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Role of the orientation of -OH groups in the sensitivity and selectivity of the interaction of M(2+) with ribosyl- and galactosyl-imino-conjugates

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Title Role of the orientation of -OH groups in the sensitivity and selectivity of the interaction of M(2+) with ribosyl- and galactosyl-imino-conjugates
 
Creator SINGHAL, NK
MITRA, A
RAJSEKHAR, G
SHAIKH, MM
KUMAR, S
GUIONNEAU, P
RAO, CP
 
Subject tetranuclear copper(ii) complexes
proton-transfer reaction
fluorescent chemosensor
metal-ions
cu(ii) complex
base ligand
oxygen-atom
hinge sugar
cu2+ ion
sensors
 
Description Three glyco-conjugates, viz., L(1), L(2) and L(3), which differ either in their carbohydrate moiety or in their aromatic moiety or both, were synthesized and characterized and were shown to have beta-anomeric form based on (1)H NMR and optical rotation studies. Metal ion interaction studies carried out in solution by emission and absorption spectral techniques exhibited selectivity towards Cu(2+) in HEPES buffer and a two fold higher sensitivity for L(2) as compared to L(1). The composition of the complexed species has been established based on ESI MS. Dinuclear-Cu(II) complexes of all these conjugates have been synthesized and characterized based on analytical and spectral methods including FTIR, (1)H NMR, FAB MS, EPR, ORD, CD and magnetism, and the structures of 1 and 3 have been established based on single crystal XRD. The structures revealed subtle differences present in the orientation of the -OH groups and also their ion binding preferences both at the molecular level as well as at the lattice levels. In the dinuclear-Cu(II) complexes, while C3-O(-) of ribosyl acts as a bridging moiety in 1, it is the C2-O(-) of galactosyl that bridges in 3 and the Cu(2)O(2) cores are stabilized by two intra-complex H-bond interactions formed using C4-OH in the case of 1 and C3-OH in the case of 3. While the glyco-moiety is poised perpendicular to the average plane of the Cu(2)O(2) core in 1, this is in plane in the case of 3.
 
Publisher ROYAL SOC CHEMISTRY
 
Date 2011-08-28T17:24:12Z
2011-12-26T12:58:08Z
2011-12-27T05:47:33Z
2011-08-28T17:24:12Z
2011-12-26T12:58:08Z
2011-12-27T05:47:33Z
2009
 
Type Article
 
Identifier DALTON TRANSACTIONS, (39), 8432-8442
1477-9226
http://dx.doi.org/10.1039/b903668g
http://dspace.library.iitb.ac.in/xmlui/handle/10054/11798
http://hdl.handle.net/10054/11798
 
Language en