錐形構(gòu)象含氟杯芳烴衍生物對(duì)銅離子的高選擇性識(shí)別

齊 琪 李 星

(寧波大學(xué)材料科學(xué)與化學(xué)工程學(xué)院，浙江省光電探測(cè)材料及器件重點(diǎn)實(shí)驗(yàn)室，寧波 315211)

0 Introduction

During the past few years，the development of efficient sensors detecting metal ions has attracted wide attention.Some metal ions are strong toxic to the human body at very low concentration，such as mercury ions and palladium ions.Although some metal ions play a central part in our daily life and are widely used in industry，excessive uptake can also have harmful effects.Therefore，it is meaningful to selectively identify related ions for human health.At present，many ion detection sensor materials have been developed，such as ion recognition responsive materials based crown ether[1]，ion recognition materials based coordination compounds[2-3]，ion recognition materials based calix[4]arene[4].

Calix[4]arenes are highly applied into many fields，such as recognition，sensors，biomedicine[5-9]，because of their adjustable conformation and easy derivatization.Calix[4]arenes are especially prominent in sensors and selective receptors due to their functionalized structures and complexation possibilities[10-12].In the field of reco-gnition of ions，the design of highly selective and multifunctional calix[4]arene derivatives has become an important branch and is also an interesting aspect of supramolecular chemistry[13-18].Chemical modification of calix[4]arenes is one of the methods to prepare derivatives[19-20].Calix[4]arene derivatives modified by different functional moieties areobtained by introd-ucing characteristic groups，such as optical active groups and electrical active groups.Wong et al.[21]investigated the property dependence of phenyl-calix[4]crown-4 on the upper rim substituent of methyl，fluorine or trimethylsilyl.Chawla et al.[22]synthesized a series of para-substituted receptors which show selectivity to Cs+and Rb+ions by introducing arylazo，thiazolylazo，pyridylazo and β-naphthylazo groups into tetrathiacalix[4]arene.However，it was rarely reported that fluorine groups were introduced on the upper rim of calix[4]arene. It is due to the special properties of fluorine groups[23-24]that few researchers synthesize fluorinated calix[4]arene derivatives.Herein，we synthesized fluorinated calix[4]arene derivatives by using Suzuki coupling reaction to modify the up-rim of calix[4]arenes and introduce fluorine and trifluoro-methyl groups into calix[4]arenes，and we studied their recognition properties.

1 Experimental

1.1 General

1H NMR spectra in CDCl3were detected on a Bruker 400 MHz spectrometer.FT-IR spectra were obtained by a Nicollet 6700 FT-IR spectrometer.UVVis spectral studies were carried out by using a TU-1901 spectrophotometer (Beijing Purkinje General Instrument).Fluorescence spectra were recorded on a Hitachi F-4600 fluorescence spectrometer.All the reagents and chemicals were commercially available and analytical pure.

1.2 Synthesis of compound 1

5，11，17，23-Tetrabromo-25，26，27，28-tetraethoxycalix[4]arene (a，0.425 7 g，0.5 mmol)，4-(trifluoromethyl)phenylboronic acid(0.372 5 g，2.0 mmol)and sodium carbonate(0.424 0 g，4 mmol)were mixed in the mixed solvent of toluene/ethanol/water(20 mL/10 mL/2 mL).The mixture was added tetrakis(triphenylphosphine)palladium((β-4)-platinum)after pumping vacuum and purging with nitrogen gas for three times.Subsequently，the mixture was heated at 80℃to reflux under nitrogen protection and stirred for 24 h.The solution was stratified statically after the reaction completed.The inorganic layer was extracted with dichloromethane(6 mL ×3)，and the organic layer was washed with saturated salt water(6 mL×3).Successively，organic phases merged into one phase，which was dried with anhydrous sodium sulfate and concentrated by rotary evaporator.The raw solid was obtained.After the purification process by a silica gel column，the white solids of 5，11，17，23-tetra(4-trifluoromethylphenyl)-25，26，27，28-tetraethoxycalix[4]arene were obtained(0.110 g，Yield:19.8%).Elemental Anal.Calcd.C64H52F12O4(%):C，69.06；H，4.70.Found(%):C，70.20；H，4.94.IR(KBr，cm-1): νmax1 328(CF3).1H NMR(400 MHz，CDCl3):δ7.39(d，J=7.9 Hz，4H，ArH)，7.27～7.18(m，5H，ArH)，6.95(s，4H，ArH)，4.59(d，J=13.1 Hz，2H，ArCH2Ar)，4.12(q，J=6.8 Hz，4H，CH2)，3.31(d，J=13.2 Hz，2H，ArCH2Ar)，1.55(t，J=6.7 Hz，7H，CH3).

