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2-(4 ',4 '-dimethyl-3 ',4 '-dihydrooxazol-2 '-yl)phenol: Some first-row transition metal complexes of this naturally occurring binding group

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Title 2-(4 ',4 '-dimethyl-3 ',4 '-dihydrooxazol-2 '-yl)phenol: Some first-row transition metal complexes of this naturally occurring binding group
 
Creator MUGESH, G
SINGH, HB
BUTCHER, RJ
 
Subject cobalt(ii)-substituted zinc metalloenzymes
monomeric selenolato complexes
im = imidazole
structural characterization
crystal-structures
coordination behavior
r= ch3
ligands
se
n,n-dimethylbenzylamine
oxazolines
metal assisted hydrolysis
hydrogen bonds
chirality
siderophores
 
Description The synthesis and characterization of monomeric Mn-III, Co-II Ni-II, Cu-II, and Zn-II phenolates derived from a biologically relevant ligand, 2-(4',4'-dimethyl-3',4'-dihydrooxazol-2'-yl)phenol (1), are described. The addition of Mn(OAc)(2). 4H(2)O to an ethanolic solution of 1 affords an unexpected 1:3 complex [Mn(OR){O(Ox)}(2)] (2) [R = C6H4CONHC(Me-2) CH2OH, Ox = 2-(4,4-dimethyl-2-oxazolinyl)phenyl] in which one of the five-membered oxazoline rings is partially hydrolyzed. The complexes [M{O(Ox)}(2)] [M = Co (3), Ni (4), Cu (6), or Zn (7)] were prepared in good yield by the reactions of 1 with the corresponding metal acetates. Novel formation of the six-coordinate NP complex 5 with neutral acetic acid was observed during the crystallization process. The complexes were characterized by elemental analysis, magnetic susceptibility, as well as EPR, H-1 NMR, electronic, and mass spectral techniques. Complexes 2, 3, 5, 6, and 7 were characterized by single crystal X-ray diffraction studies. Complex 2 is six-coordinate whereas complexes 3, 6, and 7 are four-coordinate with two oxazoline bidentate Ligands. The geometry around the metal center is found to be distorted tetrahedral for all of the four-coordinate complexes. Complex 5 is octahedral with four coordination sites occupied by the two bidentate oxazoline Ligands and the other two are occupied by two neutral acetic acid molecules. The hydroxy groups of the coordinated acetic acid are hydrogen-bonded to the phenolate oxygen atoms of the oxazoline ligands. The variable-temperature H-1 NMR spectroscopic studies of complex 7 indicate that the interconversion between the (M) and (P) helix is slow at low temperatures.
 
Publisher WILEY-V C H VERLAG GMBH
 
Date 2011-09-01T13:50:38Z
2011-12-26T12:59:40Z
2011-12-27T05:52:18Z
2011-09-01T13:50:38Z
2011-12-26T12:59:40Z
2011-12-27T05:52:18Z
2001
 
Type Article
 
Identifier EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, (3), 669-678
1434-1948
http://dspace.library.iitb.ac.in/xmlui/handle/10054/12795
http://hdl.handle.net/10054/12795
 
Language en