以5-甲基-3-吡唑甲酸和菲咯啉為配體的錳和鎘的配合物的合成、晶體結(jié)構(gòu)和熒光性能

翟長偉 程美令 韓偉 劉琦＊,,2

以5-甲基-3-吡唑甲酸和菲咯啉為配體的錳和鎘的配合物的合成、晶體結(jié)構(gòu)和熒光性能

翟長偉1程美令1韓偉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)國家重點(diǎn)實(shí)驗(yàn)室，南京210093)

以5-甲基-3-吡唑甲酸和菲咯啉為配體，合成了一個單核錳(Ⅱ)配合物[Mn(HMPCA)2(phen)]·2H2O(1)和一個具有雙核結(jié)構(gòu)單元的一維鎘(Ⅱ)的配位聚合物[Cd2(HMPCA)2(phen)2(H2O)2]·2H2O(2)(H2MPCA=5-甲基-3-吡唑甲酸，phen=菲咯啉)，并用元素分析、紅外光譜、X-射線單晶衍射結(jié)構(gòu)分析、熱重分析等對其進(jìn)行了表征。配合物1屬于三斜晶系，空間群為P1，配合物2屬于正交晶系，空間群為Pccn。配合物1中的錳(Ⅱ)離子位于一個畸變的八面體配位環(huán)境中，獨(dú)立結(jié)構(gòu)單元間通過分子間氫鍵作用構(gòu)成一個三維的超分子結(jié)構(gòu)。而在2中，每個鎘(Ⅱ)離子位于一個五角雙錐體中，來自5-甲基-3-吡唑甲酸根的氧原子橋聯(lián)2個相鄰的鎘(Ⅱ)離子，形成一個一維鏈；這些一維鏈和水分子通過分子間氫鍵進(jìn)一步形成一個三維的超分子結(jié)構(gòu)?？疾炝伺浜衔?和2的熱穩(wěn)定性和熒光性能。

錳；鎘；5-甲基-3-吡唑甲酸；菲咯啉；晶體結(jié)構(gòu)；熒光

The design and synthesis ofnovel supramolecular frameworks and coordination polymers have received considerable attention due to theirtopologically diverse structures[1-2],and potential applications in gas storage and separation[3-6],catalysis[7-8],sensors[9],lithium-ion batteries[10-13],magnetic and optical properties,etc[14-16]. Synthesis of supramolecular frameworks and coordination polymers through self-assembly is a complicated process,highly influenced by a lot of factors,such as the coordination geometry of metal ions,the nature of organic ligands,the ratio between metal salt and ligand,solvent system,pH value of the solution, temperature,the templates and the counter anions. Without a doubt,among these factors,the rational design and reasonable use of the characteristic ligand occupies the capital,because the slight change of the ligands,such as symmetry,flexibility,and the number ofcoordinated atoms,may resultin dramatic differences in structures and properties[17].The previous work of us and other research groups has indicated that the 5-methyl-1H-pyrazole-3-carboxylic acid(H2MPCA)ligand has multiple coordination sites,such as Npyrazole and Ocarboxylic acid,and have both bridging and chelating coordination modes to bind metalcenters[18-22].Moreover, phenanthroline(phen)is a good candidate formolecular building blocks[23].But,the complexes containing H2MPCA and phen have been rarely documented to date[24].As the continuation of our research,and motivated by ourinterestin functionalmetalcomplexes[25-30], we carried out the reactions of H2MPCA,phen and coorresponding metal salts in different conditions,and isolated two new complexes,namely[Mn(HMPCA)2(phen)]·2H2O(1)with mononuclear structure and a [Cd2(HMPCA)2(phen)2(H2O)2]·2H2O(2)with 1D structure.Herein,we reportthe syntheses,crystal structures of 1 and 2.In addition,IR spectra,thermal decomposition and fluorescence property of them will be discussed.

1 Experimental

1.1 Materials and methods

All chemicals for synthesis were purchased commercially and were used as received unless otherwise noted.5-methyl-1H-pyrazole-3-carboxylic acid(H2MPCA)was synthesized and purified according to the modified literature method[31].The elemental analyses(C,H and N)were performed on a Perkin-Elmer 2400 SeriesⅡelement analyzer.FTIR spectra were recorded on a Nicolet 460 spectrophotometer in the form of KBr pellets.Single-crystal X-ray diffraction measurement of the compounds were carried outwith a Bruker ApexⅡCCD diffractometer. Thermogravimetric analysis(TGA)experiments were carried out on a Dupont thermal analyzer with a heating rate of 10℃·min-1under N2atmosphere.The luminescent spectra of the solid samples were recorded with a Varian Cary Eclipse spectrometer.

