Boron Analogue of Vinylidene Dication Supported by Phosphines.

In the presence of a catalytic amount of heavier tetrylene dichlorides, an allenic diborene 1 undergoes a 1,3-hydrogen shift to afford a terminal diborene 2, which can be deemed a boron analogue of vinylidene dication stabilized by Lewis bases. X-ray diffraction analysis and computational studies re...

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Published in:Journal of the American Chemical Society Vol. 140; no. 4; pp. 1255 - 1259
Main Authors: Lu, Wei, Li, Yongxin, Ganguly, Rakesh, Kinjo, Rei
Format: Article
Published: American Chemical Society 1/31/2018
Subjects:
Online Access:View this record in EBSCOhost
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      dt: 1/31/2018
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        10.1021/jacs.7b13068
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        atl: Boron Analogue of Vinylidene Dication Supported by Phosphines.
      aug:
        au:
          Lu, Wei
          Li, Yongxin
          Ganguly, Rakesh
          Kinjo, Rei
        affil:
          NTU-CBC Crystallography Facility, Nanyang Technological University, 637371, Singapore
          Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences
      su:
        Boron
        Lewis pairs (Chemistry)
        Phosphine
        Density functional theory
        Vinylidene compounds
      sug:
        subj:
          Boron
          Lewis pairs (Chemistry)
          Phosphine
          Density functional theory
          Vinylidene compounds
      ab: In the presence of a catalytic amount of heavier tetrylene dichlorides, an allenic diborene 1 undergoes a 1,3-hydrogen shift to afford a terminal diborene 2, which can be deemed a boron analogue of vinylidene dication stabilized by Lewis bases. X-ray diffraction analysis and computational studies revealed that 2 involves a conjugative interaction between the C= C and B=B π-orbitals. The reaction of 2 with ZnBr[sub 2]afforded the corresponding isolable complex 3, in which two boon centers coordinate to the Zn atom asymmetrically.
      pubtype: Academic Journal
      doctype: Article
      src: R
    language: English
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          year: 2018
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