基于4-氨基-1，2，4-三唑和多金屬氧酸鹽為雜化配體的CuⅡ和CuⅠ配合物的水熱合成及光催化性能

劉媛媛 張慧敏 王鑫蕊 丁 波 劉正宇 丁 斌,2

0 Introduction

In recent years, hybrid inorganic-organic complexes are a new generation of solid-state materials owing to their chemical and structural diversities[1].Polyoxometalates(POMs),a unique class of metal-oxide clusters,have been intensively investigated in many important aspects such as catalysis,electrical conductivity,medicine,magnetism,materials science,and biologicalchemistry[2].The wide application range is mainly based on (i)the ability of polyoxometalates to act as electron and proton reservoirs;and (ii)the extreme variability of their molecular properties including shape,size,acidity,and charge[3].Recently,many remarkable works about constructing metal-organic frameworks (MOFs)with desired properties is the use of the coordination abilityof polyanionstocombinewith differenttransitionmetal organic units have been presented in coordination polymers[4-6].This method may bring the merits of each row-material together,such as structural diversity and unique physical and chemical properties[7].

For the construction of these POM-based CPs,the choice of organic ligands is very critical.The organic ligands can be subdivided into two classes:pre-synthesized and in situ synthesized ligands[8].The former have been used extensively in the POM-based reaction systems,including N-donor ligands,polycarboxylate ligands and so on[9].Among these Nitrogencontaining heterocyclic organic molecules,1,2,4-triazole and its derivatives are interesting ligands because they combine the coordination geometries of both pyrazoles and imidazoles with regard to the arrangement of their three heteroatoms.For example,these organic linkers have been used to construct these open MOFs,which contain unsaturated metal clusters and possess high thermal stability and even framework flexibility[10-11].As the 1,2,4-triazole derivative,4-amino-1,2,4-triazole (4-NH2-trz)is a multidentate ligand containing one amino and one triazole group,which can provide strong nitrogen coordination donors to metal centers.It can be expected that 4-NH2-trz ligand is able to be effectively imprinted onto the metal coordination centers,affording versatile and structural tunable inorganic-organic POM-based hybrid materials[12].

Previously we are also interested in exploiting the coordination chemistry and application of nitrogen-containing heterocyclic ligands and its derivatives[13].In this work,under hydrothermal conditions two novel CuⅡand CuⅠpolyoxometalate(POM)-based hybrid materials,namely[Cu2(4-NH2-trz)4(Mo8O26)(H2O)4]·5H2O(1)and[Cu4(4-NH2-trz)4Mo8O26](2)have been designed and synthesized through simply tuning the molar ratio of reactant.

1 Experimental

1.1 General

All the reagents were purchased commercially and used without further purification.Deionized water was used as solvent in this work.The solvents were distilled from the appropriate drying agents prior to use.C,H and N microanalyses were carried out with a Perkin-Elmer 240 elemental analyzer.Elemental analysis (Mo)was performed on the X7 Series inductively coupled plasma mass spectrometer(ICPMS)(Thermo Electron Corporation,U.S.A.).Powder X-ray diffraction analysis has been determined on a D/Max-2500 X-ray diffractometer using Cu Kαradiation(λ=0.154 1 nm,U=40 kV,I=40 mA)with a 2θrange of 5°～50°.The UV-Vis diffuse reflectance spectra were obtained with a Lamdba 900 UV-Vis-NIR spectroscopy at room temperature.

1.2 Preparation of coordination complexes 1 and 2

1.2.1 [Cu2(4-NH2-trz)4(Mo8O26)(H2O)4]·5H2O(1)

A mixture of MoO3(0.086 g,0.60 mmol),CuSO4·5H2O (0.051 g,0.2 mmol),4-NH2-trz (0.016 g,0.2 mmol)and H2O(10 mL)(nCuⅡ∶n4-NH2-trz∶nMoO3=2∶2∶6)was heated at 160℃for 72 hours under autogenous pressure,followed by cooling slowly(5℃·h-1)to room temperature.Blue-green long shape crystals were isolated manually from blue unidentified powder,washed with water,and dried in air.Yield:0.17 g(ca.46%based on Cu).Anal.Calc.for C8H34Cu2Mo8N16O35(%):C,5.30;H,0.19;N,12.38;Mo,42.43.Found(%):C,5.28;H,0.15;N,12.42;Mo,42.45.IR(KBr,cm-1):3116(bs),2 675(w),1 517(m),1 425(m),1 305(m),1 025(s),903(s),825(m),606(m).

