1992
DOI: 10.1021/j100198a035
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Solvent effects on the photochromic reactions of diarylethene derivatives

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Cited by 199 publications
(184 citation statements)
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“…For the typical structure (R 1 =R 2 =CH 3 ), we notice that the theoretical λ max (551 nm) correctly produces Irie's reference of 551 nm (in hexane) [25]. For R 1 =R 2 = CN, CH 3 , OCH 3 series, the trend is similar to the bathochromic effect experimentally observed [30].…”
Section: Substitution Effects On the Reactive Carbon Atomssupporting
confidence: 70%
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“…For the typical structure (R 1 =R 2 =CH 3 ), we notice that the theoretical λ max (551 nm) correctly produces Irie's reference of 551 nm (in hexane) [25]. For R 1 =R 2 = CN, CH 3 , OCH 3 series, the trend is similar to the bathochromic effect experimentally observed [30].…”
Section: Substitution Effects On the Reactive Carbon Atomssupporting
confidence: 70%
“…Maleic anhydride DA derivatives ( Figure 1) have initially been synthesized by Irie's group [7,25,26]. In these works, absorption spectra (λ max values) of closed and open DA containing X 1,2 = Se, S, N-Me are reported, with some inconsistencies for the λ max of the open form.…”
Section: Resultsmentioning
confidence: 99%
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“…Further measurements with shorter laser pulses are required for a more precise determination of the ring-closing time constant. We do not exclude that in solvents with different polarity CF5-TSC might display different time of cyclization reaction [15,35].…”
Section: Resultsmentioning
confidence: 99%
“…Therefore, the cyclization reaction dynamics, which involves the process of π -π molecular orbitals (MO) redistribution within the photochromic core, may have quite different time scale. Moreover, such reaction may be sensitive to the pump wavelength [18] and solvent polarity [15,35].…”
Section: Resultsmentioning
confidence: 99%