TY - JOUR
T1 - The coordination polymers poly[μ-4,4′-bipyrid-yl-di-μ-formato- copper(II)] and catena-poly[[[diaqua-(1-benzofuran-2,3-dicarboxyl-ato)copper(II) ]-μ-1,2-di-4-pyridylethane] dihydrate]
AU - Koner, Rajesh
AU - Goldberg, Israel
PY - 2009
Y1 - 2009
N2 - The title compounds, [Cu(CHO2)2(C10H8N2)] n , (I), and {[Cu(C10H4O5) (C12H12N2)(H2O)2]·2H2O} n , (II), are composed of one-dimensional linear coordination polymers involving copper(II) ions and bidentate bipyridyl species. In (I), the polymeric chains are located on twofold rotation axes at (x, x, 0) and are arranged in layered zones centered at z = 0, , and parallel to the ab plane of the tetra-gonal crystal. Weak coordination of the formate anions of one layer to the copper centers of neighboring layers imparts a three-dimensional connectivity to this structure. In (II), the polymeric chains propagate parallel to the a axis of the crystal. Noncoordinated water mol-ecules link the chains through O - H⋯O hydrogen bonding in directions perpendicular to c, imparting to the entire structure three-dimensional connectivity. The metal ions adopt distorted octa-hedral and square-based pyramidal environments in (I) and (II), respectively. This study indicates that, under the given conditions, extended coordination involves CuII centers associating with the bipyridyl ligands rather than with the competing benzofuran-dicarboxyl-ate entities.
AB - The title compounds, [Cu(CHO2)2(C10H8N2)] n , (I), and {[Cu(C10H4O5) (C12H12N2)(H2O)2]·2H2O} n , (II), are composed of one-dimensional linear coordination polymers involving copper(II) ions and bidentate bipyridyl species. In (I), the polymeric chains are located on twofold rotation axes at (x, x, 0) and are arranged in layered zones centered at z = 0, , and parallel to the ab plane of the tetra-gonal crystal. Weak coordination of the formate anions of one layer to the copper centers of neighboring layers imparts a three-dimensional connectivity to this structure. In (II), the polymeric chains propagate parallel to the a axis of the crystal. Noncoordinated water mol-ecules link the chains through O - H⋯O hydrogen bonding in directions perpendicular to c, imparting to the entire structure three-dimensional connectivity. The metal ions adopt distorted octa-hedral and square-based pyramidal environments in (I) and (II), respectively. This study indicates that, under the given conditions, extended coordination involves CuII centers associating with the bipyridyl ligands rather than with the competing benzofuran-dicarboxyl-ate entities.
UR - http://www.scopus.com/inward/record.url?scp=65549166066&partnerID=8YFLogxK
U2 - 10.1107/S0108270109011299
DO - 10.1107/S0108270109011299
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AN - SCOPUS:65549166066
SN - 0108-2701
VL - 65
SP - m185-m189
JO - Acta Crystallographica Section C: Crystal Structure Communications
JF - Acta Crystallographica Section C: Crystal Structure Communications
IS - 5
ER -