Formation of polyrotaxane crystals driven by dative boron–nitrogen bonds

Author:

Xiao Xuedong12ORCID,Xiao Ding12ORCID,Sheng Guan3ORCID,Shan Tianyu12,Wang Jiao12,Miao Xiaohe4ORCID,Liu Yikuan3,Li Guangfeng12ORCID,Zhu Yihan3ORCID,Sessler Jonathan L.5ORCID,Huang Feihe12ORCID

Affiliation:

1. Stoddart Institute of Molecular Science, Department of Chemistry, Zhejiang University, Hangzhou 310058, P. R. China.

2. ZJU-Hangzhou Global Scientific and Technological Innovation Center–Hangzhou Zhijiang Silicone Chemicals Co. Ltd. Joint Lab, Zhejiang-Israel Joint Laboratory of Self-Assembling Functional Materials, ZJU-Hangzhou Global Scientific and Technological Innovation Center, Zhejiang University, Hangzhou 311215, P. R. China.

3. Center for Electron Microscopy, Institute for Frontier and Interdisciplinary Sciences, State Key Laboratory Breeding Base of Green Chemistry Synthesis Technology and College of Chemical Engineering, Zhejiang University of Technology, Hangzhou 310014, P. R. China.

4. Instrumentation and Service Center for Physical Sciences, Westlake University, Hangzhou 310024, P. R. China.

5. Department of Chemistry, The University of Texas at Austin, Austin, TX 78712-1224, USA.

Abstract

The integration of mechanically interlocked molecules (MIMs) into purely organic crystalline materials is expected to produce materials with properties that are not accessible using more classic approaches. To date, this integration has proved elusive. We present a dative boron–nitrogen bond-driven self-assembly strategy that allows for the preparation of polyrotaxane crystals. The polyrotaxane nature of the crystalline material was confirmed by both single-crystal x-ray diffraction analysis and cryogenic high-resolution low-dose transmission electron microscopy. Enhanced softness and greater elasticity are seen for the polyrotaxane crystals than for nonrotaxane polymer controls. This finding is rationalized in terms of the synergetic microscopic motion of the rotaxane subunits. The present work thus highlights the benefits of integrating MIMs into crystalline materials.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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