以5-甲基-3-吡唑甲酸為配體的鈷(Ⅱ)、鎳(Ⅱ)配合物的合成、晶體結(jié)構(gòu)和性質(zhì)

程美令　王沈　唐李志鵬　劉琦,(常州大學(xué)石油化工學(xué)院，江蘇省綠色催化材料和技術(shù)重點(diǎn)實(shí)驗(yàn)室，常州364)(南京大學(xué)配位化學(xué)國(guó)家重點(diǎn)實(shí)驗(yàn)室，南京003)

以5-甲基-3-吡唑甲酸為配體的鈷(Ⅱ)、鎳(Ⅱ)配合物的合成、晶體結(jié)構(gòu)和性質(zhì)

程美令＊,1王沈1唐李志鵬1劉琦＊,1,2
(1常州大學(xué)石油化工學(xué)院，江蘇省綠色催化材料和技術(shù)重點(diǎn)實(shí)驗(yàn)室，常州213164)
(2南京大學(xué)配位化學(xué)國(guó)家重點(diǎn)實(shí)驗(yàn)室，南京210023)

以5-甲基-3-吡唑甲酸(H2MPCA)為主配體，橋聯(lián)配體4,4′-聯(lián)吡啶(4,4′-bpy)和吡嗪(pyz)為輔助配體，合成了2個(gè)新的配合物{[Co(HMPCA)2(4,4′-bpy)]2·5H2O}n(1)和{[Ni(HMPCA)2(pyz)]·5H2O}n(2)，并用元素分析、紅外光譜、X射線單晶衍射結(jié)構(gòu)分析、熱重分析等對(duì)其進(jìn)行了表征。配合物1屬于正交晶系，空間群為Pccn，配合物2屬于單斜晶系，空間群為P2/c。在1和2中，金屬離子都位于一個(gè)扭曲的八面體配位環(huán)境中，分別由4,4′-聯(lián)吡啶(1)和吡嗪(2)兩端的氮原子橋聯(lián)2個(gè)相鄰的金屬離子，形成一維鏈狀聚合物?？疾炝伺浜衔?和2的熱穩(wěn)定性、熒光性能和磁性。

鈷；鎳；5-甲基-3-吡唑甲酸；晶體結(jié)構(gòu)；熒光；磁性

0　Introduction

In the past decades,the design and construction ofthesupramolecularcomplexesconstructedby coordination bonds and/or other weak cooperative interactions have become a very attractive research fieldincoordinationchemistryandmaterials chemistry[1-4].The interest comes from the outstanding topologicalstructuresanduniquepotential applications in many fields,such as gas storage[5-8], heterogeneouscatalysis[9-10],sensors[11],lithium-ion batteries[12-14].Synthesis of supramolecular complexes through self-assembly is a complicated process,highly influenced by a lot of factors,such as the nature of organic ligands,the coordination geometry of metal ions,metal-ligand ratio,pH value,solvent system, temperature,template agents and counteranions. There is no doubt that selection and reasonable use of characteristic ligands is the key point in the construction of complexes[15-20].Recently,N-heterocyclic carboxylic acids with good coordination capacities in multicoordination modes by the N and O donor atoms on the N-heterocyclic rings and the carboxyl groups,are increasingly used in construction of complexes.The nitrogen atoms and carboxylic oxygen atoms can not only coordinate to metals,but also act as a donor and/ oracceptorinhydrogenbondinteractionsfor assemblingthecomplexintohigh-dimensional supramolecular networks.For example,organic ligand 5-methyl-1H-pyrazole-3-carboxylic acid(H2MPCA)has been widely used to synthesize various supramolecular architectures containing transition and main group metal ions,in which,H2MPCA ligand hasboth bridging and chelating coordination modes to bind metal centers[21-25].On the other hand,the chelate N ancillary ligands,such as 2,2′-bipyridine(2,2′-bpy) and 1,10-phenanthroline(phen),were also utilized in thesynthesisprocesses,whichcanadjustthe coordination structures by occupying the terminal position[23].As we all known,bipyridine(4,4′-bpy)[26]and pyrazine(pyz)[25]are good candidates for molecular building blocks,due to their rod-like rigidity and length.But,the researches of using these bridging N ancillary ligands to construct H2MPCA containing complexes have been less explored,only two 1D coordination polymers,{[Cu2(4,4′-bpy)2(2,2′-bpy)(MPCA)2]· 6H2O}n[21]and{[Co(HMPCA)2(pyz)]·5H2O}nwere reported[25].As the continuation of our research in constructing functional metal complexes containing N-heterocyclic carboxylic acids[22-25,27-30],we carried out the reactions of H2MPCA with corresponding metal salts and bridging N ancillary 4,4′-bpy and pyz,and isolated two new complexes,{[Co(HMPCA)2(4,4′-bpy)]2·5H2O}n(1)and{[Ni(HMPCA)2(pyz)]·5H2O}n(2).In this paper,thesynthesis,crystalstructures, photoluminescentandmagneticpropertiesofthe coordination polymers 1 and 2 were described.