1.2 Synthesis

1.2.1 Synthesis of[Mn(HMPCA)2(phen)]·2H2O(1)

To a solution containing H2MPCA(0.025 2 g,0.2 mmol)and imidazole(0.017 0 g,0.25 mmol)and phen (0.039 6 g,0.2 mmol)in EtOH(5 mL)was added a solution of Mn(OAC)2·4H2O(0.049 0 g,0.2 mmol)in water(5 mL).The resulting solution was stirred for one hour and allowed to stand at room temperature for three months.Yellow block crystals suitable for X-ray diffraction analysis were obtained.Anal.Calcd.for C22H22MnN6O6(%):C,50.63;H,4.22;N,16.11.Found (%):C,50.14;H,4.55;N,15.76.IR(KBr,cm-1): 3 349(w),3 190(w),3 129(w),3 141(w),3 102(w), 3 060(m),2 933(w),2 849(w),2 602(w),1 964(w), 1 814(w),1 679(s),1 573(s),1 515(m),1 493(m), 1 470(w),1 449(w),1 419(s),1 379(m),1 344(s), 1 330(m),1 306(w),1 286(s),1 220(w),1 196(w), 1 179(m),1 144(w),1119(w),1 100(m),1 091(w), 1 025(s),1 012(s),982(w),864(m),847(vs),829 (s),793(m),773(m),727(vs),684(m),651(w),639 (m),544(m),508(w),474(w),439(m),420(m).

1.2.2 Synthesis of[Cd2(HMPCA)2(phen)2(H2O)2]·2H2O (2)

To a solution containing H2MPCA(0.012 6 g,0.1 mmol)and phen(0.019 8 g,0.1 mmol)in EtOH(3 mL)was added a solution of Cd(NO3)2·4H2O(0.030 8 g,0.10 mmol)in water(3 mL).The resulting solution was stirred for 30 minutes and transferred to a Teflonlined stainless steel vessel for 72 hours with atemperature of120℃.Then the resulting solution was allowed to stand at room temperature for two weeks. Yellow block crystals suitable for X-ray diffraction analysis were obtained.Anal.Calcd.for C34H32Cd2N8O8(%):C,45.05;H,3.53;N,12.37.Found(%):C,44.85; H,3.15;N,12.46.IR(KBr,cm-1):3 442(s,br),3 134 (s),1 615(s),1 613(vs),1 432(s),1 431(s),1 383(s), 1 344(s),1 031(s),1 003(m),748(m).

1.3 X-ray crystallography

Single-crystal X-ray diffraction measurements of 1 and 2 were carried out with a Bruker Smart ApexⅡCCD diffractometer at 293(2)K and 291(2)K. Intensities ofreflections were measured using graphite -monochromatized Mo Kαradiation(λ=0.071 073 nm) with theφ-ωscans mode in the range of 1.38°～25.50° (for 1)and 2.34°～27.68°(for 2).The structures were solved by directmethods using SHELXS-97[32]computer program and refined by full-matrix least-squares methods on F2with the SHELXL-97 program package. Anisotropic thermal factors were assigned to all the non-hydrogen atoms.Hydrogen atoms were included in calculated position and refined with isotropic thermal parameters riding on the parent atoms.H atoms bonded to O or N were located in difference Fourier maps.Crystallographic data parameters for structuralanalyses are summarized in Table 1.

CCDC:1044243,1;1044244,2.

Table 1 Crystal structure parameters of the compounds 1 and 2

2 Results and discussion

2.1 Synthesis and IR spectrum

Complex 1 can be obtained by slow evaporation of a mixed solution of EtOH and deionized water of Mn(OAC)2·4H2O/H2MPCA/phen/imidazole with molar ratios of1∶1∶1∶1.25.Imidazole molecule is not includedin 1,indicating it may be play a role of base/template. Under same solvent system,when the molar ratio of Cd(NO3)2·4H2O/H2MPCA/phen was 1∶1∶1,complex 2 was obtained via slow evaporation of the resulting solution obtained by solvothermal reaction.The IR spectra of complexes 1 and 2 reflect the binding patterns of phen and H2MPCA(see Supplementary materials Fig.S1 and S2).The strong and broad absorption band around 3 000～3 600 cm-1region is assigned as characteristic peak of OH vibration, indicating thatwater molecules existin 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 at1 679(1),1 613 cm-1(2)and 1 379(1),1 383 cm-1(2)are theνas(COO-), andνs(COO-)stretching mode of the coordinated HMPCA-ligand,respectively.The difference of 300 (1),230 cm-1(2)betweenνas(COO-)andνs(COO-) indicates that HMPCA-ligand adoptmonodentate coordination[33-35].While bands assigned to the conjugated C=N stretching vibrations appearat1 573～1 330 cm-1. These assignments are consistent with the X-ray crystalstructures ofthe complexes.

