Supramolecular-jack-like guest in ultramicroporous crystal for exceptional thermal expansion behaviour

被引:167
作者
Zhou, Hao-Long [1 ]
Zhang, Yue-Biao [1 ,2 ]
Zhang, Jie-Peng [1 ]
Chen, Xiao-Ming [1 ]
机构
[1] Sun Yat Sen Univ, Sch Chem & Chem Engn, MOE Key Lab Bioinorgan & Synthet Chem, Guangzhou 510275, Guangdong, Peoples R China
[2] ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
来源
NATURE COMMUNICATIONS | 2015年 / 6卷
关键词
METAL-ORGANIC FRAMEWORK; GAS-ADSORPTION SITES; COORDINATION FRAMEWORKS; SPIN-CROSSOVER; NETWORK; FLEXIBILITY; TRANSITION; TOPOLOGY; DRIVEN; DIMER;
D O I
10.1038/ncomms7917
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The dynamic behaviours of host frameworks and guest molecules have received much attention for their great relevance with smart materials, but little has been developed to control or understand the host-guest interplay. Here we show that the confined guest can utilize not only molecular static effects but also bulk dynamic properties to control the host dynamics. By virtue of the three-dimensional hinge-like framework and quasi-discrete ultramicropores, a flexible porous coordination polymer exhibits not only drastic guest-modulation effect of the thermal expansion magnitude (up to 422 x 10(-6) K-1) and even the anisotropy but also records positive/negative thermal expansion coefficients of +482/-218 x 10(-6) K-1. Moreover, single-crystal X-ray diffraction analyses demonstrate that the jack-like motion of the guest supramolecular dimers, being analogous to the anisotropic thermal expansion of bulk van der Waals solids, is crucial for changing the flexibility mode and thermal expansion behaviour of the crystal.
引用
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页数:7
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