1　Experimental

1.1Materials and methods

All solvents and starting materials for synthesis werepurchasedcommerciallyandwereusedas received.H2MPCAwaspreparedfollowingthe literature method[31].The elemental analysis(C,H and N)was performed on a Perkin-Elmer 2400 SeriesⅡelement analyzer.FTIR spectra were recorded on a Nicolet 460 spectrophotometer in the form of KBr pellets in the range of 4 000～400 cm-1.Single-crystal X-ray diffraction measurements of 1 and 2 were carried out with a Bruker Smart ApexⅡCCD diffractometer at 296(2)K.Thermogravimetric analysis (TGA)experiments were carried out on a Dupont thermal analyzer from room temperature to 800℃at a heating rate of 10℃·min-1under N2atmosphere. Powder X-ray diffraction(PXRD)determinations were performed on an X-ray diffractometer(D/max 2500 PC,Rigaku)with Cu Kα radiation(0.154 06 nm).The operating voltage and current were 60 kV and 300 mA,respectively.The luminescent spectra of the solid samples were recorded with a Cary Eclipse spectrometer.The magnetic susceptibility measurements for crystalline sample were measured over the temperature range of 1.8～300 K with a Quantum Design MPMS-XL7 SQUID magnetometer using an applied magnetic field of 2 000 Oe.Data were corrected for the diamagnetic contribution calculated from Pascalconstants.

1.2Preparation of{[Co(HMPCA)2(4,4′-bpy)]2· 5H2O}n(1)

To a solution containing H2MPCA(0.025 2 g,0.2 mmol)and 4,4′-bpy·2H2O(0.076 8 g,0.4 mmol)in DMF(2.0 mL)was added a solution of Co(OAc)2· 4H2O(0.024 9 g,0.1 mmol)in MeOH(4.0 mL).The resulting solution was stirred for 30 min,followed by being placed into 15 mL Teflon-lined autoclave under autogenous pressure and heated at 120℃for 24 h,then the solution was cooled to the ambient temperature at the rate of 5℃·h-1.After filtration,the product was washed with deionized water and then dried,and red crystals of 1(0.026 5 g,52%,based on H2MPCA) suitable for X-ray diffraction analysis were obtained. Anal.Calcd.for C40H44Co2N12O13(%):C,47.16;H,4.35; N,16.50;Found(%):C,46.01;H,4.82;N,16.07.IR spectrum(cm-1,KBr pellet):3 431(s),3 182(m),3 132 (m),3 084(m),2920(m),2 854(m),1 681(s),1 605 (vs),1 535(m),1 495(m),1 420(s),1 383(m),1 343 (s),1 293(s),1 217(w),1 191(w),1 089(w),1 067(w), 1 027(m),1 013(m),818(m),796(m),688(w),634 (m),576(w),528(w),455(w).

