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First ionization potential, charge transfer interactions

The relatively low first ionization potential of 6 compared to fulvene can be rationalized by assuming a charge transfer due to the interaction of the symmetric le" orbital of the cyclopropane ring with the corresponding a orbital of the five-membered ring as discussed in case of spiro[4.2)heptatriene... [Pg.206]

See other pages where First ionization potential, charge transfer interactions is mentioned: [Pg.712]    [Pg.647]    [Pg.292]    [Pg.580]    [Pg.552]    [Pg.434]    [Pg.648]    [Pg.423]    [Pg.423]    [Pg.712]    [Pg.648]    [Pg.305]    [Pg.90]    [Pg.68]    [Pg.275]    [Pg.228]    [Pg.236]    [Pg.371]    [Pg.283]    [Pg.647]    [Pg.440]    [Pg.647]    [Pg.7]    [Pg.176]    [Pg.187]    [Pg.86]    [Pg.21]    [Pg.80]    [Pg.162]    [Pg.116]    [Pg.241]   
See also in sourсe #XX -- [ Pg.292 ]



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Charge ionization

Charge potential

Charge transfer first ionization potential

Charge transfer ionization

Charge transfer potentials

Charge transfer potentials interactions

Charge-transfer interactions

Charging potential

First interactions

First ionization potential

Ionization potential

Ionization transfer

Transfer Interactions

Transferable interaction potentials

Transferable potential

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