Kinetic trapping of 3D-printable cyclodextrin-based poly(pseudo)rotaxane networks

被引:44
|
作者
Lin, Qianming [1 ]
Li, Longyu [1 ]
Tang, Miao [1 ]
Uenuma, Shuntaro [2 ]
Samanta, Jayanta [1 ]
Li, Shangda [1 ]
Jiang, Xuanfeng [3 ]
Zou, Lingyi [1 ]
Ito, Kohzo [2 ]
Ke, Chenfeng [1 ]
机构
[1] Dartmouth Coll, Dept Chem, Hanover, NH 03755 USA
[2] Univ Tokyo, Dept Adv Mat Sci, 5-1-5 Kashiwanoba, Chiba, Chiba 2778561, Japan
[3] Hubei Univ, Sch Mat & Engn, Key Lab Green Preparat & Applicat Funct Mat, Minist Educ, Wuhan 430062, Peoples R China
来源
CHEM | 2021年 / 7卷 / 09期
关键词
ALPHA-CYCLODEXTRIN; INCLUSION COMPLEXES; DRIVEN; GLYCOL;
D O I
10.1016/j.chempr.2021.06.004
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Synthetically trapping kinetically varied (super)structures of molecular assemblies and amplifying them to the macroscale is a promising, yet challenging, approach for the advancement of meta-stable materials. Here, we demonstrated a concerted kinetic trapping design to timely resolve a set of transient polypseudorotaxanes in solution and harness a crop of them via micro-crystallization. By installing stopper or speed bump moieties on the polymer axles, meta-stable polypseudorotaxanes with segmented cyclodextrin blocks were hierarchically amplified into crystalline networks of different crosslinking densities at mesoscale and viscoelastic hydrogels with 3D-printability in bulk. We demonstrated simultaneous 3D-printing of two polypseudorotaxane networks from one reactive ensemble and their conversion to heterogeneous polyrotaxane monoliths. Spatially programming the macroscale shapes of these heterogeneous polyrotaxanes enabled the construction of moisture-responsive actuators, in which the shape morphing originated from the different numbers of cyclodextrins interlocked in these polyrotaxane networks.
引用
收藏
页码:2442 / 2459
页数:18
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