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Carbones as Ligands in Novel Main‐Group Compounds E[C(NHC)<sub>2</sub>]<sub>2</sub> (E=Be, B<sup>+</sup>, C<sup>2+</sup>, N<sup>3+</sup>, Mg, Al<sup>+</sup>, Si<sup>2+</sup>, P<sup>3+</sup>): A Theoretical Study
90
Citations
91
References
2016
Year
Quantum chemical calculations of the main-group compounds E[C(NHC<sup>Me</sup> )<sub>2</sub> ]<sub>2</sub> (E=Be, B<sup>+</sup> , C<sup>2+</sup> , N<sup>3+</sup> , Mg, Al<sup>+</sup> , Si<sup>2+</sup> , P<sup>3+</sup> ) have been carried out using density functional theory at the BP86/def2-TZVPP and BP86-D3(BJ)/def2-TZVPP levels of theory. The geometry optimization at BP86/def2-TZVPP gives equilibrium structures with two-coordinated species E and bending angles C-E-C between 152.5° (E=Be) and 110.5° (E=Al). Inclusion of dispersion forces at BP86-D3(BJ)/def2-TZVPP yields a three-coordinated beryllium compound Be[C(NHC<sup>Me</sup> )<sub>2</sub> ]<sub>2</sub> as the only energy minimum form. Three-coordinated isomers are found besides the two-coordinated energy minima for the boron and carbon cations B[C(NHC<sup>Me</sup> )<sub>2</sub> ]<sub>2</sub><sup>+</sup> and C[C(NHC<sup>Me</sup> )<sub>2</sub> ]<sub>2</sub><sup>2+</sup> . The three-coordinated form of the boron compound is energetically lower lying than the two-coordinated form, while the opposite trend is calculated for the carbon species. The theoretically predicted bond dissociation energies suggest that all compounds are viable species for experimental studies. The X-ray structure of the benzoannelated homologue of P[C(NHC<sup>Me</sup> )<sub>2</sub> ]<sub>2</sub><sup>3+</sup> that was recently reported by Dordevic et al. agrees quite well with the calculated geometry of the molecule. A detailed bonding analysis using charge and energy decomposition methods shows that the two-coordinated neutral compounds Be[C(NHC<sup>Me</sup> )<sub>2</sub> ]<sub>2</sub> and Mg[C(NHC<sup>Me</sup> )<sub>2</sub> ]<sub>2</sub> possess strongly positively charged atoms Be and Mg. The carbodicarbene groups C(NHC<sup>Me</sup> )<sub>2</sub> serve as acceptor ligands in the compounds and may be sketched with dative bonds (NHC<sup>Me</sup> )<sub>2</sub> C←E→C(NHC<sup>Me</sup> )<sub>2</sub> (E=Be, Mg). Dative bonds in which the carbones C(NHC<sup>Me</sup> )<sub>2</sub> are donor ligands are suggested for the cations (NHC<sup>Me</sup> )<sub>2</sub> C→E←C(NHC<sup>Me</sup> )<sub>2</sub> (E=B<sup>+</sup> , Al<sup>+</sup> ). The dications and trications possess electron-sharing bonds in which the bonding situation is best described with the formula [(NHC<sup>Me</sup> )<sub>2</sub> C]<sup>+</sup> -E-[C(NHC<sup>Me</sup> )<sub>2</sub> ]<sup>+</sup> (E=C, Si, N<sup>+</sup> , P<sup>+</sup> ).
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