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Robust Ordered Bundles of Porous Helical Nanotubes Assembled from Fully Rigid Ionic Benzene‐1,3,5‐tricarboxamides
Authors:Xibo Wu  Dr Daoliang Wang  Mingming Chen  Chengsha Wei  Shenghui Wei  Prof?Dr Ningdong Huang  Prof?Dr Liangbin Li  Prof?Dr Guobing Zhang
Institution:1. National Synchrotron Radiation Lab and College of Nuclear Science and Technology, University of Science and Technology of China, No 96, JinZhai Road, Hefei, Anhui, 20026 (P.R. China), Fax: (+86)?551‐5141078;2. Hefei Institute for Public Safety Research and Tsinghua University (P.R. China);3. CAS Key Laboratory of Soft Matter Chemistry, Department of Polymer Science and Engineering, University of Science and Technology of China (P.R. China)
Abstract:Size‐controlled and ordered assemblies of artificial nanotubes are promising for practical applications; however, the supramolecular assembly of such systems remains challenging. A novel strategy is proposed that can be used to reinforce intermolecular noncovalent interactions to construct hierarchical supramolecular structures with fixed sizes and long‐range ordering by introducing ionic terminals and fully rigid arms into benzene‐1,3,5‐tricarboxamide (BTA) molecules. A series of similar BTA molecules with distinct terminal groups and arm lengths are synthesized; all form hexagonal bundles of helical rosette nanotubes spontaneously in water. Despite differences in molecular packing, the dimensions and bundling of the supramolecular nanotubes show almost identical concentration dependence for all molecules. The similarities of the hierarchical assemblies, which tolerate certain molecular irregularities, can extend to properties such as the void ratio of the nanotubular wall. This is a rational strategy that can be used to achieve supramolecular nanotubes in aqueous environments with precise size and ordering at the same time as allowing molecular modifications for functionality.
Keywords:nanotubes  noncovalent interactions  self‐assembly  supramolecular chemistry  X‐ray diffraction
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