金屬氯化物-苯并噻唑有機(jī)-無機(jī)雜化化合物的合成、表征及熒光性質(zhì)

劉 慶 魏振宏 于 慧 郝艷歡 蔡 琥

金屬氯化物-苯并噻唑有機(jī)-無機(jī)雜化化合物的合成、表征及熒光性質(zhì)

劉 慶 魏振宏＊于 慧 郝艷歡 蔡 琥＊

（南昌大學(xué)化學(xué)學(xué)院，南昌 330031）

金屬鹵化物MCl2（M=Pb2+,Cd2+,Co2+）分別與苯并噻唑（btz）在濃鹽酸中、80℃下反應(yīng),合成了3種有機(jī)-無機(jī)雜化化合物:（btzH）［（PbCl3）]（1）,（btzH）2［CdCl4]·2H2O （2）和（btzH）2［CoCl4]·2H2O （3）,其中化合物 2 和 3 結(jié)構(gòu)相似。對化合物 1～3 進(jìn)行了粉末衍射、紅外和紫外光譜、元素分析、熱重分析以及X射線單晶衍射表征。熒光測試發(fā)現(xiàn):化合物1～3在393 nm處有發(fā)射峰,該熒光來源于苯并噻唑環(huán)中電子的π…π躍遷。

金屬氯化物；苯并噻唑；有機(jī)-無機(jī)雜化；晶體結(jié)構(gòu)；熒光性質(zhì)

0 Introduction

Organic-inorganic hybrid perovskite functional materials are a new type of crystal materials，in which the inorganic perovskite layer works as a skeleton and the organic molecular functional groups are connected to the inorganic perovskite layer through intermolecular hydrogen bonds［1-4].The organic and inorganic components form a long-range ordered single crystal through the alternating stacking，in which the inorganic parts supply the hybrid structure with thermal stability and hardnessaswellasoptical，electricaland magnetic properties［5-8]，and the organic materials offer thehybridswith softness，flexibility，and highly efficient luminescence［9]and structural diversity［10-13].Over the pastdecade，organic-inorganic hybrid compounds have exhibited good development and application in the solar semiconductor batteries［14]，light-emitting diodes［15]，ferroelectric properties［9]and other fields［16-18].

In organic-inorganic hybrid materials，the organic ligands not only play a role as the template［19-21]，but also the key to determining the properties of inorganic components［22-24]，such as in photoelectric field，the organic-inorganic hybrids constructed with organic amines and lead halide have shown good fluorescence performance［25-27].Thisisbecausethehybridperovskiteis a type of semiconductor quantum well structure，typically with small band gap inorganic sheets （carrier）alternating with larger band gap organic layer［28-30].For example，the new reported 2D lead bromide perovskite （DMEN）PbBr4（DMEN=2-（dimethylamino）ethylamine）incorporating a bifunctional ammonium dication as template was found to have white-light，broad-band emission in the visible range［25].

In this article，an aromatic heterocycle organic template benzothiazole （btz）was selected to react with the main and transition metal halides MCl2（M=Pb2+，Cd2+，Co2+）in the concentrated HCl acid，and three inorganic-organic hybrid compounds:（btzH）［PbCl3]（1），（btzH）2［CdCl4]·2H2O （2）and （btzH）2［CoCl4]·2H2O （3）were obtained.Herein，we reported the syntheses，characterizations and fluorescent properties of compounds 1，2 and 3.

1 Experimental

1.1 Instrument and materials

The starting materials PbCl2，CdCl2，CoCl2·6H2O，benzothiazole and the concentrated hydrochloric acid are commercially available and were used as received.FT-IR spectra were recorded using KBr pellets in the range of 4 000～400 cm-1on an ALPHA spectrometer.UV-Vis spectra were collected on a UV-Vis Curry 60 spectrophotometer.Powder X-ray diffraction （PXRD）patterns were collected on a glass sheet in the 2θ range of 5°～50°with a scan rate of 2°·min-1on a D8 ADVANCE diffractometerequippedwithCu Kα radiation （λ=0.154 18 nm，U=40 kV，I=40 mA）at 298 K.Thermo-gravimetry （TG）were carried out between 30 and 800℃ at a scan rate of 10℃·min-1in a N2atmosphere on a TGA Mettler-Toledo Gmbh thermogravimetric analyzer.Micro-analysis service was recorded on a Heraeus CHN-O-Rapid.Fluorescent spectra were carried on a Hitachi F-4600 spectrophotometer.

