李中峰　張振偉　崔洋哲　劉敏　楊玉平　金瓊花＊,(首都師范大學(xué)化學(xué)系，北京0008)(首都師范大學(xué)物理系，北京0008)(北京工業(yè)大學(xué)材料科學(xué)與工程學(xué)院，北京00)(中央民族大學(xué)理學(xué)院，北京0008)

兩種基于硫醇配體的銀(Ⅱ)配合物的合成、表征和晶體結(jié)構(gòu)

李中峰1張振偉2崔洋哲1劉敏3楊玉平4金瓊花＊,1
(1首都師范大學(xué)化學(xué)系，北京100048)
(2首都師范大學(xué)物理系，北京100048)
(3北京工業(yè)大學(xué)材料科學(xué)與工程學(xué)院，北京100124)
(4中央民族大學(xué)理學(xué)院，北京100081)

通過AgCl、PPh3和MBT以1∶2∶1的物質(zhì)的量之比反應(yīng)得到2種不同的配合物[AgCl(PPh3)2(BTZT)]·CH3OH(1)和[AgCl(PPh3)2(BTZT)]2(2)(PPh3=三苯基膦；MBT=2-巰基苯并噻唑；BTZT=苯并噻唑-2-硫酮)(其中2已報(bào)道)。配合物[AgBr(PPh3)2(BTZT)]·CH3OH (3)和[AgBr(PPh3)2(BTZT)]2(4)改用AgBr以相似的反應(yīng)獲得(其中4已報(bào)道)。通過紅外光譜、元素分析、核磁共振氫譜、X射線單晶衍射、熒光光譜對配合物1和3進(jìn)行了分析和表征。我們發(fā)現(xiàn)在不同的化學(xué)環(huán)境中，MBT配體可以轉(zhuǎn)化為BTZT配體，原因是其具有化學(xué)活性基團(tuán)。熒光光譜表明1和3的發(fā)射峰均源于配體中的π-π*躍遷。

三苯基膦；2-巰基苯并噻唑；苯并噻唑-2-硫酮；配合物

0　Introduction

Currently,quite a few novel coordination complexes are reported[1-2].With the rapid development of coordination complexes,complexes with closed-shell d10metals have attracted considerable attention due to important applications in catalysis[3-4]and biochemistry[5-6].In particular,complexes bearing the Ag-S bond have raised continuously increasing interest,owing to their use in pharmacology[7]and thin films[8],as well as glass and ceramic technology[9].In coordination chemistry,it is one of the most interesting phenomena that two or more stable products are synthesized by the same reactions.The success of designed synthesis and separation of materials still look upon as something of challenge[10-11].

Herein,we set out to design,prepare,and characterize silver(Ⅱ)complexes of silver halides AgX (X=Cl,Br),using same phosphine moieties and taking into account the coordination versatility of the thiol ligand(Scheme 1),namely[AgCl(PPh3)2(BTZT)]· CH3OH(1),[AgCl(PPh3)2(BTZT)]2(2)[12],and[AgBr (PPh3)2(BTZT)]·CH3OH(3),[AgBr(PPh3)2(BTZT)]2(4)[13](PPh3=triphenylphosphine;BTZT=benzothiazoline-2-thione).The BTZT ligand was transformed from MBT ligand in different chemical environment because of chemically active groups of MBT(MBT=2-mercaptobenzothiazole)[14].Complexes 1 and 3 have been synthesized and characterized by IR,elemental analysis,1H NMR spectroscopyand single-crystalX-raydiffraction.

Scheme 1 Routine of synthesis for complexes 1～4

1　Experimental

1.1Materials and measurements

All chemical reagents are commercially available and used without furthermore treatment.FT-IR spectra(KBr pellets)were measured on a Perkin-Elmer Infrared spectrometer.C,H and N elemental analysis were carried out on an ElementarVario MICRO CUBE(Germany)elemental analyzer.1H NMR was recorded at room temperature with a Bruker DPX 600 spectrometer.

1.2Synthesis of[AgCl(PPh3)2(BTZT)]·CH3OH (1)

A mixture of AgCl(0.2 mmol,0.0291g),PPh3(0.4 mmol,0.104 9 g)and MBT(0.2 mmol,0.033 3 g) were dissolved in a mixture of CH3OH(5 mL)and CH2Cl2(5 mL),stirred for 6 h and filtered.Colorless crystal 1 was obtained from the filtrate after standing at the room temperature for several days.Yield:56%. Element analysis Calcd.for C44H39AgClNOP2S2(%):C, 60.89;H,4.50;N,1.61;Found(%):C,61.08;H,4.39; N,1.52.IR data(KBr pellets,cm-1):3 418w,3 049w, 2937w,2815w,1598w,1583w,1495m,1478m,1432 s,1 328m,1 092m,1 077w,1 028m,1 012w,743s, 693s,604w,512m.1H NMR(600 MHz,CDCl3,298 K):δ 7.51～7.23(m,CHbenzene).

