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    Syntheses,Structures and Magnetic Analysis of Co(Ⅰ),Ni(Ⅱ)Coordination Polymers Based on Pyridine-2,4,6-tricarboxylic Acid

    2017-07-05 14:55:49YINXiuJuLIAOBeiLingWUHanMinPANGYiLinLIShiXiong
    關(guān)鍵詞:吡啶配位配體

    YIN Xiu-JuLIAO Bei-LingWU Han-MinPANG Yi-LinLI Shi-Xiong*,,2

    (1College of Chemistry and Biological Engineering,Hechi University,Yizhou,Guangxi 546300,China) (2School of Environment and Energy,South China University of Technology,Guangzhou 510006,China)

    Syntheses,Structures and Magnetic Analysis of Co(Ⅰ),Ni(Ⅱ)Coordination Polymers Based on Pyridine-2,4,6-tricarboxylic Acid

    YIN Xiu-Ju1LIAO Bei-Ling1WU Han-Min1PANG Yi-Lin1LI Shi-Xiong*,1,2

    (1College of Chemistry and Biological Engineering,Hechi University,Yizhou,Guangxi 546300,China) (2School of Environment and Energy,South China University of Technology,Guangzhou 510006,China)

    The title coordination polymers of{[M3(pyta)2(H2O)8]·4H2O}n(M=Co(1),Ni(2))based on H3pyta(H3pyta= pyridine-2,4,6-tricarboxylic acid)had been synthesized under hydrothermal synthesis conditions with same temperature,molar ratio and solvent,but different metal salts.X-ray diffraction analysis shows that these two polymers are hetero-isomorphic and belong to the monoclinic system,P21/c space group.The magnetic investigation shows that polymers 1 and 2 exhibit a ferromagnetic coupling between M(Ⅱ)ions.CCDC:1524314,1;1000880,2.

    coordination polymer;pyridine-2,4,6-tricarboxylic acid;magnetic

    0 Introduction

    Since“single-molecule magnets”(SMMs)were discovered,design and synthesis of the paramagnetic transitionpolymetallicclusterareattractiveto researchers[1-5].Recently many different directions have being pursued in the research field of SMMs[6-11],in which an important direction has been found that the intermolecular interaction with different correlation in the whole molecular arrangement,though very weak, can perturb the intrinsic properties of individual SMMs[12].In our previous work[13-14],we have reported and studied antiferromagnetic(AF)coupling interaction betweenmagneticcenters.Ligands3-/4-pyridinecarboxylateandpyridinecarboxylatehave recently been found to act as excellent buildingblocks with charge and multi-connecting ability in the construction of functional coordination polymers with porosity,photolumineseent or magnetic properties[15-16]. Comparedwiththepreviouslyinvestigated pyridinecarboxylateligands,pyridine-2,4,6-tricarboxylic acid(H3pyta)have the advantages of multiple bridging moieties,which leads to a variety of connection modes with transition metal centers and provides abundant structural motifs.It can act not only as N-donors but also as Ocarboxylate-donors to chelate or bridge metal ions to form coordination polymers[17], and some complexes can act as SMMs[18].In this paper,we report Co(Ⅰ)and Ni(Ⅱ)polymers based on pyridine-2,4,6-tricarboxylic acid(H3pyta):{[M3(pyta)2(H2O)8]·4H2O}n,and analyze their thermogravimetric and magnetic properties.

    1 Experimental

    All solvents and chemicals were commercial reagentsandusedwithoutfurtherpurification. pyridine-2,4,6-tricarboxylicacidwassynthesized according to the reference[17].Elemental analyses (carbon,hydrogen,and nitrogen)were performed with a Perkin-Elmer 240 elemental analyzer.IR spectra were measured from KBr pellets on a Nicolet 5DX FTIR spectrometer.XRD was performed using Rigaku D/max 2500 X-ray diffractometer(Cu Kα radiation, λ=0.156 04 nm,U=40 kV,I=150 mA,2θ=5°~65°). The TGA was determined by Perkin Elmer Pyris Diamond TG-DTA.The magnetic measurements were carried out with a Quantum Design MPMS-XL7 and a PPMS-9 ACMS magnetometer.

