2016
DOI: 10.1002/zaac.201600193
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Synthesis, Characterization, and Luminescent Properties of Silver(I) Complexes based on Diphosphine Ligands and 2,9‐Dimethyl‐1,10‐phenanthroline

Abstract: Five mono-nuclear silver(I) complexes with the ligand 2,9dimethyl-1,10-phenanthroline, namely [Ag(DPEphos)(dmp)]BF 4 (1), (4), and [Ag(dppb)(dmp)]NO 3 ·CH 3 OH (5) {DPEphos = bis[2-(diphenylphosphanyl)phenyl]ether, dppb = 1,2bis(diphenylphosphanyl)benzene, dmp = 2,9-dimethyl-1,10-phenanthroline} were characterized by X-ray diffraction, IR, 1 H NMR, 31 P NMR and fluorescence spectroscopy. Their terahertz (THz) time-

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Cited by 10 publications
(12 citation statements)
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“…Due to the difference of the diphosphine ligand, the Ag–P distances in complex 2 (2.417 Å and 2.503 Å) are longer than those in {[Ag(μ‐dppe)(dicnq)](BF 4 ) · (DMF)} n (2.399 Å and 2.438 Å). Meanwhile, the angle P–Ag–P (114.3°) in 2 is smaller than that in the complex above (140.0°) , The angle N–Ag–N (70.0°) in 2 is smaller than that in the complex [Ag(DPEphos)(dmp)]ClO 4 (71.4°) …”
Section: Resultsmentioning
confidence: 68%
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“…Due to the difference of the diphosphine ligand, the Ag–P distances in complex 2 (2.417 Å and 2.503 Å) are longer than those in {[Ag(μ‐dppe)(dicnq)](BF 4 ) · (DMF)} n (2.399 Å and 2.438 Å). Meanwhile, the angle P–Ag–P (114.3°) in 2 is smaller than that in the complex above (140.0°) , The angle N–Ag–N (70.0°) in 2 is smaller than that in the complex [Ag(DPEphos)(dmp)]ClO 4 (71.4°) …”
Section: Resultsmentioning
confidence: 68%
“…Probably due to the different anion, the asymmetric unit in 1 consists of two crystallographic‐separate molecules forming two mono‐nuclear structures with AgP 2 N 2 coordination environment (Figure a), but the asymmetric unit in 2 only consists of one molecule (Figure a). Compared to the similar silver(I) complex early reported, the average Ag–P bond lengths of 2.455 Å and Ag–N bond lengths of 2.370 Å in complex 1 are distinctly shorter than in [Ag(DPEphos)(dmp)]NO 3 (average Ag–P 2.489 Å) and (average Ag–N 2.444 Å), which is assigned to the influence of the different N‐donor ligands.…”
Section: Resultsmentioning
confidence: 88%
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“…Thus, following precedent luminescent copper compounds, various silver compounds have been prepared by applying the corresponding ligand combination, and in several cases, the silver complexes comprising the same coordination environment as that of the copper complexes have been obtained. By expecting that these compounds should have a similar electronic structure, their photophysical properties have been examined. The findings revealed that several silver compounds exhibited luminescence related to the same ES as that of the copper congeners, whereas others either showed luminescence of different origin or were nonemissive. ,, Because Ag 4d orbitals are more energetically stable than Cu 3d orbitals, the MLCT ES of Ag I complexes has higher energy than that of the corresponding Cu I complexes, resulting in the phosphorescence from LLCT or LC ESs for the Ag I complexes in contrast to the 3 MLCT emission of the Cu I complexes. ,,, Fluorescence from the ligand has also been observed when orbitals related to the Ag I center are adequately stable …”
Section: Introductionmentioning
confidence: 99%