二維網(wǎng)狀Pd（Ⅱ）配合物的合成、晶體結(jié)構(gòu)及電化學(xué)性質(zhì)

劉 瑕 劉金明 孫亞光 高恩君 熊 剛 郭美妍

(沈陽(yáng)化工學(xué)院應(yīng)用化學(xué)學(xué)院，沈陽(yáng) 110142)

研究簡(jiǎn)報(bào)

二維網(wǎng)狀Pd（Ⅱ）配合物的合成、晶體結(jié)構(gòu)及電化學(xué)性質(zhì)

劉 瑕＊?jiǎng)⒔鹈?孫亞光 高恩君 熊 剛 郭美妍

(沈陽(yáng)化工學(xué)院應(yīng)用化學(xué)學(xué)院，沈陽(yáng) 110142)

鈀（Ⅱ）配合物； 2，2′-聯(lián)吡啶-3，3′-二羧酸； 晶體結(jié)構(gòu)； 電化學(xué)性質(zhì)

2,2′-bipyridine-3,3′-dicarboxylic acid(H2bpdc)is a typical example of multidentate ligand.In it,nitrogen atom of bipyridyl moiety and oxygen atom of dicarboxyl functional group can act not only as hydrogen bond donors but as acceptors,which make it a wonderful candidate forthe construction ofsupramolecular networks.2,2′-bipyridine-3,3′-dicarboxylic acid has been proved to be a suitable ligand for the formation of 1D,2D and 3D network structures[1-4].In addition,some studies have revealed that its complexes have potential applications as spectroscopic,electrochemical and magnetic materials[5-7].But there are very few reports on ternary transition metal complexes coordinated with it.In this paper,a novel mixed ligand complex with 2,2′-bipyridine-3,3′-dicarboxylic acid and amino acid is synthesized,the crystal structure is determined by single-crystal X-ray diffraction,the electrochemical property of the complex is also further investigated.

1 Experimental

1.1 Reagents and apparatuses

All reagents are analytically pure.IR spectra wereperformed on a NEXUS 470 spectrometer with KBr pellets.Crystal structure determination was carried out on a Rigaku Saturn CCD X-ray diffractometer.The electron transfer behavior of the complex was examined using cyclic voltammogram on a CHI-660c electrochemical analysis system.C,H and N analyses were recorded on a Finnigan EA1112 elemental analyzer.

1.2 Synthesis of the complex

2,2′-bipyridine-3,3′-dicarboxylic acid and Pd(H2bpdc)Cl2were synthesized according to literature[8-9].0.421 g(1 mmol)Pd(H2bpdc)Cl2,was suspended into 20 mL water,and 0.089 g(1 mmol)L-alanine was added.The mixture was stirred for 2 h,then the solution was concentrated in a rotary evaporator.Finally the buff crystals were obtained after four weeks.Anal.Calcd.for C15H20ClN3O9Pd(%):C 34.10,H 3.79,N 7.96;found(%):C 34.25,H 3.24,N 8.23.IR (KBr,cm-1):3516s,3195 w,3099m,1670vs,1570m,1458m,1421m,1362vs,1286m,1243w,1119 m,859 w,831 m,772 m,694 m,517m.

1.3 Structure determination of the complex

All measurements were made on a Rigaku Saturn CCD detector with graphite monochromatized Mo Kα radiation (λ＝0.071 073 nm).The data were collected using φ-ω scans at 113(2)K.A total of 8 144 reflections were collected in the range of 1.54°≤θ≤27.87°,of which 4 179 (Rint＝0.028 1)were independent and 830 were observed(I＞2σ(I)).The structures were solved by direct methods and refined by full matrix least squares on F2with SHELXTL program.All-non hydrogen atoms were refined anisotropically.

CCDC:792221.

2 Results and discussion

2.1 Crystal structure determination

The crystalparametersand detailsofdata collection are summarized in Table 1.The selected bond lengths and bond angles are listed in Table 2.The molecular structure and 2D net structure of the complex are shown in the Fig.1 and 2.

