A stibium bond, i.e., a non-covalent interaction formed by covalently or coordinately bound antimony, occurs in chemical systems when there is evidence of a net attractive interaction between the electrophilic region associated with an antimony atom and a nucleophile in another, or the same molecular entity. This is a pnictogen bond and are likely formed by the elements of the pnictogen family, Group 15, of the periodic table, and is an inter- or intra-molecular non-covalent interaction. This overview describes a set of illustrative crystal systems that were stabilized (at least partially) by means of stibium bonds, together with other non-covalent interactions (such as hydrogen bonds and halogen bonds), retrieved from either the Cambridge Structure Database (CSD) or the Inorganic Crystal Structure Database (ICSD). We demonstrate that these databases contain hundreds of crystal structures of various dimensions in which covalently or coordinately bound antimony atoms in molecular entities feature positive sites that productively interact with various Lewis bases containing O, N, F, Cl, Br, and I atoms in the same or different molecular entities, leading to the formation of stibium bonds, and hence, being partially responsible for the stability of the crystals. The geometric features, pro-molecular charge density isosurface topologies, and extrema of the molecular electrostatic potential model were collectively examined in some instances to illustrate the presence of Sb-centered pnictogen bonding in the representative crystal systems considered.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9099767PMC
http://dx.doi.org/10.3390/ijms23094674DOI Listing

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  • * The study evaluated interaction energy through comparisons with spectroscopic data, geometric properties, and other factors to uncover correlations, particularly focusing on the C═O stretching frequency and nuclear magnetic resonance changes.
  • * While the interaction energy can be estimated from experimental measurements, standard AIM measurements correlate less effectively, and the σ-hole depth on the Lewis acid does not strongly relate to bond strength due to the limitations of electrostatic metrics.
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