<p> In an effort to better understand the nature of noncovalent carbon-bonding interactions, we undertook accurate high-resolution X-ray diffraction analysis of single crystals of 1,1,2,2-tetracyanocyclopropane. We selected this compound to study the fundamental characteristics of carbon-bonding interactions, because it provides accessible sigma holes. The study required extremely accurate experimental diffraction data, because the interaction of interest is weak. The electron-density distribution around the carbon nuclei, as shown by the experimental maps of the electrophilic bowl defined by a (CN)(2)CC(CN)(2) unit, was assigned as the origin of the interaction. This fact was also evidenced by plotting the (2)(r) distribution. Taken together, the obtained results clearly indicate that noncovalent carbon bonding can be explained as an interaction between confronted oppositely polarized regions. The interaction is, thus electrophilic-nucleophilic (electrostatic) in nature and unambiguously considered as attractive.</p> <p> </p>
Anglès
ab initio calculations; charge density; noncovalent carbon bonding; supramolecular chemistry; sigma-hole interactions; chalcogen-chalcogen; interactions; sigma-hole; small-molecule; halogen bonds; hydrogen; tetrel; derivatives; refinement; complexes; quality
WILEY-V C H VERLAG GMBH
Chemphyschem
SEV-2013–0319
CTQ2014– 56295-R
MINECO with FEDER funds
Severo Ochoa Excellence Accreditation 2014– 2018
Programa Estatal de I+D+i Orientada a los Retos de la Sociedad
SENSOSALUD
© 2015 Wiley-VCH Verlag GmbH & Co. KGaA
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