馬　　雁　畢凱倫　崔洋哲劉　　敏　李中峰　金瓊花（首都師范大學(xué)化學(xué)系，北京　00048）（北京工業(yè)大學(xué)材料科學(xué)與工程學(xué)院，北京　004）

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基于吡啶基苯甲酸鹽的兩個銀(Ⅱ)配合物的合成、晶體結(jié)構(gòu)及熒光性質(zhì)

馬雁1畢凱倫1崔洋哲1劉敏2李中峰1金瓊花＊，1
（1首都師范大學(xué)化學(xué)系，北京100048）
（2北京工業(yè)大學(xué)材料科學(xué)與工程學(xué)院，北京100124）

摘要：合成了2個含有吡啶基苯甲酸鹽的銀(Ⅱ)配合物，即［Ag2（PPh3）2（4，4-pybz）2（H2O）2］n（1）和［Ag2（PPh3）2（4，3-pybz）2］·2CH3OH（2）（PPh3=三苯基膦，4，4-pybz=4-吡啶-4-基-苯甲酸根，4，3-pybz=4-吡啶-3-基-苯甲酸根），并通過紅外光譜、元素分析和熒光光譜進(jìn)行分析和表征，它們的結(jié)構(gòu)由X射線單晶衍射測定。在不同的溶劑下，2個配合物由AgBF4、PPh3和不同的吡啶苯甲酸在氨水作用下，以1∶1∶1的比例反應(yīng)而成。在配合物1中，所有的銀原子由吡啶基苯甲酸橋連形成一維鏈狀結(jié)構(gòu)。在配合物2中，2個銀原子通過2個4-吡啶-3-基-苯甲酸根配體形成雙核結(jié)構(gòu)。在熒光光譜中，在發(fā)射狀態(tài)下所有的峰均來源于配體的π-π*躍遷。

關(guān)鍵詞：銀；三苯基膦；4-吡啶-3-基-苯甲酸；4-吡啶-4-基-苯甲酸

0　Introduction

In recent year，the research of coordination polymers have been of considerable interests due to important applications in gas storage［1-2］，heterogeneous catalysis［3-4］，sensing［5-6］，high photosensitivity material［7］

國家自然科學(xué)基金（No.21171119，81573832）、863國家高技術(shù)研究發(fā)展計劃（No.2012AA063201）、北京教育委員會基金（No.KM201210028020）、北京市優(yōu)秀人才項目（No.2010D005016000002）和北京市自然科學(xué)基金（No.7122015）資助。

＊通信聯(lián)系人。E-mail：jinqh@cnu.edu.cn；會員登記號：S06N3669M1105。andmagneticmaterial［8］.Thepreparationof coordination polymers or complexes can be controlled by many factors，including temperature，solution，and concentration.Closed-shell d10metal（Cu，Ag，Au）irons used for the construction of compound have also attracted attention on their coordination geometry，especiallyAg(Ⅱ)ions.Owingtotheirvariable coordinationnumberandflexiblegeometryand properties，they have been widely used［9］.

Pyridylbenzoateligandisausefulkindof bridging ligand because it contains unsymmetrical bifunctional groups.In view of this character，it has a chance of generating chiral coordination polymers［10］. 4-pyridin-4-yl-benzoic acid（4，4-Hpybz）and 4-pyridin-3-yl-benzoic acid（4，3-Hpybz）are two rigid linear kinds of ligands，which have the O and N donors on the opposite sides.In the previous studies，a numbe of group 11 or heterometallic organic frameworks with 1D，2D and 3D have reported［11-14］.

Basedontheseconsiderations，wechoos pyridylbenzoate ligand and report in this paper tw coordinationcomplexesderivedfrom triphenylphosphineligandandpyridylbenzoat ligands，namely［Ag2（PPh3）2（4，4-pybz）2（H2O）2］n（1）and ［Ag2（PPh3）2（4，3-pybz）2］·CH3OH（2） （4，4-pybz=4 pyridin-4-yl-benzoate，4，3-pybz=4-pyridin-3-yl benzoate）.They were synthesized and characterized by IR，elemental analysis and fluorescence spectrum，and their structures were elucidated by single-crystal X ray diffraction.

Scheme 1　Ligands used in the present work

Scheme 2　Routine of synthesis for complexes 1 and 2

1　Experimental

1.1Materials and measurement

All chemical reagents are commercially available and used without furthermore treatment.FTIR spectra （KBrpellets）weremeasuredonaPerkin-Elmer Infrared spectrometer.C，H and N elemental analysis were carried out on an ElementarVario MICRO CUBE （Germany）elemental analyzer.

