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Article: Supramolecular self-assembly of dinuclear alkynylplatinum(II) complexes into highly ordered crystalline hexagonal bipyramid superstructures

TitleSupramolecular self-assembly of dinuclear alkynylplatinum(II) complexes into highly ordered crystalline hexagonal bipyramid superstructures
Authors
Keywords2D hexagonal crystalline framework
dinuclear platinum(II) complexes
hexagonal bipyramid superstructure
nonclassical crystallization
Other
SDG9: Industry, innovation, and infrastructure
supramolecular self-assembly
Issue Date14-Dec-2023
PublisherCell Press
Citation
Chem, 2023, v. 9, n. 12, p. 3573-3587 How to Cite?
AbstractWe demonstrate the formation of highly symmetric crystalline hexagonal bipyramid-shaped superstructures in the self-assembly of dinuclear Pt(II) terpyridine complexes and show that it proceeds via a nonclassical crystallization (NCC) growth mechanism, which has not been reported in the supramolecular self-assembly of metal-organic complexes previously. Instead of identifying the classical hexagonal-shaped nuclei, we observed the intermediates of nanorods and pseudo-hexagonal shapes, establishing a previously unreported growth pattern of crystallization with direct experimental evidence for the NCC mechanism, which is the first of its kind in organic/organometallic supramolecular self-assembly. In addition, the crystal structures of the hexagonal bipyramids were found to be constructed from a weaving-like trimeric motif that elongates into a 2D hexagonal network by Pt···Pt, π-π, and hydrophobic interactions. It is envisaged that the current molecular packing strategy and the discovery of this NCC pathway will provide new insights into the rational design of geometric-shaped crystalline materials via supramolecular self-assembly.
Persistent Identifierhttp://hdl.handle.net/10722/348250
ISSN
2023 SCImago Journal Rankings: 6.556

 

DC FieldValueLanguage
dc.contributor.authorWang, Huai Zhen-
dc.contributor.authorChan, Michael Ho Yeung-
dc.contributor.authorChen, Zhen-
dc.contributor.authorChen, Zi Yong-
dc.contributor.authorLeung, Ming Yi-
dc.contributor.authorYam, Vivian Wing Wah-
dc.date.accessioned2024-10-08T00:31:14Z-
dc.date.available2024-10-08T00:31:14Z-
dc.date.issued2023-12-14-
dc.identifier.citationChem, 2023, v. 9, n. 12, p. 3573-3587-
dc.identifier.issn2451-9308-
dc.identifier.urihttp://hdl.handle.net/10722/348250-
dc.description.abstractWe demonstrate the formation of highly symmetric crystalline hexagonal bipyramid-shaped superstructures in the self-assembly of dinuclear Pt(II) terpyridine complexes and show that it proceeds via a nonclassical crystallization (NCC) growth mechanism, which has not been reported in the supramolecular self-assembly of metal-organic complexes previously. Instead of identifying the classical hexagonal-shaped nuclei, we observed the intermediates of nanorods and pseudo-hexagonal shapes, establishing a previously unreported growth pattern of crystallization with direct experimental evidence for the NCC mechanism, which is the first of its kind in organic/organometallic supramolecular self-assembly. In addition, the crystal structures of the hexagonal bipyramids were found to be constructed from a weaving-like trimeric motif that elongates into a 2D hexagonal network by Pt···Pt, π-π, and hydrophobic interactions. It is envisaged that the current molecular packing strategy and the discovery of this NCC pathway will provide new insights into the rational design of geometric-shaped crystalline materials via supramolecular self-assembly.-
dc.languageeng-
dc.publisherCell Press-
dc.relation.ispartofChem-
dc.subject2D hexagonal crystalline framework-
dc.subjectdinuclear platinum(II) complexes-
dc.subjecthexagonal bipyramid superstructure-
dc.subjectnonclassical crystallization-
dc.subjectOther-
dc.subjectSDG9: Industry, innovation, and infrastructure-
dc.subjectsupramolecular self-assembly-
dc.titleSupramolecular self-assembly of dinuclear alkynylplatinum(II) complexes into highly ordered crystalline hexagonal bipyramid superstructures-
dc.typeArticle-
dc.identifier.doi10.1016/j.chempr.2023.08.002-
dc.identifier.scopuseid_2-s2.0-85179606718-
dc.identifier.volume9-
dc.identifier.issue12-
dc.identifier.spage3573-
dc.identifier.epage3587-
dc.identifier.eissn2451-9294-
dc.identifier.issnl2451-9294-

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