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Mononuclear and Dinuclear Manganese(II) Complexes from the Use of Methyl(2-pyridyl)ketone Oxime
Author(s) -
Constantinos G. Efthymiou,
V. Nastopoulos,
Catherine P. Raptopoulou,
Anastasios J. Tasiopoulos,
Spyros P. Perlepes,
Constantina Papatriantafyllopoulou
Publication year - 2010
Publication title -
bioinorganic chemistry and applications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.865
H-Index - 35
eISSN - 1565-3633
pISSN - 1687-479X
DOI - 10.1155/2010/960571
Subject(s) - chemistry , oxime , ketone , manganese , ligand (biochemistry) , crystal structure , medicinal chemistry , chelation , single crystal , stereochemistry , crystallography , inorganic chemistry , organic chemistry , receptor , biochemistry
The reactions of methyl(2-pyridyl)ketone oxime, (py)C(Me)NOH, with manganese(II) sulfate monohydrate have been investigated. The reaction between equimolar quantities of MnSO 4 · H 2 O and (py)C(Me)NOH in H 2 O lead to the dinuclear complex [Mn 2 (SO 4 ) 2 {(py)C(Me)NOH} 4 ] · (py)C(Me)NOH, 1 · (py)C(Me)NOH, while employment of NaOMe as base affords the compound [Mn(HCO 2 ) 2 {(py)C(Me)NOH} 2 ] ( 2 ). The structures of both compounds have been determined by single crystal X-ray diffraction. In both complexes, the organic ligand chelates through its nitrogen atoms. The IR data are discussed in terms of the nature of bonding and the structures of the two complexes.

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