Literature DB >> 12513078

"True" inorganic heterocycles: structures and stability of group 13-15 analogues of benzene and their dimers.

Alexey Y Timoshkin1, Gernot Frenking.   

Abstract

Group 13-15 inorganic analogues of benzene, [HMYH](3) (M = B, Al, Ga; Y = N, P, As), mixed heterocycles of the type [BAlGaNPAs]H(6) and their dimers have been theoretically examined at the B3LYP/TZVP level of theory. Six different isomers have been structurally characterized for the mixed compounds [BAlGaNPAs]H(6). B-N bonding strongly (about approximately 90-100 kJ mol(-)(1)) stabilizes the mixed heterocycles, followed by the preference of the Al-N bonded structures over Ga-N bonded ( approximately 30-40 kJ mol(-1)), while B-P bonding is slightly (5-10 kJ mol(-1)) more favorable compared to B-As. Thus, the bonding pattern is predicted to be the most stable, followed by the core. Processes of [HMYH](3) formation from donor-acceptor complexes H(3)MYH(3) are predicted to be thermodynamically favorable for all MY combinations. Dimerization reactions of the coordinationally unsaturated [HMYH](3) heterocycles yielding hexamer clusters [HMYH](6) are found to be exothermic, with the exception of borazine, for which, as for benzene, dimerization is strongly endothermic due to the aromaticity of C(6)H(6) and [HBNH](3). Despite the high endothermicity of [HBNH](3) dimerization, the B-N bond formation is the driving force of the dimerization of mixed species [BAlGaNPAs]H(6). The dimerization enthalpies of [BAlGaNPAs]H(6) may be both exo- and endothermic, depending on the bonding pattern of the isomers. A complete set of mean MY bond energies in four- and six-membered cycles of [HMYH](6) was derived. The MY energies were found to be transferable quantities and may serve for a qualitative prediction of the relative stability of different isomers of mixed cluster compounds. [BAlGaNPAs](2)H(12) clusters are promising synthetic targets, they are expected to serve as single-source precursors for the stoichiometry-controlled CVD processes of the group 13-15 composites. A strategy of their synthesis and the most suitable starting systems have been also predicted.

Entities:  

Year:  2003        PMID: 12513078     DOI: 10.1021/ic020361a

Source DB:  PubMed          Journal:  Inorg Chem        ISSN: 0020-1669            Impact factor:   5.165


  2 in total

1.  Stable planar six-pi-electron six-membered N-heterocyclic carbenes with tunable electronic properties.

Authors:  Carsten Präsang; Bruno Donnadieu; Guy Bertrand
Journal:  J Am Chem Soc       Date:  2005-07-27       Impact factor: 15.419

2.  Aromatic nature of neutral and dianionic 1,4-diaza-2,3,5,6-tetraborinine derivatives.

Authors:  Kei Ota; Rei Kinjo
Journal:  RSC Adv       Date:  2021-01-04       Impact factor: 3.361

  2 in total

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