TY - JOUR
T1 - Phosphorescent Soft Salt Based on Platinum(II) Complexes: Photophysics, Self-Assembly, Thermochromism, and Anti-counterfeiting Application
AU - Ma, Yun
AU - Chen, Kexin
AU - Lu, Jinyu
AU - Shen, Jiandong
AU - Ma, Chenxi
AU - Liu, Shujuan
AU - Zhao, Qiang
AU - Wong, Wai Yeung
N1 - Funding Information:
National Funds for Distinguished Young Scientists (61825503) and the National Natural Science Foundation of China (51873176, 52073242, 62075101, 21701087, and 61775101) and the Natural Science Foundation of Jiangsu Province of China (BK20200095) were gratefully acknowledged. W.-Y.W. also thanks the financial support from the Hong Kong Research Grants Council (PolyU 153058/19P and C6009-17G), the Hong Kong Polytechnic University (1-ZE1C), and Clarea Au for the Endowed Professorship in Energy (847S).
Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/5/17
Y1 - 2021/5/17
N2 - 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-πstacking, 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.
AB - 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-πstacking, 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.
UR - http://www.scopus.com/inward/record.url?scp=85106432237&partnerID=8YFLogxK
U2 - 10.1021/acs.inorgchem.1c00826
DO - 10.1021/acs.inorgchem.1c00826
M3 - Journal article
C2 - 33896189
AN - SCOPUS:85106432237
SN - 0020-1669
VL - 60
SP - 7510
EP - 7518
JO - Inorganic Chemistry
JF - Inorganic Chemistry
IS - 10
ER -