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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 75 (1989), S. 99-110 
    ISSN: 1432-2234
    Keywords: Carbosilanes ; Structure ; Bonding ; Population analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Results of extended basis set treatments on the SCF level of theory are reported for all C-chlorinated, Si-chlorinated, symmetrically C- and Si-chlorinated silaethanes, and some chlorinated 1,3-disilapropanes. These molecules are considered as models for carbosilane compounds in general. Computed geometric structure constants are in good agreement with experiment as far as a comparison is possible. The stability and reactivity of molecules considered is discussed by means of computed bond distances, isodesmic reaction energies, and especially by results of population analysis. Si-chlorination yields a stabilization of the Si-C skeleton in carbosilanes whereas C-chlorination reduces this stability to a large extent.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2234
    Keywords: Population analysis ; Bond energies ; Hypervalency
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The population analysis based on occupation numbers, originally proposed by Davidson, is briefly reviewed. A new way is proposed to determine modified AOs and to characterize hypervalent contributions. This is discussed in application to the molecules NSF, NSF3, SF6, OPCl, OPCl2, O2PCl, SO2, ClO 4 − . It is the main objective of this work to investigate the connection between shared electron numbers σ — considered as a measure of covalent bond strength — and bond energies, σ is found to be a reliable measure of bond energies.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 42 (1976), S. 33-45 
    ISSN: 1432-2234
    Keywords: Population analysis ; Occupation numbers ; Modified AOs
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A new interpretational scheme is proposed for the analysis of molecular wavefunctions. Starting from the molecular density operator we first construct a minimal set of MAOs from the requirement that the MOs can be represented as closely as possible by the MAOs. We then use the MAOs to compute atomic occupation numbers N and shared electron numbers σ. The molecular density is then discussed in terms of N and σ. This approach has the following advantages: 1) it is generally applicable, 2) the quantities N and σ are virtually basis set independent, 3) the quantities N and σ fulfil the intuitively expected boundary conditions, 4) the simultaneous consideration of N and σ allows for a more reliable description of chemical bonding than consideration of atomic charges only.
    Type of Medium: Electronic Resource
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