Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/100069
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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.contributorMainland Development Officeen_US
dc.creatorMa, Yen_US
dc.creatorChen, Ken_US
dc.creatorLu, Jen_US
dc.creatorShen, Jen_US
dc.creatorMa, Cen_US
dc.creatorLiu, Sen_US
dc.creatorZhao, Qen_US
dc.creatorWong, WYen_US
dc.date.accessioned2023-08-08T01:51:51Z-
dc.date.available2023-08-08T01:51:51Z-
dc.identifier.issn0020-1669en_US
dc.identifier.urihttp://hdl.handle.net/10397/100069-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rights© 2021 American Chemical Societyen_US
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in Inorganic Chemistry, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.inorgchem.1c00826.en_US
dc.titlePhosphorescent soft salt based on platinum(II) complexes : photophysics, self-assembly, thermochromism, and anti-counterfeiting applicationen_US
dc.typeJournal/Magazine Articleen_US
dc.description.otherinformationTitle in author's file: A Phosphorescent Soft Salt Based on Platinum(II) Complexes: Photophysics, Self-Assembly, Thermochromism, and Anti-Counterfeiting Applicationen_US
dc.identifier.spage7510en_US
dc.identifier.epage7518en_US
dc.identifier.volume60en_US
dc.identifier.issue10en_US
dc.identifier.doi10.1021/acs.inorgchem.1c00826en_US
dcterms.abstractA new platinum(II) complex-based soft salt S1, ([Pt(tpp)(ed)]+[Pt(pba) (CN)2]-) (tpp = 2-(4-(trifluoromethyl)phenyl)pyridine, ed = ethane-1,2-diamine, pba = 4-(2-pyridyl)benzaldehyde), was designed and synthesized. UV-visible absorption and photoluminescence (PL) spectra were studied to elucidate the nature of ground and excited states. The soft salt complex was found to show self-assembly properties with the assistance of electrostatic, π-π stacking, and Pt···Pt interactions, resulting in the remarkable emergence of low-energy absorption and PL bands. Morphological transformation of S1 from undefined nanosized aggregates to nanofibers with different solvent compositions has been demonstrated. Interestingly, a luminescent polymer film was prepared by doping S1 into a polyethylene glycol matrix. The film displayed distinctive emission color change from yellow to red upon heating. Eventually, a high-level anti-counterfeiting application was accomplished using a time-resolved imaging technique based on the thermochromic luminescence property and long emission decay time displayed by S1. It is anticipated that this work can provide deep insights into the control of intermolecular interactions between cationic and anionic complexes of soft salt upon exposure to different external stimuli, resulting in the development of smart luminescent materials for various applications.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationInorganic chemistry, 17 May 2021, v. 60, no. 10, p. 7510-7518en_US
dcterms.isPartOfInorganic chemistryen_US
dcterms.issued2021-05-17-
dc.identifier.scopus2-s2.0-85106432237-
dc.identifier.pmid33896189-
dc.description.validate202308 bckwen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberABCT-0104-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNSFC; National Funds for Distinguished Young Scientists; Natural Science Foundation of Jiangsu Province of China; Hong Kong Polytechnic University; Clarea Au for the Endowed Professorship in Energyen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS52397749-
dc.description.oaCategoryGreen (AAM)en_US
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