期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 55, 期 6, 页码 2007-2011出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201508257
关键词
noncovalent interactions; self-assembly; structure elucidation; supramolecular chemistry; X-ray diffraction
资金
- Basic Science Research program through the National Research Foundation of Korea [2013R1A1A2006859, 2014R1A1A2007897]
- NRF [2009-0093818]
- Research and Development Program of KIER [B5-2513]
- Grants-in-Aid for Scientific Research [15H02025] Funding Source: KAKEN
- National Research Foundation of Korea [2014R1A1A2007897, 2013R1A1A2006859] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
A molecular Solomon link was synthesized in high yield through the template-free, coordination-driven self-assembly of a carbazole-functionalized donor and a tetracene-based dinuclear ruthenium(II) acceptor. The doubly interlocked topology was realized by a strategically chosen ligand which was capable of participating in multiple CH and - interactions, as evidenced from single-crystal X-ray analysis and computational studies. This method is the first example of a two-component self-assembly of a molecular Solomon link using a directional bonding approach. The donor alone was not responsible for the construction of the Solomon link, and was confirmed by its noncatenane self-assemblies obtained with other similar ruthenium(II) acceptors.
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