首页> 外文期刊>Acta crystallographica. Section F, Structural biology communications >Synthesis and characterization of a cadmium(II)-organic supramolecular coordination compound based on the multifunctional 2-amino-5-sulfobenzoic acid ligand
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Synthesis and characterization of a cadmium(II)-organic supramolecular coordination compound based on the multifunctional 2-amino-5-sulfobenzoic acid ligand

机译:基于多官能2-氨基-5-磺苯甲酸配体的镉(II) - 多辐射共同配位化合物的合成与表征

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Much attention has been paid by chemists to the construction of supramolecular coordination compounds based on the multifunctional ligand 5-sulfosalicylic acid (H(3)SSA) due to the structural and biological interest of these compounds. However, no coordination compounds have been reported for the multifunctional amino-substituted sulfobenzoate ligand 2-amino-5-sulfobenzoic acid (H(2)asba). We expected that H2asba could be a suitable building block for the assembly of supramolecular networks due to its interesting structural characteristics. The reaction of cadmium(II) nitrate with H2asba in the presence of the auxiliary flexible dipyridylamide ligand N,N'-bis[(pyridin-4-yl)-methyl]oxamide (4bpme) under ambient conditions formed a new mixed-ligand coordination compound, namely bis(3-amino-4-carboxybenzenesulfonato-kappa O-1)-diaquabis{N,N'-bis[(pyridin-4-yl)methyl]oxamide-kappa N}cadmium(II)-N,N'-bis-[(pyridin-4-yl)methyl]oxamide-water (1/1/4), [Cd(C7H6NO5S)(2)(C14H14-N4O2)(2)(H2O)(2)]center dot C14H14N4O2 center dot 4H(2)O, (1), which was characterized by single crystal and powder X-ray diffraction analysis (PXRD), FT-IR spectroscopy, thermogravimetric analysis (TG), and UV-Vis and photoluminescence spectroscopic analyses in the solid state. The central Cd-II atom in (1) occupies a special position on a centre of inversion and exhibits a slightly distorted octahedral geometry, being coordinated by two N atoms from two monodentate 4bpme ligands, four O atoms from two monodentate 4-amino-3-carboxybenzene-sulfonate (Hasba(-)) ligands and two coordinated water molecules. Interestingly, complex (1) further extends into a threefold polycatenated 0D-->2D (0D is zero dimensional and 2D is two-dimensional) interpenetrated supramolecular two-dimensional (4,4) layer through intermolecular hydrogen bonding. The inter layer hydrogen bonding further links adjacent threefold polycatenated two-dimensional layers into a three-dimensional network. The optical properties of complex (1) indicate that it may be used as a potential indirect band gap semiconductor material. Complex (1) exhibits an irreversible dehydration-rehydration behaviour. The fluorescence properties have also been investigated in the solid state at room temperature.
机译:由于这些化合物的结构和生物学兴趣,化学家基于多官能配体5-磺化水杨酸(H(3)SSA)的基于多官能配体5-磺化水杨酸(H(3)SSA),所关注的注意力很大。然而,没有向多官能氨基取代的磺苯甲酸配体2-氨基-5-磺苯甲酸(H(2)ASBA)报道任何配位化合物。由于其有趣的结构特征,我们预计H2ASBA可以是用于组装超分子网络的合适构建块。在环境条件下在辅助柔性双吡啶胺配体N,N'-BIS [(Pyridin-4-基) - 甲基]氧酰胺(4BPME)下,柠檬酸镉与H2ASBA的反应形成了新的混合配体配位化合物,即双(3-氨基-4-羧基苯磺酸氟磺酰-Kappa O-1) - Diaquabis {N,N'-Bis [(吡啶-4-基)甲基]氧酰胺-Kappa n}镉(II)-N,n '-BIS - [(吡啶-4-基)甲基]氧酰胺 - 水(1/1/4),[Cd(C7H6NO5)(2)(2)(C14H14-N4O2)(2)(2)(H2O)(2)]中心点C14H14N4O2中心点4H(2)O,(1),其特征在于单晶和粉末X射线衍射分析(PXRD),FT-IR光谱,热重分析(TG)和UV-Vis和光致发光光谱分析固态。 (1)中的中央CD-II原子占据了反转中心的特殊位置,并且表现出略微扭曲的八面体几何形状,由来自两个单齿4bpme配体的两个n原子协调,来自两个单常液4-氨基-3的四个O原子 - 羧苯甲酸盐(HASBA())配体和两个配位水分子。有趣的是,复合物(1)进一步延伸到三折叠的0d - > 2d(0d为零尺寸,2d是二维)穿过分子间氢键相互间隔的超分子二维(4,4)层。间氢键合相邻的三折叠多升二维层进一步连接到三维网络中。复合物(1)的光学性质表明它可以用作潜在的间接带隙半导体材料。复合物(1)表现出不可逆的脱水再水合行为。还在室温下在固态中研究了荧光性质。

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