2008
DOI: 10.1016/j.poly.2008.01.022
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Near IR luminescent rare earth 3,4,5,6-tetrafluoro-2-nitrophenoxide complexes: Synthesis, X-ray crystallography and spectroscopy

Abstract: Near IR luminescent rare earth 3,4,5,6-tetrafluoro-2-nitrophenoxide complexes: Synthesis, X-ray crystallography and spectroscopy

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Cited by 13 publications
(15 citation statements)
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“…Therefore, we finally chose ErTPM as the monomer to synthesize the target product through free radical polymerization with GMA. As shown in Fig.3B, GETPM 2 (curve b′) emits stronger characteristic luminescence than GETPM 3 (curve a′), and GETPM 1 (curve c′) in solid states were 25 excited at 390 nm.…”
Section: Luminescence Characterization Of Er Complexesmentioning
confidence: 87%
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“…Therefore, we finally chose ErTPM as the monomer to synthesize the target product through free radical polymerization with GMA. As shown in Fig.3B, GETPM 2 (curve b′) emits stronger characteristic luminescence than GETPM 3 (curve a′), and GETPM 1 (curve c′) in solid states were 25 excited at 390 nm.…”
Section: Luminescence Characterization Of Er Complexesmentioning
confidence: 87%
“…As shown in Fig. 4, the emission spectrum of ErTPM (curve a) exhibits almost identical characteristics: emission peak is broad (1500-1600 nm) and peak position is at 1530 nm for Er complexes [25][26][27][28] . However, an interesting phenomenon occurred to 35 the polymer (curves b, c, and d).…”
Section: Luminescence Characterization Of Erbium Polymersmentioning
confidence: 99%
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“…In this context, simple nitrophenolderived aromatics represent a potentially useful class of comparable chromophores [15]. Indeed poly-fluorinated nitrophenoxide ligands have been exploited in sensitized near-IR emitting species [16]. Substituted acetophenone chromophores with varying elements of charge-transfer character have also been employed to sensitise Eu III [17].…”
mentioning
confidence: 99%