2022
DOI: 10.1016/j.molstruc.2021.131439
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Mono- and oligonuclear complexes based on a o-vanillin derived Schiff-base ligand: Synthesis, crystal structures, luminescent and electrochemical properties

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Cited by 8 publications
(9 citation statements)
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“…The involvement of the phenolic oxygen atoms in the metal-ligand bonding is confirmed by the strong doublet bands observed at 1251 cm −1 , 1218 cm −1 1 and 1248 cm −1 , 1219 cm −1 2, respectively. The typical absorption band of the ν aryl -O vibration is identified in the free ligand spectrum at 1233 cm −1 [4,13,[38][39][40][41][42][43][44]. All these spectroscopic features are confirmed by the X-ray structures.…”
Section: Infrared Spectramentioning
confidence: 55%
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“…The involvement of the phenolic oxygen atoms in the metal-ligand bonding is confirmed by the strong doublet bands observed at 1251 cm −1 , 1218 cm −1 1 and 1248 cm −1 , 1219 cm −1 2, respectively. The typical absorption band of the ν aryl -O vibration is identified in the free ligand spectrum at 1233 cm −1 [4,13,[38][39][40][41][42][43][44]. All these spectroscopic features are confirmed by the X-ray structures.…”
Section: Infrared Spectramentioning
confidence: 55%
“…In recent years, much progress in the synthesis and investigation of heteronuclear 3d-4f Schiff base coordination compounds has been observed [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18]. Their crystal structures and properties are determined by several factors, e.g., type of the metal ions, metal-to-ligand stoichiometry, the nature and position of the ligands, methods of synthesis (a stepwise reaction or one-pot reaction, Figure 1), type of solvents, kind of coligands, etc.…”
Section: Introductionmentioning
confidence: 99%
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“…The IR spectrum of the ligand H 2 AD1Me exhibited a strong band at 1636 cm –1 assignable to the azomethine ν(C=N) group. 24 , 25 Upon complexation, the ν(C=N) and ν(C–N) shifted to lower frequencies by of 26–28 cm –1 and 7–13 cm –1 , respectively, a strong indicator that imine nitrogen is involved in coordination with metal ions. 3 This was also supported by the appearance of new peaks of 568 and 545 cm –1 assignable to ν(Pd–N) and ν(Ni–N), respectively.…”
Section: Resultsmentioning
confidence: 99%
“…The IR spectrum of the ligand H 2 AD1Me exhibited a strong band at 1636 cm −1 assignable to the azomethine ν(C�N) group. 24,25 Upon complexation, the ν(C�N) and ν(C−N) shifted to lower frequencies by of 26−28 cm −1 and 7−13 cm −1 , respectively, a strong indicator that imine nitrogen is involved in coordination with metal ions. 3 This was also supported by the appearance of new peaks of 568 and 545 cm −1 assignable to ν(Pd−N) and ν(Ni−N), respectively.…”
Section: Physicochemical and Spectroscopic Characterizationmentioning
confidence: 99%