兩個d10金屬配位聚合物的合成、結構及對2，4，6-三硝基苯酚的選擇性檢測

徐 涵 潘兆瑞

(1黃山學院化學化工學院，黃山 245041)

(2南京曉莊學院環境科學學院，南京 211171)

兩個d10金屬配位聚合物的合成、結構及對2，4，6-三硝基苯酚的選擇性檢測

徐 涵1潘兆瑞＊,2

(1黃山學院化學化工學院，黃山 245041)

(2南京曉莊學院環境科學學院，南京 211171)

以 4，4′-二(1-咪唑基)苯硫醚(BIDPT)，4，4′-羧基二苯胺(H2aba)，5-氧乙酸間苯二酸(H3OABDC)，Zn(NO3)2·6H2O 和 Cd(NO3)2·6H2O為原料，用溶劑熱法合成了2個配位聚合物[Zn(BIDPT)(aba)]n(1)和[Cd(BIDPT)(HOABDC)]n(2)。利用X射線單晶衍射、紅外、元素分析、熱重分析和X射線粉末衍射對其進行了表征。單晶X射線衍射研究發現配合物1為具有二重穿插的三維dia拓撲網絡結構；配合物2為3-連接六邊形的hcb二維拓撲結構，再通過氫鍵堆積作用形成三維超分子結構。1和2具有很好的熒光性質，硝基苯化合物對配合物1和2的熒光性質有不同程度的淬滅作用。它們都對2，4，6-三硝基苯酚的檢測具有很好的靈敏性。對其淬滅機理進行了深入的研究。

配位聚合物；晶體結構；熒光；硝基苯類爆炸物

Rapid and selective detection of nitroaromatic explosiveshasimmense interestbecause ofthe increasing concern about environment security.Many traditionalwayshave been developed to detectnitroaromatic explosives, such as ion mobility spectrometry,gas chromatography coupled with mass spectrometry,surface-enhanced Raman spectroscopy,X-ray imaging and other analysis methods[1-3].These methods usually have high sensitivity and selectivity,but the defects are time-consuming,not easy to operate and high cost.Recently,significant progress has been made in the application of luminescent metal-organic frameworks (MOFs)for detection of nitroaromatic explosives due to their low cost,easy synthesis,and easy modification.For example,Zhou et al.reported a luminescent EuバMOF,which exhibited selective sensing of 2,4-dinitrotolunen(2,4-DNT)with a high Ksvvalue(1.58×103L·mol-1)[4].Wang et al.reported a Cd MOF for the detection of 4-nitrophenol(4-NP)with the high Ksvvalue(6.74×104L·mol-1)and low detection limit(34.48 μg·L-1)[5].Shi et al.reported two stable Zn MOFs for the detection of picric acid (PA)with Ksvvalues of 2.40×104L·mol-1and 2.46×104L·mol-1,respectively[6].

Herein,two luminescent compounds[Zn(BIDPT)(aba)]n(1)and[Cd(BIDPT)(HOABDC)]n(2),have been successfully synthesized for sensitive detection of nitroaomative explosives through photoluminescence quenching.Notably,1 and 2 exhibit highly selective detection of PA.Quenching mechanism also has been studied deeply herein.

1 Experimental

1.1 Materials and measurement

All starting materials and solvents used during the experiments were purchased commercially without further purification.Ligand BIDPT was synthesized as reported in the literature[7].Elemental analyses(C,H and N)were carried out on a Perkin-Elmer model 240C elemental analyzer.The FT-IR spectra were obtained on a Bruker Vector 22 FTIR spectrophotometer by using KBr pellets in the range of 400～4 000 cm-1.Thermogravimetric analysis (TGA)was conducted on a NETZSCH STA 449C analyzer.Powder X-ray diffraction (PXRD)measurements were performed on a Bruker D8 Advance X-ray diffraction using Cu Kα radiation(λ=0.154 18 nm,2θ=5°～50°)in which the X-ray tube was operated at 40 kV and 40 mA.Solid-state luminescent spectra were recorded with a SHIMADZU VF-320 X-ray fluorescence spectrophotometer at room temperature.

1.2 Syntheses of compounds

[Zn(BIDPT)(aba)]n(1).A mixture of Zn(NO3)2·6H2O(29.5 mg,0.1 mmol),BIDPT(34.0 mg,0.1 mmol)and H2aba(25.6 mg,0.1 mmol)was dissolved in 9 mL H2O/CH3OH (1∶2,V/V).The final mixture was placed in a Parr Teflon-lined stainless steel vessel(15 mL)under autogenous pressure and heated at 120℃for three days.Light brown prism crystals were obtained.The yield of the reaction was ca.41%based on BIDPT ligand.Anal.Calcd.for C32H22ZnN5O4S(%):C,60.19;H,3.45;N,10.97.Found(%):C,60.32;H,3.32;N,10.81.IR (KBr,cm-1):3 403(m),3 131(s),1 687(s),1 596(s),1 518(m),1 400(s),1 304(m),1 173(m),1 127(w),1 063(m),964(m),879(m),827(m),780(s),655(w),551(w).