1.3Synthesis of[AgBr(PPh3)2(BTZT)]CH3OH(3)

Complex 3 was prepared in a manner similar to that described for 1,using AgBr(0.2 mmol,0.037 0 g),PPh3(0.4 mmol,0.104 8 g)and MBT(0.2 mmol, 0.033 2 g)as starting materials.Yield:51%.Element analysis Calcd.for C44H39AgBrNOP2S2(%):C,57.92;H, 4.27;N,1.53.Found(%):C,57.81;H,4.02;N,1.46. IR data(KBr pellets,cm-1):3 434w,3 052w,3 001w, 2 935w,2 875w,2 825w,1 596w,1 492m,1 478m, 1 432s,1 323m,1 093m,1 076w,1 030m,1 012w, 996w,743s,694s,606w,513m.1H NMR(600 MHz, CDCl3,298 K):δ 7.51～7.23(m,CHbenzene).

1.4Structure determ ination

Single crystals of the title complexes were mounted on a Bruker Smart 1000 CCD diffractometer equipped with a graphite-monochromated Mo Kα(λ= 0.071 073 nm)radiation at 298 K.Semi-empirical absorption corrections were applied using SADABS program[15a].All the structures were solved by direct methods using SHELXS program of the SHELXTL-97 package and refined with SHELXL-97[15b].Metal atom centers were located from the E-maps and other nonhydrogen atoms were located in successive difference Fourier syntheses.The final refinements were performed by full matrix least-squares methods withanisotropic thermal parameters for non-hydrogen atoms on F2.The hydrogen atoms were generated geometrically and refined with displacement parameters riding on the concerned atoms.

Crystallographic data and experimental details for structural analysis are summarized in Table 1,and selected bond lengths and angles of complexes 1 and 3 are summarized in Table 2.The bond lengths and angles of hydrogen bonds of complexes 1 and 3 are listed in Table 3.

CCDC:1407305,1;1407306,3.

Table 1 Crystallographic data for com p lexes 1 and 3

Table 2 Selected bond distances(nm)and bond angles(°)for complexes 1 and 3

Table 3 Hydrogen bonds of com p lexes 1 and 3

2　Results and discussion

2.1Synthesis of comp lexes

As is known to all,many factors can influence the structures of the compounds,such as temperature, solvent and molar ratio of the starting materials.We obtain two kinds of complexes 1 and 2 by the reactions of AgCl,PPh3,and BTZT in 1∶2∶1 molar ratio in mixed solvent(CH3OH/CH2Cl2).Complex 1 crystallizes in the monoclinic system with space group P21/n,while 2[12]crystallizes in the triclinic system with space group P1.

3 and 4 were obtained by the reactions of AgBr with PPh3in the presence of 2-mercaptobenzothiazole (MBT)in 1∶2∶1 molar ratio in mixed solvent(CH3OH/ CH2Cl2).3 crystallizes in the monoclinic system with space group P21/n,while 4[13]crystallizes in the triclinic system with space group P1.

Complexes 2 and 4 were synthesized in winter, but 1 and 3 were obtained in summer.So we think that the temperature of volatilization may influence the structures of the compounds.

2.2Infrared spectroscopy

The infrared spectra of complexes 1 and 3 show the absorption around 1 459～1 495 cm-1due to C-C stretch vibration of the phenyl rings and the middle absorption around 3 049 or 3 052 cm-1is caused by C-H vibration of the phenyl rings.The C-H out-ofplane bending vibrations of the phenyl rings are found around 743 and 694 cm-1.The absorption of the N-H stretch vibration is in the range of 3 418～3 434 cm-1. The C=N bond vibration is found in 1 432 cm-1.

2.3Description of the crystal structure

Single-crystal X-ray diffraction analysis of 1 reveals the Ag(Ⅱ)metal adopts four-coordinated mode, which is bonded to two P atoms from two PPh3ligands,one chlorine atom and one S atom from the C=S fragment of the BTZT ligand peripherally establishing a distorted tetrahedral geometry about the metal.In particular,the complex 2 contains two same moieties in each asymmetric unit[12].

In complex1(Fig.1),theAg-Pbond distance issimilar to that in previous literature.The Ag-Cl bond distance is comparable with those observed in related complexes[AgCl(κ1-S-C3H5NS(NeMe))(PPh3)2](0.257 0(1) nm)[16]and[AgCl(κ1-S-C3H5NS(NePrn)(PPh3)2)] (0.257 51(5)nm)[16].The Ag-S bond distance is longer than that found in[Ag(imdt)Cl]n[17](0.248 66(14)nm), but it is shorter than that of complex 2[12].The angles around the Ag atom are in the range of 100.50(3)°～129.27(3)°.The Cl-Ag-S bond angle is smaller than that of[AgCl(TPP)2(MTZD)](102.68(3)°)and{[AgCl (TPP)2(MBZT)]·(MBZT)·2(toluene)}(104.91(4)°)[18].

Fig.1 Perspective view of complex 1 with thermal ellipsoids drawn at the 30%probability level

Moreover,intramolecular N-H…Cl hydrogen bonds are observed(N…Cl 0.311 6(3)nm,N-H…Cl 170.0°)in the complex 1.The main structure of 1 links free CH3OH by hydrogen bonding interactions.

