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Article: Supramolecular assembly of amphiphilic platinum(ii) Schiff base complexes: diverse spectroscopic changes and nanostructures through rational molecular design and solvent control

TitleSupramolecular assembly of amphiphilic platinum(ii) Schiff base complexes: diverse spectroscopic changes and nanostructures through rational molecular design and solvent control
Authors
Issue Date10-May-2024
PublisherRoyal Society of Chemistry
Citation
Chemical Science, 2024, v. 15, n. 22, p. 8545-8556 How to Cite?
AbstractA new class of amphiphilic tetradentate platinum(ii) Schiff base complexes has been designed and synthesized. The self-assembly properties by exploiting the potential Pt⋯Pt interactions of amphiphilic platinum(ii) Schiff base complexes in the solution state have been systematically investigated. The presence of Pt⋯Pt interactions has further been supported by computational studies and non-covalent interaction (NCI) analysis of the dimer of the complex. The extent of the non-covalent Pt⋯Pt and π-π interactions could be regulated by a variation of the solvent compositions and the hydrophobicity of the complexes, which is accompanied by attractive spectroscopic and luminescence changes and leads to diverse morphological transformations. The present work represents a rare example of demonstration of directed cooperative assembly of amphiphilic platinum(ii) Schiff base complexes by intermolecular Pt⋯Pt interactions in solution with an in-depth mechanistic investigation, providing guiding principles for the construction of supramolecular structures with desirable properties using platinum(ii) Schiff base building blocks.
Persistent Identifierhttp://hdl.handle.net/10722/348288
ISSN
2023 Impact Factor: 7.6
2023 SCImago Journal Rankings: 2.333

 

DC FieldValueLanguage
dc.contributor.authorZhang, Huilan-
dc.contributor.authorChan, Michael Ho Yeung-
dc.contributor.authorLam, Jonathan-
dc.contributor.authorChen, Ziyong-
dc.contributor.authorLeung, Ming Yi-
dc.contributor.authorWong, Eric Ka Ho-
dc.contributor.authorWu, Lixin-
dc.contributor.authorYam, Vivian Wing Wah-
dc.date.accessioned2024-10-08T00:31:26Z-
dc.date.available2024-10-08T00:31:26Z-
dc.date.issued2024-05-10-
dc.identifier.citationChemical Science, 2024, v. 15, n. 22, p. 8545-8556-
dc.identifier.issn2041-6520-
dc.identifier.urihttp://hdl.handle.net/10722/348288-
dc.description.abstractA new class of amphiphilic tetradentate platinum(ii) Schiff base complexes has been designed and synthesized. The self-assembly properties by exploiting the potential Pt⋯Pt interactions of amphiphilic platinum(ii) Schiff base complexes in the solution state have been systematically investigated. The presence of Pt⋯Pt interactions has further been supported by computational studies and non-covalent interaction (NCI) analysis of the dimer of the complex. The extent of the non-covalent Pt⋯Pt and π-π interactions could be regulated by a variation of the solvent compositions and the hydrophobicity of the complexes, which is accompanied by attractive spectroscopic and luminescence changes and leads to diverse morphological transformations. The present work represents a rare example of demonstration of directed cooperative assembly of amphiphilic platinum(ii) Schiff base complexes by intermolecular Pt⋯Pt interactions in solution with an in-depth mechanistic investigation, providing guiding principles for the construction of supramolecular structures with desirable properties using platinum(ii) Schiff base building blocks.-
dc.languageeng-
dc.publisherRoyal Society of Chemistry-
dc.relation.ispartofChemical Science-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleSupramolecular assembly of amphiphilic platinum(ii) Schiff base complexes: diverse spectroscopic changes and nanostructures through rational molecular design and solvent control-
dc.typeArticle-
dc.identifier.doi10.1039/D3SC06094B-
dc.identifier.scopuseid_2-s2.0-85192798903-
dc.identifier.volume15-
dc.identifier.issue22-
dc.identifier.spage8545-
dc.identifier.epage8556-
dc.identifier.eissn2041-6539-
dc.identifier.issnl2041-6520-

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