1.2 Syntheses of compounds 1～3

1.2.1 Synthesis of （btzH）［（PbCl3）] （1）

To a solution of PbCl2（0.20 g，0.72 mmol）in concentrated HCl（18 mL，47%）was added a solution of benzothiazole （0.20 g，1.52 mmol）in concentrated HCl（18 mL，47%）.The mixed solution was heated to 80℃and kept stirring for half hour.Cooling down the reaction to room temperature gave colorless needle crystals.Yield:144 mg，44% （based on PbI2）.Anal.Calcd.for C7H6NSCl3Pb（%）:C 18.69，H 1.34，N 3.11.Found （%）:C 18.36，H 1.69，N 3.33.IR （KBr，cm-1）:3 740（w），3 440 （s），3 094 （m），3 046（w），2 948 （m），2 865（m），2 802（m），2 742（m），2 646（m），1 852（m），1 716（m），1 596（m），1 580（m），1 458（m），1 428（m），1 271（m），1 241（m），952（s），888（s），800（w），755（w），721（m），686（m），554（w），503（w），423（w）.

1.2.2 Synthesis of （btzH）2［CdCl4]·2H2O （2）

According to the similar procedure to synthesis of compound 1 based on CdCl2（0.359 g，1.96 mmol）and benzothiazole （0.396 g，2.93 mmol）in concentrated HCl（18 mL，47%）gave the light gray prismatic crystals of 2.Yield:124 mg，72%.Anal.Calcd.for C14H16N2O2S2Cl4Cd（%）:C 29.89，H 2.87，N 4.98.Found （%）:C 29.64，H 2.43，N 4.72.IR （KBr，cm-1）:3 424（s），3 102（m），3 052 （w），2 963 （m），2 895（m），2 813（m），2 745 （m），2 359 （s），1 811 （w），1 603（w），1 579（s），1 461（s），1 429（m），1 244（s），825（s），761（w），722（s），566（w），504（w），413（w）.

1.2.3 Synthesis of （btzH）2［CoCl4]·2H2O （3）

According to the similar procedures to synthesis of compound 1 based on CoCl2·6H2O （0.50 g，1.83 mmol）and benzothiazole （0.49 g，3.63 mmol）in concentrated HCl （18 mL，47%）gave the deep blue block crystals of 3.Yield:400 mg，43%.Anal.Calcd.for C14H16N2O2S2Cl4Co（%）:C 33.03，H 3.17，N 5.50%.Found （%）:C 33.47，H 3.31，N 5.13.IR （KBr，cm-1）:3 738（w），3 411（w），3 076（w），3 029（m），2 946（m），2 878 （w），2 809 （w），2 744 （m），2 658 （m），2 365 （s），1 833（w），1 702（s），1 626（s），1 586（s），1 460（m），1 413（m），1 294（s），1 266（s），1 244（s），1 168（s），1 046（s），912（m），822（s），757（w），721（m），685（s），538（w），497（w），418（s）.

1.3 X-ray crystallography

In the crystallographic data collection of compounds 1～3，standard procedures were used for mounting the crystals on a Bruker SMART CCD diffractometer with graphite-monochromated Mo Kα radiation （λ=0.071 073 nm）.The structures were solved by the direct methods routines in the SHELXS program and refined on F2in SHELXL［31].Non-hydrogen atoms were first refined isotropically followed by anisotropic refinement by full matrix least-squares calculations based on F2using SHELXL-97［32].All hydrogen atoms exceptthatin watermoleculeswere placed in idealized positionsand treated asriding atoms.Hydrogen atoms in water molecules were first located in the difference Fouriermaps then positioned geometrically and allowed to ride on their respective parent atoms.Details of the data collection and refinement are given in Table 1.

CCDC:1571943，1;1571944，2;1571945，3.

Table 1 Crystal data and structure refinement for compounds 1～3

2 Results and discussion

2.1 Synthesis and characterization

Compounds 1～3 were obtained by reactions of MX2（M=Pb，Cd，Co）and btz with molar ratio of 1∶2 in concentrated HCl solution. After heating and evaporation，the reactions led to the formation of colorless needle crystals of 1，light gray plate crystals of 2 and deep blue block crystals of 3 in moderate yields，respectively.Crystals were then filtered and washed with methanol and acetonitrile and dried in vacuo.The phase purities of a mass of 1～3 were verified using the powder X-ray diffraction （PXRD）patterns which matched very well with the simulated ones in terms of the single-crystal X-ray data as shown in Fig.S1.