1.2Synthesis of［Ag2（PPh3）2（4，4-pybz）2（H2O）2］n（1）

A mixture of AgBF4（0.2 mmol，0.038 6 g），triphenylphosphine（PPh3）（0.2 mmol，0.052 2 g）and 4-pyridin-4-yl-benzoic acid（4，4-Hpybz，0.2 mmol， 0.040 0 g）with a little ammonia water were dissolved in a mixture of CH3CN（5 mL）and H2O（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:54%.Element analysis Calcd for C60H50Ag2N2O6P2（%）:C，61.40；H，4.26；N，2.39 Found（%）:C，59.59；H，4.16；N，2.57.IR data（cm-1KBr pellets）:3 647w，3 356m，3 048m，1 669w，1 593s 1558s，1478m，1434m，1375s，1228w，1181w，1 096w 1 067w，1 027w，997w，870w，832m，781s，753s，694s 561w，520m，506m，477m.

1.3Synthesisof［Ag2（PPh3）2（4，3-pybz）2］·2CH3OH（2）

Complex 2 was prepared in a manner similar tthat described for 1，using AgBF4（0.2 mmol，0.039 2 g），PPh3（0.2 mmol，0.052 4 g）and 4-pyridin-3-ylbenzoic acid（4，3-Hpybz，0.2 mmol，0.039 8 g）with a little ammonia water as starting materials in a mixture of CH3OH （5mL）and CH2Cl2（5 mL）.Yield:49%. Element analysis Calcd.for C62H54Ag2N2O6P2（%）:C，61.96；H，4.50；N，2.33.Found（%）:C，62.14；H，4.45；N，2.21.IRdata（cm-1，KBrpellets）:3324w，3053w，2 918w，2 811w，1 585m，1 535m，1 477m，1 433m，1388s，1332w，1309w，1179w，1152w，1095m，1068w，1 040m，1 007w，870w，844w，813w，786m，747s，695s，559w，520m，507m，495m，463w.

1.4Structure determination

Singlecrystalsofthetitlecomplexeswere 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 SHELXS-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 with anisotropic 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 1～2 are summarized in Table 2.The hydrogen bonds of complexes 1～2 are listed in Table 3.

CCDC:890642，1；890650，2.

Table 1　Crystallographic data for complexes 1～2

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

Table 3　Hydrogen bonds of complexes 1～2

2　Results and discussion

2.1Synthesis of the complex

As is known to all，ligand and solvent are factors of influencing the structures of the compounds.In the preparation of title complexes，the ligands 4-pyridin-4-yl-benzoic acid（4，4-Hpybz）and 4-pyridin-3-yl-benzoic acid（4，3-Hpybz）influence the coordination modes of the silver atom.Complex 1 is obtained by the reaction of AgBF4，PPh3and 4，4-Hpybz with ammonia water in 1∶1∶1 molar ratio in mixed solvent（CH3CN/H2O）generating an infinite chain structure.Complex 2 is obtained by the reaction of AgBF4，PPh3and 4，3-Hpybz with ammonia water in 1∶1∶1 molar ratio in mixed solvent（CH3OH/CH2Cl2）generating a binuclear structure.In the synthesis process，NH3·H2O is used as a critical material of deprotonation，which makes 4，4-Hpybz and 4，3-Hpybz transformed into 4，4-pybz and 4，3-pybz.

2.2Infrared spectroscopy

The infrared spectra of complex 1～2 show the absorptions around 1 434 cm-1are due to C-C stretch vibrationofthephenylringsandthemiddle absorptions around 3 048 cm-1are caused by C-H vibration of the phenyl rings.The absorptions of the COO-stretch vibration are around 1 388 cm-1.

2.3Description of the crystal structure

Single-crystal X-ray diffraction analysis reveals that 1 crystallizes in the Orthorhombic system with space group P212121.The asymmetric unit（Fig.1）is comprised of two Ag(Ⅱ) ions，two PPh3ligands，two water ligands and two 4-pyridin-4-yl-benzoate（4，4-pybz）ligands，which is further linked by 4，4-pybz to generate a 1D coordination polymer（Fig.2）.The metal whichadoptsfour-coordinatedmode，isuniquely bonded to one of oxygen atoms of a carboxyl fragment and a N atom from the pyridine ring fragment of the 4，4-pybz ligand establishing a distorted tetrahedral geometry about the metal，just as in the complex｛［Ag（PPh3）2（bpp）］（BF4）｝n［16］.Ag-N（0.2325（3），0.2253（3）nm）and Ag-P bond lengths（0.2368 6（10），0.235 99（9）nm）are typical Ag(Ⅱ)-Npyand Ag(Ⅱ)-P distances，respectively［17］.Ag(Ⅱ)-Npybond distances are longer than that observed in［Ag（pycz）（H2O）］·3H2O（pycz=4-（4-pyridyl）benzonate）（0.214 5（3）nm）［18］.Moreover，the intramolecular O-H…O hydrogen bond is observed（O …O 0.267 5（4）nm，O-H…O 137.8°）in the complex 1.

