Self-assembled, optically-active {naphthalene diimide}U{cucurbit[8]uril} ensembles in an aqueous environment.

Higginbotham, HF; Maniam, S; Hsia, T; Isaacs, L; Langford, SJ; Bell, TDM

Self-assembled, optically-active {naphthalene diimide}U{cucurbit[8]uril} ensembles in an aqueous environment.

Higginbotham, HF Maniam, S Hsia, T Isaacs, L Langford, SJ Bell, TDM

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Publisher:: ROYAL SOC CHEMISTRY
Publication Type:: Journal Article
Citation:: Phys Chem Chem Phys, 2021, 23, (24), pp. 13434-13439
Issue Date:: 2021-06-23

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Field	Value	Language
dc.contributor.author	Higginbotham, HF
dc.contributor.author	Maniam, S
dc.contributor.author	Hsia, T
dc.contributor.author	Isaacs, L
dc.contributor.author	Langford, SJ
dc.contributor.author	Bell, TDM
dc.date.accessioned	2022-06-26T22:58:24Z
dc.date.available	2022-06-26T22:58:24Z
dc.date.issued	2021-06-23
dc.identifier.citation	Phys Chem Chem Phys, 2021, 23, (24), pp. 13434-13439
dc.identifier.issn	1463-9076
dc.identifier.issn	1463-9084
dc.identifier.uri	http://hdl.handle.net/10453/158382
dc.description.abstract	Naphthalene diimides (NDIs) are shown to arrange spontaneously co-facially with cucurbit[8]uril (CB[8]) in an aqueous environment through purely non-covalent interactions. The resultant 2 : 2 supramolecular complex of NDI and CB[8] is highly fluorescent (>30 times more than the constituent NDIs) due to the formation of NDI-NDI excimers within the supramolecular complex.
dc.format	Print
dc.language	eng
dc.publisher	ROYAL SOC CHEMISTRY
dc.relation	http://purl.org/au-research/grants/arc/DP170104477
dc.relation.ispartof	Phys Chem Chem Phys
dc.relation.isbasedon	10.1039/d1cp00659b
dc.rights	info:eu-repo/semantics/closedAccess
dc.subject	02 Physical Sciences, 03 Chemical Sciences, 09 Engineering
dc.subject.classification	Chemical Physics
dc.title	Self-assembled, optically-active {naphthalene diimide}U{cucurbit[8]uril} ensembles in an aqueous environment.
dc.type	Journal Article
utslib.citation.volume	23
utslib.location.activity	England
utslib.for	02 Physical Sciences
utslib.for	03 Chemical Sciences
utslib.for	09 Engineering
pubs.organisational-group	/University of Technology Sydney
pubs.organisational-group	/University of Technology Sydney/Faculty of Science
pubs.organisational-group	/University of Technology Sydney/Faculty of Science/School of Mathematical and Physical Sciences
utslib.copyright.status	closed_access	*
dc.date.updated	2022-06-26T22:58:22Z
pubs.issue	24
pubs.publication-status	Published
pubs.volume	23
utslib.citation.issue	24

Abstract:

Naphthalene diimides (NDIs) are shown to arrange spontaneously co-facially with cucurbit[8]uril (CB[8]) in an aqueous environment through purely non-covalent interactions. The resultant 2 : 2 supramolecular complex of NDI and CB[8] is highly fluorescent (>30 times more than the constituent NDIs) due to the formation of NDI-NDI excimers within the supramolecular complex.

Please use this identifier to cite or link to this item:

http://hdl.handle.net/10453/158382