趙素琴　顧金忠（青海民族大學物理與電子信息工程學院，西寧　80007）（蘭州大學化學化工學院，蘭州　730000）

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配位聚合物［Fe（HL）（H2O）］n的合成、晶體結(jié)構(gòu)及磁性質(zhì)

趙素琴＊，1顧金忠＊，2
（1青海民族大學物理與電子信息工程學院，西寧810007）
（2蘭州大學化學化工學院，蘭州730000）

摘要：通過水熱方法，采用H3L（H3L=2-（4-carboxypyridin-3-yl）terephthalic acid）與FeSO4·7H2O反應(yīng)，合成了一個具有二維結(jié)構(gòu)的配位聚合物［Fe（HL）（H2O）］n（1），并對其結(jié)構(gòu)和磁性質(zhì)進行了研究。結(jié)構(gòu)分析結(jié)果表明該聚合物的晶體屬于正交晶系，Pnna空間群，a=1.454 65（11）nm，b=2.474 23（15）nm，c=0.735 65（4）nm，V=2.647 7（3）nm3，Dc=1.802 g·cm-3，Z=8，R=0.046 8，wR=0.125 6（I 2σ（I）。HL2-配體交替連接相鄰的鐵(Ⅱ)離子形成了一維鏈結(jié)構(gòu)單元，這些鏈又通過配體與鐵(Ⅱ)離子的配位作用形成了二維層。最后這些層通過氫鍵作用形成了一個復雜的三維超分子框架。拓撲分析表明，配合物1具有一個雙節(jié)4，4-連接的拓撲網(wǎng)絡(luò)結(jié)構(gòu)其拓撲符號為（43.62.8）。研究表明，該聚合物中相鄰鐵(Ⅱ)離子之間存在反鐵磁相互作用。

關(guān)鍵詞：配位聚合物；鐵(Ⅱ)配合物；磁性

青海省應(yīng)用基礎(chǔ)研究計劃項目（No.2015-ZJ-738）資助。

＊通信聯(lián)系人。E-mail：qhzhsq@sina.com，gujzh@lzu.edu.cn；會員登記號：S06N5892M1004。

0　Introduction

Recently，the design and synthesis of transition metal functional coordination polymers have received enormousattentionfortheirappealingstructural topologies as well as potential applications such as gas storage，magnetism，luminescence and catalysis，etc［1-6］.However，it is still a great challenge to generate compounds with desirable structural features and properties，since a lot of factors can influence the result，such as coordination geometries of metal ions，main organic ligands，introduction of auxiliary ligands，variation in reaction temperatures，ratios of reagents，types of solvents，pH values，crystallization conditions，etc［7-12］.In this regard，diverse multicarboxylic or heterocyclic carboxylic acids are frequently used as multifunctional building blocks in generating coordination polymers，not only because of their ability to lead to different coordination modes and exhibit high thermal stability，but also due to their possibility to act as good H-bond donors and acceptors［3-5，13-16］.In order to extend our investigations in this field，we chose 2-（4-carboxypyridin-3-yl）terephthalic acid（H3L）as a functional ligand，based on the following considerations:first，H3L should be an excellent bridging ligand for the construction of coordination polymers，sinceithasdiversifiedcoordinationmodesand flexible conformation，in which pyridyl and phenyl rings can rotate around the C-C bond；second，to the best of our knowledge，H3L ligand has not been adequately explored in the construction of coordination polymers.Herein，we report the synthesis，crystal structure，magnetic properties of Fe(Ⅱ)compound with H3L ligand.

1　Experimental

1.1Reagents and physical measurements

All chemicals and solvents were of AR grade and used without further purification.Carbon，hydrogen and nitrogen were determined using an Elementar VarioELelementalanalyzer.IRspectrawere recorded using KBr pellets and a Bruker EQUINOX 55 spectrometer.Thermogravimetric analysis（TGA） data were collected on a LINSEIS STA PT1600 thermal analyzer with a heating rate of 10℃·min-1. PowderX-raydiffractionpatterns（PXRD）were determined with a Rigaku-Dmax 2400 diffractometer using Cu Kα radiation（λ=0.154 060 nm）and 2θ ranging from 5°to 45°，in which the X-ray tube was operated at 40 kV and 40 mA.Magnetic susceptibility data were collected in the 2～300 K temperature range with a Quantum Design SQUID Magnetometer MPMS XL-7 with a field of 0.1 T.A correction was made for the diamagnetic contribution prior to data analysis.