1.3Preparationof{[Ni(HMPCA)2(pyz)]·5H2O}n(2)

To a solution containing H2MPCA(0.025 2 g,0.2 mmol)and pyz(0.016 0 g,0.2 mmol)in deionized water (5.0 mL)was added a solution of Ni(OAc)2·4H2O (0.049 9 g,0.2 mmol)in deionized water(5.0 mL).The resulting solution was stirred for 30 min,followed by being placed into 25 mL Teflon-lined autoclave under autogenous pressure and heated at 180℃for 24 h,then is was cooled to the ambient temperature at the rate of 5℃·h-1.After filtration,the product was washed with deionized water and then dried,and blue crystals of 2 (0.028 7g,60%,based on H2MPCA)suitable for X-ray diffraction analysis were obtained.Anal.Calcd.for C14H24NiN6O9(%):C,35.10;H,5.05;N,17.54;Found (%):C,35.01;H,5.31;N,17.23.IR spectrum(cm-1, KBr pellet):3 379(m),3 200(m),3 140(m),3 110(m), 2 969(w),2 850(w),1 610(vs),1 493(w),1 418(s), 1 324(m),1 281(s),1 212(m),1 118(w),1 160(w), 1 050(m),1 025(m),843(w),794(m),688(w),563 (w),483(m),446(w).

1.4X-ray crystallography

Single-crystal X-ray diffraction measurements of 1 and 2 were carried out with a Bruker Smart ApexⅡCCD diffractometer at 296(2)K(1)and 293(2)K (2).Intensities of reflections were measured using graphite-monochromatizedMoKαradiation(λ= 0.071 073 nm)with the φ-ω scans mode in the range of 2.809°～28.071°(1)and 2.433°～27.631°(2).The structure was solved by direct methods using the SHELXS program of the SHELXTL package and refined with SHELXL[32].For 1,the lattice water molecule(O4)was fixed with constrained parameters and refined with an occupancy factor of 0.25.In the case of 2,two free water molecules bearing O3 and O4 atoms were found to be disordered over two positions with an occupancy ratio of 0.5/0.5 for O(3)/O (3A)and O(4)/O(4A).Another lattice water molecule (O5)wasfixedwithconstrainedparametersand refined with an occupancy factor of 0.5.Anisotropic thermal factors were assigned to all the non-hydrogen atoms.Hydrogen atoms on O4 atom in 1 were not located.All other hydrogen atoms attached to C were placedgeometricallyandallowedtorideduring subsequent refinement with an isotropic displacement parameter fixed at 1.2 times Ueqof the parent atoms. H atoms bonded to O or N atoms were first located in difference Fourier maps and then placed in the calculatedsitesandincludedintherefinement. Crystallographicdataparametersforstructural analyses are summarized in Table 1.

CCDC:1445391,1;1445392,2.

Table 1Crystal structure parameters of the compounds 1 and 2

Continued Table 1

2　Results and discussion

2.1IR spectrum

The IR spectra of complexes 1 and 2 reflect the binding patterns of H2MPCA,4,4′-bpy and pyz(Fig.S1 in supplementary materials).The strong and broad absorption band around 3 200～3 600 cm-1region is assigned as characteristic peak of OHvibration, indicating that water molecules exist in the complexes. The absorption peak between 1 690 cm-1and 1 730 cm-1is not observed,showing all carboxylic groups are deprotonated.The strong peaks at 1 605 cm-1(1),1 610cm-1(2),and 1 420 cm-1(1),1 418 cm-1(2)are the νas(COO-)andνs(COO-)stretching mode of the coordinated HMPCA-ligand,respectively[33-35].For complex 1,the weak absorption at 3 000 cm-1is the νas(C-H)bent vibration of 4,4′-bpy.For complex 2,the absorbances between 1 050 and 1 212 cm-1are assignable to pyz bands[36].

Fig.1Coordination environment of Co(Ⅱ)ion in 1 with thermal ellipsoid at 30%probability level

