張奇龍 王煥宇 胡鵬 朱必學

(1貴陽醫(yī)學院化學教研室，貴陽550004)

(2貴州省大環(huán)化學及超分子化學重點實驗室，貴陽550025)

1,3-雙(2-(2,2-二氰乙烯基)苯氧基)-2-丙醇及其銀(Ⅱ)配合物的合成、晶體結(jié)構(gòu)及其熒光性質(zhì)

張奇龍＊，1王煥宇1胡鵬1朱必學2

(1貴陽醫(yī)學院化學教研室，貴陽550004)

(2貴州省大環(huán)化學及超分子化學重點實驗室，貴陽550025)

用1,3-雙(2-甲酰基苯氧基)-2-丙醇和丙二腈進行反應得到1,3-雙(2-(2,2-二氰乙烯基)苯氧基)-2-丙醇配體L，然后將配體與AgSbF6進行配位反應，得到配合物[AgLSbF6]n·nCHCl3(1)，并用元素分析,FTIR和X-射線單晶衍射進行了表征。結(jié)果表明，配體L屬于單斜晶系，空間群P21/n，晶體學參數(shù)：a=0.990 2(11)nm,b=2.181(2)nm,c=1.012 2(11)nm,β=109.374(10)°,V=2.062(4) nm3,Z=4,Dc=1.277 g·cm-3,Mr=396.40,μ=0.087 mm-1,F(000)=824,R1=0.064 2,wR2=0.117 4(I＞2σ(I))。配合物1屬于單斜晶系，空間群P21/n，晶體學參數(shù)：a=1.270 57(11)nm,b=1.456 44(13)nm,c=1.669 85(14)nm,β=105.643(3)°,V=2.975 6(4)nm3,Z=4,Dc= 1.918 g·cm-3,Mr=859.39,μ=1.907 mm-1,F(000)=1 664,R1=0.0417,wR2=0.1 032(I＞2σ(I))。在配合物1中，配體L表現(xiàn)為四齒配體分別與4個銀(Ⅱ)離子配位，同時，每一個銀(Ⅱ)離子與4個相鄰配體配位形成2D層狀結(jié)構(gòu)。同時，研究了配體和配合物的固體熒光性質(zhì)。

1,3-雙(2-(2,2-二氰乙烯基)苯氧基)-2-丙醇；晶體結(jié)構(gòu)；Ag(Ⅰ)配合物；熒光性質(zhì)

0 Introduction

The assembly of coordination polymers(CPs), consisting of metal ions and organic polymers,with specific network topologies has attracted significant researchinterestinrecentyearsowingtotheir tremendous potential applications as functional solidstate materials[1-4]in material science and engineering. However,the rational design and fabrication of CPs withspecificstructuresandtunablephysical properties is a challenging task.The diverse structures of such materials always depend on several factors, such as type of metal ion,template,metal-ligand ratio, pH value,counter anion,and number of coordination sites provided by organic ligands[5-6].Silver(I)-based CPs(AgCPs)have attracted remarkable attention becauseoftheirdistinctmolecularstructures. Moreover,theyactaspromisingcandidatesfor conductive,luminescent,andmagneticmaterials. Interestingly,Ag(I)exhibits strong preference toward coordination to nitrogen donor than to harder oxygencontaining ligands.Therefore,it is extremely important to explore and rationalize the effect of different ligands on the topology of AgCPs.

An outstanding aspect of the AgCPs is that they possessuniqueluminescencefeaturesthathave attractedsignificantinterestoftheresearchers. Therefore,extensiveresearcheffortshavebeen devoted to the AgCPs.Great affinity of Ag ions leads to dynamic coordination range varying from two to six, even to seven and eight,showing strong tendency to displayversatilecoordinationspheres,partly attributed to the d10electronic configuration of Ag[7-10]. Moreover,there are numerous ligands with rational design and reasonable use to compose functional CPs with excellent structures and properties[11-12].Based on the fact that flexible organic molecules adopt different conformations under different conditions[13-16],in this study,interaction of the flexible ligand 1,3-bis(2-(2,2-dicyanovinyl)phenoxy)-2-propanol(L,Scheme 1)with Ag(I)was investigated.Herein,we describe the synthesis,crystal structure,and fluorescent properties of Ag(I)complex coordinated to flexible,ether-bridgin g,tetradentate ligand L.

Scheme 1 Schematic representation of the formation of ligand L

1 Experimental

1.1 Materials and measurements

All chemicals from commercial sources were of reagent grade and used without purification.Elemental (C,H,N)analysis data were obtained with a Vario ELⅢelemental analyzer.IR spectra were recorded by KBr pellets on Bio-Rad FTIR spetrophotometer(in the 400～4 000 cm-1range).1H NMR spectra were recorded on a JEOLECX 500MHz spectrometer using DMSO solutionatroomtemperature.Thermogravimetric measurements were carried out in a nitrogen stream using a Netzsch STA449C apparatus with a heating rate of 10℃·min-1.X-Ray powder diffraction(XRPD) was carried out on a RIGAKU DMAX2500 apparatus.

