1985
DOI: 10.1016/0040-6090(85)90421-3
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J-aggregation of photochromic spiropyran in Langmuir-Blodgett films

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Cited by 161 publications
(78 citation statements)
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“…The monomeric PMC band and a bathochromic narrow and intense band assigned to that of J-PMC [2,12,13] were observed at around 571 and 613 nm, respectively, regardless of the R value. From the absorbance (A) changes in both bands with R, it was suggested that the J-PMC formation tends to increase with the increase in R up to ca.…”
Section: Measurementsmentioning
confidence: 99%
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“…The monomeric PMC band and a bathochromic narrow and intense band assigned to that of J-PMC [2,12,13] were observed at around 571 and 613 nm, respectively, regardless of the R value. From the absorbance (A) changes in both bands with R, it was suggested that the J-PMC formation tends to increase with the increase in R up to ca.…”
Section: Measurementsmentioning
confidence: 99%
“…Experimental 2.1. Materials SP 1822 was synthesized according to the method of Ando et al [2]. 2C18N+2C1 was obtain from Tokyo Kasei Kogyo Co. and recrystallized from ethyl acetate.…”
Section: Introductionmentioning
confidence: 99%
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“…Careful investigation of light-induced J-aggregation in mixed LB films of SP1822 and alkanes shows that J-aggregates are formed at temperatures above the melting point of the mixture 22 . At temperatures below the melting point, alkanes pack with the alkyl chains of SP1822 and those of its merocyanine form to hinder J-aggregation, which explains the temperaturedependent photoreactions of mixed LB films of SP1822 and octadecane reported by Ando et al 17 . Langmuir films of SP1822 show thermal hysteresis of light-induced J-aggregation, which is related to the phase transition that occurs in bulk SP1822 23 .…”
mentioning
confidence: 93%
“…Ando et al first reported the UV irradiation-induced isomerization of spiropyran to merocyanine followed by the formation of J-aggregates 17 . Room temperature UV irradiation of six-layer LB films of an amphiphilic spiropyran, 1 ,3 -dihydro-3 ,3 -demethyl-6-nitro-1 -octadecyl-8-docosanoyloxymethyl spiro 2H-1-benzopyran-2,2 -2H -indole SP1822 , mixed with octadecane leads to the isomerization of SP1822 to its merocyanine form without the formation of J-aggregates.…”
mentioning
confidence: 99%