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    Synthesis, Crystal Structure and Properties of a New Coordination Polymer Constructed with 3-(4-hydroxypyridinium-1-yl)phthalic Acid

    2014-12-15 08:58:08LIFuAnBAISuZhenLIXingWuCHENQun
    結(jié)構(gòu)化學 2014年5期

    LI Fu-An BAI Su-Zhen LI Xing-Wu CHEN Qun

    ?

    Synthesis, Crystal Structure and Properties of a New Coordination Polymer Constructed with 3-(4-hydroxypyridinium-1-yl)phthalic Acid

    LI Fu-Ana①BAI Su-ZhenaLI Xing-WuaCHEN Quanb①

    a(467000)b(471023)

    3-(4-hydroxypyridinium-1-yl) phthalic acid, polymer, binuclear nickel unit

    1 INTRODUCTION

    The construction of new supramolecular coordina- tion polymers attracts fast growing interest in the fields of coordination chemistry, not only for the creation of various interesting structures, but also for the potential applications of new functional ma- terials[1-5]. Tactical selection of the organic ligand is a key factor for designing metal-organic coordina- tion polymers. In general, structural motifs of the coordination polymers are closely related to the geometry and the number of coordination sites pro- vided by organic ligands, and some characteristics of the supramolecules are related to noncovalent interactions such as hydrogen bonding[6-7]interaction. Therefore, both structure of the organic ligand and the presence of noncovalent interactions are very important factors for the construction of supramo- lecular coordination polymers.

    Since carboxylate groups can adopt different bin- ding modes to construct exciting networks, organic aromatic polycarboxylate ligands have been exten- sively employed in the preparation of coordination polymers[8]. As an important family of multidentate O-donor ligands, 3-(4-hydroxyl-pyridinium-1-yl) phthalic acid (H2dpa) is a very good candidate for building supramolecular coordination polymers. Firstly, the abundant functional groups on this ligand can adopt various coordinate modes such as terminal monodentate, chelating one metal ion, bridging two metal ions in,and, and in a tridentate form to build interesting polymer archi- tectures, as well as act as hydrogen-bond acceptor to give rise to supramolecular networks;Secondly, this organic ligand has a good water-solubility and is beneficial to investigate the nature of this ligand in hydrothermal conditions. Thirdly, only a few coor- dination polymers constructed from H2dpa have been reported by the literatures[9], and much work is still necessary to understand the coordination che- mistry of H2dpa.

    One good approach for the construction of coor- dination polymers is to perform reactions with mi- xed-ligands such as polycarboxylate and N-contai- ning ligands in the same system, and a great number of new intriguing structures have been obtained[10], which indicates that the introduction of N-containing auxiliary ligands into a metal-polycarboxylate sys- tem often leads to structural changes and affords new networks. From this point of view, we focus on the self-assembly of Ni(II) and carboxylate incor- porating bpe as an auxiliary ligand to intrigue struc- ture and obtained a new metal-organic framework, {[Ni(dpa)(bpe)(H2O)]2}(1), and its thermal analy- sis and UV-vis absorption spectrahave also been investigated. In this paper, we should report the coordination polymer 1.

    2 EXPERIMENTAL

    2. 1 Materials and measurements

    3-(4-Hydroxypyridinium-1-yl) phthalic acid was synthesized according to the literature[11]. The single crystal of complex 1 was obtained through hydro- thmaerl method in a Teflon-lined stainless steel container. Other starting materials were of reagent grade and obtained commercially without further purification. Elemental analyses for C, H and N were performed on a Perkin-Elmer 240 elemental analyzer. Thermal analysis was carried out on a SDT 2960 thermal analyzer from room temperature to 800 ℃at a heating rate of 20 ℃/min under nitrogen flow. The FT-IR spectra were recorded from KBr pellets in the range of 4000~400 cm?1on a Nicolet NEXUS 470-FTIR spectrometer. Solid UV-visible spectra were obtained in the 200~800 nm range on a JASCO UVIDEC-660 spectrophotometer.

    2. 2 Synthesis of complex 1

    Complex 1 was synthesized hydrothermally in a Teflon-lined stainless steel container by heating a mixture of H2dpa (0.0130 g, 0.05 mmol), bpe (0.0091 g, 0.05 mmol), Ni(NO3)2·6H2O (0.0145 g, 0.05 mmol) and KOH (0.0056 g, 0.1 mmol) in 7 mL of distilled water at 150 ℃ for 3 d. Subsequent cooling to room temperature yielded block crystals of 1 (75% yield based on nickel). C25H19N3NiO6(516.14): calcd. (%) C, 58.17; H, 3.71; N, 8.14. Found (%): C, 58.25; H, 3.64; N, 8.23. IR/cm?1(KBr): 3427(m), 2924(w), 1637(s), 1607(s), 1584(s), 1559(s), 1384(s), 1339(w), 1285(w), 1191(m), 1114 (s), 893(w), 839(w), 618(w).

