Conformations of large macrocycles and ring-in-ring complexes
MetadataShow full item record
A kinetically directed, stepwise approach towards molecular Borromean links enabled the isolation and structural characterization of synthetic intermediates along the way. Here we report the synthesis and crystal structures of three flexible macrocyclic intermediates and a new ring-in-ring complex, anchored together through ruthenium(ii) centers, which contains open terpyridine caps in the inner Ring II. Terpyridines circumvent the conformational cis/trans limitations of bipyridines and the new ring-in-ring complex forms tetrametallic complexes with Zn(ii), Pt(ii) and Ru(iii) metal ions. Analysis of the four macrocyclic structures provides a good foundation for the conformational flexibility in these complexes and demonstrates the robust applicability of the terpyridine design elements towards the engineered synthesis of ring-in-ring topologies.
Klosterman , J K , Veliks , J , Frantz , D K , Yasui , Y , Loepfe , M , Zysman-Colman , E , Linden , A & Siegel , J S 2016 , ' Conformations of large macrocycles and ring-in-ring complexes ' Organic Chemistry Frontiers , vol 3 , no. 6 , pp. 661-666 . DOI: 10.1039/C6QO00024J
Organic Chemistry Frontiers
© 2016 The Authors. Open Access article. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.
This work was supported by the Swiss National Science Foundation.
Items in the St Andrews Research Repository are protected by copyright, with all rights reserved, unless otherwise indicated.