    1.1 Synthesis of{[Co3(pyta)2(H2O)8]·4H2O}n(1)

    CoCl2·6H2O(0.072 4 g,3 mmol),H3ptc(0.021 1 g, 1 mmol)were mixed in 7 mL distilled H2O water and 3 mL ethanol.The pH value of the solution was adjusted to 7 with 1 mol·L-1NaOH,and then sealed in a 23 mL Teflon-lined stainless steel autoclave.The mixture was heated in an oven at 100℃for two days, and cooled to room temperature at a rate of 10℃·h-1. Red massive crystals of 1 were obtained.Yield:95% (based on H3ptc).Anal.Calcd.for C16H28Co3N2O24(%): C,23.74;H,3.46;N,3.46.Found(%):C,23.77;H, 3.40;N,3.48.IR(cm-1):3 448s,1622s,1 509w,1 444w, 1 378s,1 312w,1 256w,1 114w,926w,747m,512m.

    1.2 Synthesis of{[Ni3(pyta)2(H2O)8]·4H2O}n(2)

    The procedures were similar to the synthesis of 1 except that the metal salts was NiCl2·6H2O.Green massive crystals of 2 were obtained.Yield:86%. (based on H3ptc).Anal.Calcd.for C16H28Ni3N2O24(%): C,23.75;H,3.46;N,3.46.Found(%):C,23.81;H, 3.41;N,3.52.IR(cm-1):3 853m,3 749m,3 438s, 2 348w,1 622s,1 430w,1 378s,1 289w,1 113w, 926w,747m,512m.

    1.3 X-ray diffraction

    Single-crystal X-ray diffraction data were collected on a Agilent supernova diffractometer equipped with graphite-monochromated Mo radiation with radiation wavelength 0.071073 nm,by usingthex-scan technique.For 1 and 2,the structures were solved by direct methods using the SHELXS-2013[19],and refined by full-matrix least-squares on F2using the Olex2program[20].All non-hydrogen atoms were refined anistropically.Hydrogenatomsweregenerated geometrically and refined isotropically with the riding mode.Crystallographiccrystaldataandstructure processing parameters for polymers 1~2 are summarized in Table 1.Selected bond lengths and bond angles for polymers 1~2 are listed in Table 2,and hydrogen bonds for polymers 1~2 are listed in Table 3.

    CCDC:1524314,1;1000880,2.

    Table 1Crystal data and structure parameters for polymers 1~2

    Continued Table 1

    Table 2Selected bond lengths(nm)and bond angles(°)for polymers 1~2

    Continued Table 2

    Table 3Hydrogen bonds parameters for polymers 1 and 2

    2 Results and discussion

    2.1 Crystal structures of 1 and 2

    X-ray single-crystal diffraction analysis reveals that polymers 1 and 2 crystallizes in monoclinic system,space group P21/c,they are hetero-isomorphic andtwo-dimensionalstructurepolymers.The coordination environment of M(Ⅱ)in 1 and 2 is shown in Fig.1a.The asymmetric unit consists of three M(Ⅱ)ions,two pyta3-ligand,eight coordinated water molecules,and four free water molecules.

    There are three separate M(Ⅱ)ions and two coordinationmodesinthepolymers.Thefirst coordination mode is that the M(Ⅱ)ion is coordinated by one nitrogen atom(N1)and three oxygen atoms(O1, O2,O6)from pyta3-ligand and two coordinated water molecules(O7,O8).The other one is that the M(Ⅱ)ion is coordinated by six oxygen atoms(O5,O5B from two different pyta3-ligand and O9,O9A,O10,O10A from four coordinated water molecules).These two different M(Ⅱ)ions in 1 and 2 both are six-coordinated.For polymer 1,the Co-O distances fall in the range of 0.202 16(15)~0.226 94(16)nm.The Co-N distance is 0.205 40(17)nm.The bond angles of N1-Co1-O2 and O10-Co2-O10B are 73.87(6)°and 180.0°,respectively. For polymer 2,the Ni-O distances fall in the range of 0.200 10(18)~0.229 56(19)nm.The Ni-N distance is 0.199 6(2)nm.The bond angles of N1-Ni1-O2 and O9B-Ni2-O9 are 74.62(7)°and 180.0°,respectively. These bond angles and bond distances all fall in the normal ranges[17,21].

    Fig.1(a)Coordination environment of M(Ⅱ)(M=Co,Ni)ions in 1~2;(b)2-D network structure of polymers 1~2 viewed along a axis; (c)Hydrogen bonds in 1~2;(d)3D structure of 1~2 formed by hydrogen bonds viewed along b axis

    In polymers 1 and 2,the five coordination sites on the ligand all coordinate with metal ions.So,the pyta3-ligand adopts a μ5-η1:η2:η2bridging style to coordinate with M(Ⅱ)ions.Two O atoms from carboxyl of ligand coordinate with two M(Ⅱ)ions,so carboxyl adopts a μ2-η1:η1bridging style to coordinate with M(Ⅱ)ions.As the ligand adopts a μ5-η1:η2:η2bridging style and carboxyl takes a μ2-η1:η1bridging style,the polymers1and2exhibitaveryspecialtwodimensional network structure along a axis(Fig.1b).

