Valence and extra-valence orbitals in main group and transition metal bonding
Copyright (c) 2006 Wiley Periodicals, Inc.
Veröffentlicht in: | Journal of computational chemistry. - 1984. - 28(2007), 1 vom: 15. Jan., Seite 198-203 |
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Format: | Aufsatz |
Sprache: | English |
Veröffentlicht: |
2007
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Zugriff auf das übergeordnete Werk: | Journal of computational chemistry |
Schlagworte: | Journal Article |
Zusammenfassung: | Copyright (c) 2006 Wiley Periodicals, Inc. We address the issue first raised by Maseras and Morokuma with regard to the questionable treatment of empty p-orbitals in the algorithm for natural atomic/bond orbitals (NAOs, NBOs) and associated natural population analysis. We quantify this issue in terms of the numerical error (root-mean-square density deviation) resulting from the two alternative treatments of empty p-sets, leading to distinct NAOs, atomic charges, and idealized Lewis structural representations. Computational application of this criterion to a broad spectrum of main group and transition group species (employing both single- and multi-structure resonance models) reveals the interesting general pattern of (i) relatively insignificant differences for normal-valent species, where a single resonance structure is usually adequate, but (ii) clear superiority of the standard NAO algorithm for hypervalent species, where multi-resonance character is pronounced. These comparisons show how the divisive issue of "valence shell expansion" in transition metal bonding is deeply linked to competing conceptual models of hypervalency (viz., "p-orbital participation" in skeletal hybridization vs. 3c/4e resonance character). The results provide a quantitative measure of superiority both for the standard NAO evaluation of atomic charges as well as the general 3c/4e (A: B-C<-->A-B :C resonance) picture of main- and transition-group hypervalency |
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Beschreibung: | Date Completed 25.01.2007 Date Revised 12.12.2006 published: Print Citation Status PubMed-not-MEDLINE |
ISSN: | 1096-987X |