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Highest occupied molecular orbital general reactivity

The Sc -promoted photoinduced electron transfer can be generally applied for formation of the radical cations of a variety of fullerene derivatives, which would otherwise be difficult to oxidize [135]. It has been shown that the electron-transfer oxidation reactivities of the triplet excited states of fullerenes are largely determined by the HOMO (highest occupied molecular orbital) energies of the fullerenes, whereas the triplet energies remain virtually the same among the fullerenes [135]. [Pg.267]

See other pages where Highest occupied molecular orbital general reactivity is mentioned: [Pg.74]    [Pg.797]    [Pg.541]    [Pg.26]    [Pg.8]    [Pg.521]    [Pg.26]    [Pg.797]    [Pg.279]    [Pg.538]    [Pg.231]    [Pg.67]    [Pg.168]    [Pg.8]    [Pg.797]    [Pg.245]    [Pg.114]    [Pg.143]    [Pg.221]    [Pg.26]    [Pg.179]    [Pg.26]    [Pg.107]    [Pg.966]    [Pg.181]    [Pg.593]    [Pg.578]    [Pg.324]    [Pg.34]    [Pg.34]    [Pg.161]    [Pg.127]    [Pg.3]    [Pg.185]    [Pg.352]   
See also in sourсe #XX -- [ Pg.106 , Pg.107 , Pg.108 , Pg.109 , Pg.110 , Pg.111 , Pg.112 , Pg.113 ]

See also in sourсe #XX -- [ Pg.106 , Pg.107 , Pg.108 , Pg.109 , Pg.110 , Pg.111 , Pg.112 , Pg.113 ]



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General reactivity

Highest

Highest occupied molecular

Highest occupied molecular orbital

Molecular orbital occupied

Molecular orbitals highest occupied

Molecular reactivity

Molecular, generally

Molecular, generally orbitals

Occupied molecular orbitals

Occupied orbital

Occupied orbitals

Orbitals highest occupied

Orbits general

Reactive Molecular

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