Mechanically‐Driven Vase–Kite Conformational Switch in Cavitand Cross‐Linked Polyurethanes
Dr. Martina Torelli,
Prof. Francesca Terenziani,
Dr. Alessandro Pedrini,
Dr. Francesca Guagnini,
Dr. Ilaria Domenichelli,
Prof. Chiara Massera,
Prof. Enrico Dalcanale
Affiliations
Dr. Martina Torelli
Department of Chemistry, Life Sciences and Environmental Sustainability and INSTM UdR Parma University of Parma Parco Area delle Scienze 17/A Parma 43124 Italy
Prof. Francesca Terenziani
Department of Chemistry, Life Sciences and Environmental Sustainability and INSTM UdR Parma University of Parma Parco Area delle Scienze 17/A Parma 43124 Italy
Dr. Alessandro Pedrini
Department of Chemistry, Life Sciences and Environmental Sustainability and INSTM UdR Parma University of Parma Parco Area delle Scienze 17/A Parma 43124 Italy
Dr. Francesca Guagnini
Department of Chemistry, Life Sciences and Environmental Sustainability and INSTM UdR Parma University of Parma Parco Area delle Scienze 17/A Parma 43124 Italy
Dr. Ilaria Domenichelli
Department of Chemistry, Life Sciences and Environmental Sustainability and INSTM UdR Parma University of Parma Parco Area delle Scienze 17/A Parma 43124 Italy
Prof. Chiara Massera
Department of Chemistry, Life Sciences and Environmental Sustainability and INSTM UdR Parma University of Parma Parco Area delle Scienze 17/A Parma 43124 Italy
Prof. Enrico Dalcanale
Department of Chemistry, Life Sciences and Environmental Sustainability and INSTM UdR Parma University of Parma Parco Area delle Scienze 17/A Parma 43124 Italy
Abstract The eligibility of tetraquinoxaline cavitands (QxCav) as molecular grippers relies on their unique conformational mobility between a closed (vase) and an open (kite) form, triggered in solution by conventional stimuli like pH, temperature and ion concentration. In the present paper, the mechanochemical conformational switching of ad hoc functionalized QxCav covalently embedded in an elastomeric polydimethylsiloxane and in a more rigid polyurethane matrix is investigated. The rigid polymer matrix is more effective in converting mechanical force into a conformational switch at the molecular level, provided that all four quinoxaline wings are covalently connected to the polymer.