Coordination of NO(2) to Cu and Mg in M(NO(2))(2) Complexes. A Theoretical Study

Luis Rodríguez-Santiago; Xavier Solans-Monfort; Mariona Sodupe; Vicenç Branchadell

doi:10.1021/ic980187j

Coordination of NO(2) to Cu and Mg in M(NO(2))(2) Complexes. A Theoretical Study

Inorg Chem. 1998 Sep 7;37(18):4512-4517. doi: 10.1021/ic980187j.

Authors

Luis Rodríguez-Santiago¹, Xavier Solans-Monfort, Mariona Sodupe, Vicenç Branchadell

Affiliation

¹ Departament de Química, Universitat Autònoma de Barcelona, Edifici Cn, 08193 Bellaterra, Spain.

PMID: 11670595
DOI: 10.1021/ic980187j

Abstract

The geometries, vibrational frequencies, and metal-ligand bond dissociation energies of 18 different structures of the Cu(NO(2))(2) complex have been studied. Mg(NO(2))(2) and Cu(NO(3))(2) have also been studied for comparison. The most stable structure of Cu(NO(2))(2) and Cu(NO(3))(2) corresponds to a D(2)(h)() one with a coplanar eta(2)-O,O coordination for the two NO(2) ligands. For Mg(NO(2))(2) the most stable structure is a D(2)(d)() one. The bonding in the D(2)(h)() and D(2)(d)() structures of Cu(NO(2))(2) is analyzed. For the MNO(2) systems the binding energy is very similar with both metals, while for the M(NO(2))(2) complexes the difference when changing the metal is very important. This behavior is related to the first and second ionization potentials of Cu and Mg. The computed vibrational frequencies are in good agreement with the available experimental data.