2.2Crystal structures of 1 and 2

X-ray crystal structure analysis reveals that 1 crystallizes in the orthorhombic system space group Pccn.The asymmetric unit of 1 contains a half of Co(Ⅱ)ion,one HMPCA-anion,half of a 4,4′-bpy,one and a half lattice water molecules.The coordination sphere of Co(Ⅱ)is defined by two carboxylate oxygen atoms,two nitrogen atoms from two HMPCA-anions, and two nitrogen atoms from two 4,4′-bpy ligands, leading to a hexa-coordinated octahedral geometry. The equatorial position are occupied by O1,O1A,N1, and N1A atoms,proved by that the sum of the bond anglesof O1A-Co1-N1A(78.48(11)°),N1-Co1-O1 (78.48(11)°),N1-Co1-O1A(101.52(11)°)and O1-Co1-N1A(101.52(11)°)is equal to 360°,and N3 and N3A atoms are located in the axial positions(Fig.1 and Table 2).As a bidentate ligand,the HMPCA-anion chelates one Co(Ⅱ)atom with pyrazole N atom and carboxyl O atom to form a five membered ring.As shown in Fig.2,two crystallographically equivalent ions,Co1 and Co1A are linked by two N atoms(N3 and N3A)from 4,4′-bpy in a bridging fashion, generating an infinite 1D chain.The length of Co-O1 bond is 0.207 6(3)nm,and the Co-N bonds are in the range of 0.214 4(3)～0.216 5(3)nm,which are close to those Co-O(Co1-O1 0.211 6(5)nm),Co-N(Co1-N1 0.208 2(5)nm)in the reported Co(Ⅱ)complex[CoCl4(Athpp)2]·2H2O(Athpp=3-amino-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole)[37].The average bond length of Co-N is longer than that of Co-O,showing that the strength of cobalt ion coordinated with nitrogen atoms are weaker than that of oxygen atoms from HMPCA-ligands in 1.By the function of the hydrogen bond O3-H3X…O2C(Symmetry codes:C:x,1+y,-1+z) and O3-H3Y…O1D(Symmetry codes:D:1-x,1/2+y, 3/2-z),the solvent water molecules are embedded in the chain.Finally,these 1D chains are extended into 3D structure by the N2-H2…O2B(Symmetry codes: B:x,1/2-y,-1/2+z)hydrogen-bonding interactions (Fig.3).

2 crystallizes in the monoclinic system space group P2/c.The asymmetric unit of 2 contains half of one Ni(Ⅱ)ion,one HMPCA-anion,half of one pyz,

Table 2Selected bond lengths(nm)and angles(°)for the compounds 1 and 2

Table 3Hydrogen bond parameters(°)for the compound 1

Fig.2One-dimension chain of 1

Fig.3Three-dimension structure of 1

two and half free water molecules.As illustrated in Fig.4,Ni(Ⅱ)ion is located in a distorted octahedral geometry,coordinating with two N atoms(N1,N1A), two O atoms(O1,O1A)from two chelating HMPCA-anions,and two N atoms(N3,N4)from two pyz ligands.The equatorial position are occupied by O1, O1A,N1,and N1A atoms,proved by that the sum of the bond angles of O1A-Ni1-N1A(79.85(7)°),N1-Ni1-O1(79.85(7)°),N1-Ni1-O1A(100.15(7)°)and O1-Ni1-N1A(100.15(7)°)is equal to 360°,and N3 and N4 atoms are located in the axial positions(Table 2).The length of Ni-O bond are 0.207 04(18)nm,and the Ni-N bonds are in the range of 0.206 19(19)～0.216 6(3)nm, which are close to those Ni-O(Ni1-O1 0.209 80(13) nm),Ni-N(Ni1-N1 0.206 82(14)nm)in the reported Ni(Ⅱ)complex[Ni(HMPCA)2(ImH)2]·2H2O[24].Theaverage bond length of Ni-N is longer than that of Ni-O,showing that the strength of Ni(Ⅱ)ion coordinated with nitrogen atoms are weaker than that of oxygen atoms from HMPCA-ligands in 2.Adjacent Ni(Ⅱ)centers are linked by one pyz ligand in a bridging mode to form an infinite 1D chain(Fig.5),in which the Ni1…Ni1B separation is 0.709 2(2)nm.Five halves of solvent water molecules(O3,O3A,O4,O4A and O5)are not discussed about the hydrogen bond interactions.

