Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/100069
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Title: Phosphorescent soft salt based on platinum(II) complexes : photophysics, self-assembly, thermochromism, and anti-counterfeiting application
Authors: Ma, Y 
Chen, K
Lu, J
Shen, J
Ma, C
Liu, S
Zhao, Q
Wong, WY 
Issue Date: 17-May-2021
Source: Inorganic chemistry, 17 May 2021, v. 60, no. 10, p. 7510-7518
Abstract: A 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.
Publisher: American Chemical Society
Journal: Inorganic chemistry 
ISSN: 0020-1669
DOI: 10.1021/acs.inorgchem.1c00826
Rights: © 2021 American Chemical Society
This 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.
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