[Cd(BIDPT)(HOABDC)]n(2).A mixture of Cd(NO3)2·6H2O (30.8 mg,0.1 mmol),BIDPT (34.0 mg,0.1 mmol)and H3OABDC (24.0 mg,0.1 mmol)was dissolved in 5 mL of DMF/CH3CN/H2O(VDMF∶VCH3CN∶VH2O=1 ∶2∶2).The final mixture was placed in a Parr Teflon-lined stainless steel vessel (15 mL)under autogenous pressure and heated at 95℃for three days.Colorless block crystals were obtained.The yield of the reaction was ca.46%based on BIDPT ligand.Anal.Calcd.for C28H20CdN4O7S(%):C,50.23;H,2.99;N,8.37.Found(%):C,50.20;H,3.04;N,8.32.IR(KBr,cm-1):3 405(m),3 130(s),1 715(m),1 662(m),1 587(m),1 513(s),1 401(s),1 386(s),1 307(m),1 277(m),1 127(m),1 063(w),962(w),936(w),827(m),779(w),766(w),649(w),551(w).

1.3 Single crystal X-ray crystallography

Intensity data were collected with a Bruker SMART CCD diffractometer using graphite-monochromated Mo Kα radiation(λ=0.071 073 nm)for 1 and 2.All absorption corrections were performed using the SADABS program[8].The structures were solved by direct methods and all non-hydrogen atoms were refined anisotropically on F2by the full-matrix leastsquares technique using the SHELXL-97 crystallog-raphic software package[9].All the hydrogen atoms were generated geometrically and refined isotropically using a riding model.The details of the crystal parameters,data collection and refinements for 1 and 2 are listed in Table 1,selected bond lengths and angles are summarized in Table 2.

CCDC:1538448,1;1416600,2.

Table1 Crystallographic data for 1 and 2

Table2 Selected bond distances(nm)and bond angles(°)of 1 and 2

2 Results and discussion

2.1 Structures description

2.1.1 Crystal structure analysis of[Zn(BIDPT)(aba)]n(1)

The X-ray crystallographic analysis shows that compound 1 crystallizes in the orthorhombic crystal system with the Pbca space group.The asymmetric unit contains one Znギcation,one BIDPT ligand and one aba2-ligand.As shown in Fig.1,the Znギcation locates in a {ZnN2O3}distorted square-pyramidal geometry made up of two nitrogen atoms and three carboxylate oxygen atoms from two aba2-ligands.The Zn-O lengths are in the range of 0.193 2(4)～0.238 2(4)nm,while the Zn-N bond lengths are in the range of 0.202 8(4)～0.203 3(4)nm,which are in the normal range[10-11].The aba2-anions join neighboring Znギcations center to generate a 1D right-handed helical chain structure.The BIDPT ligands link the Znギcations to form another 1D right-handed helical chain structure (Fig.2).Both of the adjacent right-handed helical chains are arranged like a cross shape,leading to the formation of a 3D framework (Fig.3a).The 3D structure can be clarified as a 4-connected diamond(dia)lattice by considering Znギ cations as the connected nodes and all ligands as the 2-connected spacers (Fig.3b).Therefore,the whole structure can thus be represented as a dia topology with a point symbol of{66}.

Fig.1 Coordination environment of the Znギcation in 1

Fig.2 View of two types of right-handed helical chains constructed by aba2-and Znギ,BIDPT and Znギ

Fig.3 (a)View of the 3D framework of 1 along the b axis;(b)Two-fold interpenetrating 3D dia-type topology of 1

2.1.2 Crystal structure analysis of

[Cd(BIDPT)(HOABDC)]n(2)

