Fluorescent Probe for H+:Synthesis,Spectroscopic and Electrochemical Studies of Exocyclic Ring-Fused Boron Dipyrromethene Dyes

XU Hai-YunSHEN Zhen

(1School of Chemistry and Chemical Engineering,State Key Laboratory of Coordination Chemistry, Nanjing University,Nanjing 210093,China)

(2Department of Chemistry,Shangqiu Normal College,Shangqiu,Henan 476000,China)

Fluorescent Probe for H+:Synthesis,Spectroscopic and Electrochemical Studies of Exocyclic Ring-Fused Boron Dipyrromethene Dyes

XU Hai-Yun1,2SHEN Zhen＊,1

(1School of Chemistry and Chemical Engineering,State Key Laboratory of Coordination Chemistry, Nanjing University,Nanjing210093,China)

(2Department of Chemistry,Shangqiu Normal College,Shangqiu,Henan476000,China)

Three new exocyclic ring-fused boron-dipyrromethene (BDP)dyes with N,N-dimethylaniline,pmethoxyphenyl or phenyl subunit at meso-position were synthesized.Their absorption,steady-state fluorescence and electrochemical properties were investigated.The spectrofluorometric titrations were performed to examine their responsive abilities to H+in strong polar solvent.The dimethylanilino-substituted BDP dye 1 showed a large fluorescence enhancement upon adding H+to its CH3CN-H2O(1∶1,V/V)solution.BDP 1 can be used as a fluorescent probe for H+in the acidic pH range excited with visible light.

Boron-dipyrromethene(BDP)dyes;fused exocyclic rings;H+recognition;electron transfer,fluorescent sensor

In recent years,boron-dipyrromethene(BDP)dyes have received increasing attentions because of their superior photostability to fluorescein[1],insensitivity towards pH value and solvent polarity[2],and sufficiently high lipophilicity to permeate cell membranes,as well as high molar extinction coefficients,high fluorescence quantum yields approaching unit,photoexcitation with visible light and accessible structural modification[3]. These valuable properties have brought out various applications in the field of laser dyes[4],fluorescentsensors[5],opticaldevices[6]and dopants in liquid crystals[7].A lot of BDP derivatives substituted with phenolic,naphtholic,dialkylaminopheny,calix[4]-arene subunits at meso-position show interesting photoinduced electron transfer(PET)mediated fluorescence off/on switch,thus acting as probes for pH sensing in the alkaline region,the acidic region and the near neutral region,respectively[8].To the best of our knowledge,examples of BDP analogous fused with exocyclic rings,especially at positions 1,2,6,7 are very rare[9-10].As our increasing interest in BDP-based fluorescent molecular sensors or switches and an extension of our previous research work[9-12],we report here three new exocyclic ring-fused boron-dipyrromethene(BDP)dyes substituted with N,N-dimethylaniline (1), pmethoxyphenyl (2)or phenyl(3)subunit at mesoposition.Their photophysical properties have been investigated by steady-state absorption and emission spectroscopy.Moreover,the binding behavior of 1 and 2 with H+in acetonitrile-H2O (1∶1,V/V)has been spectroscopically examined and their redox features have been also studied.

1 Experimental

1.1 Instruments

Elemental analyses for C,H and N were performed on a Perkin-Elmer 240C elemental analyzer.Melting points were determined with a Reichert Thermover apparatus without correction.1H NMR and13C NMR spectra were recorded on a Bruker DRX500 spectrometer and referenced to the residual proton signals of the solvent.The Mass spectra were measured with a Bruker Daltonics AutoflexⅡTMMALDI-TOF spectrometer.IR spectra were recorded on Bruker Vector 22 spectrometer with KBr pellets in the 4 000～400 cm-1region.UV-Visible spectra were carried out on a UV-3100 spectrophotometer.Fluorescence spectra were measured on an Aminco Bowman 2 Luminescence spectrophotometer with a xenon arc lamp as the light source.The fluorescence quantum yields (Φf)were determined relative to rhodamine 6G in water(λex=488 nm,Φf=0.76)with an absorbance below 0.1 at the excitation wavelength)[13].The reported complex stability constant Ksof probe 1 with H+was determined by gradually adding microliter of H+(c=10-2mol·L-1of HClO4)to a dilute solution(typically c=10-5mol·L-1)of dye 1 in CH3CN-H2O (1∶1,V/V).Cyclic voltammetry were carried out in 0.1 mol·L-1TBAP(tetra-nbutylammonium perchlorate)in acetonitrile on a Perkin-Elmer electrochemical analysis system model 283 with a platinum disk as the working electrode,Ag/ AgCl as the quasi-reference electrode,and a platinum wire as the counterelectrode.Redox potentials were referenced internally against ferrocenium/ferrocene(Fc+/Fc).All measurements were performed under an inert atmosphere with a scan rate of 250 mV·s-1at room temperature.

