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On the Versatility of BH 2 X (X=F, Cl, Br, and I) Compounds as Halogen‐, Hydrogen‐, and Triel‐Bond Donors: An Ab Initio Study
Author(s) -
Bauzá Antonio,
Frontera Antonio
Publication year - 2016
Publication title -
chemphyschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.016
H-Index - 140
eISSN - 1439-7641
pISSN - 1439-4235
DOI - 10.1002/cphc.201601044
Subject(s) - halogen , front cover , halide , halogen bond , hydrogen bond , cover (algebra) , boron , ab initio , crystallography , chemistry , ab initio quantum chemistry methods , hydrogen , computational chemistry , molecule , inorganic chemistry , organic chemistry , engineering , mechanical engineering , alkyl
The front cover artwork is provided by the group of Prof. Antonio Frontera (Universitat de les Illes Balears). The image shows the versatility of boron halides in establishing σ‐ and π‐hole interactions. Read the full text of the article at 10.1002/cphc.201600683.

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