Theoretical Investigation of Intermolecular Dihydrogen Bonds in C2H2···HM and C2H4···HM (M = Li, Na and K) Complexes: A DFT and ab initio Study

This study aims to investigate the dihydrogen bond formation in ethyne (C2H2) and ethene (C2H4) with alkali metal hydrides (HM; M = Li, Na and K) complexes using density functional theory (DFT) and ab initio methods. It mainly focuses on the comparison of the performances of different functionals of DFT and ab initio method on the intermolecular dihydrogen bonded complexes. The geometrical parameter and energy values agree with the formation of dihydrogen bonds in the complexes. Among the ethyne and ethene complexes, the smallest dihydrogen bond distance was formed by C2H2···HK and C2H4···HK, respectively. The C2H2 is found to form better dihydrogen bond (DHB) with alkali metal hydrides than C2H4. Among all the functionals, M06L was observed to predict shortest H···H bond distance, while M062X the longest. Natural bond orbital (NBO), quantum theory of atom in molecules (QTAIM) along with molecular electrostatic potential (MEP) analysis further confirms the dihydrogen bond formation.

Facile cyclization of sodium aminodiboranate to construct a boron–nitrogen–hydrogen ring

One-step cyclization of aminodiboranate can be used to prepare aminodiborane efficiently, where the dihydrogen bond plays an important role.

Dihydrogen Bond in the Aminoborane Complex of a Nicergoline Intermediate

An aminoborane side product from the nicergoline manufacture process was identified by single-crystal X-ray diffraction. As boranes of pharmaceutical molecules are quite rare, the binding potential of the BH3 group was investigated and compared with similar compounds using Cambridge Structural Database (CSD). Surprisingly, the packing was stabilized by a dihydrogen bond, which triggered a false alert for too-short contact of hydrogen atoms in IUCR checkCIF. As the dihydrogen bond concept is not widely known, such an alert might mislead crystallographers to force –CH3 optimal geometry to –BH3 groups. The B–H distances equal to or less than 1.0 Å (17% of the CSD structures) are substantially biased when analyzing the structures of aminoborane complexes in CSD. To conduct proper searching, B–H bond length normalization should be applied in the CSD search.

Unconventional dihydrogen-bond interaction induced cyanide-bridged chiral nano-sized magnetic molecular wheel: synthesis, crystal structure and systematic theoretical magnetism investigation

The new chiral nano-size compounds showing SMM characteristic have been structurally and magnetically investigated in detail.