Fig.4Coordination environment of Ni(Ⅱ)ion in 2 with thermal ellipsoid at 30%probability level

Fig.5One-dimension chain government of the coordination compound 2

2.3Thermogravimetric analysis

So as to examine the thermal stability of the compounds 1 and 2,the thermogravimetric analysis were carried out from ambient temperature up to 800℃(Fig.S2).For 1,the first weight loss of 8.89% between 50 and 206℃is attributed to the loss of lattice water molecules(Calcd.8.84%).The second degradation stage is in the range of 206～230℃with weight loss of 30.76%,corresponding to the loss of 4,4′-bpy molecules(Calcd.30.66%).The third degradation stage is in the range of 230～460℃, corresponding to the loss of HMPCA-ligands,and the remaining material finally degrades to CoO(Calcd. 14.71%,Found 14.96%).For 2,the first weight loss of 8.02%between 110 and 224℃is attributed to the loss of two lattice water molecules(Calcd.7.52%). The second degradation stage is in the range of 224～356℃with weight loss of 26.20%,corresponding to the loss of three lattice water molecules and one pyz molecule(Calcd.27.99%).Above 356℃,theremaining material decomposes gradually.

2.4Powder X-ray diffraction

ThePXRDpatternsoftitlecomplexesare measured at room temperature for checking the phase purity of the complexes(Fig.S3).The operating voltage and current were 60 kV and 300 mA,respectively. PeaksoftheexperimentalandsimulatedPXRD patterns are in accordance with each other,indicating the superior phase purity of the complexes.The dissimilarities in intensity may be on account of the preferredorientationofthecrystallinepowder samples.

2.5Fluorescence properties

The solid-state fluorescence of two complexes andfreeH2MPCAwereinvestigatedatroom temperature(Fig.S4).The strongest emission peaks for 1 and 2,and free ligand all appear at ca.425 nm (λex=376 nm).According to the position and band shape,the emission bands for 1 and 2 are very similar to that of the free ligand,indicating that the emission bands of complexes 1 and 2 may be attributable to the internal charge transfer(π→π*/n→π*transitions)of the ligand.

2.6Magnetic properties

Fig.6Temperature dependence of χMT((Ⅱ))and χM-1(○)for(1)

Fig.7Temperature dependence of χMT((Ⅱ))and χM-1(○)for(2)

With an applied magnetic field of 2 000 Oe,the variable-temperature(1.8～300K)magneticsusceptibility data were collected for a crystal sample of complexes 1 and 2(Fig.6,7).For complex 1,the experimental χMT value is 2.497 emu·K·mol-1,which is much larger than the spin-only value of 1.875 emu·K·mol-1for an uncoupled high-spin cobalt(Ⅱ)ion(with S=3/2), indicating that an important orbital contribution is involved.The χMT value is different from the value of 2.972 emu·K·mol-1for the complex{[Co(HMPCA)2(pyz)]·5H2O}n[25]and that of 2.985 emu·K·mol-1for the complex[Co(pyz)(H2O)4](NO3)2·2H2O[36],also different from the value of 2.1 emu·K·mol-1for[Co (acac)2(pyz)][38].AsshowninFig.6,whenthe temperatureislowered,theχMTvaluedecreases continuously to 1.443 emu·K·mol-1at 1.8 K.Such behavior suggests the existence of antiferromagnetic interaction behavior even if the single-ion effects, such as spin-orbit coupling,distortion from regular stereochemistry,electron delocalization,and crystal field mixing of excited states into the ground state, may also be present[39].The Curie-Weiss law(χM=C/ (T-θ))was used to fit the magnetic susceptibilities between 300 and 1.8 K.According to the fitting result,Curie constant of C=2.59 emu·K·mol-1and Weiss constant of θ=-8.67 K can be obtained, indicating further that a antiferromagnetic coupling between Co(Ⅱ)ions.For complex 2,the experimental χMT value at 300 K is 1.327 emu·K·mol-1,which is higher than that expected for spin-only value of Ni(Ⅱ)ion(1.0 emu·K·mol-1with g=2.0)(Fig.7).As the temperature lowers to 1.8 K,the χMT value increases slowly to a maximum of about 1.405 emu·K·mol-1at 30 K,then decreases rapidly to a value of 0.524 emu· K·mol-1at 1.8 K.This behavior suggests that ferromagnetic interactions are operating in 2 in the high-temperature region of 30～300 K,which origins frommagneticexchangeinteractionsNi(Ⅱ)ions between pyz ligand within the 1D chain.Similarferromagnetic interactions also exist in reported nickle complexes[Ni(SCN)2(pyrazine)2]nand[Ni(SCN)2(pyrazine)2][40].The sharp decrease of χMT value at lowertemperaturesmaybeaconsequenceof interchains antiferromagnetic interactions in the 3D lattice,which favor a long-range antiferromagnetic ordering.The magnetic susceptibilities above 30 K follow the Curie-Weiss law χM=C/(T-θ)with Curie constant of 1.32 emu·K·mol-1and Weiss constant of 1.935 K.The positive θ value also reveal the presence offerromagneticinteractionin2inthehightemperature region.The magnetic susceptibilities of 30～2 K follow the Curie-Weiss law with Curie constant of 1.548 emu·K·mol-1and Weiss constant of -3.482 K.The negative θ value also reveal the presence of antiferromagnetic interaction in 2 in the low-temperature region.