1.2 Reagents and materials

All air-and moisture-sensitive reactions were carried out under an atmosphere of nitrogen in ovendried glassware.Unless otherwise noted,all reagents or solvents were obtained from commercial suppliers and used as received without further purification.Dry dichloromethane was obtained by refluxing and distilling over CaH2.Dry tetrahydrofuran (THF)was distilled from sodium/benzophenone.Triethylamine was obtained by simple distillation.Acetonitrile used for the electrochemical studies was distilled from CaH2.The solvents used for photophysical measurement were of spectroscopic grade without further purification.Chromatographic purifications were conducted by using 40～200 μm silica gel obtained from Merck.Thin-layer chromatography (TLC)was performed on silica gel plates coated with fluorescent indicator.2-Ethoxycarbonyl-4,5,6,7-tetrahydroisoindole (a)was synthesized according to the literature[14].

1.3 Synthesis

1.3.1 2 -methyl-4,5,6,7-tetrahydro-2H-isoindole(b)

Scheme 1 Synthetic route for 1,2 and 3

LiAlH4(1.14 g,30 mmol)powder was added in small portions to a stirred solution of ethyl 4,5,6,7-tetrahydro-2H-isoindole-1-carboxylate a (579 mg,3 mmol)in dry THF (200 mL)under nitrogen.The reaction mixture was refluxed for 3 h.After cooling to room temperature,water(50 mL)was added dropwise and the resulting mixture was filtered through a Celite pad,which was washed with EtOAc (3×30 mL).The organic layer was separated and the aqueous layer was extracted with EtOAc (2×20 mL).The combined organic layer was washed with water(5×30 mL)and brine (30 mL),dried over Na2SO4,and concentrated under reduced pressure.The residue was purified by chromatography on silica using CHCl3as solvent.The first fraction was collected to give b (0.27 g)as a pale red liquid with a 67%yield.

1.3.2 General procedure for the preparation of 1～3

Compound b (2 mmol)and aldehyde [4-(dimethylamino)benzaldehyde (1),4-methoxybenzaldehyde(2),or benzaldehyde(3)](1 mmol)were dissolved in dry CH2Cl2(120 mL)under nitrogen.One drop of trifluoroacetic acid (TFA)was added,and the solution was stirred at room temperature in the dark for 2～4 h (until TLC showed complete consumption of aldehyde).A solution of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone(DDQ,1 mmol)in dry CH2Cl2(20 mL)was added, and the stirring was continued for additional 1 h.The reaction mixture wasthen treated with absolute triethylamine (3 mL)and boron trifluoride etherate(3 mL).After the mixture was stirred for another 1 h,a deep green fluorescence was observed in the mixture. The reaction mixture was washed with water(3×50 mL) and brine(50 mL),dried over Na2SO4,and the solvent was evaporated at reduced pressure.The crude product was purified by column chromatography on silica-gel and recrystallization from CHCl3/hexane.