1.3 Synthesis of compound 2

Compound a (0.426 7 g，0.5 mmol)and 4-fluorophenylboronic acid (0.826 9 g，2 mmol)were stirred in 32 mL of mixed solvents(Vtoluene∶Vethanol∶Vwater=10∶5∶1)at ambient temperature.The sodium carbonate solution (2 mL，2 mol·L-1)was added to the mixture.Then the mixture was added (β-4)-platinum after vacuuming and sparging nitrogen gas several times and heated at 80 ℃ to reflux for 24 h.Finally，the reaction mixture was extracted with CH2Cl2and washed with saturated salt water.The product was purified by a silica gel column to give compound 2 as a white solid (0.100 g，yield 21.92%).Elemental Anal.Calcd.for C60H52F4O4(%):C，78.93；H，5.74.Found(%):C，79.95；H，6.56.IR (KBr，cm-1):νmax1 227(Ar-F).1H NMR(400 MHz，CDCl3):δ7.04(dd，J=8.5，5.4 Hz，2H，ArH)，6.86(s，2H，ArH)，6.80(t，J=8.7 Hz，2H，ArH)，4.55(d，J=13.1 Hz，1H，ArCH2Ar)，4.08(q，J=7.0 Hz，2H，CH2)，3.26(d，J=13.2 Hz，1H，ArCH2Ar)，1.53(dd，J=13.5，6.4 Hz，6H，CH3).

Scheme 1 Synthetic routes for compounds 1～3

1.4 Synthesis of compound 3

A mixture of a(0.851 2 g，1.0 mmol)and 3，5-bis(trifluoromethyl)benzeneboronic acid (1.038 8 g，4 mmol)in the presence of Na2CO3(2.218 9 g)as the templating base under nitrogen in mixed solvent was stirred.(β-4)-Platinum was added in the solution after vacuuming three times.After all reagents were added，the resulting mixture was refluxed at 90℃under the protection of nitrogen for 24 h.The solution was extracted with CH2Cl2and washed with saturated salt water three times after reaction.The solution was dried with anhydrous sodium sulfate.Then，the crude product was obtained by concentrating with rotary evaporator.Compound 3 was obtained by the purification process(0.130 g，Yield:9.40%).Elemental Anal.Calcd.for C68H48F24O4(%):C，58.97；H，3.49.Found(%):C，59.03；H，3.51.IR(KBr，cm-1):νmax1 272(CF3).1H NMR(400 MHz，CDCl3):δ7.58(s，1H，ArH)，7.43(s，2H，ArH)，6.94(s，2H，ArH)，4.60(d，J=13.2 Hz，1H，ArCH2Ar)，4.12(q，J=7.0 Hz，2H，CH2)，3.35(d，J=13.3 Hz，1H，ArCH2Ar)，1.63～1.50(m，8H，CH3).

1.5 General procedure for UV-Vis study and fluorescence study

Standard stock solutions(0.01 mol·L-1)of metal acetate salts and chloride salts (NaCl，KCl，CsCl，Cu(Ac)2·H2O，BaCl2·2H2O，Zn(Ac)2，Mg(Ac)2·4H2O，Cd(Ac)2·2H2O，Mn(Ac)2·4H2O，Co(Ac)2·4H2O，Ni(Ac)2·4H2O，F(xiàn)eCl3，CaCl2)were prepared in CH3OH.The stock solutions(0.1 mmol·L-1)of compounds 1～3 were prepared with CH2Cl2.The solution concentration of compounds 1～3 is 5 μmol·L-1with different concentrations of metal ions in the mixed solvent(VCH2Cl2∶VCH3OH=1∶1)in the titration experiments for UV-Vis and fluorescent studies.

