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Ramos, L.A., Ulic, S.E., Romano, R.M., Erben, M.F., Lehmann, C.W., Bernhardt, E., Beckers, H., Willner, H. and Della Vedova, C.O. (2010) Vibrational Spectra, Crystal Structures, Constitutional and Rotational Isomerism of FC(O)SCN and FC(O)NCS. Inorganic Chemistry, 49, 11142-11157.
https://doi.org/10.1021/ic101741e

has been cited by the following article:

• TITLE: Chalcogen Bonds in Small-Organic Molecule Compounds Derived from the Cambridge Structural Database (CSD)

  AUTHORS: Albert S. Lundemba, Dikima D. Bibelayi, Philippe V. Tsalu, Peter A. Wood, Jason Cole, Jean S. Kayembe, Zephirin G. Yav

  KEYWORDS: Chalcogen Bond, CSD, Ab Initio Calculation, Interaction Geometry, Interaction Energy

  JOURNAL NAME: Crystal Structure Theory and Applications, Vol.10 No.4, November 11, 2021

  ABSTRACT: Growing interest in non-covalent interactions involving chalcogen atoms has been ascribed to their importance in crystal engineering, molecular recognition and macromolecular edifices. The present study is dealing with chalcogen bonds involving divalent Sulphur, Selenium and Tellurium atoms, acting as sigma-hole donors, in small-molecule compounds using the Cambridge Structural Database (CSD) in conjunction with ab initio calculations. Results derived from CSD surveys and computational study revealed that nucleophiles formed complexes with the chalcogen-bond donors R1-X-R2 (X = S, Se or Te). The main forces stabilizing the complexes were chalcogen bonds, enhanced by dispersion interactions. Complexation pattern and energetics show that nucleophile bonding at divalent S, Se and Te atoms is a relatively strong and directed interaction. The bond consists of a charge transfer from a nucleophile atom lone pair to an X-R1 or X-R2 antibonding orbital.