TheTGA curvesforcompounds1～3 were provided in Fig.S2.Complex 1 occurrs two weight loss steps between 180 and 750℃.The first weight loss，observed between 180 and 200℃，is ascribed to the decomposition of the btz ligand （30%loss）.The second weight loss，occurring between 550 to 750 ℃ ，is attributed to the loss of halide anions or sublimation of newly formed PbCl2compound.While complex 2 is not stable，it firstly decomposes at 100 ℃ due to the loss of solvated water （6%）.The second and third weight loss between 150 to 280℃are ascribed to the loss of btz ligand （49%）.The last weight loss began at 560 ℃ is corresponded to the loss of CdCl2，which is consistent with its melting point at 568℃.The residue（1.5%）may belong to the high boiling impurities.The weight loss of compound 3 is somewhat familiar to complex 2，but the weight loss curve is not as clear as that in complex 2.

In FT-IR spectra of compounds 1～3，the strong absorption bands at 1 580 and 1 596 cm-1for 1，1 579 and 1 603 cm-1for 2，1 586 and 1 626 cm-1for 3 are ascribed to the C=C and C=N stretching vibrations of aromatic rings.The middle absorptions at 3 094，3 046 cm-1for 1，at 3 102，3 052 cm-1for 2 and at 3 076，3 029 cm-1for 3 are corresponded to the vibration of C-H bond in benzothiazole ring.The C-S stretching vibration in compounds 1～3 is about at 722 cm-1.Due to the formation of hydrogen bond，the vibration of NH in benzothiazole ring becomes very weak.The broad and strong bands at about 3 400 cm-1in compounds 2 and 3 indicate the presence of co-crystallized water molecules.

2.2 Structure description

Complex 1 crystallizes in the triclinic system with a space group of P1 and the asymmetric unit contains one （btzH）+cation，one ［PbCl3]-anion （Fig.1a）.Based on the connectivity of the chlorine atoms to the Pb atoms，there are three types of chlorine atoms:the terminal Cl（3），the double bridging Cl（1），and the triple-bridging Cl（2）.The inorganic part of 1 is composed of ［PbCl6]octahedrons by sharing three edges along a axis direction to give 1D double-strand（Fig.1b）.The protonated （btzH）+cations are connected to the double-strands by intermolecular hydrogen bond N-H…Cl along c axis direction （Table 4）.In ［PbCl6]octahedron，the Pb-Cl bond lengths vary from 0.275 6（2）to 0.304 3（2）nm，and the maximum angle of Cl-Pb-Cl is at 174.53（6）°，revealing the octahedron was seriously distorted （Table 2）.

Complex 2 crystallizes in the triclinic system with a space group of P1 and the asymmetric unit contains two protonated （btzH）+cations，one ［CdCl4]2-anion and two solvated water molecules （Fig.2a）.The coordination geometry around the Cd(Ⅱ)atom adopts a slightly distorted tetrahedron with the Cd-Cl bond lengths varying from 0.244 34（7）to 0.245 39（6）nm，and the angles varying from 105.89（4）°to 114.25（3）°（Table 3）.In the whole structure，two water molecules act as μ2-connecting nods linking the ［CdCl4]tetrahedrons by two pairs of hydrogen bonds（Owater-H…Cl，Table 4）along a and b directions to form a 2D layer （Fig.2b）.At the same time，the cationic （btzH）+suspends on the 2D layer using the other type of hydrogen bond （N-H…Owater）along c direction，（Table 4，F(xiàn)ig.3c）.

Fig.1 （a）Asymmetric unit of 1 drawn with 30%thermal ellipsoids;（b）Protonated （btzH）+cations connected to 1D double-strands by N-H…Cl hydrogen bonds

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

Fig.2 （a）Asymmetric unit of 2 drawn with 30%thermal ellipsoids;（b）［CdCl4]tetrahedrons connected with water molecules using hydrogen bonds O-H…Cl along a and b directions;（c）（btzH）+cations connected to the 2D layers using hydrogen bond N-H…O along c direction

Complex 3 crystallizes in the monoclinic system with a space group of C2/c and the asymmetric unit contains one protonated （btzH）+cations，half ［CoCl4]2-anion and one solvated water molecules （Fig.3a）.As shown in Fig.3b and 3c，the structure of compound 3 is very similar to that of complex 2，so the structure of compound 3 is not described in detail herein.To be noted，the Co-Cl bond lengths in complex 3 are shorter than the Cd-Cl bond lengths in complex 2 due to that the radius of Co2+ion is smaller than that of Cd2+（Table 3）.But the average bond angle Cl-Co-Clat 109.5°in tetrahedron ［CoCl4]is similar to that of Cl-Cd-Cl（109.44°）in ［CdCl4].

