2000
DOI: 10.1562/0031-8655(2000)071<0071:casaip>2.0.co;2
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Chlorophyll a Self-assembly in Polar Solvent–Water Mixtures†

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Cited by 58 publications
(45 citation statements)
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“…The evident relevance of the pigment ability to mutate its physico-chemical properties upon aggregation has induced several laboratories to investigate the conditions at which long-wavelength absorbing forms of chlorophyll can be formed in vitro, in polar and nonpolar solvents and in a series of membrane mimetic systems [14][15][16]. Due to the complexity of the system under investigation and the number of parameters that can influence the Chl a aggregation processes, any study on the equilibrating species in solution may be rather difficult, and needs a large number of techniques to be carried out.…”
Section: Resultsmentioning
confidence: 99%
“…The evident relevance of the pigment ability to mutate its physico-chemical properties upon aggregation has induced several laboratories to investigate the conditions at which long-wavelength absorbing forms of chlorophyll can be formed in vitro, in polar and nonpolar solvents and in a series of membrane mimetic systems [14][15][16]. Due to the complexity of the system under investigation and the number of parameters that can influence the Chl a aggregation processes, any study on the equilibrating species in solution may be rather difficult, and needs a large number of techniques to be carried out.…”
Section: Resultsmentioning
confidence: 99%
“…Chl a in solution is known to exhibit both self-quenching and the formation of complexes and aggregates, all of which may perturb the electronic spectra. 14 To check for such effects measurements were made in 0.2 mm and 1 mm cells both with an OD of 0.3 at the maximum of the S0 S1 transition, thus varying the concentration by a factor of 5. The main features of the molecular response were independent of concentration confirming that we are studying monomeric Chl a.…”
Section: Methodsmentioning
confidence: 99%
“…The average decay lifetime of the aggregates is then as short as 144 ps. By comparing this number with the decay lifetime of Chl a molecules in acetone of 6.1 ns (44,45), we conclude that IsiA aggregates have an ∼50 times faster average decay lifetime than Chl a in acetone and should therefore have an emission yield of ∼2% compared to that of Chl a in acetone.…”
Section: Time-resolved Emissionmentioning
confidence: 98%