex I Wixtrom; Alexander M Spokoyny
Journal:  Inorg Chem       Date:  2018-02-21       Impact factor: 5.165

3.  Rapid Synthesis of Redox-Active Dodecaborane B12(OR)12 Clusters Under Ambient Conditions.

Authors:  Alex I Wixtrom; Yanwu Shao; Dahee Jung; Charles W Machan; Shaunt N Kevork; Elaine A Qian; Jonathan C Axtell; Saeed I Khan; Clifford P Kubiak; Alexander M Spokoyny
Journal:  Inorg Chem Front       Date:  2016-03-03       Impact factor: 6.569

4.  New ligand platforms featuring boron-rich clusters as organomimetic substituents.

Authors:  Alexander M Spokoyny
Journal:  Pure Appl Chem       Date:  2013-05       Impact factor: 2.453

5.  Metal-catalyzed cross-coupling chemistry with polyhedral boranes.

Authors:  Rafal M Dziedzic; Alexander M Spokoyny
Journal:  Chem Commun (Camb)       Date:  2019-01-03       Impact factor: 6.222

6.  Sterically Unprotected Nucleophilic Boron Cluster Reagents.

Authors:  Xin Mu; Jonathan C Axtell; Nicholas A Bernier; Kent O Kirlikovali; Dahee Jung; Alexander Umanzor; Kevin Qian; Xiangyang Chen; Katherine L Bay; Monica Kirollos; Arnold L Rheingold; K N Houk; Alexander M Spokoyny
Journal:  Chem       Date:  2019-08-22       Impact factor: 22.804

7.  Iridium-catalysed regioselective borylation of carboranes via direct B-H activation.

Authors:  Ruofei Cheng; Zaozao Qiu; Zuowei Xie
Journal:  Nat Commun       Date:  2017-03-16       Impact factor: 14.919

8.  Magnesium-mediated sp3 C-H activation in cascade cyclization of 1-arylethynyl-2-alkyl-o-carboranes: efficient synthesis of carborane-fused cyclopentanes.

Authors:  Jie Zhang; Cen Tang; Zuowei Xie
Journal:  Chem Sci       Date:  2020-09-02       Impact factor: 9.825

9.  Tri-insertion with dearomatization of terminal arylalkynes using a carborane based frustrated Lewis pair template.

Authors:  Jian Zhang; Zuowei Xie
Journal:  Chem Sci       Date:  2020-11-28       Impact factor: 9.825

10.  Synthesis, structure and aromaticity of carborane-fused carbo- and heterocycles.

Authors:  Tek Long Chan; Zuowei Xie
Journal:  Chem Sci       Date:  2018-01-16       Impact factor: 9.825

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