1:red crystals(214 mg,yield 48%).m.p.＞250℃;1H NMR (500 MHz,CDCl3):δ 7.07(d,2H,J=8.1 Hz), 6.79(broad s,2H),3.06(s,6H),2.49(s,6H),2.35(t, 4H,J=6.1 Hz),1.72(m,4H),1.62(m,4H),1,44(t,4H, J=2.8 Hz);13C NMR(500 MHz,CDCl3):151.8,150.1, 141.3,139.6,131.0,129 3,128.6,128.3,112.7,40.84, 24.66,23.63,22.97,21.79,12.68;IR (KBr):νmax/cm-11 547,1 482(C=C,C=N),1 200(B-F);MS(MALDITOF):m/z:448.20 [M+H]+;elemental analysis calcd.(%)for C27H32BF2N3:C 72.49,H 7.21,N 9.39;found:C 72.42,H 7.29,N 9.32.

Compound 2 was prepared from the reaction of b (0.27 g,2 mmol)with 4-methoxybenz-aldehyde(0.14 g, 1m mol)in dry CH2Cl2(120 mL)under nitrogen atmosphere and purified by flash chromatography (silica gel,5%EtOAc/petroleum ether),followed by recrystallization from CHCl3/hexane to give red crystals in 18%yield.m.p.194℃;1H NMR(500 MHz,CDCl3): δ=7.16(d,2H,8.6Hz),6.99(d.2H,8.6Hz),3.90(s,3H), 2.49(s.6H),2.35(t.4H,6.2Hz),1.65(t,4H,3.9Hz),1.61 (m,4H),1.43(m,4H);13CNMR (500 MHz,CDCl3): 156.42,153.17,141.23,139.66,130.64,129.88,128.69, 128.11,116.30,52.65,24.58,23.46,22.88,21.74, 12.74;IR(KBr):νmax/cm-11548,1480(C=C,C=N),1201 (B-F);MS(EI):m/z(%):434.71(100)[M+];elemental analysis calcd.(%)for C27H29BF2N2O:C 71.90,H 6.73, N 6.49;found:C 71.82,H 6.70,N 6.54.

Compound 3 was synthesized analogously by the reaction of benzaldehyde(0.11 g,1 mmol)with b(0.27 g,2 mmol)in dry CH2Cl2(120 mL),and purified by column chromatography (silicagel,5% EtOAc/ petroleum ether),recrystallized from CHCl3/hexane to give red solid in 30%yield.m.p.170℃;1H NMR(500 MHz,CDCl3):δ=7.28～7.49(m,5H),2.47(s,6H),2.34 (t,4H,J=6.0 Hz),1.75(t,4H,J=10 Hz),1.59(m,4H); 1.40(m,4H);IR(KBr):νmax/cm-11 549,1 480(C=C,C= N),1 202(B-F);MS(EI):m/z(%):404.23(100)[M+]; elemental analysis calcd.(%)for C25H27BF2N2:C 72.27, H 6.73,N 6.93;found:C 72.14,H 6.82,N,6.88.

2 Results and discussion

2.1 Spectroscopic properties

The absorption and emission properties of BDPs 1～3 in nonpolar and polar solvents are listed in Table 1,and the absorption and steady-state fluorescence emission spectra of dye 1 in the determined solvents are shown in Fig.1.

Table 1 Absorption and emission properties of 1～3 in hexane and acetonitrile at 298 K

Fig.1 Absorption spectra of dye 1 in hexane(a)and CH3CN(b)and the emission spectra of 1 in hexane(c)and CH3CN(d)at 298 K (λex=490 nm)

Ascan beseen from Table1,themolar absorption coefficients (εmax)for these exocyclic ringfused BDP derivatives are relatively high and lie in 35000～111300 mol-1·L-1·cm-1range,and the nature of the para-substituent(R)in the phenyl group at mesoposition of BDPs 1～3 has no essential effect on their absorption and emission maxima.In addition,the maximal band positions in the absorption and emission spectra do not show any particular trend as a function of solvent polarity, only being slightly shifted hypsochromically with increasing the solvent polarity, which is consistent with the general behavior of BDP chromophore.On the other hand,the longest absorption or emission bands for BDPs 1～3 are shifted to the red of 10～20 nm relative to those described BDP dyes carrying only alkyl substituents on the BDP core[15]owe to the introduction of the fused exocyclic rings on the pyrrole side.