1.6 X-ray diffraction data collection and refinement

Crystallographic data for 1 and 2 were collected at room temperature on a Bruker Smart CCD area detector diffractometer equipped with a graphite monochromated Mo Kα radiation (λ=0.071 073 nm)by ω-2θscan mode.All absorption corrections were applied using the SADABSprogram[25].The Lp factor and empirical absorption were performed to correct the data，and to restore the data and correct the unit cell parameters by using SANIT and SMART software.The structures were solved by direct method and refined on F2by full-matrix least-squares using the SHELXTL-97 program package[26].All non-hydrogen atoms were refined with anisotropic displacement parameters. All hydrogen atoms were placed geometrically and were refined in a riding-model approximation.The crystallographic data of compound 1 and 2 are summarized in Table 1.

CCDC:1900304，1；1900303，2.

Table 1 Crystallographic data for compounds 1 and 2

2 Results and discussion

2.1 Synthesis of compounds 1～3

Modifying up-rim of calix[4]arene was implemented according to the Scheme 1.Compound a as raw materials can be prepared by published procedure[27].Thus，the Suzuki coupling reaction of tetrabromocalix[4]arene with fluorine-containing phenylboronic acid produced fluorine-containing calix[4]arene derivatives.The structures of compounds 1～3 were proved by respective IR，X-ray diffraction and1HNMR spectra.

1H NMR spectroscopy can be used as a marker to identify the conformation of calix[4]arene derivatives because there are different characteristics with different conformations in1H NMR spectra[28-30].The conical conformation of the compound 1 can be confirmed by the presence of doublets atδof 3.31 and 4.59 as an AB type proton signal of ArCH2Ar in the1H NMR spectra.In the1H NMR spectra of compound 2，there were two doublets atδof 3.26 and 4.45 for ArCH2Ar，which confirmed the compound 2 is in the cone conformation.Compound 3 adopts the coneconformation due to the proton signal of methylene bridges atδof 3.35 and 4.60 in1H NMR spectra.The IR spectra of compounds 1～3 show characteristic bands at 1 328 cm-1(CF3)，1 227 cm-1(Ar-F)and 1 272 cm-1(CF3)，respectively.

2.2 Single crystal structure

We successfully obtained colorless single crystals of compounds 1 and 2 from the mixed solvent(ethyl acetate/petroleum ether)and collected their structure data by single crystal X-ray diffractometer.As shown in Fig.1 and 2，X-ray diffraction analysis revealed that compound 1 and 2 adopts conical conformations.Single crystals suitable for X-ray diffraction analysis of 3 were not obtained presently.

Compound 1 shows an asymmetric distorted cone conformation，in which the relatively long distance between the aromatic ring C1…C6 and C29…C34 is about 1.44 nm，and the short distance between the aromatic ring C15…C20 and C43…C48 is about 0.37 nm(Fig.1).The nearest distance(0.37 nm)is attributed to the strong π-π stacking interactions in 1.The distance about 0.49 nm between the aromatic ring C21…C26 and C49…C54 displays hardly the π-π stacking interactions.The aromatic ring C21…C26 are rotated relative to the aromatic ring C15…C20，and torsion angle of C19-C18-C21-C26 is 37.2°.Similarly，torsion angle of C45-C46-C49-C50 is 40.5°.

Compound 2 with a cone conformation was obtained through substituents of 4-fluorophenyl groups on upper rim，similar to compound 1.The distance between the aromatic rings C1…C6 and C1A…C6A is about 0.35 nm，which results from strong π-π interactions in 2 (Fig.2).Torsion occurs between fluorophenyl-substituted aromatic rings C1…C6 and C7…C12，and torsion angle of C3-C4-C7-C8 is about 45.3°.

Fig.1 Crystal structure(a)and π-π stacking interaction(b)of compound 1

Fig.2 Crystal structure(a)and π-π stacking interaction(b)of compound 2

2.3 UV-Vis spectroscopic studies

Calix[4]arenes are considered to be perfect compounds for forming stable complexation with metal ions，such as Fe3+，Ni2+，Cu2+.Therefore，we studied and explored the fluorinated calix[4]arene for binding ability.The titration experiments were implemented to explore the interplay of compounds 1～3 with various metal ions and investigate its selectivity.

