毛盼東 吳偉娜 楊 苗 楊慶雯 王 元

（河南理工大學(xué)化學(xué)化工學(xué)院，焦作 454000）

The complexes with the amide group have gained much attention due to their structural diversities,intriguing propertiesand applicationsin various fields[1-2].Such ligands with flexible structure,could form stable complexes with varies of transition metal or rare earth metal ions[3-6].To the best of our knowledge,however,the investigations on the complexes with main-group metal ions are relatively scarce.Thus,in this work,Liガ/Naガ complexes were obtained via the reaction of 2-（5-chloroquinolin-8-yloxy）-1-（pyrrolidin-1-yl）ethanone （L）with Liガ/Naガ perchlorate,which have been characterized by X-ray diffraction.In CH3CN solution,both complexes show similar fluorescence emission as L.However,under the same synthetic conditions, （HL）ClO4·H2O was accidentally produced in the case of Alバ perchlorate,which exhibits quite different fluorescence spectra from that of L.

1 Experimental

1.1 Materials and measurements

Solvents and starting materials for synthesis were purchased commercially and used as received.Elemental analysis was carried out on an Elemental Vario EL analyzer.The IR spectra （ν=4000～400 cm-1）were determined by the KBr pressed disc method on a Bruker V70 FTIR spectrophotometer.The UV spectra were recorded on a Purkinje General TU-1800 spectrophotometer.Fluorescence spectra were determined on a Varian CARY Eclipse spectrophotometer,in the measurements of emission and excitation spectra the pass width is 5 nm.

1.2 Preparations of 1,2 and(HL)ClO4·H2O

The ligand L[7-8]（0.1 mmol）and LiClO4,NaClO4or Al（ClO4）3（0.1 mmol）were dissolved in the ethyl acetate/acetone （10 mL,1∶2,V/V）solution,respectively.The mixture was filtered and spontaneously volatilized at room temperature to obtain crystals of 1,2 and （HL）ClO4·H2O,respectively.

1：Colorless needles.Anal.Calcd.for C30H30Cl3LiN4O8（%）：C,52.38;H,4.40;N,8.14.Found（%）：C,52.27;H,4.52;N,7.9.FT-IR （cm-1）：ν（C=O）1 650,ν（C=N）1 588,ν（Ar-O-C）1 236.

2：Colorless plates.Anal.Calcd.for C30H30Cl3NaN4O8（%）：C,51.19;H,4.30;N,7.96.Found（%）：C,51.07;H,4.45;N,7.78.FT-IR （cm-1）：ν（C=O）1 656,ν（C=N）1 593,ν（Ar-O-C）1 238.

（HL）ClO4·H2O：Yellow rods.Anal.Calcd.for C15H15Cl2N2O7（%）：C,44.35;H,3.72;N,6.90.Found（%）：C,44.13;H,3.96;N,6.67.FT-IR （cm-1）：ν（C=O）1 641,ν（C=N）1 594,ν（Ar-O-C）1 231.

1.3 X-ray crystallography

The X-ray diffraction measurements for 1,2 and（HL）ClO4·H2O were performed on a Bruker SMART APEXⅡCCD diffractometer equipped with a graphite monochromatized Mo Kα radiation （λ=0.071 073 nm）by using φ-ω scan mode.Semi-empirical absorption correction was applied to the intensity data using the SADABS program[9].The structures were solved by direct methods and refined by full matrix least-square on F2using the SHELXTL-97 program[10].All nonhydrogen atoms were refined anisotropically.The C13 and C14 atoms of 1 occupied two positions,with the occupancy value of C13（C14）/C13B（C14B）being 0.692/0.308.The similar feature of C14 atom in 2 is observed,with the occupancy value of C14/C14B being 0.717/0.283.The H atoms for water molecule in（HL）ClO4·H2O are located from difference Fourier map and refined with restraints in bond length and thermal parameters.All the other H atoms were positioned geometrically and refined using a riding model.Details of the crystal parameters,data collection and refinements for 1,2 and （HL）ClO4·H2O are summarized in Table 1.

