共 47 条
Light-fueled rapid macroscopic motion of a green fluorescent organic crystal
被引:11
作者:

Giri, Prasenjit
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Jadavpur Univ, Dept Chem, Kolkata 700032, India Jadavpur Univ, Dept Chem, Kolkata 700032, India

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Garani, Souvik
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Jadavpur Univ, Dept Chem, Kolkata 700032, India Jadavpur Univ, Dept Chem, Kolkata 700032, India

Raveendran, Anju
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KAHM Unity Womens Coll, Mallapuram 676122, Kerala, India Jadavpur Univ, Dept Chem, Kolkata 700032, India

Panda, Manas K.
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Jadavpur Univ, Dept Chem, Kolkata 700032, India Jadavpur Univ, Dept Chem, Kolkata 700032, India
机构:
[1] Jadavpur Univ, Dept Chem, Kolkata 700032, India
[2] KAHM Unity Womens Coll, Mallapuram 676122, Kerala, India
关键词:
DIMENSIONAL COORDINATION POLYMER;
MOLECULAR-CRYSTALS;
THERMAL-EXPANSION;
SINGLE-CRYSTALS;
SHAPE-MEMORY;
DRIVEN;
COCRYSTAL;
D O I:
10.1039/d1ce00460c
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
We 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.
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页码:5876 / 5881
页数:6
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