2011
DOI: 10.1007/s10973-011-2134-0
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Synthesis, structural, spectroscopic characterization, and structural comparison of 3-hydroxybenzoate and nicotinamide/N,N-diethylnicotinamide mixed ligand complexes with Zn(II)

Abstract: The mixed-ligand 3-hydroxybenzoic acid complex of Zn(II) with nicotinamide and N,N-diethylnicotinamide were synthesized and characterized (colorless single crystals, [Zn(3-hba) 2 (H 2 O) 2 (na) 2 ] and [Zn(3-hba) 2 (H 2 O) 2 (dena) 2 ]). The chemical, FT-IR, thermal, mass spectral analyses, and X-ray data results revealed that both of the compounds contain two water molecules, two 3-hydroxybenzoate (3-hba) and two nicotinamide (na) or two N,N-diethylnicotinamide (dena) ligands per formula unit. 3-hba and na or… Show more

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Cited by 18 publications
(6 citation statements)
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“…As a result of spectral investigation of complexes between nicotinamide and these metals, it was determined that it has ability to bind as monodentate ligand through pyridine nitrogen. [19][20][21].…”
Section: Introductionmentioning
confidence: 99%
“…As a result of spectral investigation of complexes between nicotinamide and these metals, it was determined that it has ability to bind as monodentate ligand through pyridine nitrogen. [19][20][21].…”
Section: Introductionmentioning
confidence: 99%
“…The maximum adsorption band of broaden spectrum owned by Cu II (VII) complex corresponded to the wavelength of approximately 677.49 nm ( 2 E g → 2 T 2g ) [28,29]. There was no any d-d electronic transition for an octahedral splitting possible to occur because fully occupied d orbitals in the last orbit of Zn II (VIII) complex with the diamagnetic feature as seen from the magnetic susceptibility data ( Figure 5) [30][31][32].…”
Section: Solid-state Uv-vis Spectroscopymentioning
confidence: 99%
“…Schemes 2 and 3 show the synthesis reaction scheme of Co(II) cation and Cd(II) cation centered nicotinic S C H E M E 1 Synthesis reaction scheme of sodium salt nicotinicate S C H E M E 2 Synthesis reaction scheme of Co(II) cation centered nicotinic acid/N,Ndiethylnicotinamide mixed ligand complex acid/N,N-diethylnicotinamide mixed ligand complex, respectively. The final total solution was stirred on a magnetic stirrer hot-plate at 60 C for 5 h. [25,55] The beaker in which it was transferred was covered with a perforated paraffin film and left to stand until crystal formation. After about 10-15 days, the respective metal cation complexes were allowed to aggregate as crystals of dark-pink for Co(II) and pale white for Cd(II) and stored for structural analysis.…”
Section: Introductionmentioning
confidence: 99%