1.2Synthesis of the title complex

A mixture of FeSO4·7H2O（0.083 g，0.3 mmol），H3L（0.073 g，0.3 mmol），NaOH（0.024 g，0.6 mmol），and H2O（10 mL）was stirred at room temperature for 15 min，and then sealed in a 25 mL Teflon-lined stainless steel vessel，and heated at 160℃for 3 days，followed by cooling to room temperature at a rate of 10℃·h-1.Red block-shaped crystals of 1 were isolated manually，and washed with distilled water.Yield:60% （based on Fe）.Anal.Calcd.for C14H9FeNO7（%）:C 46.83，H 2.53，N 3.90；Found（%）:C 46.52，H 2.51，N 3.95.IR（KBr，cm-1）:3 601m，3 422m，1 716s，1 588s，1548s，1480w，1 388vs，1 290w，1 238m，1 170w，1 124 w，1 038w，946w，860w，814w，784w，744m，698m，664 w，566w，486w.

The compound is insoluble in water and common organic solvents，such as methanol，ethanol，acetone，and DMF.

1.3Structure determination

Single-crystal data of compound 1 were collected at 293（2）K on a Bruker Smart Apex 1000 CCD diffractometer with Cu Kα radiation（λ=0.154 184 nm）.A summary of the crystallography data and structure refinement is given in Table 1，and selected bond lengthsandanglesarelistedinTable2.The structures were solved using direct methods，which yielded the positions of all non-hydrogen atoms.These were refined first isotropically and then anisotropically.All the hydrogen atoms were placed in calculated positions with fixed isotropic thermal parameters and included in structure factor calculations in the final stage of full-matrix least-squares refinement.Allcalculations were performed using the SHELXTL-97 system［17］.

CCDC:1437796.

Table 1　Crystal data for compound 1

Table 2　Selected bond distances（nm）and bond angles（°）for compound 1

Table 3　Hydrogen bond lengths（nm）and angles（°）of complex 1

2　Results and discussion

2.1Crystal structure

The X-ray crystallography analysis reveals that the compound 1 crystallizes in the orthorhombic system space group Pnna.As shown in Fig.1，the asymmetric unit of 1 contains two crystallographically unique Fe(Ⅱ)atoms（half occupancy），one HL2-ligand and one coordinated H2O molecule.Both Fe1 and Fe2 atoms possess a distorted octahedral coordination environment.The Fe1 center is coordinated by four O and two N atoms from the four different HL2-blocks The Fe2 center is also bound by four O atoms from the four different HL2-ligands and two O atoms from two coordinated water molecules.The Fe-O（0.205 0（3 ～0.229 2（4）nm）and Fe-N（0.220 3（3）nm）bond lengths are in good agreement with those observed insome other related Fe(Ⅱ)compounds［18-20］.In 1，the HL2-spacer exhibits a μ4-coordination mode（Scheme 1），in which the two deprotonated carboxylate groups show the μ2-η1∶η1and μ2-η2∶η0bidentate modes.The dihedral angle between the pyridyl and phenyl rings in the HL2-is 57.54°.The HL2-moieties alternately link the adjacent Fe(Ⅱ) centers to form a 1D chain motif with the Fe…Fe separation of 0.391 4（4）nm （Fig.2）.These 1D motifs are arranged into a 2D sheet structure by further coordination interactions of the HL2-ligands to Fe(Ⅱ) ions（Fig.2）.For topological analysis［21-22］，the 2D metal-organic network in 1 was simplified（terminal H2O ligands omitted，μ4-HL2-moieties reduced to centroids）to give an underlying binodal 4，4-connected layer（Fig.3）.It is built from the 4-connected topologically equivalent Fe1/Fe2 and μ4-HL2-nodes and features an topology［21-22］defined by the point symbol of（43.62.8）.Furthermore，the neighboring metal-organic sheets in 1 are assembled，through the O-H…O hydrogen bonds，into a 3D supramolecular framework（Fig.4）

Scheme 1　Coordination mode of HL2-ligand in compound 1

Fig.1　Drawing of the asymmetric unit of compound 1

Fig.2　Perspective of the 2D metal-organic sheet parallel to the ac plane

Fig.3　Perspective of the 3D supramolecular framework parallel to the ab plane

Fig.4　Topological representation of the underlying 2D metal-organic network showing a binodal 4，4-connected layer with the unique topology defined by the point symbol of（43.62.8）

2.2TGA analysis and PXRD result

Thethermalstabilityofcompound1was investigated under nitrogen atmosphere by thermogravimetric analysis（TGA）.As shown in Fig.5，the TGA curve of the compound 1 indicates that there is one distinct thermal effect in the 122～270℃ range，which corresponds to the removal of one coordinated H2O molecule（Obsd.5.1%；Calcd.5.0%）.Further heating up to 416℃ leads to the decomposition of dehydrated sample.

