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Article: Solvent‐Induced Cluster‐to‐Cluster Transformation of Homoleptic Gold(I) Thiolates between Catenane and Ring‐in‐Ring Structures

TitleSolvent‐Induced Cluster‐to‐Cluster Transformation of Homoleptic Gold(I) Thiolates between Catenane and Ring‐in‐Ring Structures
Authors
Keywordscatenanes
gold
metallophilic interactions
supramolecular chemistry
thiolates
Issue Date2019
PublisherWiley - VCH Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www3.interscience.wiley.com/journal/26737/home
Citation
Angewandte Chemie (International Edition), 2019, v. 58 n. 45, p. 16297-16306 How to Cite?
AbstractSupramolecular ensembles adopting ring‐in‐ring structures are less developed compared with catenanes featuring interlocked rings. While catenanes with inter‐ring closed‐shell metallophilic interactions, such as d10–d10 AuI–AuI interactions, have been well‐documented, the ring‐in‐ring complexes featuring such metallophilic interactions remain underdeveloped. Herein is described an unprecedented ring‐in‐ring structure of a AuI‐thiolate Au12 cluster formed by recrystallization of a AuI‐thiolate Au10 [2]catenane from alkane solvents such as hexane, with use of a bulky dibutylfluorene‐2‐thiolate ligand. The ring‐in‐ring AuI‐thiolate Au12 cluster features inter‐ring AuI–AuI interactions and underwent cluster core change to form the thermodynamically more stable Au10 [2]catenane structure upon dissolving in, or recrystallization from, other solvents such as CH2Cl2, CHCl3, and CH2Cl2/MeCN. The cluster‐to‐cluster transformation process was monitored by 1H NMR and ESI‐MS measurements. Density functional theory (DFT) calculations were performed to provide insight into the mechanism of the “ring‐in‐ring⇌ [2]catenane” interconversions.
Persistent Identifierhttp://hdl.handle.net/10722/282884
ISSN
2023 Impact Factor: 16.1
2023 SCImago Journal Rankings: 5.300
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorXu, GT-
dc.contributor.authorWu, LL-
dc.contributor.authorChang, XY-
dc.contributor.authorAng, WH-
dc.contributor.authorWong, WY-
dc.contributor.authorHuang, JS-
dc.contributor.authorChe, CM-
dc.date.accessioned2020-06-05T06:22:42Z-
dc.date.available2020-06-05T06:22:42Z-
dc.date.issued2019-
dc.identifier.citationAngewandte Chemie (International Edition), 2019, v. 58 n. 45, p. 16297-16306-
dc.identifier.issn1433-7851-
dc.identifier.urihttp://hdl.handle.net/10722/282884-
dc.description.abstractSupramolecular ensembles adopting ring‐in‐ring structures are less developed compared with catenanes featuring interlocked rings. While catenanes with inter‐ring closed‐shell metallophilic interactions, such as d10–d10 AuI–AuI interactions, have been well‐documented, the ring‐in‐ring complexes featuring such metallophilic interactions remain underdeveloped. Herein is described an unprecedented ring‐in‐ring structure of a AuI‐thiolate Au12 cluster formed by recrystallization of a AuI‐thiolate Au10 [2]catenane from alkane solvents such as hexane, with use of a bulky dibutylfluorene‐2‐thiolate ligand. The ring‐in‐ring AuI‐thiolate Au12 cluster features inter‐ring AuI–AuI interactions and underwent cluster core change to form the thermodynamically more stable Au10 [2]catenane structure upon dissolving in, or recrystallization from, other solvents such as CH2Cl2, CHCl3, and CH2Cl2/MeCN. The cluster‐to‐cluster transformation process was monitored by 1H NMR and ESI‐MS measurements. Density functional theory (DFT) calculations were performed to provide insight into the mechanism of the “ring‐in‐ring⇌ [2]catenane” interconversions.-
dc.languageeng-
dc.publisherWiley - VCH Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www3.interscience.wiley.com/journal/26737/home-
dc.relation.ispartofAngewandte Chemie (International Edition)-
dc.rightsThis is the peer reviewed version of the following article: Angewandte Chemie (International Edition), 2019, v. 58 n. 45, p. 16297-16306, which has been published in final form at https://doi.org/10.1002/anie.201909980. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.-
dc.subjectcatenanes-
dc.subjectgold-
dc.subjectmetallophilic interactions-
dc.subjectsupramolecular chemistry-
dc.subjectthiolates-
dc.titleSolvent‐Induced Cluster‐to‐Cluster Transformation of Homoleptic Gold(I) Thiolates between Catenane and Ring‐in‐Ring Structures-
dc.typeArticle-
dc.identifier.emailWu, LL: llwusx@hku.hk-
dc.identifier.emailChang, XY: xychang@hku.hk-
dc.identifier.emailHuang, JS: jshuang@hku.hk-
dc.identifier.emailChe, CM: chemhead@hku.hk-
dc.identifier.authorityWu, LL=rp02732-
dc.identifier.authorityHuang, JS=rp00709-
dc.identifier.authorityChe, CM=rp00670-
dc.description.naturepostprint-
dc.identifier.doi10.1002/anie.201909980-
dc.identifier.pmid31486262-
dc.identifier.scopuseid_2-s2.0-85074042262-
dc.identifier.hkuros310310-
dc.identifier.volume58-
dc.identifier.issue45-
dc.identifier.spage16297-
dc.identifier.epage16306-
dc.identifier.isiWOS:000487405800001-
dc.publisher.placeGermany-
dc.identifier.issnl1433-7851-

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