| Literature DB >> 26605477 |
Tao Zeng1, Dmitri G Fedorov2, Michael W Schmidt3, Mariusz Klobukowski1.
Abstract
The orbital-based natural language describing the complexity of chemistry ( Stowasser , R. ; Hoffmann , R. J. Am. Chem. Soc. 1999 , 121 , 3414 ) was extended by us recently to the definition of spin-orbit natural spinors ( Zeng , T. et al. J. Chem. Phys. 2011 , 134 , 214107 ). This novel method gives chemical insights into the role of spin-orbit coupling in covalent bonding and in the Jahn-Teller effect. The natural spinors are used to explain antibonding spin-orbit effects on TlH and Tl2: it is found that the spin-orbit induced charge transfer from the bonding to the nonbonding or antibonding orbitals has a large effect on the bond strength. The natural spinors are also used to explain the spin-orbit quenching of the Jahn-Teller effect in WF5: the spin-orbit interaction can stabilize the totally symmetric electron distribution so that the high-symmetry molecular structure becomes more stable than its distortions. A general discussion of the role of the spin-orbit coupling in covalent bonding and Jahn-Teller effect is given in terms of the competition between the rotational nature of the spin-orbit coupling and the directionality of the two effects. The natural spinors offer the advantage of providing a simple and clear pictorial explanation for the profound relativistic spin-dependent interactions in chemistry often appearing as a black box answer.Entities:
Year: 2011 PMID: 26605477 DOI: 10.1021/ct200457q
Source DB: PubMed Journal: J Chem Theory Comput ISSN: 1549-9618 Impact factor: 6.006