2014
DOI: 10.1002/ejic.201402422
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Photoluminescence of Zinc Complexes: Easily Tunable Optical Properties by Variation of the Bridge Between the Imido Groups of Schiff Base Ligands

Abstract: International audienceA series of organic–metal chelate complexes of symmetric tetradentate Schiff base ligands derived from salicylaldehyde and 2-hydroxy-1-naphthaldehyde were designed and investigated. The combination of five nonconjugated flexible spacers and five conjugated rigid spacers with four salicylaldehyde derivatives provided a series of forty complexes. The series of blue to red photoluminescent complexes was investigated by UV/Vis absorption and luminescence spectroscopy in solution and in the so… Show more

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Cited by 68 publications
(66 citation statements)
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“…Although an enhancement of the quantum yield of luminescence was observed for Schiff base ligand, no significant variation of the luminescence lifetime was observed. In particular, the lifetimes were determined to be in the nanosecond timescale, which is consistent with values previously determined for fluorescent zinc complexes [ 13 ].…”
Section: Resultssupporting
confidence: 86%
See 1 more Smart Citation
“…Although an enhancement of the quantum yield of luminescence was observed for Schiff base ligand, no significant variation of the luminescence lifetime was observed. In particular, the lifetimes were determined to be in the nanosecond timescale, which is consistent with values previously determined for fluorescent zinc complexes [ 13 ].…”
Section: Resultssupporting
confidence: 86%
“…In addition, luminescent properties of zinc(II) complexes are determined only by the organic ligand because the d-shell of the central ion is completely filled. The luminescent properties of these compounds can be easily varied by changing the nature of substituents in the composition of the ligands [ 13 ].…”
Section: Introductionmentioning
confidence: 99%
“…The solution spectrum of [Zn(sal)](H 2 O) displayed two absorption bands. The first absorption band centered in the range of 260-300 nm could be assigned to a π-π* transition of the aromatic part and n-π* electronic transitions of the nonbonding electrons of the azomethine nitrogen atoms [76]. The second absorption band in the range of 320-400 nm could be attributed to intermolecular metal-ligand interactions within the whole complex (metal-ligand (d-π*) charge transfer (MLCT band)) [77,78].…”
Section: Synthesis and Spectroscopic Characterizationmentioning
confidence: 99%
“…To illustrate the difference of costs, the Pt precursor (PtCl 2 ) is approximately 1100 times more expensive than Zn(OAc) 2 .2H 2 O (0.15 €/gram) which is the standard reagent for the synthesis of Schiff base Zn(II) chelates, and IrCl 3 .2H 2 O is 450 times more expensive than Zn(OAc) 2 .2H 2 O [73]. Considering that reaction yields for the synthesis of Schiff base Zn(II) chelates range between 60% and 90% [74], and that zinc is clearly less toxic than Ru, Ir, and Pt, Schiff base Zn(II) chelates have been thus examined for photopolymerization [75]. However, contrarily to the previous complexes that were phosphorescent materials, meaning that these complexes exhibit long-living excited states in the microsecond timescale, a different situation is found for Zn complexes.…”
Section: Zinc Complexesmentioning
confidence: 99%