As shown in Fig.3，it can be found that the maximum ultraviolet absorption wavelength of compounds 1～3 are in a range of 220～270 nm in the mixed solvent(VCH2Cl2∶VCH3OH=1∶1).The ultraviolet spectrum of compound 1 displayed strong peaks at 230 and 270 nm owing toπ→π*and n→π*transitions.There were two peaks at 232 and 258 nm in the ultraviolet spectrum of compound 2，and the UV-Vis spectrum of 3 exhibited strong peaks at 225 and 266 nm.

Fig.3 UV-Vis spectra of compounds 1～3 in mixed solvent CH2Cl2/CH3OH

The selectivity of 1～3 in mixed solvent(5 μmol·L-1)to different metal ions (0.5 mmol·L-1，excepted Fe3+)was preliminarily measured by UV-Vis spectroscopy.The wavelength with maximum absorbance upon the metal ion addition was listed in Table 2.On the basis of titration experiments，compound 1 exhibited a new band at 361 nm after adding Fe3+(10 equiv.)(Fig.4).After adding copper ions(100 equiv.)，the new band appeared at 246 nm while the original peaks disappeared as shown in Fig.4.Compared with the compound 1 in the absence of metal ions，the absorbance of the band enhanced greatly.Other metal ions，unlike iron or copper ions，only caused slight changes in absorption bands.Moreover，the color of compound 1 changed to yellow green after adding Cu2+for 24 h (Fig.4).The result reflects that 1 is more selective for Cu2+ions.

Fig.4 UV-Vis spectra of 1 with different metal ions(100 equiv.excepted Fe3+)in the mixed solvent CH2Cl2/CH3OH

Table 2 Maximum absorbance wavelength of compounds 1～3 after titration with metals ions

The UV-Vis spectrum of compound 2 exhibited a significant increase of absorbance with the addition of Cu2+(Fig.5)，and the bands shifted to 237 nm.The change of bands indicates that compound 2 has the ability to interact with copper ions.With the addition of nickel ions，the absorbance of compound 3 enhanced remarkably at 226 nm and decreased at 266 nm，although the absorption bands did not shift significantly(Fig.6).In the presence of iron ions，the spectra showed gentle absorption peaks.In addition，it was visible that the new absorption band appeared at 246 and 362 nm，respectively，after copper and iron ions were added in the solution of compound 3 as shown in Fig.6.The results show that copper ions，iron ions and nickel ions can interact with compound 3，especially copper ions have the most pronounced response.

Fig.5 UV-Vis spectra of compound 2 with different metal ions(100 equiv.，excepted Fe3+)in the mixed solvent CH2Cl2/CH3OH

Fig.6 UV-Vis spectra of compound 3 with different metal ions(100 equiv.，excepted Fe3+)in the mixed solvent CH2Cl2/CH3OH

Compounds 1～3 show different binding abilities to metal ions，which possibly result from the following two factors:different substituents and substitution sites on the upper edge of calix[4]arenes.It can be seen that the factors affecting the selectivity of ligands to metal ions are not only the hard or soft properties of metal ions，but also the radius of ions，the size of holes and even the conformation of compounds.Many factors lead to the selectivity of different compounds to specific ions[31-35].

The selectivity of compounds 1～3 to copper ions was tested in existence of interfering ions by experiments adding Cu2+ions and the other ions(1∶1)(Fig.7～9).It was found that other ions did not obviously interfere absorption spectra of the compounds with Cu2+.In addition，the interference of other ions on the binding of compound 3 to iron ions was also examined(Fig.10).Other ions except Cu2+did not affect the absorption spectra of compound 3 with iron ions.Adding copper ions broke down the binding of compound 3 to iron ions，which may be due to the higher binding efficiency of compound 3 to copper ions.

