形状变换p-环面作为门户开关,传感,交付和逻辑操作在水中†

Chao-Yi Yao , Hong-Yu Lin , Brian Daly , Ze-Qing Chen , Hannah S.N. Crory , H. Q. Nimal Gunaratne , Eric V. Anslyn , A. Prasanna de Silva
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引用次数: 1

摘要

对环乙烷中亚苯基单元之间的碳原子的杂化状态显示出控制这些主体的客体结合性质。二聚环乙烷可以通过氧化还原进行形状转换,从而捕获或释放小的芳烃。三元环乙烷在聚吡啶Ru(ii)配合物上具有类似的功能。控制捕获和释放是交付此类货物的关键。在这些过程中被调制的发光和电化学信号用作传感功能。其中一些调制非常强,因此可以应用布尔逻辑方案。可以看到时序逻辑和组合逻辑的小规模串行集成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Shape-shifting p-cyclophanes as portals to switching, sensing, delivery and logic operations in water†

The hybridization state of carbon atoms between phenylene units in p-cyclophanes is shown to control the guest binding properties of these hosts. Dimeric cyclophanes can be shape-switched by redox so that small aromatics can be captured or released. Trimeric cyclophanes perform similar functions on polypyridineRu(ii) complexes. Controlled capture and release are key to delivery of such cargos. The luminescence and electrochemical signals which are modulated during these processes serve as sensing functions. Some of these modulations are so strong that Boolean logic schemes can be applied. Small-scale serial integration of sequential and combinational logic is seen.

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Synthesis of biologically active [1,5]diazocino[2,1-b]quinazolinones through [4 + 4] cycloaddition of 2-alkynyl quinazolinones with aza-ortho-quinone methides† Synthesis of fluorinated allylic alcohols via photoinduced decarboxylative cross-coupling of α-fluoroacrylic acids and alcohols† Aromatization-driven cascade [1,5]-hydride transfer/cyclization for synthesis of spirochromanes† Playing with the cavity size of exTTF-based self-assembled cages† An alternative approach to triazatruxene synthesis and derivatization to a boron difluoride complex†
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