Bonding in Heavier Group 14 Zero-Valent Complexes-A Combined Maximum Probability Domain and Valence Bond Theory Approach

Jan Turek, Benoit Braïda, Frank De Proft

Onderzoeksoutput: Articlepeer review

12 Citaten (Scopus)

Samenvatting

The bonding in heavier Group 14 zero-valent complexes of a general formula L2E (E=Si–Pb; L=phosphine, N-heterocyclic and acyclic carbene, cyclic tetrylene and carbon monoxide) is probed by combining valence bond (VB) theory and maximum probability domain (MPD) approaches. All studied complexes are initially evaluated on the basis of the structural parameters and the shape of frontier orbitals revealing a bent structural motif and the presence of two lone pairs at the central E atom. For the VB calculations three resonance structures are suggested, representing the “ylidone”, “ylidene” and “bent allene” structures, respectively. The influence of both ligands and central atoms on the bonding situation is clearly expressed in different weights of the resonance structures for the particular complexes. In general, the bonding in the studied E0 compounds, the tetrylones, is best described as a resonating combination of “ylidone” and “ylidene” structures with a minor contribution of the “bent allene” structure. Moreover, the VB calculations allow for a straightforward assessment of the π-backbonding (E→L) stabilization energy. The validity of the suggested resonance model is further confirmed by the complementary MPD calculations focusing on the E lone pair region as well as the E–L bonding region. Likewise, the MPD method reveals a strong influence of the σ-donating and π-accepting properties of the ligand. In particular, either one single domain or two symmetrical domains are found in the lone pair region of the central atom, supporting the predominance of either the “ylidene” or “ylidone” structures having one or two lone pairs at the central atom, respectively. Furthermore, the calculated average populations in the lone pair MPDs correlate very well with the natural bond orbital (NBO) populations, and can be related to the average number of electrons that is backdonated to the ligands.
Originele taal-2English
Pagina's (van-tot)14604-14613
Aantal pagina's10
TijdschriftChem. Eur. J.
Volume23
Nummer van het tijdschrift58
DOI's
StatusPublished - 17 okt 2017

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