Table 3 Selected bond lengths （nm）and angles （°）for 2 and 3

Fig.3 （a）Asymmetric unit of 3 drawn with 30%thermal ellipsoids;（b）［CoCl4]tetrahedrons connected by water molecules using hydrogen bonds O-H…Cl along a and b directions to form 2D layer;（c）（btzH）+cations suspended on the 2D layers using hydrogen bond N-H…Owateralong c direction

2.3 Absorption and fluorescence

As shown in Fig.4，compounds 1～3 in the solid states showed the similar absorption wavelengths in the range of 200～300 nm.The absorption peaks at 260 and 300 nm both come from the π … π*transition of btz ring which can be proved by the absorptions of free ligand btz in solution （Fig.4，inset）.Due to the strong absorption of organic part，the absorptions originated from inorganic parts［PbCl6]in complex 1 and ［CdCl4]in complex 2 are not obvious.In 3，the tetrahedrally coordinated Co2+ions show the obvious absorption band in the range of 600～750 nm which belong to the spin allowed d-d transitions of Co2+ion.While in complex 2，the d-d transition is not found due to that the d orbits in Cd2+ions are full.

Table 4 Hydrogen bonds for compounds 1,2 and 3

Fig.4 UV-Vis spectra of compounds 1～3 in solid states

The solid fluorescent spectra of compounds 1～3 were showed in Fig.5.At the excitation wavelength of 320 nm，all compounds show the similar emissions at 393 nm.In order to clarify the fluorescence source of the compounds 1～3，we carried out the fluorescence test of free ligand btz in solution，but it was found that there was no fluorescence response in dichloromethane solution.According to the literatures，we know that benzothiazole has a large π-conjugated system，and manybenzothiazolederivativeshave exhibited good fluorescence properties［33-35].According to the above analysis，we still believe that the fluorescence emission peaks of compounds 1～3 are derived from the π … π transition of the btz ring.This is because the benzothiazole is protonated and hydrogenbonded to the chloride atoms in polyhedron，and its fluorescence performance turns from original quenching into enhancement.

Fig.5 Emission spectra of compounds 1～3 in the solid states

3 Conclusions

Three organic-inorganic hybrid compounds were isolated by reactions of btz with MCl2（M=Pb2+，Cd2+，Co2+）in concentrated HCl aqueous solution.The single X-ray diffraction investigation demonstrated that the inorganic part in complex 1 is a 1D two stranded chain，and those in compounds 2 and 3 are the ［MCl4]（M=Cd，Co）tetrahedrons，which are both linked with the solvated water molecules by the hydrogen bond.Fluorescent spectra reveal that compounds 1～3 show the similar emission peaks at 393 nm，which are ascribed to the π…π transition of the protonated btz ring.

Supporting information is available at http://www.wjhxxb.cn

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Syntheses,Characterization and Optical Properties of Three Organic-Inorganic Hybrid Compounds Based on Metal Chlorides and Benzothiazole

LIU Qing WEI Zhen-Hong＊YU HuiHAO Yan-Huan CAI Hu＊
（College of Chemistry,Nanchang University,Nanchang 330031,China）

The reaction of three divalent metal (Ⅲ) halides MCl2（M=Pb2+，Cd2+，Co2+）with two equivalents of benzothiazole （btz）in the concentrated acid HCl at 80 ℃ resulted in the formation of the corresponding organicinorganic hybrid compounds: （btzH）［（PbCl3）] （1），（btzH）2［CdCl4]·2H2O （2）and （btzH）2［CoCl4]·2H2O （3），in which the structures of compounds 2 and 3 are similar.All compounds have been characterized by XRD，IR，UV-Vis，EA，TG and single X-ray diffraction.Fluorescent investigation reveals that compounds 1～3 exhibit similar emission peaks at 393 nm，which are ascribed to the π…π transition of the btz ring.CCDC:1571943，1;1571944，2;1571945，3.

metal chloride;benzothiazole;organic-inorganic hybrid;crystal structure;fluorescent property

O614.43+3；O614.24+2；O614.81+2

A

1001-4861（2017）11-2139-08

10.11862/CJIC.2017.258

2017-09-09。收修改稿日期:2017-10-15。

國家自然科學(xué)基金（No.21571094,21661021）和江西省科技廳項目（No.20161BAB203073）資助。

＊通信聯(lián)系人。E-mail:weizh@ncu.edu.cn,caihu@ncu.edu.cn