    Owing to the introduction of water molecules,the crystals of polymers 1 and 2 have a large number of hydrogen bonds.The O atoms in carbonyl group on the ligand form O-H…O intramolecular hydrogen bonds with coordinated water molecules.The free water molecules in polymers 1 and 2 form O-H…O intermolecular hydrogen bonds with coordinated water molecules(Fig.1c).These hydrogen bonds finallygenerate a three-dimensional network structure by bridgingthetwo-dimensionalplaneswith intermolecular hydrogen bonds(Fig.1d).

    2.2 PXRD and thermal gravimetric analysis

    In order to check the purity of polymers 1 and 2, powder X-ray diffraction of the as-synthesized samples was measured at room temperature.The peak positions of experimental patterns are in good agreement with the simulated ones,which clearly indicates good purity of the polymers 1 and 2(Fig.2).

    Fig.2PXRD patterns for polymers 1(a)and 2(b)

    The thermal stabilities of polymers 1 and 2 were tested in the range of 45~1 000℃under a nitrogen atmosphere at a heating rate of 5℃·min-1and TGA curves of polymers 1 and 2 were shown in Fig.3.The TGA curve of 1 show that polymer 1 first loses twelve water molecules(Obsd.27.59%,Calcd.26.69%)in the range of 45~236℃.The second weight loss is responsibleforthedecompositionofallorganic components in the range of 236~556℃.The residue withweightof31.72%mightbeCo2O3(Calcd. 30.75%).The TGA curve of 2 show that polymer 2 first loses twelve water molecules(Obsd.23.52%,Calcd. 23.75%)in the range of 45~123℃.Further weight loss is responsible for the decomposition of all organic components in the range of 123~503℃.The residue with weight of 28.79%might be NiO(Calcd.27.71%).

    2.4 Magnetic analysis for polymers 1~2

    Co(Ⅰ)(d7)of polymer 1 and Ni(Ⅱ)(d8)of polymer 2haveunpairedelectrons,sotheirmagnetic properties are studied.The magnetic susceptibilities, χmof 1 and 2 were measured in the 2~300 K temperature range,and shown as plots of χmandχmT versus T in Fig.4a and Fig.4b,respectively.As shown in Fig.4a,the molar magnetic susceptibility χmof polymer 1 increases gradually as the temperature lowers,and more rapidly increases below 25 K,then reaches a maximum value of 2.24 cm3·mol-1at 2 K.It can be seen from the χmT curve that the χmT value is 9.56 cm3·mol-1·K at 300 K,which is significantly higher than the theoretical value 5.64 cm3·mol-1·K of the high-spin triplet Co2+,indicating a great spin-orbit coupling contribution.As the decrease of temperature,the χmT begin to decrease slowly,and the decrease in the range of 300~25 K could be attributed to the single ion behavior of Co2+.But the χmT more rapidly reduces below 25 K,then reaches a minimum value of 4.46 cm3·mol-1·K at 2 K.Combined with the decrease in the χmT value when cooling,this result indicates the presence of weak antiferromagnetic interactions in polymer 1[22].At 300K,the magnetic moment(μeff)of cobalt(Ⅱ),which is determined by the equation μeff=2.828(χmT)1/2,reaches the peak value of 8.74μB.This value is slightly higher than that expected for an isolated divalent high-spin Co(Ⅰ)system with μeff= 3.87μB.

    Fig.3TGA curves of polymers 1(a)and 2(b)

    AsshowninFig.4b,themolarmagnetic susceptibility χmof polymer 2 increases gradually as the temperature lowers,and more rapidly increases below 25 K,then reaches a maximum value of 0.48 cm3·mol-1at 2 K.It can be seen from the χmT curve that the χmT value is 3.76 cm3·mol-1·K at 300 K, which is equal to the theoretical value of the highspin binuclear Ni2+.As the decrease of temperature, the χmT decrease slowly,and the decrease in the range of 300~25 K could be attributed to the single ion behavior of Ni2+.But there is more rapidly reduction for χmT below 25 K,then it reaches a minimum value of 0.96 cm3·mol-1·K at 2 K.At 300 K,the magnetic moment(μeff)of nickel(Ⅱ)reaches the peak value of 5.48μB.This value is slightl yhigher than that expected for an isolated divalent high-spin Ni(Ⅱ)system with μeff=2.83μB.From magnetic data of the polymers,it is clear that AF coupling mainly occurs between intrachain metal ions.