Fig.7 Interference test of other ions on compound 1 with Cu2+in the mixed solvent CH2Cl2/CH3OH

Fig.8 Interference test of other ions on compound 2 with Cu2+in the mixed solvent CH2Cl2/CH3OH

Fig.9 Interference test of other ions on compound 3 with Cu2+in the mixed solvent CH2Cl2/CH3OH

Fig.10 Interference test of other ions on compound 3 with Fe3+in the mixed solvent CH2Cl2/CH3OH

2.4 Fluorescence studies

The fluorescence spectra of compounds 1～3(5 μmol·L-1)were measured as shown in Fig.11.The emission peak of 1 was 360.4 nm under the excitation of 294 nm，and there was a fluorescence peak of 2 at 348.4 nm when the exciting wavelength is 289 nm，while that of 3 was at 383.0 nm with excitation at 292 nm.The results from the fluorescence spectroscopy show that there is similarity in the optimum excitation wavelengths of the compounds.

Fig.11 Fluorescence spectra of compounds 1～3 in the mixed solvent CH2Cl2/CH3OH

The binding of compounds 1～3 (5 μmol·L-1)towards various ions (100 equiv.，excepted Fe3+)was tested by fluorescence spectroscopy as showed in Fig.12～14.The results of tests are consistent with those of ultraviolet spectra.The fluorescence intensity of compound 1 decreased sharply after adding copper ions，and there was obvious quenching in emission.The intensity of compound 2 decreased obviously in the existence of Cu2+ions，while the other ions did not lead to remarkable changes.In the existence of copper and iron ions，the fluorescence intensity of compound 3 decreased.The intensity of compound 3 towards Cu2+showed stronger quenching than that of compound 3 to Fe3+.Compound 3 is more compatible to Cu2+than Fe3+.Upon addition of metal ions(100 equiv.，except Fe3+)，all metal ions more or less affect the emission intensity of compounds 1～3 despite no changing in the band of compound 1～3.In particular，the addition of copper and iron ions causes remarkable quenching in emission intensity.These results indicate that 1 and 2 only show high selectivity to Cu2+，and 3 is highly selective to iron and copper ions due to their different groups.

Fig.12 Selectivity of compound 1 towards Cu2+upon addition of various metal ions

Fig.13 Selectivity of compound 2 towards Cu2+upon addition of various metal ions

Fig.14 Selectivity of compound 3 towards Cu2+and Fe3+upon addition of various metal ions

The selectivity of compounds 1～3 towards Cu2+is further studied.The fluorescence quenching of compound 2 is more prominent，i.e. “Off state” (Fig.13)，compared to “On state” (Fig.11)，which has the highest selectivity to copper ions among compounds 1～3.Quenching of fluorescence in emission caused by Cu2+is owing to reverse photo-induced electron transfer(reverse PET)[36-37].

In order to further observe the practical applicability of compounds 1～3 as fluorescent sensors for Cu2+or Fe3+，we explored the interference of other ions.The competitive experiments were carried out on compounds 1～3 in the presence of copper ions(100 equiv.)or iron ions(10 equiv.)with an equal proportion of co-existing ions(Fig.15～18).The results show that the fluorescence responses of compounds 1～3 to copper ions do not change significantly in the existence of other ions，and the fluorescence response of compound 3 to iron ions except copper ions shows small changes.

Fig.15 Competitive selectivity of compound 1 towards Cu2+in the presence of different cations in the mixed solvent CH2Cl2/CH3OH

Fig.16 Competitive selectivity of compound 2 towards Cu2+in the presence of different cations in the mixed solvent CH2Cl2/CH3OH

Fig.17 Competitive selectivity of compound 3 towards Cu2+in the presence of different cations in the mixed solvent CH2Cl2/CH3OH

Fig.18 Competitive selectivity of compound 3 towards Fe3+in the presence of different cations in the mixed solvent CH2Cl2/CH3OH

3 Conclusions

In conclusion，we synthesized fluorinated calix[4]arene derivatives 1～3 in the cone conformation.The calix[4]arene derivatives were characterized by1H NMR，F(xiàn)T-IR，UV-Vis，fluorescence spectra analysis and so on.Compounds 1～3 show high significant selective nature to copper ions，which is indicated by UV-Vis and fluorescence techniques.The ultraviolet intensity of compounds 1～3 increased，new bands appeared and fluorescence quenching occurred in the presence of copper ions.At the same time，compound 3 exhibits higher selectivity to copper ions than iron ions.This kind of molecular switch may be utilized as a Cu2+selective sensor.