CCDC：1573564,1;1573565,2;1573566,（HL）ClO4·H2O.

Table 1 Selected crystallographic data for 1,2 and(HL)ClO4·H2O

Continued Table 1

2 Results and discussion

2.1 Crystal structures

A diamond drawing of 1,2 and （HL）ClO4·H2O is shown in Fig.1.Selected bond distances are summarized in Table 2.Complexes 1 and 2 are isostructural and crystallize in the monoclinic,space group P2/n.Thus the structure of 1 is discussed in detail for an example.As shown in Fig.1a,the asymmetric unit of 1 contains a half of coordination cation with the Liガion lying on the two-fold rotate axis,and a half of free perchlorate anion for charge balance.The Liガion in 1 is surrounded by two acetamide ligands with N2O4donor set,thus giving a distorted octahedron geometry[11-12]. As expected,there exist no classic hydrogen bonds in both complexes.

Fig.1 Diamond drawing of 1 （a）,2 （b）and （HL）ClO4·H2O （c）with 30%thermal ellipsoids

Table 2 Selected bond lengths(nm)and angles(°)in 1,2 and(HL)ClO4·H2O

In （HL）ClO4·H2O,the distances of C=N and C=O are slightly shorter than those in 1 and 2,probably due to the protonation of quinoline N atom and the formation of hydrogen bonds,respectively.In the crystal,the cation （HL）+and free perchlorate anion are linked by crystal water molecule via intermolecular N-H…O （N1-H1A…O7,with D…A distance being 0.261 1（5）nm,D-H…A angle being 163.0°）and O-H…O hydrogen bonds （O7-H7C…O2,with D…A distance being 0.267 3（5）nm,D-H…A angle being 173.0°;O7-H7B…O5,with D…A distance being 0.295 3（4）nm,D-H…A angle being 160.0°）.

2.2 IR spectra

The spectral regions for both complexes are more or less similar due to the similarity in coordination modes of the ligand with the metal centre.The free ligand L exhibit three absorption bands at 1 682,1 598 and 1 241 cm-1,assigned to ν（C=O）,ν（C=N）and ν（CO-C）,respectively[13-16].However,in complexes 1 and 2,such three absorption bands shift evidently to lower frequency,indicating that the oxygen atoms of the carbonyl group,quinoline nitrogen atoms and ethereal oxygen atoms take part in coordination to the central metal ion.In addition,compared with that of the ligand,the stretching vibration frequency of the C=O（at 1 641 cm-1）and C=N （at 1 594 cm-1）of （HL）ClO4·H2O shifted by 41 cm-1and 4 cm-1,indicating the existence of hydrogen bonds involving carbonyl group and the protonation of the quinoline nitrogen atom[17].

2.3 UV spectra

Fig.2 UV spectra of L （a）,1 （b）,2 （c）and （HL）ClO4·H2O（d）in CH3CN solution at room temperature

The UV spectra of 1,2 and （HL）ClO4·H2O in CH3CN solution （concentration：10 μmol·L-1）were measured at room temperature （Fig.2）.The spectra of L features two main band located around 244 nm （ε=156 000 L·mol-1·cm-1）and 316 nm （ε=19 500 L·mol-1·cm-1）,which could be assigned to characteristic ππ*transition centered on quinoline ring and the acetamide unit, respectively[18].Similar bands are observed in 1 （242 nm,ε=26 948 L·mol-1·cm-1;314 nm,ε=3 389 L·mol-1·cm-1）and 2 （243 nm,ε=26 072 L·mol-1·cm-1;314 nm, ε=3 198 L·mol-1·cm-1）.The hyperchromicities indicate that the ligand L take part in the coordination in 1 and 2.However,a significant red-shift （254 nm,ε=32 400 L·mol-1·cm-1;371 nm,ε=1 850 L·mol-1·cm-1）can be observed in the case of（HL）ClO4·H2O,probably due to the protonation of quinoline N atom[19].

