Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1823
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dc.contributor.authorKumar, Pravesh-
dc.contributor.authorSrivastava, A.-
dc.contributor.authorSah, C.-
dc.contributor.authorDevi, Sudha-
dc.contributor.authorVenkataramani, Sugumar-
dc.date.accessioned2020-11-18T10:44:17Z-
dc.date.available2020-11-18T10:44:17Z-
dc.date.issued2019-
dc.identifier.citationChemistry - A European Journal, 25(51), pp.11924-11932.en_US
dc.identifier.otherhttps://doi.org/10.1002/chem.201902150-
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/chem.201902150-
dc.identifier.urihttp://hdl.handle.net/123456789/1823-
dc.description.abstractReversibly photoswitchable phenylazo‐3,5‐dimethylisoxazole and 37 aryl‐substituted derivatives were synthesized. Excellent photoswitching ability of these compounds in solution and the solid state was demonstrated. Through kinetics studies by means of NMR spectroscopy, high Z‐isomer stability was demonstrated. Interestingly, the majority of the derivatives showed light‐induced contrasting color changes in solution and the solid state. Besides, many of the derivatives exhibit partial phase transition upon UV irradiation. The highlight of this class of photoswitches is the reversible light‐induced phase transition between solid and liquid phases in the parent compound, which can be used in patterned crystallization. These results show that this new class of azoheteroarene based photoswitches has opportunities to be useful in various domains.en_US
dc.language.isoenen_US
dc.publisherWiley‐VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.subjectAzo compoundsen_US
dc.subjectIsomerizationen_US
dc.subjectPhase transitionsen_US
dc.subjectPhotochromismen_US
dc.titleArylazo‐3,5‐dimethylisoxazoles: Azoheteroarene Photoswitches Exhibiting High Z‐Isomer Stability, Solid‐State Photochromism, and Reversible Light‐Induced Phase Transitionen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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