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Cover Picture: 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 (ChemPhysChem 20/2016)
Author(s) -
Bauzá Antonio,
Frontera Antonio
Publication year - 2016
Publication title -
chemphyschem
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 1.016
H-Index - 140
eISSN - 1439-7641
pISSN - 1439-4235
DOI - 10.1002/cphc.201601045
Subject(s) - halogen bond , front cover , moiety , cover (algebra) , chemistry , hydrogen bond , halogen , non covalent interactions , nanotechnology , ab initio , crystallography , computational chemistry , stereochemistry , organic chemistry , molecule , materials science , mechanical engineering , alkyl , engineering
The Front Cover picture illustrates the study on the versatility of haloborane compounds to establish hydrogen, halogen, and triel bonding interactions in homodimeric systems. In the cover this is exemplified by the presence of a haloborane moiety turning on the lights of the noncovalent chemistry. More information can be found in the Full Paper by A. Bauzá and A. Frontera on page 3181 in Issue 20, 2016 (DOI: 10.1002/cphc.201600683.