TY - JOUR

T1 - All-electron CASPT2 study of Ce(eta(8)-C8H6)(2)

AU - Kerridge, Andrew

AU - Kaltsoyannis, Nikolas

PY - 2010/6

Y1 - 2010/6

N2 - CASSCF wave functions and CASPT2 energies are presented for the ground and 15 and 31 excited states of the D-2d and D-2h conformers respectively of the f-element sandwich molecule CePn(2) (Pn =eta(8)-C8H6) The ground states of both conformers are found to be strongly multiconfigurational, analogous to cerocene, CeCOT2 (COT = eta(8)-C8H8), as reported in Journal of Physical Chemistry A 113 (2009) 2896 Investigation of the nature of the multiconfigurational character shows that the analogy with cerocene is indeed strong It is shown that the occupations of the natural orbitals produce a more reliable description of the CePn(2) ground state than does the configurational admixture, and that these occupations can be used to deduce a value for the total f-density in the system. This density is found to be slightly lower than that of cerocene, and is in good agreement with that found experimentally. A density functional theory calculation of the same system is able to broadly capture the important features of the electronic structure, but is unable to replicate the experimental value of the total f-density CASPT2 calculations reproduce the energy of the first band in the UV/Vis spectrum of CePn*(2) (Pn* =eta(8)-(CMe6)-Me-8) to within 0 01 eV Although this extremely good agreement is probably somewhat fortuitous, it highlights the fact that multiconfigurational methods are required in order to model systems such as CePn(2) to a high level of accuracy. (C) 2010 Academie des sciences. Published by Elsevier Masson SAS. All rights reserved

AB - CASSCF wave functions and CASPT2 energies are presented for the ground and 15 and 31 excited states of the D-2d and D-2h conformers respectively of the f-element sandwich molecule CePn(2) (Pn =eta(8)-C8H6) The ground states of both conformers are found to be strongly multiconfigurational, analogous to cerocene, CeCOT2 (COT = eta(8)-C8H8), as reported in Journal of Physical Chemistry A 113 (2009) 2896 Investigation of the nature of the multiconfigurational character shows that the analogy with cerocene is indeed strong It is shown that the occupations of the natural orbitals produce a more reliable description of the CePn(2) ground state than does the configurational admixture, and that these occupations can be used to deduce a value for the total f-density in the system. This density is found to be slightly lower than that of cerocene, and is in good agreement with that found experimentally. A density functional theory calculation of the same system is able to broadly capture the important features of the electronic structure, but is unable to replicate the experimental value of the total f-density CASPT2 calculations reproduce the energy of the first band in the UV/Vis spectrum of CePn*(2) (Pn* =eta(8)-(CMe6)-Me-8) to within 0 01 eV Although this extremely good agreement is probably somewhat fortuitous, it highlights the fact that multiconfigurational methods are required in order to model systems such as CePn(2) to a high level of accuracy. (C) 2010 Academie des sciences. Published by Elsevier Masson SAS. All rights reserved

KW - Electronic structure

KW - Cerium

KW - Computer chemistry

KW - Ab Initio calculations

KW - Density functional calculations

KW - Metallocenes Lanthanides

KW - SANDWICH COMPLEXES

KW - PHOTOELECTRON-SPECTRA

KW - MOLECULAR-STRUCTURE

KW - OXIDATION-STATE

KW - APPROXIMATION

KW - ORBITALS

KW - CEROCENE

KW - ENERGY

KW - CERIUM(III)

KW - EXCHANGE

U2 - 10.1016/j.crci.2010.02.006

DO - 10.1016/j.crci.2010.02.006

M3 - Journal article

VL - 13

SP - 853

EP - 859

JO - Comptes Rendus Chimie

JF - Comptes Rendus Chimie

SN - 1631-0748

IS - 6-7

ER -