    2. 3 Crystallographic data collection and structure determination

    Single-crystal X-ray diffraction data of 1 were collected on a Bruker Smart Apex CCD diffracto- meter[12]equipped with graphite-monochromatized Moradiation (= 0.71073 ?) at room tempe- rature using the-scan technique. Empirical absorp- tion corrections were applied to the intensities using the SADABS program[13]. The structure was solved by direct methods using SHELXS-97[14]computer program and refined by full-matrix least-squares methods on2with the SHELXL-97[15]program package. All non-hydrogen atoms were subjected to anisotropic refinement. The hydrogen atoms of organic ligands and the coordination water mole- cules were included in the structure factor calcu- lation at the idealized positions using a riding model and refined isotropically. The selected bond distan- ces and bond angles for complex 1 are listed in Table 1.

    Table 1. Selected Bond Lengths (?) and Bond Angles (°)

    Symmetry transformations used to generate the equivalent atoms: #1: –+1, –+2, –

    3 RESULTS AND DISCUSSION

    3. 1 Crystal structure description

    In 1, {[Ni(dpa)(bpe)(H2O)]2}n, the asymmetric unit consists of one Ni center, one bpe (two one-half BPE) molecule, one coordination water and one completely deprotonated dpa2-anion (Fig. 1). As illustrated in Fig. 2, the coordinated environment around the Ni(II) center can be described as a distor- ted octahedron coordination geometry [NiN2O4], where each Ni ion is six-coordinated by three car- boxylate oxygen atoms (O(1), O(2) and O(4#1)) from two different dpa2-ligands, one coordinated water molecule (O(1W) and two nitrogen atoms (N(1) and N(2)) from two different bpe ligands. The Ni-N bond lengths are 2.090(3) and 2.098(3) ?, and the Ni-O bond lengths fall in the range of 2.062(3)~2.189(3) ?, which are in good agreement with those reported in other Ni(II) complexes with N,O-mixed ligands[16]. As shown in Fig. 2, the carboxylate groups adopt the chelating bidentate and monodentate coordination modes to connect the two Ni ions and form a dinuclear unit with the Ni···Ni distance about 5.267(2) ?. The dinuclear units are linked by the bpe ligands to give rise to a metal-organic layer (Fig. 3).

    Fig. 1. (a) Coordination modes of dpa2-ligand. (b) Coordination modes of the bpe ligand. All of the hydrogen atoms are omitted for clarity

    Fig. 2. Coordination environment of Ni(II) ion and the binuclear structure unit in complex 1. The hydrogen atoms are omitted for clarity. Symmetric code: #1: –+1, –+2

    Fig. 3. Two-dimensional structure of complex 1. The hydrogen atoms are omitted for clarity

    Hydrogen bonding interactions are generally very important for generating supramolecular architec- tures[17]. In 1, the coordinated water molecule O(1W) is hydrogen-bonded to carboxyl group O(3)#1 through the O(1W)···O(3)#1 to consolidate the 2D sheet, and intersheet hydrogen bonding O(1W)···O(2)#4 further extends the 2D sheet into a 3D supra- molecular framework (Fig. 4, Table 2).

    Fig. 4. 3D net connected by hydrogen bonding (dotted lines) interactions. Symmetry code: #4: –, 2–, –

    Table 2. Hydrogen-bond geometry (?, °)

    Symmetry codes: #1: –+1, –+2, –; #4: –, –+2, –

    3. 2 Thermal analysis

    Thermogravimetric analysis (TGA) was con- ducted to study the thermal stability of complex 1, which is an important aspect of metal-organic frame- work. TGA was performed on crystalline samples of 1 in the range of 40~800 ℃, as depicted in Fig. 5. The framework of 1 can be stable up to 80 ℃. The compound loses its coordinated water molecules from 80to 190 ℃ (obsd. 4.42%, calcd. 3.49%). Then the compound begins to rapidly decompose at 310 ℃, as shown in Fig. 5.

    3. 3 Electronic spectra

    The diffuse-reflectance UV-vis spectra reveal the absorption features of complex 1, the ligand H2dpa and auxiliary ligand bpe (Fig. 6), and the three spectra consist of absorption components in the UV and Vis regions. In the three cases, the intense absorption peaks at 235, 266 and 262 nm for 1, the ligand H2dpa and auxiliary ligand bpe can be ascribed to* transitions of the ligands, whereas the main UV absorption bands at 331 nm for 1 can be attributed to ligand-to-metal charge transfer (LMCT). In the case of complex 1, additional clear peaks in the visible region are observed at 647 nm, which probably respectively originate from thespin-allowed transition of the Ni2+(8) ion in a dis- torted octahedral coordination configuration. The patterns of coordination polymer 1 correspond well with other Ni(II) complexes with N,O-mixed li- gands[18].

    Fig. 5. TGA curve of the title complex

    Fig. 6. UV-vis absorption spectra for complex 1 and the H2dpa and bpe ligands

    ACKNOWLEDGEMENTS

    The authors express thanks to Key Laboratory of Applied Chemistry of Pingdingshan University for financial support.

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    18 October 2013;

    26 December 2013 (CCDC 935130)

    Li Fu-An, born in 1967, majoring in functional coordination chemistry.Fax: +86-375-3718265, E-mail: lifuanpds@163.com Dr. Q. Chen, Fax: +86-379-64232193, E-mail: chenquan05@126.com

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