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  • 1
    Publication Date: 2015-08-08
    Description: Two new coordination polymers (CPs) formed from 5-iodobenzene-1,3-dicarboxylic acid (H 2 iip) in the presence of the flexible 1,4-bis(1 H -imidazol-1-yl)butane (bimb) auxiliary ligand, namely poly[[μ 2 -1,4-bis(1 H -imidazol-1-yl)butane-κ 2 N 3 : N 3′ ](μ 3 -5-iodobenzene-1,3-dicarboxylato-κ 4 O 1 , O 1′ : O 3 : O 3′ )cobalt(II)], [Co(C 8 H 3 IO 4 )(C 10 H 14 N 4 )] n or [Co(iip)(bimb)] n , (1), and poly[[[μ 2 -1,4-bis(1 H -imidazol-1-yl)butane-κ 2 N 3 : N 3′ ](μ 2 -5-iodobenzene-1,3-dicarboxylato-κ 2 O 1 : O 3 )zinc(II)] trihydrate], {[Zn(C 8 H 3 IO 4 )(C 10 H 14 N 4 )]·3H 2 O} n or {[Zn(iip)(bimb)]·3H 2 O} n , (2), were synthesized and characterized by FT–IR spectroscopy, thermogravimetric analysis (TGA), solid-state UV–Vis spectroscopy, single-crystal X-ray diffraction analysis and powder X-ray diffraction analysis (PXRD). The iip 2− ligand in (1) adopts the (κ 1 ,κ 1 -μ 2 )(κ 1 , κ 1 -μ 1 )-μ 3 coordination mode, linking adjacent secondary building units into a ladder-like chain. These chains are further connected by the flexible bimb ligand in a trans – trans – trans conformation. As a result, a twofold three-dimensional interpenetrating α-Po network is formed. Complex (2) exhibits a two-dimensional (4,4) topological network architecture in which the iip 2− ligand shows the (κ 1 )(κ 1 )-μ 2 coordination mode. The solid-state UV–Vis spectra of (1) and (2) were investigated, together with the fluorescence properties of (2) in the solid state.
    Print ISSN: 0108-2701
    Electronic ISSN: 1600-5759
    Topics: Chemistry and Pharmacology , Geosciences , Physics
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  • 2
    Publication Date: 2015-06-16
    Description: Copper(II) coordination polymers have attracted considerable interest due to their catalytic, adsorption, luminescence and magnetic properties. The reactions of copper(II) with 2-amino-4-sulfobenzoic acid (H 2 asba) in the presence/absence of the auxiliary chelating ligand 1,10-phenanthroline (phen) under ambient conditions yielded two supramolecular coordination polymers, namely (3-amino-4-carboxybenzene-1-sulfonato-κ O 1 )bis(1,10-phenanthroline-κ 2 N , N ′)copper(II) 3-amino-4-carboxybenzene-1-sulfonate monohydrate, [Cu(C 7 H 6 N 2 O 5 S)(C 12 H 8 N 2 ) 2 ](C 7 H 6 N 2 O 5 S)·H 2 O, (1), and catena -poly[[diaquacopper(II)]-μ-3-amino-4-carboxylatobenzene-1-sulfonato-κ 2 O 4 : O 4′ ], [Cu(C 7 H 6 N 2 O 5 S)(H 2 O) 2 ] n , (2). The products were characterized by FT–IR spectroscopy, thermogravimetric analysis (TGA), solid-state UV–Vis spectroscopy and single-crystal X-ray diffraction analysis, as well as by variable-temperature powder X-ray diffraction analysis (VT-PXRD). Intermolecular π–π stacking interactions in (1) link the mononuclear copper(II) cation units into a supramolecular polymeric chain, which is further extended into a supramolecular double chain through interchain hydrogen bonds. Supramolecular double chains are then extended into a two-dimensional supramolecular double layer through hydrogen bonds between the lattice Hasba − anions, H 2 O molecules and double chains. Left- and right-handed 2 1 helices formed by the Hasba − anions are arranged alternately within the two-dimensional supramolecular double layers. Complex (2) exhibits a polymeric chain which is further extended into a three-dimensional supramolecular network through interchain hydrogen bonds. Complex (1) shows a reversible dehydration–rehydration behaviour, while complex (2) shows an irreversible dehydration–rehydration behaviour.
    Print ISSN: 0108-2701
    Electronic ISSN: 1600-5759
    Topics: Chemistry and Pharmacology , Geosciences , Physics
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