2010
DOI: 10.1016/j.saa.2009.10.018
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Synthesis, spectral, crystallography and thermal investigations of novel Schiff base complexes of manganese (III) derived from heterocyclic β-diketone with aromatic and aliphatic diamine

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Cited by 58 publications
(18 citation statements)
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“…The measurements of molecular electronic spectra were used to assign the stereochemistries of metal ions in the metal chelates depending on the sites and number of d–d transition peaks. The electronic absorption spectra of ligands and their metal chelates were measured in the wavelength range 200–800 nm and at 298 K. The ligand exhibits an absorption band in UV–visible area around 400 nm which is attributed to n → π* transition originating from azomethine group of the ligand . The absorption bands of complexes at λ max = 318–484 nm correspond to charge transfer from HNA imine ligand to the metal ion.…”
Section: Resultsmentioning
confidence: 99%
“…The measurements of molecular electronic spectra were used to assign the stereochemistries of metal ions in the metal chelates depending on the sites and number of d–d transition peaks. The electronic absorption spectra of ligands and their metal chelates were measured in the wavelength range 200–800 nm and at 298 K. The ligand exhibits an absorption band in UV–visible area around 400 nm which is attributed to n → π* transition originating from azomethine group of the ligand . The absorption bands of complexes at λ max = 318–484 nm correspond to charge transfer from HNA imine ligand to the metal ion.…”
Section: Resultsmentioning
confidence: 99%
“…[15] The strong band in the Schiff base at 1634 cm --1 underwent a negative shift of about 10--15 cm --1 in the complexes, confirming the coordination of the azomethine N atoms to the metal atoms. [16] The intense absorption at 2079 cm --1 in the spectrum of 2 is due to the vibration of the thiocyanate ligands. The weak absorption …”
Section: Resultsmentioning
confidence: 99%
“…Kompleks 1'de ise görünür bölgede maksimum 452 nm dalga boyunda mor emisyon bandı görülmektedir. Kompleks 1 ile H2L ligandı benzer emisyon bandları gösterdiği için, kompleksin gözlenen emisyonuna da ligand kaynaklı nπ* veya ππ* elektronik geçişi katkıda bulunmaktadır [38,39].…”
Section: Kompleks 1 'In Fotolüminesans öZellikleriunclassified
“…Kompleks 1 ile H2L ligandının emisyon spektrumları karşılaştırıldığında, ligand ile metal atomunun koordinasyon etkisinden dolayı maksimum emisyon bandının yeşilden mor bölgeye kaydığı görülmektedir [39,40]. Kompleks 1'in emisyon bandı H2L ligandına göre daha şiddetlidir.…”
Section: Kompleks 1 'In Fotolüminesans öZellikleriunclassified
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