Single-crystal X-ray structural analysis reveals that compound 2 crystallizes in the monoclinic crystal system with the P21/c space group and features a 2D undulated layered structure.The asymmetric unit of 2 is composed of one crystallographically independent Cdギcation,one BIDPT ligand and one partially deprotonated HOABDC2-ligand(Fig.4).Cdギis coordinated by two nitrogen atoms from two BIDPT ligands(Cd-N 0.222 6(2)～0.223 9(2)nm),two oxygen atoms from one rigid carboxyl group and one oxygen atom from one flexible carboxyl group of two individual HOABDC2-ligands(Cd-O 0.220 4(2)～0.245 6(2)nm).The Cd-O/N bong lengths are all normal and comparable to other Cdギ compounds[12-13].The rigid and flexible carboxylate groups of HOABDC2-ligand link the Cdギcations to form one infinite 1D zigzag chain with the Cd…Cd distance of 0.686 2(4)nm and Cd…Cd…Cd angle of 151.256(4)°(Fig.5a).Two BIDPT ligands link two Cdギcations to form an approximately rhombus[Cd2(BIDPT)2]32-membered metallamacrocycle (Fig.5b).The supplementary interior angles are 80.966°and 99.034°,respectively.In the metallamacrocycle,the N…Cd…N angle is 100.1°.Furthermore,a 2D undulated network is formed by the cross-link between the metallamacrocycles and the 1D zigzag chains (Fig.6a).By taking Cdギions as 3-connected nodes,and organic ligands as linkers,this 2D sheet can be viewed as a 3-connected hcb net with the point symbol of {63} (Fig.6b).Further,these layers stack in an AAA model to construct a 3D supramolecular framework by intermolecular hydrogen bond(O6-H6A…O1#1)formed in the adjacent layers(Fig.7).

Fig.4 Coordination environment of the Cdギcation in 2

Fig.5 (a)Infinite 1D linear chain formed by Cdギcations and HOABDC2-ligands;(b)Rhombus[Cd2(BIDPT)2]metallamacrocycle

Fig.6 (a)2D network of 2 viewed from the b axis direction(b)Schematic representation of 3-connected hcb net

Fig.7 View of the 3D supramolecular framework incorporating hydrogen bonds of 2

2.2 Thermal stability and powder X-ray diffraction(PXRD)

To examine the thermal stabilities of these two compounds,TGA were carried out.As shown in Fig.8,the TGA study of compound 1 indicates no obvious weight loss from 25 to 250℃,suggesting that the frameworks are thermally stable.For 2,no obvious weight loss is observed from 25 to 330℃,after that the decomposition of 2 starts.This phenomenon may be attributed to the coexistence of strong hydrogen bonding interaction and coordination interaction[14].

Fig.8 TG curves of compounds 1 and 2

To confirm the purity of 1 and 2,powder X-ray diffraction analysis (PXRD)were carried out.The experimental spectra of them are nearly consistent with their simulated spectra (Fig.9),which indicates that 1 and 2 have been successfully obtained as pure crystalline.

Fig.9 PXRD curves of compounds 1(a)and 2(b)

2.3 Luminescent property and determination of nitroaromatic compounds

To examine their luminescence properties,the solid-state luminescence of 1 and 2 are investigated at room temperature.The emission peaks of 1 and 2 appear at 510 and 525 nm,respectively,which may be attributed to the ligation of the ligand to the metal center in d10compounds[15](Fig.10).The luminescence of 1 and 2 motivated us to investigate its potential application in the detection of sensing small molecules.Considering environmental security and the strong emission of 1 and 2,we investigate their possibility of sensing nitroaromatic explosives,including 2,4-DNT,PA,4-NP,2,4-dinitrophenol(2,4-DNP),nitrobenzene (NB),3-nitrophenol(3-NP),1,3-dintrobenzene (1,3-DNB),4-nitrotoluene (NT),1,4-dintrobenzene(1,4-DNB);in detail,a series of suspensions of 1 and 2 in dimethylformamide(DMF)with gradually increasing concentrations of nitroaromatic explosives in DMF solution(5 mmol·L-1)were prepared to monitor the photolumonescence response.As shown in Fig.11,the order of quenching efficiency for 1 is PA＞3-NP＞1,4-DNB＞NT＞2,4-DNP＞2,4-DNT＞1,3-DNB＞4-NP＞NB,and the quenching efficiency for 2 is PA＞1,4-DNB＞NT＞2,4-DNP＞4-NP＞1,3-DNB＞2,4-DNT＞NB＞3-NP.To our excitement,there were significant luminescence attenuation with quenching rate of 64.3%for 1 and 61.0%for 2 in the presence of PA with the concentration of 50 μmol·L-1.