1.2.2 [Cu4(4-NH2-trz)4Mo8O26](2)

A mixture of MoO3(0.057 g,0.40 mmol),CuSO4·5H2O (0.076 g,0.3 mmol),4-NH2-trz (0.025 g,0.3 mmol)and H2O(10 mL)(nCuⅡ∶n4-NH2-trz∶nMoO3=4∶3∶3)was heated at 160℃for 72 hours under autogenous pressure,followed by cooling slowly(5℃·h-1)to room temperature.Red block crystals were isolated manually from blue unidentified powder,washed with water,and dried in air.Yield:0.19 g(ca.35%based on Cu).Anal.Calc.for C8H16Cu4Mo8N16O26(%):C,5.40;H,0.90;N,12.62;Mo,43.27.Found(%):C,5.38;H,0.92;N,12.72;Mo,43.18.IR(cm-1):3 104(m),1 631(m),1 580(m),1 480(m),1 357(w),1 210(w),1 108(s),995(s),902(m),814(m),582(m).

1.3 Photocatalytic measurements of coordination complexes 1 and 2

The photocatalytic measurements of coordination polymers 1 and 2 were evaluated by the degradation of methylene blue (MB),rhodamine B (RhB)and methyl orange(MO)under irradiation of a 300 W high pressure mercury lamp.The experiments were carried out in typical processes,5 mg complexes 1 and 2 were dispersed in aqueous solutions of three dyes(1×10-5mol·L-1,10 mL),respectively.The mixture was stirred in the dark for 30 min for the adsorptiondesorption equilibrium, then the mixture was transferred and placed under the lighting of Hg lamp(200 W)with continuous stirring.Next,every 20 min intervals,aliquots of the mixture samples were taken out and centrifuged.Finally,the sample was analyzed by UV-Vis measurement.The degradation efficiency(D)of dye is defined as follow:

where C0and A0represents the initial concentration and absorbance of dyes solution after 30 min in the dark,Ctand Atrepresents the concentration and absorbance of the dye at time t.

1.4 X-ray crystallography

Structure measurements of complexes 1 and 2 were performed on a computer controlled Bruker SMART 1000 CCD diffractometer equipped with graphite-monochromated Mo Kαradiation with radiation wavelength 0.071 073 nm by using theω-scan technique.The structures were solved by direct methods and refined with the full-matrix least-squares technique using the SHELXS-97 and SHELXL-97 programs[14-15].Anisotropic thermal parameters were assigned to all non-hydrogen atoms.The organic hydrogen atoms were generated geometrically;the hydrogen atoms of the water molecules were located from difference maps and refined with isotropic temperature factors.Analytical expressions of neutralatom scattering factors were employed,and anomalous dispersion corrections were incorporated.Crystal data collection and refinement details for complexes 1 and 2 are summarized in Table 1.Selected bond lengths and angles for complexes 1 and 2 are listed in Table 2.Hydrogen bonds analysis was carried out using the PLATON program[16],all the hydrogen bonds distances and angles are listed in Table S1.

CCDC:1554212,1;1473507,2.

Table 1 Crystal data and structure refinement information for complexes 1 and 2

Continued Table 1

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

2 Results and discussion

2.1 Preparations of coordination polymers 1 and 2

The chemistry of copperギ-molybdenumボ oxides itself represents a unique subclass of inorganic complex,in which the combination of different oxidation states, polyhedral types, and their connectivity defines the structural variety of geometric forms[17].Coordination polymers 1 and 2 are stable in air and can retain their structural integrity at room temperature for a considerable long time.The successful isolation of complexes 1 and 2 relies on the exploitation of hydrothermal techniques.Hydrothermal reaction conditions are essential for preparing the final complexes 1 and 2.On the other hand,complexes 1 and 2 are synthesized by using the same raw materials and similar hydrothermal synthetic conditions expect only using different molar ratiosnMoO3=2∶2∶6 for 1 and 4∶3∶3 for 2).Therefore the molar ratios of reactants in the multi-component system were significant for the crystallization of products.In order to select the most appropriate hydrothermal reaction conditions to prepare these well-crystalline products 1 and 2,different molar ratios of the reactants (n4-NH2-trz/varying from 2 to 6 are sequentially used,in which the molar quality of MoO3can vary from 0.2 to 0.6 mmol.The synthetic proce-dures for complexes 1 and 2 described in the experi-mental details were selected as the most appropriate ones.The different crystal structures of 1 and 2 show the important influence of the molar ratios of starting reagents.

