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Please use this identifier to cite or link to this item: http://dspace.unitywomenscollege.ac.in/xmlui/handle/123456789/1901
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dc.contributor.authorAnju Raveendran-
dc.contributor.authorPrasenjit Giri-
dc.contributor.authorAbhrojyoti Mazumder-
dc.contributor.authorDibyendu Dey-
dc.contributor.authorSouvik Garani-
dc.contributor.authorManas K Panda-
dc.date.accessioned2024-10-14T10:09:38Z-
dc.date.available2024-10-14T10:09:38Z-
dc.date.issued2021-05-07-
dc.identifier.issn1466-8033-
dc.identifier.urihttp://dspace.unitywomenscollege.ac.in/xmlui/handle/123456789/1901-
dc.description.abstractWe report here a new green fluorescent organic crystal of an amide functionalized acrylonitrile derivative (E-ArF2) that displays various types of macroscopic response when illuminated with UV light (390 nm). The shape deformation and actuation of the E-ArF2 crystal can be controlled on-demand by shining UV-light on the specific parts of the crystal and reversing the direction of light illumination. When UV light is shone on the (001) face of a straight crystal, it rapidly bends away from the light source and can be bent to the opposite direction by reversing the illumination direction on the other face (00−1). With the aid of various analytical techniques, NMR, IR, UV-vis and X-ray diffraction, we established that the light fueled macroscopic actuation of the E-ArF2 crystal is rooted to the combined effect of E- to Z-isomerization and the [2 + 2] cycloaddition reaction in the solid state. Based on the above experimental facts, a general mechanistic model of the actuation is also proposed.en_US
dc.language.isoenen_US
dc.publisherCryst Eng Commen_US
dc.titleLight-fueled rapid macroscopic motion of a green fluorescent organic crystalen_US
dc.typeArticleen_US
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