    Fig.4Plots of χmand χmT vs T of polymers 1(a)and 2(b)

    3 Conclusions

    In summary,two coordination polymers based on pyridine-2,4,6-tricarboxylic acid had been synthesized and characterized.X-ray diffraction study reveals that the polymers 1~2 are isostructural and have twodimensionalnetworkstructure.Themagnetic measurement reveals the pyridine-2,4,6-tricarboxylic acidasbridgeligandcanmediatethe antiferromagnetic(AF)coupling interaction between magnetic centers.

    [1]Rumberger E M,Shah S J,Beedle C C,et al.Inorg.Chem., 2005,44:2742-2752

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    [6]Wang J H,Zhang S H,Wang W,et al.J.Cluster Sci.,2015, 26:1129-1142.

    [7]Huang X R,Yang L,Zhou Y J,et al.J.Cluster Sci.,2015, 26:2033-2042

    [8]Limas N G,Manz T A.RSC Adv.,2016,6:45727-45747

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    [11]LI Huan(李歡),CHEN Yun-Zhou(陳云舟),WANG Yan-Jun (王艷君),et al.Chinese J.Inorg.Chem.(無(wú)機(jī)化學(xué)學(xué)報(bào)), 2016,32:2198-2204

    [12]Miyasaka H,Yamashita M.Dalton Trans.,2007,36:399-406

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    [14]LIAO Bei-Ling(廖蓓玲),LI Shi-Xiong(李石雄),YIN Xiu-Ju (銀秀菊),et al.Chinese J.Inorg.Chem.(無(wú)機(jī)化學(xué)學(xué)報(bào)), 2016,32:1255-1260

    [15]Lu J Y.Coord.Chem.Rev.,2003,246:327-347

    [16]Zhang L Y,Zhang J P,Lin Y Y,et al.Cryst.Growth Des., 2006,6:1684-1689

    [17]Gao H L,Yi L,Zhao B,et al.Inorg.Chem.,2006,45:481-483

    [18]Li C J,Peng M X,Leng J D,et al.CrystEngComm,2008, 10:1645-1652

    [19]Sheldrick G M.Acta Crystallogr.Sect.A,2008,A64:112-122

    [20]Bourhis L J,Dolomanov O V,Gildea R J,et al.Acta Crystallogr.Sect.A,2015,A71:59-75

    [21]LI Shi-Xiong(李石雄),LIAO Bei-Ling(廖蓓玲),LUO Pei (羅培),et al.Chinese J.Inorg.Chem.(無(wú)機(jī)化學(xué)學(xué)報(bào)), 2015,31:291-296

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    基于2,4,6-吡啶三酸配體的Co(Ⅰ)、Ni(Ⅱ)配位聚合物的合成、結(jié)構(gòu)和磁性分析

    銀秀菊1廖蓓玲1吳漢民1龐毅林1李石雄*,1,2
    (1河池學(xué)院化學(xué)與生物工程學(xué)院,宜州546300) (2華南理工大學(xué)環(huán)境與能源學(xué)院,廣州510006)

    以2,4,6-吡啶三酸為配體,采取水熱合成的方法,在相同溫度、物質(zhì)的量之比、溶劑,不同金屬鹽條件下合成了{(lán)[M3(pyta)2(H2O)8]·4H2O}n(M=Co(1),Ni(2),H3pyta=2,4,6-吡啶三酸)配位聚合物。X射線單晶衍射測(cè)試分析表明2個(gè)配合物是異質(zhì)同晶結(jié)構(gòu),屬于單斜晶系,P21/c空間群。磁性測(cè)試表明在配合物的中心離子M(Ⅱ)之間存在反鐵磁耦合作用。

    配位聚合物;2,4,6-吡啶三酸;磁性

    O614.81+2;O614.81+3

    A

    1001-4861(2017)06-1043-08

    2016-12-28。收修改稿日期:2017-04-15。

    10.11862/CJIC.2017.116

    廣西高校科研項(xiàng)目(No.YB2014331)、廣西教育廳基礎(chǔ)研究(No.200807MS090)、廣西教育科學(xué)“十二五”規(guī)劃課題(No.2015C408)、國(guó)家自然科學(xué)基金(No.21563010)和廣西自然科學(xué)基金(No.2014GXNSFBA118045)資助項(xiàng)目。

    *通信聯(lián)系人。E-mail:lsx1324@163.com

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