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- W2091533123 abstract "In this work, a systematic theoretical investigation on a series of dimeric complexes formed between MH2 and HX has been carried out by employing correlated ab initio methods. It was shown that besides dihydrogen bonds, there also exists novel noncovalent X⋯H interactions between the two molecules, which have similar characteristics to traditional halogen bonds. Upon complexation, the HX bonds tend to elongate in all cases, concomitant with red-shifts of the HX stretching frequencies. X⋯H interaction energies, calculated at the MP2/aug-cc-pvtz level, range from −2.11 to −11.78 kJ/mol; the interactions are much weaker than corresponding dihydrogen bonds. The major stabilization source of dihydrogen and halogen bonds arises from the electrostatic force, while charge-transfer force plays a minor role in the formation of the complexes. AIM analyses further confirm the presence of X⋯H interactions in the systems, and the electron density at bond critical points correlates fairly well with the interaction energy." @default.
- W2091533123 created "2016-06-24" @default.
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- W2091533123 date "2010-07-01" @default.
- W2091533123 modified "2023-10-05" @default.
- W2091533123 title "Novel halogen bonding interactions between MH2 (M=Mg, Be) and HX (X=Cl, Br, I) molecules" @default.
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- W2091533123 doi "https://doi.org/10.1016/j.theochem.2010.04.028" @default.
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