†Department of Chemistry, University of Ulsan, Ulsan 680-749, Republic of Korea.
‡Energy Materials Lab, Korea Institute of Energy Research, Daejeon 305-343, Republic of Korea.
J Am Chem Soc. 2015 Apr 15;137(14):4674-7. doi: 10.1021/jacs.5b02573. Epub 2015 Apr 2.
The coordination-driven self-assembly of an anthracene-functionalized ditopic pyridyl donor and a tetracene-based dinuclear Ru(II) acceptor resulted in an interlocked metalla[2]catenane, [M2L2]2, in methanol and a corresponding monorectangle, [M2L2], in nitromethane. Subsequently, guest template, solvent, and concentration effects allowed the self-assembly to be reversibly fine-tuned among monorectangle and catenane structures.
受配位驱动,蒽功能化的双齿吡啶给体和基于四并苯的双核 Ru(II)受体发生自组装,生成了一个互锁的金属[2]索烃[M2L2]2,在甲醇中;以及相应的单.rectangle [M2L2],在硝基甲烷中。随后,客体模板、溶剂和浓度效应允许自组装在单.rectangle 和索烃结构之间进行可逆的微调。