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Phase conjugate, third-order effects

In going from benzene to 3-carotene (the second structure), the Y value increases by more than three orders of magnitude showing the importance of increase in the effective conjugation length. The third structure exhibits N-phenyl substitution in the benzimidazole type structures to introduce a two dimensional conjugation. The last structure, an organometallic polymer, has also been measured in the solution phase. Because of the resonance condition encountered, the Y value is.complex. [Pg.64]


See other pages where Phase conjugate, third-order effects is mentioned: [Pg.151]    [Pg.246]    [Pg.481]    [Pg.263]    [Pg.114]    [Pg.213]    [Pg.525]    [Pg.148]    [Pg.461]    [Pg.461]    [Pg.358]    [Pg.402]    [Pg.155]    [Pg.59]    [Pg.182]    [Pg.482]    [Pg.526]    [Pg.78]    [Pg.263]    [Pg.5103]    [Pg.198]    [Pg.1377]    [Pg.837]    [Pg.122]    [Pg.396]    [Pg.105]   


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Conjugate phase

Conjugative effects

Effects conjugation

Ordered phases

Phase effects

Phases ordering

Third-order

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