2005
DOI: 10.1021/cm048020d
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Two-Photon-Induced Photoisomerization of an Azo Dye

Abstract: The cis − trans photoisomerization of an azo dye was induced by two-photon excitation using a titanium:sapphire femtosecond laser, and was monitored by 1H NMR spectroscopy. The NMR signals of the two isomers were well separated, allowing the unambiguous identification of the photoproducts. No photoproducts other than the cis isomer were observed. The operation of a two-photon mechanism was confirmed by measurement of the dependence of the initial reaction rate on the laser power. The approach of the system to … Show more

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Cited by 58 publications
(41 citation statements)
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“…They also examined two-photon photochromic reaction of 5 in solution with femtosecond pulses at 820 nm. In the same year, Magennis also reported the two-photon photochromism in an azo dye (Scheme 10) [43]. The cis-trans photoisomerization of the commercially available azo dye in DMSO was induced by two-photon excitation employing femtosecond pulses.…”
Section: Scheme 8 Photoisomerization Of Indolylfulgidementioning
confidence: 98%
“…They also examined two-photon photochromic reaction of 5 in solution with femtosecond pulses at 820 nm. In the same year, Magennis also reported the two-photon photochromism in an azo dye (Scheme 10) [43]. The cis-trans photoisomerization of the commercially available azo dye in DMSO was induced by two-photon excitation employing femtosecond pulses.…”
Section: Scheme 8 Photoisomerization Of Indolylfulgidementioning
confidence: 98%
“…Aiming at applications in data storage devices, polymeric materials doped with azochromophores, presenting photoinduced birefringence, have been produced [4][5][6][7][8]. In such case, the guest-host strategy adopted to incorporate the azochromophore into the polymer led to low residual birefringence due to the high mobility of the chromophore in the polymeric matrix [9,10].…”
Section: Introductionmentioning
confidence: 99%
“…Thus absorption spectroscopy can be conveniently used to measure the cis fraction in the steady state Fischer, 1967), and the subsequent thermal relaxation to an all-trans state (Beltrame et al, 1993;Hair et al, 1990;Eisenbach, 1980a;Gabor and Fischer, 1971). Nuclear magnetic resonance (NMR) spectroscopy can also be used (Magennis et al, 2005). Under moderate irradiation, the composition of the photostationary state is predominantly cis for azobenzenes, mixed for aminoazobenzenes, and predominantly trans for pseudo-stilbenes.…”
Section: Introduction To Azobenzenementioning
confidence: 99%