2011
DOI: 10.1021/om2008937
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Turning On MLCT Phosphorescence of Iridium(III)–Borane Conjugates upon Fluoride Binding

Abstract: The heteroleptic complexes (C ∧ N) 2 Ir III (C ∧ N: ppy, 2; btp, 3), bearing a 4-(dimesitylboryl)benzoate (Bbz) auxiliary ligand, and their fluoride adducts were prepared and characterized. While the PL spectra of 2 and 3 exhibit very weak emission in solution, the addition of fluoride turned on (C ∧ N) 2 Ir-centered phosphorescence (λ em 527 nm for 2 and 617 nm for 3). Experimental and DFT calculations suggest that the weak emission is ascribable to a photoinduced electron transfer from the MLCT state of the … Show more

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Cited by 43 publications
(28 citation statements)
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“…7,8 Hence, the regulation and detection of uoride attracted considerable attention. Over the past decade a number of uoride ion sensors based on different signaling mechanisms, such as intramolecular charge transfer, 9,11,12 photo-induced electron transfer, [13][14][15][16][17][18][19][20][21][22] uorescence resonance energy transfer, [23][24][25][26][27] twisted intramolecular charge transfer, 28,29 excited state proton transfer, [30][31][32][33][34][35][36][37][38][39][40][41] metal-ligand charge transfer, [42][43][44][45][46] and excimer/exciplex [47][48][49] formation, have been used. However most of the reported probes suffer from low sensitivity (or) slow response, turn-off uorescence response and complicated synthetic procedures.…”
Section: Introductionmentioning
confidence: 99%
“…7,8 Hence, the regulation and detection of uoride attracted considerable attention. Over the past decade a number of uoride ion sensors based on different signaling mechanisms, such as intramolecular charge transfer, 9,11,12 photo-induced electron transfer, [13][14][15][16][17][18][19][20][21][22] uorescence resonance energy transfer, [23][24][25][26][27] twisted intramolecular charge transfer, 28,29 excited state proton transfer, [30][31][32][33][34][35][36][37][38][39][40][41] metal-ligand charge transfer, [42][43][44][45][46] and excimer/exciplex [47][48][49] formation, have been used. However most of the reported probes suffer from low sensitivity (or) slow response, turn-off uorescence response and complicated synthetic procedures.…”
Section: Introductionmentioning
confidence: 99%
“…The development of selective and efficient sensors is of prime importance owing to their applications in biological, and analytical processes. 1-8 A number of sensors or probes have been reported for the detection of different analytes based on intramolecular charge transfer, 9,10 photoinduced electron transfer, [11][12][13][14][15] uorescence resonance energy transfer, [16][17][18][19][20] excimer/exciplex formation, [21][22][23] metal-ligand charge transfer, [24][25][26][27] and twisted intramolecular transfer. 28 Another unique process known as excited state intramolecular proton transfer (ESIPT) has given promising materials with applications ranging from organic light emitting diodes to uorescent probes.…”
Section: Introductionmentioning
confidence: 99%
“…Most of the sensor-anion interactions are based on hydrogen bonding interaction and some of them are followed by sensor deprotonation [4][5][6]. Furthermore, the chemosensor sensing mechanisms have been suggested as intramolecular charge transfer (ICT) [7], photoinduced electron transfer (PET) [8], excited states proton transfer (ESPT) [9], and metal-ligand charge transfer (MLCT) [10]. Chalcone derivative, 3-(4-hydroxy-3-methoxy phenyl)-1-phenyl-2-propen-1-one (1), is promising candidate for anion chemosensor because of its ability for proton donating in hydrogen bonding interaction and its conjugation system through phenol ring and enone group [11][12].…”
Section: Introductionmentioning
confidence: 99%