In particular,as a d9metal,CuⅡion can be easily converted into CuⅠion in the presence of different types of reducer.The changeable oxidation states and versatile coordination geometries make copper ion can be used as a controllable linker.It is noted that CuⅡion in complex 2 was reduced to CuⅠunder hydrothermal conditions.Bond valence sum calculations for 1 and 2 show that all Mo atoms are in+6 oxidation state,while Cu atoms are in+1 oxidation state in 2 and the+2 oxidation state in 1.Additionally,the oxidation state of the Cu atoms in 1 and 2 is further confirmed by their coordination environments and crystal color(blue-green long shape crystals for 1 and red block crystals for 2).

2.2 Structural description

Single-crystal X-ray diffraction analysis reveals that complex 1 crystallizes both in P1 space groups and triclinic crystal system.complexe 1 consists of two Cuギions,four 4-amino-1,2,4-triazol(4-atrz)ligands,one Mo8O264-anion,four coordinated water molecules and five interstitial water molecules.As shown in Fig.1a,in complexe 1,4-atrz ligands adopt pyrazolate-like[N-N]-bidentate bridging coordination mode.The CuⅡcenter (Cu1)is six-coordinated by three N atoms(N1A,N2 and N5)from triazolyl groups and three Oxygen atoms (O7,O14 and O15).These Oxygen atoms O(14),O(15)act as the terminal coordinated water molecules,while the oxygen atom O(7)come from Mo8O264-anions further linked Cu1 atoms.Two sixcoordinated Cuギatoms(Cu1 and Cu1A)are linked by two bi-dentate 4-atrz ligands forming binuclear CuⅡstructural units.Further the dual-core structural units are linked by Mo8O264-ions through bridging O7 atom,which are arranged into the 1D hybrid metalorganic framework along the crystallographic b axis(Fig.1b).Numerous N-H…O and O-H…O hydrogenbonding interactions(N(7)-H(7A)…O(1),0.305 7(7)nm;N(7)-H(7B)…O(10),0.300 5(6)nm;O(14)-H(14A)…O(16),0.269 8(6)nm;O(15)-H(15A)…O(17),2.681(7)nm;O(16)-H(16A)…O(11),0.279 5(6)nm)also can be observed in the coordination framework of 1,which also further extend 1 into a 3D supramolecular network(Fig.1c).

Single-crystal X-ray diffraction analysis reveals that complex 2 also crystallizes in P1 space groups and triclinic crystal system.Complex 2 consists of four Cuガions (Cu1,Cu2,Cu2A and Cu3),four 4-amino-1,2,4-triazol(4-atrz)ligands and one Mo8O264-anion.As shown in Fig.2a,in complex 2,Cu(1)is six-coordinated by two triazole nitrogen atoms and four oxygen atoms from Mo8O264-anions forming the octahedral coordination mode,Cu3 is four-coordinated by two triazole nitrogen atoms and two oxygen atoms from Mo8O264-anions forming the planar coordination mode while Cu2 are four-coordinated by two triazole nitrogen atoms(N2 and N5)and two polyoxometalate oxygen atoms forming the tetrahedral coordination geometry.These 4-atrz ligands bridge neighboring CuⅠcenters forming tetra-nuclear CuⅠstructural unit.It is interestingly that,as shown in Fig.2b,1D[Cu4(4-NH2-trz)4]helical chains can be observed,in which these CuIcenters are extended by these bridging 4-atrz ligands.For 2,these 1D right-hand and left-hand helical chains are linked by(β-Mo8O26)4-anions to form the 2D hybrid framework of 2(Fig.2c).These CH…O,N-H…O and O-H…N hydrogen bonding interactions(N(4)-H(4A)…O(10),0.320 95(4)nm;O(2W)-H(2A)…N(7),0.280 8(6)nm;N(8)-H(8A)…O(10),0.315 41(4)nm;N(8)-H(8B)…O(4),0.297 13(4)nm;C(1)-H(1)…O(9),0.319 13(4)nm)further extend 2D hybrid framework of 2 to generate a 3D supramolecular architecture(Fig.2d).

Fig.1 (a)Binuclear CuII structural units of 1 with H atoms are omitted for clarity;(b)Binuclear CuII structural units extended by Mo8O264-ions forming the 1D hybrid metal-organic framework of 1;(c)3D supramolecular framework viewed along the b-axis direction(dashed lines represent hydrogen bonding interactions)

2.3 Powder X-ray diffraction(PXRD)and FT-IR characterizations

PXRD patterns of 1 and 2 are also recorded at room temperature to determine the phase purity.As shown in Fig.3,the positions of the experimental patterns are in good agreement with those of the simulated patterns,implying phase the as-synthesized samples of 1 and 2 are pure.The slight differences in reflection intensities between the simulated and the experimental patterns are due to the variation in the crystal orientation of the powder sample.

