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- W4387298990 abstract "Chalcogen bonds, which involve the interaction of an electrophilic region associated with a chalcogen atom and a nucleophilic region in an adjacent atom, have emerged as a new frontier in supramolecular chemistry. In this study, the formation of tellurium (Te)-containing chalcogen bonds along with weak hydrogen-bonds has been demonstrated, via an investigation of the crystal structures, obtained from the Cambridge Structural Database (CSD). A statistical analysis of the occurrence of short and directional tellurium-centered contacts in organic molecules, namely, Te···Te, Te···C, and Te···H–C, has been performed. This was followed by the analysis of molecular electrostatic potentials, a Hirshfeld surface analysis, the three-dimensional deformation densities, and the energetics associated with the existence of different interactions in tellurium-containing molecules, having a diverse array of functional groups. Our findings indicate that Te functions as a σ-hole chalcogen bond donor, engaging with the nucleophilic π-rich system that functions as a chalcogen bond acceptor. This is an important supramolecular feature that governs the packing of molecules in the crystalline state, in addition to the presence of other tellurium-centered contacts. Thus, the current study is an attempt to consider the potential of Te-containing compounds, showing simultaneous chalcogen bond “donor” and “acceptor” characteristics, in the design of new materials." @default.
- W4387298990 created "2023-10-04" @default.
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- W4387298990 date "2023-10-03" @default.
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- W4387298990 title "Quantitative Investigation of Intermolecular Te···A (A = π/Te/H) Interactions in Organotellurium Compounds from the Cambridge Structural Database" @default.
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- W4387298990 doi "https://doi.org/10.1021/acs.cgd.3c00703" @default.
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