期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 135, 期 6, 页码 2084-2087出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja3118812
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资金
- NSF [1212799]
- National Natural Science Foundation of China [21072039, 91127010]
- Public Welfare Technology and Application Program [2010C31042]
- Special Funds for Key Innovation Team of Zhejiang Province [2010R50017]
- Technology Planning Project of Zhejiang Province [2011C12031]
- World Class University (WCU) program [R33-2008-000-10003]
- Priority Research Centres program through the National Research Foundation of Korea (NRF) [2009-0093818]
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [1212799] Funding Source: National Science Foundation
- National Research Council of Science & Technology (NST), Republic of Korea [KIER-B32413] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
- National Research Foundation of Korea [R33-2012-000-10003-0, 2009-0093818] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
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.
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