Theoretical calculations at the MP2/6-311++G(2d,2p) level are used to analyze the interaction between HNZ (Z = O, S) and H₂XNH₂ (X = B, Al). In the most stable conformation, the complexes are cyclic, the molecules being held together by conventional NH⋯Z hydrogen bonds and by XH⋯HN dihydrogen bonds. Binding energies including ZPE- and BSSE-corrections lie in the range 6.2-6.9 kJ mol^-1 and there is little sensitivity to the nature of the X and Z atoms. In the XH⋯HN dihydrogen bonds, the NH stretching vibrations are blue-shifted in the HNO complexes and red-shifted in the H₂AlNH₂-HNS complex. In the conventional NH⋯Z hydrogen bonds, the NH stretching vibrations are red-shifted. The topological parameters at the bond critical point are in the usual range for hydrogen or dihydrogen bonds. A natural bond orbital analysis including the calculation of the atomic charges, hybridization, occupation of the antibonding orbitals and hyperconjugation energies shows that the shifts of the NH stretching vibrations in the conventional and dihydrogen bonds are mainly determined by the changes in occupation of the σ*(NH) antibonding orbitals. The mechanism of intramolecular coupling is discussed and appears to be different for the HNO and HNS complexes. The analysis of all the theoretical data reveals that the NH⋯Z bonds are stronger in the H ₂BNH₂ than in the H₂AlNH₂ systems and that the XH⋯HN dihydrogen bonds are stronger in the H ₂AlNH₂ than in the H₂BNH₂ complexes. © the Owner Societies.

Trung N.T., Hue T.T., Nguyen M.T., Zeegers-Huyskens T.

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