In coordination complexes 1 and 2,the FT-IR bands at 903,825 cm-1for 1 and 902,814 cm-1for 2 can be assigned to ν(Mo-O)and ν(Mo-O-Μo).FT-IR spectra also display typical characteristic absorption bands for triazole moieties of L.The peaks around ca.3 100 cm-1and peaks located at 1 100～1 300 cm-1,which can be related to ν(C-H)and ν(C-N)orν(N-N)of triazole moieties.The triazole out of plane ring absorption is also observed at around 600 cm-1(606 cm-1for 1 and 582 cm-1for 2)[18].

Fig.2 (a)Tetra-nuclear CuⅠstructural unit in 2 with H atoms omitted for clarity;(b)1D[Cu4(4-NH2-trz)4]helical chains with CuⅠcenters bridged by 4-amino-triazole ligands;(c)1D right-hand and left-hand helical chainslinked by(β-Mo8O26)4-anionsto formthe2Dhybrid framework of 2;(d)3Dsupramolecular framework viewed along the crystallographic b-axis direction(dashed lines represent hydrogen bonding interactions)

Fig.3 PXRD patterns for coordination framework(a)1 and(b)2

2.2 Photocatalytic capability for organic dyes of 1 and 2

As our knowns,large numbers of commercial organic dyes are devoted to our daily life,however,they are also toxic and carcinogenic to us.Therefore how to rational utilize and purified the waste water can be the burning question to solve.Some reported about coordination polymers can show excellent photocatalytic capability in the degradation of organic dyes under UV irradiation[19-20].

The photocatalytic activity of 1 and 2 in three different dye solutions is shown in Fig.4 and Fig.5.The entire six absorbance decrease obviously,moreover,the variation trend of the concentration ratios of the dyes(C/C0)against time(t)with 1 in solutions were plotted,with C0representing the initial concentration of dyes after stirred in the dark for 20 min.As depicted in Fig.4,complex 1 shows remarkable photocatalytic capacity for these three organic dyes,and could be nearly completely degraded(the degradation efficiency(D)of dye is 99.4%for MB,98.8%for RhB,and 84.6%for MO)in 100 min.Complex 2 also shows photocatalytic capacity for the three organic dyes,and could be nearly completely degraded(the degradation efficiency(D)of dye is 95.8%for MB,96.8%for RhB,and 83.2%for MO)in 100 min.The results indicate that both complexes 1 and 2 could be an excellent candidate for photocatalytic activity in the photocatalytic degradation of some organic dyes.

Fig.4 Plots of Ct/C0 against irradiation time of MB,RhB and MOwith coordination polymer 1

Fig.5 Plots of Ct/C0 against irradiation time of MB,RhB and MOwith coordination polymer 2

With a view to the coordination environment,the kinds of the central metal ions and the coordinated mode of the ligand have significant influence on the photocatalytic activities.As described in the previous literature[21-22],during the photocatalytic process of POM-based coordination polymers,UV-Vis light can induce POM/organic ligands to produce oxygen and/or nitrogenmetal charge transfer by promoting an electron from the highest occupied molecular orbital(HOMO)to the lowest unoccupied molecular orbital(LUMO).The HOMOstrongly demands one electron to return to its stable state.Therefore,one electron is captured from water molecules,which are oxygenated into the·OH active species,which can decompose certain dyes thus effectively to complete the photocatalytic process[23-24].

3 Conclusions

In summary, under similar hydrothermal conditions,only using different molar ratio for the stating materials (nCuⅡ∶n4-NH2-trz∶nMoO3=2∶2∶6 for 1 and 4∶3∶3 for 2),two novel polyoxometalate(POM)-based CuⅡand CuⅠhybrid materials,namely[Cu2(4-NH2-trz)4(Mo8O26)(H2O)4]·5H2O(1)and[Cu4(4-NH2-trz)4Mo8O26](2)(4-NH2-trz=4-amino-1,2,4-triazole)have been designed and synthesized.Their crystal structures have been determined by single crystal X-ray diffraction,FT-IR infrared spectra and powder X-ray diffraction.PXRD patterns of the bulky samples 1 and 2 also havebeen determined,which agreewell with theoretical PXRD patterns confirming pure phases.Photocatalytic activities for decomposition of different organic dyes have been investigated for complexes 1 and 2,indicating that 1 and 2 have significant photocatalytic degradation effect to these organic dye molecules.The result also reveals that great potential in the construction of these novel metal organic frameworks employing different triazole derivatives and versatile polyoxometalate(POM)-based building blocks.On the basis of this work,further syntheses,structures and properties studies of these coordination polymers using these versatile building blocks are also under way in our laboratory.

Supportinginformation isavailable at http://www.wjhxxb.cn

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