Fig.5　TGA curve of compound 1

Powder X-ray diffraction（PXRD）experiment for compound 1 has been carried out at room temperature to identify whether the crystal structure can represent the bulk samples.As shown in Fig.6，the peak positions of the PXRD pattern closely match the simulated ones，thus indicating that the as-synthesized bulk material is pure product.

Fig.6　PXRD pattern of compound 1 at room temperature

Fig.7　Temperature dependence of χMT（○）and 1/χM（□）for compound 1

2.3Magnetic properties

Variable-temperaturemagneticsusceptibility studies were carried out on powder samples of 1 in the 2～300 K temperature range.As shown in Fig.7 the χMT value at 300 K is 3.61 cm3·mol-1·K，which i larger than the spin-only value 3.00 cm3·mol-1·K for magnetically isolated high-spin Fe(Ⅱ)center（S=2，g= 2.0），as expected for the presence of an orbital contri bution in octahedral Fe(Ⅱ)［20，23］.As the temperature i lowered，the χMT values gradually decrease to 0.68 cm3·mol-1·K at 2.0 K，which indicates the presence o an antiferromagnetic interaction in 1.Between 2.0 and 300 K，the magnetic susceptibility can be fitted to the Curie-Weiss law with CM=3.64 cm3·mol-1·K and θ= -3.91 K.These results indicate an antiferromagnetic interaction between the adjacent Fe(Ⅱ)ions.According to the crystal structure of 1，compound 1 can b consideredas1Dchainfromtheviewpointo magnetism due to long distance between the chain motifs.We tried to fit the magnetic data of 1 usin the following expression for a 1D Fe(Ⅱ)chain［23-24］: Where μ is the Langevin function: And J is the parameter of exchange interaction between two Fe(Ⅱ) ions bridged by the carboxylate groups.Using this rough model，the susceptibilities for 1 were simulated，leading to J=-2.57 cm-1，g=2.04，and the agreement factor R=5.19×10-5（R=∑（χobsT-χcalcT）2∑（χobsT）2）.The negative J parameter confirms that an antiferromagnetic exchange coupling exists between the adjacent Fe(Ⅱ)centers，which is agreement with a negative θ value.There are two sets of magnetic exchange pathways within the chain motif，which consist of one carboxylate group in syn-syn fashion and one η2-O bridge from the μ2-carboxylate group，cooperatively contributed by theantiferromagnetic coupling transported by mixed bridges.

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中圖分類號：O614.81+1

文獻標識碼：A

文章編號：1001-4861（2016）05-0853-06

DOI：10.11862/CJIC.2016.114

收稿日期：2015-11-21。收修改稿日期：2016-04-02。

Synthesis，Crystal Structure and Magnetic Property of a Coordination Polymer［Fe（HL）（H2O）］n

ZHAO Su-Qin＊，1GU Jin-Zhong＊，2
（1College of Physics and Electronic Information Engineering，Qinghai University for Nationalities，Xining，Qinghai 810007，China）
（2College of Chemistry and Chemical Engineering，Lanzhou University，Lanzhou 730000，China）

Abstract：A coordination polymer，namely［Fe（HL）（H2O）］n（1），has been synthesized hydrothermally using H3L（H3L= 2-（4-carboxypyridin-3-yl）terephthalic acid）and FeSO4·7H2O.The compound crystallizes in the orthorhombic system，space group Pnna with a=1.454 65（11）nm，b=2.474 23（15）nm，c=0.735 65（4）nm，V=2.647 7（3）nm3Dc=1.802 g·cm-3，Z=8，R=0.046 8 and wR=0.125 6（I＞2σ（I）.The HL2-moieties alternately link the adjacent Fe(Ⅱ)centers to form a 1D chain motif.These 1D motifs are arranged into a 2D sheet structure by further coordination interactions of the HL2-ligands to Fe(Ⅱ) ions.Furthermore，the neighboring metal-organic sheets in 1 ar assembled，through the O-H…O hydrogen bonds，into a complex 3D supramolecular framework.For topologica analysis，the 2D metal-organic network in 1 is a binodal 4，4-connected layer，which is defined by the poin symbol of（43.62.8）.Magnetic studies for compound 1 show a weak antiferromagnetic coupling between the neares Fe(Ⅱ)centers，with g=2.04 and J=-2.57 cm-1.CCDC:1437796.

Keywords：coordination polymer；iron(Ⅱ)complex；magnetic properties