In complex 3(Fig.2),the angles around the Ag atom are in the range of 101.13(4)°～129.04(5)°.The coordination geometry around each Ag atom indicates a distorted tetrahedron.The Ag-P bond length is typical Ag-P distance[19].The Ag-Br distance is found in good agreement with the reported values[16,20],but is longer than those of complex 4.The Ag-S bond length is longer than that observed in[Ag2(μ-S-pySH)2(PPh3)2Br2](0.260 8(1)nm)[14].The P-Ag-P bond angle is all longer than those in another similar complex[21]. Moreover,intramolecular N-H…Br hydrogen bonds are observed(N…Br 0.326 9(5)nm,N-H…Br 169.2°) in the complex 3.The main structure of 3 links free CH3OH by hydrogen bonding interactions.The O-H…Br hydrogen bond to link free CH3OH and NO3-anion is observed(O…Br 0.332 9(7)nm,O-H…Br 171.2°) in the complex 3.

Fig.2 Perspective view of complex 3 with thermal ellipsoids drawn at the 30%probability level

Compared to complex 3,the complex 4 contains two same structures in each asymmetric unit.Each Ag atom adopts four-coordinated mode,which is coordinated with two P atoms from two PPh3,one Br atom and one S atom from benzothiazoline-2-thione ligand (BTZT).

2.4Fluorescence spectra

The luminescent excitation and emission spectra of complexes 1,3 and MBT ligand in the solid state at room temperature are obtained.The emission peak of PPh3is at 402 nm(λex=372 nm)[19].In the fluorescence emission spectrum of MBT ligand,the emission peak is found at 419 nm(λex=342 nm).When excited at 365 nm,a fluorescence emission peak of complex 1 is found at 431 nm.The complex 3 exhibits fluorescencesignal centered at 423 nm with an excitation maximum at 353 nm.The red-shift of emission peaks of 1 and 3 are derived from ligand-centered π-π* transition.

Fig.3 Solid-state excitation and emission spectra of 1 and 3 at 298 K

3　Conclusions

In summary,two kinds of silver(Ⅱ)halide complexes based on triphenylphosphine and benzothiazoline-2-thione,[AgCl(PPh3)2(BTZT)]·CH3OH(1),and [AgBr(PPh3)2(BTZT)]·CH3OH(3),were synthesized and characterized by IR,elemental analysis,1H NMR spectroscopy,luminescent spectra and single-crystal X-ray diffraction.However,by the same reactions two different products 2(The reaction condition was same as 1)and 4(The reaction condition was same as 3) were synthesized.Single-crystal X-ray diffraction analysis reveals that 1 and 3 crystallize in the monoclinic system with space group P21/n,while 2 and 4 crystallize in the triclinic system with space group P1.The luminescent spectra show that 1 and 3 emission peaks were assigned to the ligand centered π-π*transition.

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Syntheses,Characterizations and Crystal Structures of Two Kinds of Silver(Ⅱ)Com p lexes Derived from Thiol Ligand

LI Zhong-Feng1ZHANG Zhen-Wei2CUI Yang-Zhe1LIU Min3YANG Yu-Ping4JIN Qiong-Hua＊,1
(1Department of Chemistry,Capital Normal University,Beijing 100048,China)
(2Department of Physics,Capital Normal University,Beijing 100048,China)
(3The College of Materials Scienceand Engineering,Beijing University of Technology,Beijing 100124,China)
(4School of Science,Minzu University of China,Beijing 100081,China)

Two kinds of complexes[AgCl(PPh3)2(BTZT)]·CH3OH(1)and[AgCl(PPh3)2(BTZT)]2(2)were obtained by the reaction of AgCl,PPh3,and MBT in 1∶2∶1 molar ratio(PPh3=triphenylphosphine;MBT=2-mercaptobenzothiazole BTZT=benzothiazoline-2-thione)(2 has been reported).[AgBr(PPh3)2(BTZT)]·CH3OH(3)and[AgBr(PPh3)2(BTZT)]2(4)were prepared in a manner similar to 1 and 2 using AgBr(4 has been reported).Complexes 1 and 3 have been characterized by IR,elemental analysis,1H NMR spectroscopy,fluorescence spectrum and singlecrystal X-ray diffraction.The MBT ligand can transform into the BTZT ligand in different chemical environment because of its chemically active groups.The luminescent spectra show that emission peaks of 1 and 3 are assigned to the ligand centered π-π*transition.CCDC:1407305,1;1407306,3.

triphenylphosphine;2-mercaptobenzothiazole;benzothiazoline-2-thione;complex

O614.122

A

1001-4861(2016)01-0139-06

10.11862/CJIC.2016.023

2015-08-19。收修改稿日期：2015-11-11。

國家自然科學(xué)基金(No.21171119，11104360，11204191，81573832)、863國家高技術(shù)研究發(fā)展計(jì)劃(No.2012AA063201)、北京教育委員會基金(No.KM201210028020)和北京市優(yōu)秀人才項(xiàng)目(No.2010D005016000002)資助。

＊通信聯(lián)系人。

E-mail：jinqh@cnu.edu.cn；會員登記號：S06N3669M1105。