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Accurate density functional theory description of binding constants and NMR chemical shifts of weakly interacting complexes of C 60 with corannulene‐based molecular bowls
Author(s) -
Welsh Ivan,
Lein Matthias
Publication year - 2013
Publication title -
journal of computational chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.907
H-Index - 188
eISSN - 1096-987X
pISSN - 0192-8651
DOI - 10.1002/jcc.23455
Subject(s) - density functional theory , chemical shift , computational chemistry , ab initio , chemistry , range (aeronautics) , representation (politics) , molecular physics , statistical physics , chemical physics , physics , materials science , organic chemistry , politics , political science , law , composite material
Density functional calculations on “catch and release” complexes of C 60 with corannulene derived molecular bowls show that computationally obtained 1 H nuclear magnetic resonance (NMR) chemical shifts can be used as a reliable predictor of binding constants. A wide range of functionals was benchmarked against accurate ab initio calculations to ensure a credible representation of the weak forces that dominate the interactions in these systems. The most reliable density functional theory (DFT) results were then calibrated using experimentally observed NMR data. Careful analysis and comparison of a wide range of commonly used density functionals shows that the explicit inclusion of dispersion corrections is currently the only reliable way to accurately describe the systems investigated in our study. Moreover, we are able to show that the B97‐D and ωB97X‐D functionals are not only able to reproduce ab initio benchmark calculations, but they do so accurately with a moderately sized basis sets and without the problems of numerical integration we encountered with other functionals in this study. © 2013 Wiley Periodicals, Inc.