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Coordination Polymers Formed by the Mono- and Dinuclear Cu(II) Complexes of 1,1 '-Methylene/thio-bis(2-naphthoxy) Acetic Acid

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Title Coordination Polymers Formed by the Mono- and Dinuclear Cu(II) Complexes of 1,1 '-Methylene/thio-bis(2-naphthoxy) Acetic Acid
 
Creator BAGHEL, GS
CHINTA, JP
KAIBA, A
GUIONNEAU, P
RAO, CP
 
Subject METAL-ORGANIC FRAMEWORKS
ZEOLITIC IMIDAZOLATE FRAMEWORKS
SUPRAMOLECULAR CHEMISTRY
RETICULAR SYNTHESIS
BUILDING-BLOCKS
HOST FRAMEWORKS
MOLECULES
LIGANDS
NETWORK
DESIGN
 
Description A series of five new Cu2+ coordination polymers, namely, {[CuLCH2(DMF)] (DMF)}(n) (1), {[CuLCH2(DMF)(2,2'-bipy)](CH3OH)}(n) (2), {[CuLCH2(2,2'-bipy)](2H(2)O)}(n) (3), {[CuLCH2(H2O)(2,2'-bipy)](2H(2)O)}(n) (5), [Cu-2(L-s)(2)(DMF)(2)](DMF)(CH3OH)(2H(2)O)}(n) (6), and three discrete coordination complexes {[Cu2LCH2(2,2'-bipy)(2)(CH3O)](ClO4)(CH3OH)} (4), {[CuLs(2,2'bipy)]-(CH3OH)} (7), and {[CuLs(1,10-phen)](DMF)} (8) have been prepared by the reaction of Cu(ClO4)(2)(center dot)6H(2)O and 1,1'-methylene-bis(2-naphthoxy acetic acid) (L-CH2) or 1,1'-thiobis(2-naphthoxy acetic acid) (L-S), with or without the presence of 2,2'-bipyridine, under varying reaction conditions or methods of crystallization or both. All the compounds were characterized by elemental analysis, IR, thermogravimetric analysis, and single crystal X-ray diffraction (XRD). The structures of L-CH2 and L-s obtained by single crystal XRD indicated anti-orientation of the pendant arms which upon metal complexation may turn into cis- orientation leading to discrete metal ion complexes or may remain in anti- orientation leading to extended multidimensional co-ordination polymers. The complexation with Cu2+ led to five different coordination spheres which in turn resulted in five different lattice structures. Thus, the present paper demonstrates the design of coordination polymers that are rich with mononuclear as well as dinuclear Cu2+ centers wherein L-CH2 or L-s coordinates in a monodentate as well as a bridging fashion leading to the formation of one-dimensional curving, helical, and two-dimensional networks.
 
Publisher AMER CHEMICAL SOC
 
Date 2014-10-17T05:23:39Z
2014-10-17T05:23:39Z
2012
 
Type Article
 
Identifier CRYSTAL GROWTH & DESIGN, 12(2)914-926
1528-7483
1528-7505
http://dx.doi.org/10.1021/cg2013683
http://dspace.library.iitb.ac.in/jspui/handle/100/16058
 
Language en