Block Co-PolyMOCs by Stepwise Self-Assembly

被引:62
作者
Wang, Yufeng [1 ]
Zhong, Mingjiang [1 ]
Park, Jiwon V. [1 ]
Zhukhovitskiy, Aleksandr V. [1 ]
Shi, Weichao [2 ]
Johnson, Jeremiah A. [1 ]
机构
[1] MIT, Dept Chem, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[2] Harvard Univ, John A Paulson Sch Engn & Appl Sci, Cambridge, MA 02138 USA
基金
美国国家科学基金会;
关键词
METAL-ORGANIC FRAMEWORKS; COORDINATION; LIGAND; COMPLEXES; CONSTRUCTION; MOLECULES; DRIVEN; NANOSTRUCTURES; METALLACYCLES; TOPOLOGIES;
D O I
10.1021/jacs.6b06712
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report a stepwise assembly strategy for the integration of metal-organic cages (MOCs) into block copolymers (BCPs). This approach creates "block co-polyMOC" (BCPMOC) materials whose microscopic structures and mechanical properties are readily tunable by adjusting the size and geometry of the MOCs and the composition of the BCPs. In the first assembly step, BCPs functionalized with a pyridyl ligand on the chain end form star-shaped polymers triggered by metal coordination-induced MOC assembly. The type of MOC junction employed precisely determines the number of arms for the star polymer. In the second step, microphase separation of the BCP is induced, physically cross-linking the star polymers and producing the desired BCPMOC networks in the bulk or gel state. We demonstrate that large spherical M12L24 MOCs, small paddlewheel M2L4 MOCs, or a mixture of both can be incorporated into BCPMOCs to provide materials with tailored branch functionality, phase separation, microdomain spacing, and mechanical properties. Given the synthetic and functional diversity of MOCs and BCPs, our method should enable access to BCPMOCs for a wide range of applications.
引用
收藏
页码:10708 / 10715
页数:8
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