Single-crystal X-ray diffraction analysis indicatesthat the complex crystallizes in P1 space group.The core structure of complex is composed of one[Pd(H2bpdc)Ala]-,one chloride ion and three molecules of H2O as lattice solvent.Pd（Ⅱ）atom is four-coordinated via N1,N2 from H2bpdc,and N3,O5 from L-alanine.From Table 2,bond lengths of N1-Pd1,N2-Pd1,N3-Pd1,O5-Pd1 are 0.199 9(3),0.200 7(3),0.205 3(3)and 0.1989(3)nm,respectively,which are close to those of some Pd（Ⅱ）complexes[10-12].Bond angles of N1-Pd1-N3 and O5-Pd1-N2 are 175.61(13)°and 174.02(12)°respectively,which shows that the coordination geometry is slightly distorted planar square.The two pyridine rings are not planar since the dihedral angle between the pyridine rings of H2bpdc is 18.81°.It is a usual feature for several complexes bridged by the ligands containing 2,2′-bipyridyl unit[13-14].

Table 1 Crystallographic date and details of the structure refinement

Table 2 Selected bond lengths(nm)and bond angles(°)for the title complex

The compl ex is involved in intramolecular π-π stacking and hydrogen bonding interactions,which plays an important role in the formation of the twodimensional supramolecular networks.There are offset face-to-face π-π stacking interactions between the pyridine ring containing N2 and the same pyridine ring positioned in the nearest parallel molecule.Cg1,Cg2 and Cg3 are the centroid of three parallel pyridine ring.They interact via π-π stacking interactions with distance of Cg1-Cg2 0.370 5 nm and Cg2-Cg3 0.370 89 nm,perpendicular distance of the three plane are 0.324 8 nm and 0.3528 nm.Due to these π-π stacking the complex has a 1D zigzag chain structure.The adjacent zigzag chains are linked each other by the hydrogen bond interactions between the uncoordinated carboxyl oxygen atom (O6)of L-alanine and the carbon atom (C9)of the pyridine rings of the adjacent zigzag chain,which lead to a 2D network(Fig.2).

2.2 Electrochemical property

The standard three-electrode system with Au disk working electrode,a Pt rod auxiliary electrode,and the SCE reference electrode was used for electrochemical detection.The cyclic voltammogram of the complex was obtained with 0.001 mol·L-1the complex in water.The scanning rate was 0.1 V·s-1,at the range from 0 to 1.3 V.From the voltammogram curves(Fig.3),it shows only one pair of oxidation-reduction peaks corresponding to the oxidation-reduction couple of Pd2+/Pd,Epa=0.470 V,Epc=1.119 V.The average formal potential(E1/2)is 0.795 V.The peak-to-peak separation between the corresponding anodic and cathodic peak is 0.649 V,exhibiting a irreversible electrode process.

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Synthesis,Crystal Structure and Electrochemical Properties of 2D Network Palladium（Ⅱ）Complex

LIU Xia＊LIU Jin-Ming SUN Ya-Guang GAO En-Jun XIONG Gang GUO Mei-Yan
(Faculty of Applied Chemistry,Shenyang Institute of Chemical Technology,Shenyang 110142)

A novel palladium（Ⅱ） complex[Pd(H2bpdc)Ala]Cl·3H2O(where H2bpdc is 2,2′-bipyridine-3,3′-dicarboxylic acid and Ala is L-alanine)has been synthesized and characterized by IR spectra and elemental analysis.The crystal structure of the complex has been determined by single-crystal X-ray diffraction analysis.It crystallizes in triclinic system,space group P1 with a=0.685 5(2)nm,b=0.988 4(4)nm,c=1.349 6(4)nm,α=98.375(8)°,β=97.900(15)°,γ=90.118(15)°,V=0.8959(5)nm3,Z=2.In the molecule,Pd（Ⅱ） atom is four-coordinated and located at the centre of a planar quadrangle.The complex is assembled via intramolecular π-π stacking interactions and hydrogen bonds,which forms 2D network.The cyclic voltammetric behavior of the complex was also investigated.CCDC:792221.

palladium（Ⅱ） complex;2,2′-bipyridine-3,3′-dicarboxylic acid;crystal structure;electrochemical propert

O614.82+3

A

1001-4861(2010)11-2109-04

2010-05-10。收修改稿日期：2010-08-09。

沈陽(yáng)化工學(xué)院青年科研啟動(dòng)基金(No.200303)資助。

＊通訊聯(lián)系人。 E-mail：laura-lx@163.com

劉 瑕，女，40歲，博士研究生，副教授；研究方向：配位化學(xué)。