2.2 Crystalstructures of 1 and 2

X-ray crystal structure analysis reveals that 1 crystallizes in the triclinic system space group P1. The asymmetric unit of 1 contains one Mn(Ⅱ)ion,two HMPCA-anions,one phen,two free water molecules. As illustrated in Fig.1,the coordination sphere of Mn(Ⅱ)is defined by two carboxylic oxygen atoms (O(1),O(3)),two nitrogen atoms(N(1),N(5))from two HMPCA-anions,and two nitrogen atoms(N(2),N(3)) from one phen ligand,leading to a distorted octahedral geometry.The equatorial position are occupied by N (1),N(3),N(5),and O(1)atoms,O(3)and N(2)atoms are located in the axial positions,and the bond angles of O(3)-Mn(1)-N(2),N(3)-Mn(1)-O(1)are 157.30(18)°, and 154.00(17)°respectively,deviating from 180° (Table 2).The bond distances of Mn(1)-N and Mn(1)-O are in the range of 0.226 5(4)～0.228 3(5)nm,and 0.213 4(4)～0.218 0(4)nm,respectively,which are close to the values observed in other Mn(Ⅱ)complexes based pyrazole derivative ligands[24].

Fig.1 Coordination environment of Mn(Ⅱ)ion in 1 with thermal ellipsoid at 50%probability level

Independent components[Mn(HMPCA)2(phen)] and H2O are linked by three kinds of hydrogen bonds (O-H…O,N-H…O and C-H…O)(Table 3),as shown in Fig.2,resulting in the production of a three dimensional supramolecular framework.It is worth to note that complex 1 has same molecular formula with [Mn(HMPCA)2(phen)]·2H2O reported by us recently[24], but they have different crystal system,space group, cell parameters and network superstructures et al,so they are two true supramolecular isomers[36-38].

Fig.2 3D framework of 1(Dash lines:hydrogen bonds)

Coordination polymer 2 crystallizes in the orthorhombic system space group Pccn.The asymmetric unit of 2 contains one[Cd2(HMPCA)2(phen)2(H2O)2] molecule and two free water molecules.As illustrated in Fig.3,the coordination sphere of Cd1(Ⅱ)is defined by three carboxylic oxygen atoms(O(1),O(3),O(4)) and one nitrogen atom N(5)from two HMPCA-anions, two nitrogen atoms(N(1),N(2))from a phen ligand,and an oxygen atom(O(1W)from a water molecule, leading to a pentagonal bipyramid geometry with seven coordination.The five atoms(O(3),O(4),O(1W), N(1),O(1))form the equator plane of the pentagonal bipyramid,while the two axial positions are occupied by two nitrogen atoms(N(5),N(2)).Selected bond lengths and angles are given in Table 2.The bond angles of O(1W)-Cd(1)-N(1),N(1)-Cd(1)-O(1),O(4)-Cd (1)-O(1),O(1W)-Cd(1)-O(3),O(4)-Cd(1)-O(3)are added up to equal to 375°,close to 360°,showing that O(3), O(4),O(1W),N(1)and O(1)atoms are in the equatorial position.Moreover,the bond angle of N(5)-Cd(1) -N(2)is 166.11°,deviates from 180°,again revealing that the coordination polymer 2 has a distorted

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

Fig.3 Coordination environment of Cd(Ⅱ)ion in 2 with thermal ellipsoid at 50%probability level

Table 3 Bond lengths(nm)and angles(°)of hydrogen bonds for complexes 1 and 2

Symmetry codes:for 1:i1+x,y,z;ii1-x,1-y,1-z;iii-x,2-y,1-z;iv-x,2-y,-z;for 2:i3/2-x,y,-1/2+z;ii3/2-x,3/2-y,z;iii-1/2+x, 1-y,3/2-z pentagonal bipyramid geometry.The bond distances of Cd1-O and Cd1-N are in the range of 0.230 2(4)～0.238 6(4)and 0.230 8(5)～0.235 4(5)nm(Table 2), which are close to the values observed in other Cd(Ⅱ) complexes[29,39].The coordination sphere of Cd2(Ⅱ)is same with that of Cd1(Ⅱ),five atoms(O(1),O(2),O(3), N(4),N(7))form the equator plane of the pentagonal bipyramid,while the two axial positions are occupied by N(3)and O(2W)atoms.The bond angles of O(3)-Cd(2)-O(2),O(3)-Cd(2)-N(7),N(7)-Cd(2)-N(4),and N (3)-Cd(2)-O(2W)are 74.86°,68.81°,84.90°,and 152.59°respectively.The Cd1(Ⅱ)and Cd2(Ⅱ)ions are connected together by one carboxylic oxygen atom to form a binuclear unit,in which the distance between two Cd(Ⅱ)ions is 0.463 2 nm.These binuclear units are linked each other to form a 1D chain,as shown in Fig.4.Besides,the separation of 0.348 4 nm between the centroids of the benzene ring from phen ligands, indicates the existence ofthe significantintramolecular π-πinteractions.These 1D chains,and the lattice water molecules are interlinked via the interactions of two kinds ofintermolecular hydrogen bonds(O-H…O C-H…O),resulting in the formation of a 3D supermolecular framework,as shown in Fig.5.Thelengths and angles of the hydrogen bonds are listed in Table 3.

