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Anion-π Interaction-Directed Assembly of Polyoxometalate-Based Host-Guest Compounds and Its Contribution to Photochromism
被引:51
|作者:
Liao, Jian-Zhen
[1
,2
]
Wu, Xiao-Yuan
[1
]
Yong, Jian-Ping
[1
]
Zhang, Hai-Long
[1
,2
]
Yang, Wen-Bing
[1
]
Yu, Rongmin
[1
]
Lu, Can-Zhong
[1
]
机构:
[1] Chinese Acad Sci, Fujian Inst Res Struct Matter, Key Lab Design & Assembly Funct Nanostruct, Fuzhou 350002, Fujian, Peoples R China
[2] Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China
基金:
中国国家自然科学基金;
关键词:
METAL-ORGANIC FRAMEWORK;
CHARGE-SEPARATED STATES;
NAPHTHALENE DIIMIDES;
COORDINATION POLYMER;
OPTICAL-PROPERTIES;
ELECTRON-TRANSFER;
HYBRID CRYSTAL;
COMPLEXES;
MODULATION;
SWITCHES;
D O I:
10.1021/acs.cgd.5b00857
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Two rare copper-based host guest crystalline compounds were synthesized with different photoresponsive reversible visible light photochromism as a result of blending of distinctively different functional components, naphthalenediimides (NDIs) tectons and polyoxometalates. A slight adjustment of the substituent of the diimide nitrogens, from rigid to semirigid ligands, will result in different modes of anion-pi interactions, which eventually lead to different structures and different sensitivities to visible light. The unique anion-pi interactions impart significant impacts on the structures of the compounds and, to some extent, the ability to gain or lose electrons of the NDIs of the compounds, which is evident from subtle changes in photochromic sensitivity and reduction potentials; if compounds bear more and stronger anion-pi interactions, this might dramatically enhance the compounds' stability and diminish the pi-electron-deficient property of the core naphthalene ring of the NDIs.
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页码:4952 / 4958
页数:7
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