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Cross-Conjugation and Electronic Structure in TTF Analogs

To date, tremendous advances have been witnessed in the chemistry and physics of molecular conductors for organic electronic materials with scientific and commercial motivation [1, 2]. [Pg.301]

Cross Conjugation Dendralene, Radialene and Fulvene Chemistry, First Edition. [Pg.301]

This chapter provides an overview of recent syntheses, redox properties, and electronic structures of the multi-redox system of TTF or DT rings in cross-conjugation. [Pg.302]

Dendralenes, acyclic cross-conjugated polyenes having a nonplanar structure, containing DT rings (DT[ ]dendralenes) have received considerable attention as novel multistage redox systems. The [3]- and [4]-dendralenes containing [Pg.302]


I 8 Cross-Conjugation and Electronic Structure in TTF Analogs Table 8.6 Redox potentials of DT[5] radialenes . ... [Pg.318]


See other pages where Cross-Conjugation and Electronic Structure in TTF Analogs is mentioned: [Pg.301]    [Pg.302]    [Pg.304]    [Pg.308]    [Pg.312]    [Pg.314]    [Pg.316]    [Pg.320]    [Pg.322]    [Pg.324]    [Pg.326]    [Pg.328]    [Pg.330]    [Pg.332]    [Pg.336]    [Pg.301]    [Pg.302]    [Pg.304]    [Pg.308]    [Pg.312]    [Pg.314]    [Pg.316]    [Pg.320]    [Pg.322]    [Pg.324]    [Pg.326]    [Pg.328]    [Pg.330]    [Pg.332]    [Pg.336]   


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Conjugated electrons

Conjugated structure

Conjugation cross

Cross-/! structure

Cross-conjugated

Electronic crossing

TTF

TTF structure

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