Fig.4 1D chain structure of 2

Fig.5 3D grid-like structure of 2(Dashed lines:hydrogen bonds)

2.3 Thermogravimetric 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℃(see Supplementary materials,Fig.S2).For 1,the first weight loss of 7.41%between 126℃and 199℃is attributed to the loss of two lattice water molecules (Calcd.6.90%).The second degradation stage is in the range of 199～434℃with weight loss of 35.02%, corresponding to the loss of one phen molecule (Calcd.34.52%).The third degradation stage is in the range of 434～478℃with weight loss of 24.99%, corresponding to the loss of a HMPCA-ligand(Calcd. 23.99%).The remaining material finally degrades to MnO(Calcd.13.62%,Found 14.79%).For 2,the first weight loss of 3.53%between 50℃and 150℃is attributed to the loss of two lattice water molecules (Calcd.3.98%).The second degradation stage is in the range of 170～250℃with weight loss of 4.17%, corresponding to the loss of two coordinated water molecules(Calcd.3.98%).The third degradation stage is in the range of 250～440℃with weight loss of 38.65%,corresponding to the lossoftwo phen molecules (Calcd.35.80%).Above 440℃,the remaining material decomposes gradually.

2.4 Fluorescence properties

The solid-state fluorescence of two complexes, and free H2MPCA ligand were investigated at room temperature.As shown in Fig.6,the strongestemission peaks for free ligand,and complexes 1 and 2 all appear at ca.425 nm(λex=376 nm).Therefore the origin of the emission of complexes 1 and 2 may be attributed to the internal charge transfer(π→π*/n→π*transitions)ofthe ligand.

Fig.6 Solid-state fluorescence of compounds 1 and 2

3 Conclusion

In summary,complexes[Mn(HMPCA)2(phen)]· 2H2O(1)with mononucleatestructureand[Cd2(HMPCA)2(phen)2(H2O)2]·2H2O(2)with 1D structure containg binuclear units have been successfully synthesized. The coordination modes ofHMPCA-anionsare different in two complexes.Non-covalent bonds play an important role in the formation of three-dimensional supramolecular architectures ofthe complexes.Similar to ligand H2MPCA,complexes 1 and 2 show blue fluorescence in the solid state atroom temperature.

Supporting information is available athttp://www.wjhxxb.cn

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Syntheses,Crystal Structures and Luminescent Properties of Manganese and Cadmium Complexes Based on 5-Methyl-1H-Pyrazole-3-Carboxylic Acid and Phenanthroline Ligands

ZHAIChang-Wei1CHENG Mei-Ling1HAN Wei1LIU 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 210093,China)

One monomeric complex[Mn(HMPCA)2(phen)]·2H2O(1)and one 1D coordination polymer[Cd2(HMPCA)2(phen)2(H2O)2]·2H2O(2)with binuclear structural unit(H2MPCA=5-methyl-1H-pyrazole-3-carboxylic acid,phen= phenanthroline)have been synthesized and characterized by elemental analysis,IR spectra,thermogravimetric analysis and single crystal X-ray diffraction.Complex 1 crystallizes in the triclinic system,space group P1,while 2 in the orthorhombic system,space group Pccn.In 1,Mn(Ⅱ)ion located in a distorted octahedral coordination geometry,discrete water molecules and mononucleate units are assembled into a 3D supramolecular network.In 2,each Cd(Ⅱ)ion located in a pentagonal bipyramid geometry.Each carboxyl group from HMPA-anion bridges two adjacent Cd(Ⅱ)ions,forming a 1D chain.These chains and water molecules are connected by hydrogen bonds,forming a 3D supramolecular framework.The thermalstability and luminescentproperties of them are also investigated.CCDC:1044243,1;1044244,2.

manganese(Ⅱ);cadmium(Ⅱ);5-methyl-1H-pyrazole-3-carboxylic acid;crystal structure;photoluminescence

O614.71+1；O614.24+2

A

1001-4861(2015)07-1409-08

10.11862/CJIC.2015.193

2015-01-28。收修改稿日期：2015-05-13。

國家自然科學(xué)基金(No.20971060，21101018),南京大學(xué)配位化學(xué)國家重點(diǎn)實(shí)驗(yàn)室開放課題資助項(xiàng)目。

＊通訊聯(lián)系人。E-mail：liuqi62@163.com，Tel：0519-86330185；會員登記號：S060018987P。