2.4 Fluorescence spectra

Fig.3 Fluorescence emission spectra of L （a,e）,1 （b,f）,2 （c,g）,and （HL）ClO4·H2O （d,h）in CH3CN solution at room temperature excited at different wavelengths

The fluorescence spectra of 1,2 and （HL）ClO4·H2O in CH3CN solution （concentration：10 μmol·L-1）were measured at room temperature （Fig.3）.When excited at 310 nm,complexes 1 and 2 show a broad emission at 403 nm as the free ligand L[18],while （HL）ClO4·H2O exhibits almost no emission under the same tested conditions （Fig.3A）.On the contrary, （HL）ClO4·H2O could display intense green emission （at 525 nm）observed by naked eyes at excitation of 390 nm（Fig.3B）.The protonation of nitrogen atoms can greatly enhance the electron-withdrawing ability of quinoline,which may lead to a little bit delocalize.Meanwhile,the delocalization of the electron cloud density can help to stabilize the molecules in the excited states,which is contributed to the shifts of the fluorescence spectra to longer wavelength[20].

[1]Song X Q,Wen X G,Liu W S,et al.J.Solid State Chem.,2010,183：1-9

[2]Binnemans K.Coord.Chem.Rev.,2015,295：1-45

[3]Yan Z Z,Hou N,Wang C M.Spectrochim.Acta A,2015,137：1265-1269

[4]Song X Q,Xing D Y,Lei Y K,et al.Inorg.Chim.Acta,2013,404：113-122

[5]Song X Q,Wang Y W，Zheng J R,et al.Spectrochim.Acta A,2007,68：701-704

[6]Wu W N,Tang N,Yan L.J.Fluoresc.,2008,18：101-107

[7]Wu W N,Yuan W B,Tang N,et al.Spectrochim.Acta A,2006,65：912-918

[8]MAO Pan-Dong（毛盼東）,CHEN Liang（陳 亮）,WU Wei-Na（吳 偉 娜 ）,et al.Chinese J.Inorg.Chem.（無(wú) 機(jī) 化 學(xué) 學(xué) 報(bào) ）,2016,32（2）：336-342

[9]Sheldrick G M.SADABS,University of G?ttingen,Germany,1996.

[10]Sheldrick G M.SHELX-97,Program for the Solution and the Refinement of Crystal Structures,University of G?ttingen,Germany,1997.

[11]Huang Y Q,Zhao W,Chen J G,et al.Z.Anorg.Allg.Chem.,2012,638：679-682

[12]Huang Y Q,Wan Y,Chen H Y,et al.New J.Chem.,2016,40：7587-7595

[13]Wu W N,Tang N,Yan L.Spectrochim.Acta A,2008,71：1461-1465

[14]Wu W N,Cheng F X,Yan L,et al.J.Coord.Chem.,2008,61：2207-2215

[15]MAO Pan-Dong（毛盼東）,XU Jun（徐君）,WU Wei-Na（吳偉娜）,et al.Chinese J.Inorg.Chem.（無(wú)機(jī)化學(xué)學(xué)報(bào)）,2016,32（4）：677-682

[16]YE Xing-Pei（葉行培）,WU Wei-Na（吳偉娜）,LI Fei-Fei（李飛飛）,et al.Chinese J.Inorg.Chem.（無(wú)機(jī)化學(xué)學(xué)報(bào)）,2013,29（13）：2678-2682

[17]XU Mu-Sheng（徐 木 生）,ZHUANG Zhi-Xia（莊 峙 廈）,SUN Da-Hai（孫 大 海）,et al.Spectroscopy and Spectral Analysis（光譜學(xué)與光譜分析）,1999,19（4）：556-558

[18]Song X Q,Zang Z P,Liu W S,et al.J.Solid State Chem.,2009,182：841-848

[19]HAO Yong-Jing（郝勇靜）,XIE Juan（謝娟）,YIN Xiao-Ru（殷曉茹）.Journal of Northwest University：Nature Science（西北大學(xué)學(xué)報(bào)：自然科學(xué)版）,2016,52（5）：64-67

[20]Ma S Q,Zhang J B,Liu Y J,et al.J.Phys.Chem.Lett.,2017,8：3068-3072