| Literature DB >> 29192134 |
Qiong Wu1,2, Phillip M Rauscher1, Xiaolong Lang2, Rudy J Wojtecki2, Juan J de Pablo1,3, Michael J A Hore2, Stuart J Rowan1,2,3,4.
Abstract
As the macromolecular version of mechanically interlocked molecules, mechanically interlocked polymers are promising candidates for the creation of sophisticated molecular machines and smart soft materials. Poly[n]catenanes, where the molecular chains consist solely of interlocked macrocycles, contain one of the highest concentrations of topological bonds. We report, herein, a synthetic approach toward this distinctive polymer architecture in high yield (~75%) via efficient ring closing of rationally designed metallosupramolecular polymers. Light-scattering, mass spectrometric, and nuclear magnetic resonance characterization of fractionated samples support assignment of the high-molar mass product (number-average molar mass ~21.4 kilograms per mole) to a mixture of linear poly[7-26]catenanes, branched poly[13-130]catenanes, and cyclic poly[4-7]catenanes. Increased hydrodynamic radius (in solution) and glass transition temperature (in bulk materials) were observed upon metallation with Zn2.Entities:
Year: 2017 PMID: 29192134 DOI: 10.1126/science.aap7675
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728