3　Conclusions

In summary,we have successfully synthesized two new complexes with infinite 1D chains,{[Co (HMPCA)2(4,4′-bpy)]2·5H2O}n(1)and{[Ni(HMPCA)2(pyz)]·5H2O}n(2)by the reaction of H2MPCA and N ancillary ligands with M(OAc)2·4H2O(M=Co,Ni) respectively.The emission bands of complexes 1 and 2 may be attributable to the intraligand π→π*/n→π* transitions.Magnetic properties of the complexes show that 1 exists the interaction of anti-ferromagnetism betweentwoadjacentmetalionsand2exists ferromagneticinteractioninthehigh-temperature region and antiferromagnetic interaction in the lowtemperature region.

Supporting information is available at http://www.wjhxxb.cn

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Syntheses,Crystal Structures and Properties of Cobalt(Ⅱ)and Nickel(Ⅱ)Complexes Based on 5-Methyl-1H-pyrazole-3-carboxylic Acid Ligand

CHENG Mei-Ling＊,1WANG Shen1TANG Li-Zhi-Peng1LIU Qi＊,1,2
(1School of Petrochemical Engineering and Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, Changzhou University,Changzhou,Jiangsu 213164,China)
(2State Key Laboratory of Coordination Chemistry,Nanjing University,Nanjing 210023,China)

Two new 1D chain-typed coordination polymers,{[Co(HMPCA)2(4,4′-bpy)]2·5H2O}n(1)and {[Ni(HMPCA)2(pyz)]·5H2O}n(2)(H2MPCA=5-methyl-1H-pyrazole-3-carboxylic acid,4,4′-bpy=4,4′-bipyridine,pyz= pyrazine),have been synthesized and characterized by elemental analysis,IR spectra,single crystal X-ray diffraction and thermogravimetric analysis.Complex 1 crystallizes in the orthorhombic system,space group Pccn, and 2 crystallizes in the monoclinic system,space group P2/c.In 1 and 2,metal ions are both located in an octahedral geometry,coordinated by two nitrogen atoms and two oxygen atoms from two HMPCA-anions,and linked by two nitrogen atoms from 4,4′-bpy ligands(1)and pyz ligands(2),respectively,forming a 1D chaintyped coordination polymer.The thermal stability,luminescent properties and magnetic properties of them have also been investigated.CCDC:1445391,1;1445392,2.

cobalt(Ⅱ);nickel(Ⅱ);5-methyl-1H-pyrazole-3-carboxylic acid;crystal structure;photoluminescence;magnetic properties

圖分類號(hào)：O614.81+2；O614.81+3A

1001-4861(2016)08-1457-10

10.11862/CJIC.2016.184

2016-04-01。收修改稿日期：2016-06-02。

國(guó)家自然科學(xué)基金(No.21101018,20971060)、江蘇省高校自然科學(xué)研究面上項(xiàng)目(No.13KJB150001)、南京大學(xué)配位化學(xué)國(guó)家重點(diǎn)實(shí)驗(yàn)室開放課題和江蘇省先進(jìn)催化與綠色制造協(xié)同創(chuàng)新中心創(chuàng)新型人才支持項(xiàng)目資助。

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