1987
DOI: 10.1002/chin.198724042
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ChemInform Abstract: Charge Separation in Carotenoporphyrin‐Quinone Triads: Synthetic, Conformational, and Fluorescence Lifetime Studies.

Abstract: A series of tripartite molecules (I)‐(III) and porphyrin‐quinone analogues (IV) has been synthesized (described in schemes, no details or yields given) in order to investigate the effect of structure on the yield and lifetime of the charge‐separated state.

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Cited by 16 publications
(33 citation statements)
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“…À state at both 295 and 220 K [11,29]. This suggests that the rate constants for the relevant electron transfer steps are insensitive to the structural difference.…”
mentioning
confidence: 93%
See 1 more Smart Citation
“…À state at both 295 and 220 K [11,29]. This suggests that the rate constants for the relevant electron transfer steps are insensitive to the structural difference.…”
mentioning
confidence: 93%
“…The electronic coupling between donor and acceptor moieties has been tuned in order to alter electron transfer rate constants in favorable directions [8,[11][12][13]. The effects of medium (solvent) and temperature have also been investigated [14,15].…”
Section: Introductionmentioning
confidence: 99%
“…The process will be illustrated with PIQ dyad 1, which consists of a benzoquinone moiety joined to a tetraarylporphyrin via an amide linkage [27]. Excitation of the porphyrin moiety of 1 in dichloromethane solution leads to the series of events depicted in Figure 2.…”
Section: A Simple Covalently Linked Devicesmentioning
confidence: 99%
“…were obtained as Perchlorates by the reaction of [Co(NH 3 )^H 2 0](C10^) 3 and the sodium salts of the ligands. Recrystallization from acetone yielded analytically pure compounds.…”
Section: Synthesismentioning
confidence: 99%