1.2 Synthesis of the ligand L

1,3-bis(2-formylphenoxy)-2-propanol[17](0.3 g,1.0 mmol),excess of malononitrile(CH2(CN)2),and ammoniumacetate(NH4OAc)weremixedthoroughlyina mortar.The product so obtained was purified by column chromatography on silica gel using dichloromethane (CH2Cl2)as an eluent to afford yellow crystalline solid (0.26 g,65%).1H NMR(500MHz,DMSO-d6):8.623(s, 2H,C=CH),8.029～7.133(m,8H,C6H4),5.732(s,1H, CHOH),4.337(s,1H,OH),4.284～4.153(m,4H, OCH2CH2O).Anal.Calcd.(%)for C23H16N4O3:C,69.69; H,4.07;N,14.13;Found(%):C,69.62;H,4.00;N, 14.17.IR(KBr,cm1):3 524(m),3 046(w),2 924(w), 2 226(m),1 581(s),1 482(m),1 453(m),1 363(w),1 307 (w),1257(s),1163(w),1 116(w),1 045(w),1 006(w),947 (w),812(w),759(w),616(w),490(w).

1.3 Synthesis of[AgLSbF6]n·nCHCl3(1)

Hexafluoroantimonate(V)(AgSbF6,0.17 g,0.1 mmol)in chloroform(CHCl3,20 mL)was added dropwise with stirring to ligand L(0.2 g,0.5 mmol)in ethanol(20 mL)and stirring was continued at room temperature for several days.Slow evaporation of this solution yielded yellow block crystals suitable for X-ray analysis.The precipitate so formed was collected by filtration,and dried at room temperature to give 1(0.26 g,60%).Anal. Calcd.(%)for AgC24H17Cl3N4O3SbF6:C,33.54;H,1.99; N,6.52.Found(%):C,33.60;H,1.92;N,6.60.IR(KBr, cm-1):3 444(s),2 928(w),2 228(m),1 726(w),1 587(s), 1 483(m),1 454(m),1 362(w),1 310(w),1 253(s),1 166 (w),1115(w),1 005(w),809(w),757(s),615(s).

1.4 X-ray crystallographic study

X-ray diffraction data were collected at room temperature with graphite monochromated Mo Kα radiationonBrukerSmartApexsinglecrystal diffractometer by using a φ-ω scan method.Unit cell dimensionswereobtainedwithleast-squaresrefinements and multi-scan absorption corrections were applied by using SADABS program.The structures were solved by direct methods using the program SHELXL-97 in the winGX package[18].H atoms were placed in calculated positions,with C-H distances of 0.093～0.096 nm and NH=0.086 nm,and refined using a riding model with Uiso(H)=(1.2～1.5)Ueq(C).The ORTEP-3[19]drawing of the molecules is shown in Fig.1 and Fig.3.Crystal and experimental data are listed in Table 1,selected bond lengths and angles are given in Table 2.Hydrogen bonding geometry is given in Table 3 and Table 4.

Fig.1Molecular structure of ligand L

Fig.2Dimers formed by the ligand through O2-H2…H2-O2 hydrogen bonds

Fig.3Thermal ellipsoid plot at 25%level of the asymmetric units of the complex 1

Table 1Crystallographic data for ligand L and 1

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

Table 3Hydrogen Bond Lengths(nm)and Bond Angles(°)for ligand L

Table 4C-H…π interactions in complex 1

CCDC：1008802,L;1008804,1.

2 Results and discussion

2.1 Crystal structures of ligand L and complex1

The bond lengths and bond angles of ligand L are listed in Table 2,and its crystal structure is shown in Fig.1.The hydroxyl groups present in the flexible ligand are connected by the ether chain bridge.Fig.1 and values listed in Table 2 show that the two pairs of C(CN)2are located toward the end of the base in the same direction.However,the two benzene rings are not in a plane,and the dihedral angle between them is 168.37°.The ligand forms dimers through O2-H2…H2-O2 hydrogen bonds(Fig.2 and Table 3).

The crystal structure of the complex 1 is shown in Fig.3.Single-crystal XRD analysis reveals that compound 1 crystallizes in the monoclinic space group P21/n.The asymmetric unit is composed of a Ag(Ⅰ)center,a unique ligand L,an SbF6anion,and CHCl3solventmolecules(Fig.3).EachAg(Ⅰ)ionis tetracoordinated in a distorted tetrahedron coordination environment to three N atoms and one O atom from four different ligands.The Ag1-N1,Ag1-N2,and Ag1-N4 bond lengths are 0.240 5(4),0.217 0(4),and 0.223 1(5)nm,respectively.The Ag1-O3 bond length is 0.246 7(3)nm,N-Ag-N bond angles are in the range of 87.14(15)°～138.57(15)°,and N-Ag-O bond angles are in the range of 91.32(12)°～109.46(12)°. The ligands act as a μ4-bridge connecting four Ag(Ⅰ)ions,with three nitrogen atoms of the three cyano groups,respectively and one oxygen atom of hydroxyl group.The two cyano nitrogen atoms at one end of ligand L coordinate with two Ag(Ⅰ)ions independently. In contrast,only one of the two cyano nitrogen atoms at the other end coordinates with a Ag(Ⅰ)ion;the uncoordinatednitrogenatomundergoesweak interaction with the molecules of solvent CHCl3.The two adjacent cyano nitrogen atoms at the two ends of ligand L and the two cyano nitrogen atoms at one end of another ligand L coordinate with two Ag(Ⅰ)ions simultaneouslyandthus,forma24-member macrocycle.Such 24-member macrocycles alternately extend to either side and form a one-dimensional(1D) ribbon structure(Fig.4),in which the hydroxyl oxygen atoms of ligand L coordinate individually to Ag(Ⅰ)ion, bridgingthe1DribbonstructuresintotheCPs consisting of two-dimensional(2D)mesh structure.In this 2D mesh structure(Fig.5),C-H…π interactionsexist between the hydrogen on C4(H4)and ring Cg1, with an C4-H4…Cg(1)angle of 93.33°,a H4…Cg(1) distance of 0.315 45 nm,where Cg(1)is the centroid of the phenyl ring formed by atoms C5,C6,C7,C8,C9, and C10(Table 4).The ligands act as four-connecting nodes;the Ag atoms act as four-connecting links.

