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Density functional and post–Hartree–Fock studies on effective exchange interaction of d –π– d conjugated systems involving m ‐phenylene‐type bridge
Author(s) -
Takano Y.,
Onishi T.,
Kitagawa Y.,
Soda T.,
Yoshioka Y.,
Yamaguchi K.
Publication year - 2000
Publication title -
international journal of quantum chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.484
H-Index - 105
eISSN - 1097-461X
pISSN - 0020-7608
DOI - 10.1002/1097-461x(2000)80:4/5<681::aid-qua17>3.0.co;2-3
Subject(s) - chemistry , density functional theory , pyrimidine , delocalized electron , superexchange , hartree–fock method , exchange interaction , spin (aerodynamics) , molecular orbital , computational chemistry , spin polarization , molecular physics , atomic physics , condensed matter physics , physics , molecule , stereochemistry , quantum mechanics , ferromagnetism , ion , organic chemistry , thermodynamics , electron
Density functional and post–Hartree–Fock calculations have been carried out for the metal–π conjugated complexes involving pyrimidine as an m ‐phenylene‐type unit. Total energies for the lowest and highest spin states are used for investigation of d –π– d magnetic interactions via pyrimidine of Mn(II) 2 –pyrimidine, Cu(II) 2 –pyrimidine, and Mn(II)Cu(II)–pyrimidine. The natural orbital analysis of the unrestricted Hartree–Fock (UHF) and density functional theory (DFT) solutions of these complexes has been performed to elucidate relative contributions of spin polarization and spin delocalization (superexchange) interactions for determination of the sign of effective exchange integrals. Implications of the calculated results have been discussed in relation to the molecular magnetism of Mn(II) and Cu(II) complexes from the viewpoint of charge and spin density distributions, shapes of the natural orbitals, and their occupation numbers. © 2000 John Wiley & Sons, Inc. Int J Quant Chem 80: 681–691, 2000