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dc.contributor.authorGuagnini, Francesca
dc.contributor.authorPedrini, Alessandro
dc.contributor.authorSwager, Timothy M
dc.contributor.authorMassera, Chiara
dc.contributor.authorDalcanale, Enrico
dc.date.accessioned2022-07-21T21:37:25Z
dc.date.available2021-09-20T18:21:24Z
dc.date.available2022-07-21T21:37:25Z
dc.date.issued2019
dc.identifier.urihttps://hdl.handle.net/1721.1/132219.2
dc.description.abstract© 2019 The Royal Society of Chemistry. Stimuli-responsive supramolecular assemblies are dynamic systems that can reversibly switch between different states upon external stimuli. In this context, metal coordination offers a reliable strategy for the preparation of stimuli responsive supramolecular architectures. Herein we report the preparation of a solvent-responsive cavitand-lanthanum coordination complex. A tetra-phosphonate cavitand has been functionalized with four hydroxyl moieties at the upper rim to form a pre-organized octadentate ligand capable of binding lanthanum salts. Exploiting the orthogonal recognition sites, two different complex architectures are formed in acetonitrile and acetone, respectively. The complexes have been characterized in solution by NMR spectroscopy, ITC experiments, while at the solid state, the single crystal structure of the acetonitrile derivative has been determined. Furthermore, as observed by DOSY-NMR spectroscopy, small quantities of acetone in acetonitrile are sufficient to trigger assembly interconversion.en_US
dc.language.isoen
dc.publisherRoyal Society of Chemistry (RSC)en_US
dc.relation.isversionof10.1039/C9DT03199Een_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourceOther repositoryen_US
dc.titleSolvent-responsive cavitand lanthanum complexen_US
dc.typeArticleen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Soldier Nanotechnologiesen_US
dc.relation.journalDalton Transactionsen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2020-09-23T12:56:48Z
dspace.orderedauthorsGuagnini, F; Pedrini, A; Swager, TM; Massera, C; Dalcanale, Een_US
dspace.date.submission2020-09-23T12:56:51Z
mit.journal.volume48en_US
mit.journal.issue36en_US
mit.licenseOPEN_ACCESS_POLICY
mit.metadata.statusPublication Information Neededen_US


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