Fig.41D ribbon structure in the complex 1

Fig.5View of 2D coordination layer structure in the complex 1

2.2 PXRD analysis

To examine the phase purity of the complexes, the PXRD patterns of title complex was obtained at room temperature.As shown in Fig.6,the peak positions of the simulated and experimental PXRD patterns were in agreement,demonstrating good phase purityforthecomplex.Thedissimilaritiesin intensities may be due to the preferred orientation of the crystalline powder samples.

Fig.6PXRD patterns of complex 1

2.3 Photoluminescent properties of Ligand L and Complex 1

The photoluminescence spectra of the ligand L and complex 1 are shown in Fig.7.The ligand L exhibited photoluminescence with emission maxima at 474 nm(λex=337 nm).Presumably,the peak originated from the π*→n or π*→π transitions[20].Intense emissions occurred at 525 nm(λex=338 nm)for complex 1,which was attributed to the intraligand π→π* transitions modified by metal coordination[21].The enhancementandslightred-shiftofcomplex1 compared to that of the ligand L probably resulted from the fact that the coordination of Ag(Ⅰ)ions increased the conformational rigidity of the ligand and;thus,reduced the loss of energy by thermal vibrational decay[22-23].

Fig.7Fluorescence spectra of the ligand and complex

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Synthesis,Crystal Structures,and Fluorescent Properties of Ag(I)Complex Containing 1,3-Bis(2-(2,2-dicyanovinyl)phenoxy)-2-propanol Ligand

ZHANG Qi-Long＊，1WANG Huan-Yu1HU Peng1ZHU Bi-Xue2
(1Department of Chemistry,Guiyang Medical College,Guiyang 550004,China)
(2Key laboratory of Macrocycle and Supramolecular Chemistry,Guiyang 550025,China)

1,3-bis(2-formylphenoxy)-2-propanol underwent an ammonium acetate-catalyzed condensation reaction with dicyanomethane to afford the ligand 1,3-bis(2-(2,2-dicyanovinyl)phenoxy)-2-propanol(L).Further,the ligand L was made to react with hexafluoroantimonate(AgSbF6)which resulted in the formation of coordination polymer [AgLSbF6]n·nCHCl3(1).Complex 1 so-obtained was characterized by Fourier transform infrared spectroscopy,elemental analysis,and single crystal X-ray diffraction.The results of X-ray crystallographic analysis indicated that the ligand L crystallized in the monoclinic system,space group P21/n,with the following crystal cell parameters: a=0.990 2(11)nm,b=2.181(2)nm,c=1.012 2(11)nm,β=109.374(10)°,V=2.062(4)nm3,Z=4,Dc=1.277 g·cm-3, Mr=396.40,μ=0.087 mm-1,F(000)=824,R1=0.064 2,and wR2=0.1174(observed reflections withI＞2σ(I)). Complex 1 crystallized in the monoclinic system,space group P21/n,with the following crystallographic data:a= 1.270 57(11)nm,b=1.456 44(13)nm,c=1.669 85(14)nm,β=105.643(3)°,V=2.975 6(4)nm3,Z=4,Dc=1.918 g· cm-3,Mr=859.39,μ=1.907 mm-1,F(000)=1664,R1=0.041 7,and wR2=0.103 2(observed reflections with I＞2σ(I)). In the crystal structure,each ligand L acted as a tetradentate ligand coordinating four Ag(Ⅰ)centers,and each Ag(Ⅱ)was connected to four ligands L,forming two-dimensional layered structure.Moreover,the fluorescent properties of ligand L and complex 1 were investigated in the solid state at room temperature.CCDC：1008802,L;1008804,1.

3-bis(2-(2,2-dicyanovinyl)phenoxy)-2-propanol;crystal structure;Silver(Ⅱ)Complex;Fluorescent property

O614.81+2；O614.24+1

A

1001-4861(2015)02-0353-08

10.11862/CJIC.2015.030

2014-08-01。收修改稿日期：2014-09-17。

國家自然科學基金(No.21061003)資助項目。

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