Formation of [3]Catenanes from 10 Precursors via Multicomponent Coordination-Driven Self-Assembly of Metallarectangles

被引:161
作者
Li, Shijun [1 ,2 ]
Huang, Jianying [2 ,3 ]
Cook, Timothy R. [2 ]
Pollock, J. Bryant [2 ]
Kim, Hyunuk [4 ]
Chi, Ki-Whan [5 ]
Stang, Peter J. [2 ]
机构
[1] Hangzhou Normal Univ, Coll Mat Chem & Chem Engn, Hangzhou 310036, Zhejiang, Peoples R China
[2] Univ Utah, Dept Chem, Salt Lake City, UT 84112 USA
[3] Zhejiang Gongshang Univ, Coll Food Sci & Biotechnol, Hangzhou 310035, Zhejiang, Peoples R China
[4] Korea Inst Energy Res, Energy Mat & Convergence Res Dept, Taejon 305343, South Korea
[5] Univ Ulsan, Dept Chem, Ulsan 680749, South Korea
基金
新加坡国家研究基金会; 中国国家自然科学基金; 美国国家科学基金会;
关键词
SYNTHETIC MOLECULAR MOTORS; DONOR-ACCEPTOR; ORGANOPLATINUM(II) METALLACYCLES; 1,2-BIS(PYRIDINIUM)ETHANE AXLES; INTERLOCKED STRUCTURES; DIRECTED SYNTHESIS; OLEFIN METATHESIS; CLICK CHEMISTRY; ETHER WHEELS; CATENATION;
D O I
10.1021/ja3118812
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We describe the formation of a suite of [3]catenanes via multicomponent coordination-driven self-assembly and host-guest complexation of a rectangular scaffold comprising a 90 degrees Pt-based acceptor building block with a pseudorotaxane bis(pyridinium)ethane/dibenzo-24-crown-8 linear dipyridyl ligand and three dicarboxylate donors. The doubly threaded [3]catenanes are formed from a total of 10 molecular components from four unique species. Furthermore, the dynamic catenation process is reversible and can be switched off and on in a controllable manner by successive addition of KPF6 and 18-crown-6, as monitored by H-1 and P-31 NMR spectroscopy.
引用
收藏
页码:2084 / 2087
页数:4
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