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Ligand‐Assisted Back Energy Transfer in Luminescent Tb III Complexes for Thermosensing Properties
Author(s) -
Yamamoto Masanori,
Kitagawa Yuichi,
Nakanishi Takayuki,
Fushimi Koji,
Hasegawa Yasuchika
Publication year - 2018
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201804392
Subject(s) - denticity , excited state , ligand (biochemistry) , chemistry , luminescence , phosphine , phosphine oxide , crystallography , phosphorescence , photochemistry , crystal structure , fluorescence , materials science , atomic physics , organic chemistry , receptor , optoelectronics , quantum mechanics , catalysis , biochemistry , physics
A luminescent Tb III complex with a hexafluoroacetylacetone (hfa) ligand shows a characteristic back energy transfer (BEnT), which leads to high temperature sensitivity and potential application as a thermosensitive paint. Ligand‐assisted BEnT was observed when a phosphine oxide ligand was introduced into Tb(hfa) 3 complex, which was shown to affect the activation energy (Δ E a ) and frequency factor ( A ) in the BEnT process between Tb III ion and hfa ligands. According to temperature‐dependent emission‐lifetime measurements of mononuclear Tb(hfa) 3 complexes with monodentate phosphine oxides and polynuclear Tb(hfa) 3 complexes with bidentate phosphine oxides, the Δ E a and A values of polynuclear Tb III complexes were smaller than those of mononuclear Tb III complexes. Phosphorescence spectra and lifetimes of each Gd(hfa) 3 complex revealed that excited states of hfa ligands in Tb III complexes differed from those of the polynuclear Tb III complexes and mononuclear Tb III complexes. The differences in the Δ E a and A values between polynuclear and mononuclear Tb III complexes were caused by the formation of different excited states, such as delocalization of the excited state in the polynuclear Tb III complexes and localization of excited states in the mononuclear Tb III complexes. In particular, small Δ E a and A values of polynuclear Tb III complexes provided high, effective activation of the BEnT at low temperature, which resulted in high‐sensitive temperature‐dependent phosphor materials over a wide temperature range.