Guest-induced amorphous-to-crystalline transformation enables sorting of haloalkane isomers with near-perfect selectivity

被引:39
|
作者
Wu, Jia-Rui [1 ,2 ,3 ]
Wu, Gengxin [1 ]
Li, Dongxia [1 ]
Dai, Dihua [1 ]
Yang, Ying-Wei [1 ]
机构
[1] Jilin Univ, Coll Chem, Int Joint Res Lab Nanomicro Architecture Chem, 2699 Qianjin St, Changchun 130012, Peoples R China
[2] Jilin Univ, Key Lab Automobile Mat, Minist Educ, 5988 Renmin St, Changchun 130025, Peoples R China
[3] Jilin Univ, Sch Mat Sci & Engn, 5988 Renmin St, Changchun 130025, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
METAL-ORGANIC FRAMEWORKS; IODINE CAPTURE; SEPARATION; DESIGN; ZEOLITES;
D O I
10.1126/sciadv.abo2255
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 separation of haloalkane isomers with distillation-free strategies is one of the most challenging research topics in fundamental research and also gave high guiding values to practical industrial applications. Here, this contribution provides a previously unidentified solid supramolecular adsorption material based on a leggero pillararene derivative BrP[5]L, which can separate 1-/2-bromoalkane isomers with near-ideal selectivity. Activated solids ofBrP[5]L withinteresting amorphousand nonporousfeaturescouldadsorb 1-bromopropane and1-bromobutane from the corresponding equal volume mixtures of 1-/2-positional isomers with purities of 98.1 and 99.0%, respectively. Single-crystal structures incorporating theoretical calculation reveal that the high selectivity originates from the higher thermostability of 1-bromoalkane-loaded structures compared to its corresponding isomer-loaded structures, which could be further attributed to the perfect size/shape match between BrP[5]L and 1-bromoalkanes. Moreover, control experiments using its counterpart macrocycle of traditional pillararene demonstrate that BrP[5]L has better adsorptive selectivity, benefiting from the intrinsic free-rotation phenylene subunit on its backbone.
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页数:9
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