期刊
ACS ORGANIC & INORGANIC AU
卷 2, 期 3, 页码 252-260出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsorginorgau.1c00051
关键词
crystal engineering; noncovalent interactions; chalcogen bonds; NMR spectroscopy
资金
- Natural Sciences and Engineering Research Council of Canada
In this study, a series of new chalcogen-bonded cocrystals were described, revealing the strong interaction between selenocyanates and acceptor molecules through chalcogen bonds. It was found that the chemical shift of selenium changed upon the establishment of chalcogen bonds during cocrystallization. This work contributes to the predictability of chalcogen bonds in crystal engineering and the understanding of NMR response to chalcogen bond formation.
We describe a series of new chalcogen-bonded cocrystals featuring 1,2-bis(selenocyanatomethyl)benzene (DSN) and 1,2,4,5-tetrakis(selenocyanatomethyl)-benzene (TSN) as the donor moieties and a variety of Lewis bases such as onium halides, N-oxides, and pyridine-containing heterocycles as the acceptors. Single-crystal X-ray diffraction demonstrates that, in every case, the selenocyanates consistently interact with the acceptor molecules through strong and directional Se center dot center dot center dot X chalcogen-bonds (ChBs) (X = halides, oxygen, and nitrogen). Se-77 solid-state nuclear magnetic resonance spectroscopy was applied to measure selenium chemical shift tensor magnitudes and to explore potential correlations between these tensor elements and the local ChB geometry. In every case, the isotropic Se-77 chemical shift decreases, and the chemical shift tensor span increases upon cocrystallization of DSN with the various ChB acceptors. This work contributes to a growing body of knowledge concerning the predictability and robustness of chalcogen bonds in crystal engineering as well as the NMR response to the establishment of chalcogen bonds. In particular, among the systems studied here, highly linear chalcogen bonds are formed exclusively at the stronger sigma-hole of each and every selenium atom regardless of the size, charge, or denticity of the electron donor moiety.
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