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Electron-pairing energy

Crystal field splitting energy compared to the electron pairing energy. [Pg.620]

While the first electrochemical reduction potential provides an estimate for Ac (assuming it is a reversible process), the second and higher reduction potentials do not provide the spectrum of single electron affinity levels. Rather, they provide information about two-electron, three-electron, and higher electron reduction processes, and, therefore, depend on electron pairing energy. Thus, the utility of solution-phase reduction potentials for estimating solid-state affinity levels is... [Pg.206]

These two contributions represent the value of the one-electron integral /(Is) multiplied by two because there are two electrons in the ls-orbital, and the electron-pair energy (Is Is) between these electrons. Specifically, one has ... [Pg.298]

For a further discussion of this electron-pair energy (Is Is), one can introduce into equ. (7.56a) a hydrogenic Pu(r) radial function, and derive... [Pg.300]

Low-spin cations. The CFSE s for these cations are corrected for electron-pairing energies which approximate the A0 values. [Pg.154]

Crystal Field Splittings, Ao, and Mean Electron Pairing Energies, P, for Several Transition-metal Ions (energies in cm-1)... [Pg.565]


See other pages where Electron-pairing energy is mentioned: [Pg.74]    [Pg.590]    [Pg.94]    [Pg.131]    [Pg.133]    [Pg.74]    [Pg.212]    [Pg.746]    [Pg.299]    [Pg.299]    [Pg.243]    [Pg.365]    [Pg.335]    [Pg.212]    [Pg.41]    [Pg.212]    [Pg.735]    [Pg.84]    [Pg.992]    [Pg.181]    [Pg.377]    [Pg.64]    [Pg.401]    [Pg.560]    [Pg.106]    [Pg.992]    [Pg.593]    [Pg.1152]    [Pg.243]    [Pg.3697]    [Pg.350]    [Pg.34]    [Pg.643]    [Pg.2762]    [Pg.44]   
See also in sourсe #XX -- [ Pg.74 ]

See also in sourсe #XX -- [ Pg.74 ]




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Coupled Electron Pair Approximation potential energy surfaces

Energy-rich electron-hole pairs

Pair energy

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