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Can Fluorine form Halogen Bond? Investigation of Halogen Bonds through Steric Charge
Author(s) -
Koohi Akram Mahmudi,
Mahdavifar Zabiollah,
Noorizadeh Siamak
Publication year - 2017
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201601840
Subject(s) - steric effects , halogen , chemistry , halogen bond , fluorine , molecule , covalent bond , computational chemistry , crystallography , photochemistry , stereochemistry , hydrogen bond , organic chemistry , alkyl
Calculated steric charges ( q s r = - 1 4 π∇ 2 υ s r , where ν s is steric potential) on the molecular surfaces are used to investigate the non‐covalent interactions formed between some R−X molecules (R= NC, NCCC, CF 3 CC, FCC, CF 3 , CH 3 , and X=F, Cl, Br) and ammonia, water as well as formaldehyde. It is shown that the formation of halogen‐bonded complexes could be regarded as the interaction between a negative steric charge (steric potential depletion) on the surface of halogen atom and a positive steric charge (steric potential accumulation) region of an electron‐donor site. But the evaluated positive steric charges on the surface of fluorine atoms in R−F molecules predict no halogen bonds for these compounds. Therefore, it is suggested that the R < C - > F ⋯ Yinteractions should be renamed to “fluorine bond”, instead of halogen bond. The evaluated steric charges also successfully determine both the strength and direction of halogen bonds for those cases in which the σ‐hole concept fails.