Fig.1　Perspective view of complex 1

Fig.2　Linear chain of 1

Fig.3　Asymmetric unit of complex 2

Complex 2 is a binuclear heteroleptic complex formed with distinctly soft Ag(Ⅱ)，PPh3and 4，3-pybz in 1∶1∶1 molar ratio.Each Ag is four-coordinated，surrounded by a P atom from a PPh3ligands and two chelating O atoms and a N atom from two 4，3-pybz ligands（Fig.3）.The ligand 4，3-pybz acts as a typical multiple dentate ligand to join Ag(Ⅱ)atoms，just as in the complex［La2Cu2（ox）2L6］·4HL（HL=4-pyridin-4-ylbenzoic acid）［19］.The angles around Ag(Ⅱ) ranging from 88.70（8）°to 136.69（6）°indicate that the geometry around Ag atom is distortedly tetrahedral.In complex 2，Ag(Ⅱ)-Npy bond distance（0.234 2（2）nm）is longer than those in the complex［Ag3（CH3CN）3（L1）2Cl］（BF4）2·3CH3CN（0.218 7（18）and 0.232 0（5）nm）［20］.The main structure of 2 links free CH3OH by hydrogen bonding interactions.The O-H…O hydrogen bond to link freeCH3OH is observed（O…O 0.270 2（5）nm，O-H…O 168.6°）in the complex 2.

Fig.4　Solid-state excitation and emission spectra of 1～2 at 298 K

2.4FluorescenceSpectrum

The luminescent excitation and emission spectra of complexes 1～2 and 4，4-Hpybz，4，3-Hpybz ligand in the solid state at room temperature are obtained.The emission peak of PPh3is at 402 nm（λex=372 nm）［21］.In the fluorescence emission spectra of 4，4-Hpybz ligand，the emission peaks are found at 395 nm（λex=322 nm）. The 4，3-Hpybz ligand exhibits fluorescence signal centered at 417 nm with an excitation maximum at 341 nm.When excited at 354 nm，a fluorescence emission peak of complex 1 is found at 424 nm.The complex 2 exhibits fluorescence signal centered at 356 nm with an excitation maximum at 425 nm（Fig.4）. The red-shift of emission peaks of 1～2 are derived from ligand-centered π-π*transition.

3　Conclusions

Two new Ag(Ⅱ)complexes of phosphine-containing ligands，namely［Ag2（PPh3）2（4，4-pybz）2（H2O）2］n（1）and ［Ag2（PPh3）2（4，3-pybz）2］·2CH3OH（2），have been synthesized and characterized by elemental analysis，IR，X-raydiffractionandfluorescencespectra. Structureanalyses show that，theAg atomsare bridged by pyridylbenzoate-containing ligand to form infinite chain structure in 1.Two Ag atoms are bridged by two 4-pyridin-3-yl-benzoate ligands to form binuclear complex in 2.The luminescent spectra show that the origin of these emissions all involves emissive state derived from ligand centered π-π*transition We hope our results could offer new strategy for the characterization and design of coordination polymers.

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中圖分類號：O614.122

文獻(xiàn)標(biāo)識碼：A

文章編號：1001-4861（2016）05-0884-07

DOI：10.11862/CJIC.2016.100

收稿日期：2015-12-25。收修改稿日期：2015-03-02。

Syntheses，Crystal Structures and Fluorescence Properties of Two Silver(Ⅱ)Complexes Derived from Pyridylbenzoate Ligands

MA Yan1BI Kai-Lun1CUI Yang-Zhe1LIU Min2LI Zhong-Feng1JIN Qiong-Hua＊，1
（1Department of Chemistry，Capital Normal University，Beijing 100048，China）
（2The College of Materials Science and Engineering，Beijing University of Technology，Beijing 100124，China）

Abstract:Two silver(Ⅱ) complexes with pyridylbenzoate ligands，namely［Ag2（PPh3）2（4，4-pybz）2（H2O）2］n（1），［Ag2（PPh3）2（4，3-pybz）2］·2CH3OH（2）（PPh3=triphenylphosphine，4，4-pybz=4-pyridin-4-yl-benzoate，4，3-pybz=4-pyridin-3-yl-benzoate）were synthesized and characterized by IR，elemental analysis and fluorescence spectra，and their structures were elucidated by single-crystal X-ray diffraction.They have been made by reacting AgBF4，PPh3，different pyridylbenzoic acids in 1∶1∶1 molar ratio with ammonia water under different mixed solution conditions. In 1，the Ag atoms are bridged by pyridylbenzoate-containing ligand to form infinite chain structure.In 2，two Ag atoms are bridged by two 4-pyridin-3-yl-benzoate ligands to form binuclear complex.In fluorescence spectra，these emission peaks indicate that the origin of these emissions all involves emissive state derived from ligandcentered π-π*transition.

Keywords:silver；triphenylphosphine；4-pyridin-3-yl-benzoic acid；4-pyridin-4-yl-benzoic acid