Fig.10 Solid-state photoluminescent spectra for 1 and 2

The titration curves showed that emission intensity of 1 and 2 both decreased with increasing concentration of PA from 2.5 to 150.0 μmol·L-1(Fig.12a,c).The photoluminescence quenching efficiency can be quantitatively explained by the Stern-Volmer(SV)equation:I0/I=1+KsvcPA,where I0and I are the luminescence intensities of 1 and 2 DMF suspens-ions before and after the addition of PA,respectively;Ksvis the quenching constant (L·mol-1),and cPAis the concentration of PA.As shown in Fig.12b,d,at low concentrations,the SV plots of PA display nearly linear (R2=0.992 for 1 and R2=0.994 for 2),the Ksvvalues were calculated to be 3.46×104L·mol-1for 1 and 2.28×104L·mol-1for 2,which is comparable to those in well-designed solution base organic compounds for sensing of PA[16-19].However,at higher concentration,the SV lots subsequently deviate from linearity and bend upward,which may be due to the selfabsorption[20].Low detection concentration and high quenching constant of PA show 1 and 2 can easily detect a trace quantity of PA.The mechanism of selective sensing of explosives based on coordination polymers(CPs)is not very clear,maybe the resonance energy transfer makes PA exhibit high photoluminescence quenching compared to others.

Fig.11 Quenching rates of photoluminescence for 1 and 2 upon addition of different explosive analytes with a concentration of 50 μmol·L-1

Fig.12 (a)Concentration-dependent luminescence quenching of 1 after adding different concentrations of PA;(b)Stern-Volmer plot of I0/I versus PA concentration in the 1 aqueous suspension;(c)Concentration-dependent luminescence quenching of 2 after adding different concentrations of PA;(d)Stern-Volmer plot of I0/I versus PA concentration in the 2 aqueous suspension

2.4 Mechanism of sensing nitroaromatic explosives for 1 and 2

The possible reason for the quenching may be the resonance energy transfer mechanism[21].The nonlinearity of the SV plot for PA suggests that such an energy transfer mechanism exists in the photoluminescence quenching process.The spectraloverlap between the UV-Vis absorption spectra of nitroaromatic analytes and the emission spectra of 1 and 2 were also checked.As shown in Fig.13,the absorption spectrum of PA has an effective overlap with the emission spectra of 1 and 2,so the resonance energy transferred between CPs and PA can be proved[22].As a result,resonance energy transfer makes PA exhibits high level of photoluminescence quenching compared to other nitroaromatic analytes.

Fig.13 Spectral overlap between UV-Vis spectra of explosive analytes and the emission spectra of 1 and 2 in DMF

3 Conclusions

In summary,two new CPs with different framework structures have been successfully constructed under hydrothermal conditions.Moreover,1 and 2 show strong luminescence and their luminescence could be quenched by a series of nitroaromatic explosives.Importantly,theyexhibitsveryhighly sensitive and selective detection ofpicric acid compared to other nitroaromative explosives due to the resonance transfer.Our work provides a rational strategy fordesign and synthesisofMOF-based sensors for selective and sensitive detection of one nitroaromatic explosive from other nitroaromatic explosives.

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Syntheses,Crystal Structures and Exceptionally Selective Detection of Picric Acid of Two Luminescent d10Metal-Organic Frameworks

XU Han1PAN Zhao-Rui＊,2
(1School of Chemistry and Chemical Engineering,Huangshan University,Huangshan,Anhui 245041,China)
(2School of Environmental Science,Nanjing Xiaozhuang University,Nanjing 211171,China)

Two coordination polymers,namely[Zn(BIDPT)(aba)]n(1)and[Cd(BIDPT)(HOABDC)]n(2)(BIDPT=4,4′-bis(imidazol-l-yl)diphenyl thioether,H2aba=4,4′-azanediyldibenzoic acid,H3OABDC=5-oxyacetate isophthalic acid)have been solvothermally synthesized and characterized by infrared spectroscopy,elemental analysis,and powder X-ray diffraction.In 1,the Znギions are linked by BIDPT and aba2-ligands to give a 2-fold interpenetrating 3D frameworks with{66}dia topology.Compound 2 can be viewed as a 3-connected hcb net with the point symbol of{63}and extended into a three-dimensional supramolecule through hydrogen bonds.Complexes 1 and 2 show strong luminescence and their luminescence could be quenched by a series of nitroaromatic explosives.Importantly,they exhibit very highly sensitive and selective detection of picric acid compared to other nitroaromative explosives.The quenching mechanisms are also deeply studied.CCDC:1538448,1;1416600,2.

coordination polymer;crystal structre;photoluminescence;nitroaromatic explosives

O614.24+1；O614.24+2

A

1001-4861(2018)01-0055-08

10.11862/CJIC.2018.009

2017-06-30。收修改稿日期：2017-09-11。

國家自然科學基金青年基金(No.21301094)和安徽高校省級自然科學研究基金(No.KJHS2017B05)資助項目

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