摘要
The control of structural transformations triggered by external signals is important for the development of novel functional devices. In the present study, it is demonstrated that helicates can be designed to structurally respond to the presence of different counterions and to adopt either a compressed or an expanded structure. Reversible switching is not only possible between those two states, furthermore, the twist of the aggregate also can be controlled. Thus, three out of four possible states of a helicate (expanded/left-handed, expanded/right-handed, compressed/left-handed) based on an enantiomerically pure ester bridged dicatecholate ligand are specifically addressed by introduction, exchange, or removal of countercations. This approach is used to reversibly switch between the different states or to successively address them.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 11817-11820 |
| 页数 | 4 |
| 期刊 | Angewandte Chemie - International Edition |
| 卷 | 57 |
| 期 | 36 |
| DOI | |
| 出版状态 | 已出版 - 3 9月 2018 |
| 已对外发布 | 是 |
指纹
探究 'A Helicate-Based Three-State Molecular Switch' 的科研主题。它们共同构成独一无二的指纹。引用此
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