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

被引:3
作者
Yao, Chao-Yi [1 ]
Lin, Hong-Yu [1 ]
Daly, Brian [1 ]
Chen, Ze-Qing [1 ]
Crory, Hannah S. N. [1 ]
Gunaratne, H. Q. Nimal [1 ]
Anslyn, Eric V. [1 ,2 ]
de Silva, A. Prasanna [1 ]
机构
[1] Queens Univ, Sch Chem & Chem Engn, Belfast BT9 5AG, North Ireland
[2] Univ Texas Austin, Dept Chem, 100 24th St,Norman Hackerman Bldg Room 114A, Austin, TX 78712 USA
基金
英国工程与自然科学研究理事会;
关键词
ELECTRON-TRANSFER; RUTHENIUM(II) COMPLEXES; EXCITED-STATE; RECOGNITION; RECEPTOR; SENSORS; AGENTS;
D O I
10.1039/d2qo02043b
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
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.
引用
收藏
页码:1570 / 1576
页数:7
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