The steady-state absorption spectrum of 1 features with a strong,narrow band centered around 524 nm and a shoulder on the shorter wavelength side centered at about 496 nm,which is typical for the conventional BDP derivatives carrying only alkyl substitutes on the indacene core[2a].A considerably weaker and broad absorption band is observed at about 390 nm,which can be attributed to the s0-s2transition[16].The absorption spectra of 2 and 3 are,in general,similar to those of 1 in the used solvents.

Excitation of 2 yields the typical fluorescence spectra (Fig.2)features of the classical BDP,with a narrow and slightly Stokes-shifted band of mirror image shape.The intensity and position of the fluorescent spectra are almost independent of the solvent polarity, indicating that emission occurs from the weakly polar, relaxed Franck-Condon excited state.The emission spectra of 3 are almost the same as those of 2 in the determined solvents

Fig.2 Absorption of dye 2 in hexane(dotted line)and CH3CN(solid line)and emission spectra of 2 in CH3CN(dashed line)(λex=490 nm),the emission spectra of dye 2 in hexane,similar to that in CH3CN,are omitted for better clarity

In contrary to its absorption spectra,the emission spectra of 1 are strongly solvent-dependent.In hexane, the localized,narrow LE emission maximum around 542 nm is strong and shaped like the mirror image of the absorption spectra,which strongly resemble those of 2 and 3.In acetonitrile,the fluorescence of 1 from this LE emission is strongly quenched (Fig.1)due to the photoinduced electron transfer(PET)from the nitrogen atom of the p-dimethylamino-substituted phenyl group to the excited BDP chromophore,while dye 2 or dye 3 display a strong fluorescence emission independent of the nature of the studied solvents.

2.2 Fluorimetric titrations of 1 and 2 with H+

In acetonitrile-water solvent,all of the features (including position,shape,height)of the absorption spectra of dye 1 and dye 2 are essentially H+independent,indicating that the effect of protonation on the absorption behavior of 1 and 2 is only barely,with a slight bathochromic shift in the absorption maxima. However,the effect of H+binding on the emission spectrum of 1 is very large.

As seen from Fig.3,the fluorescence emission intensity (F)is only dependent on H+and increases significantly with increasing cH+while the emission maxima centered at 540 nm are almost invariant,with only a slight bathochromic shift.Upon binding of H+with the dimethylamino group, p-alkylaminosubstituted phenyl moiety on meso-position of the BDP core becomes substituted with an electron acceptor rather than with an electron donor in such a way that any PET is strongly inhibited,which means that the quenching fluorescence is again revived.The association constants Ksfor the interaction H+with 1 in acetonitrile-water is determined by the nonlinear curvefitting analysis of the fluorescence titration data(F) recorded as a function of cH+Fig.3b)according to Eq. (1),where the fluorescence signals Fminis the initial fluorescence value of 1,and Fmaxis the maximum fluorescence value in the presence of H+(Fmaxcan not be accurately determined,it can be left as a floatingparameter in the analysis).

Fig.3 (a)Variations in fluorescence intensity of a solution of dye 1 in CH3CN-H2O(1∶1,V/V)as a function of pH value; (b)Fluorescence titration curve of dye 1 in CH3CN-H2O(1∶1,V/V)as a function of cH+is obtained from Fig.3a (λem=540 nm,λex=490 nm),and the solid line represents the best fits with eq 1 to the fluorimetric titration data of dye 1

The estimated Ksvalue of a well-defined 1∶1 stoichiometry of H+binding to the aniline moiety of 1 is found to be 333 mol-1·L.Therefore,the corresponding pKa(here,Kais the acid dissociation constant of the ammonium form of 1)is determined as 2.52 including in the normal ranges of values reported for other 8-dimethylaminophenyl-substituted BDP analogues[17]or related donor-acceptor-substituted biaryl dyes,such as p-anthracene-9-yldimethyl-aminobenze (pKa=2.50 in ethanol-water 4∶1,V/V)[18]or 4-dimethyl-amino-4′-cyano-biphenyl(pKa=2.35 in ethanol-water 1∶1,V/V)[19].

To study the influence of added salt on the steadystate fluorescence of dye 1,we recorded pH valuedependent emission spectra of dye 1 under various conditions.The results are shown in Fig.4,indicating that the fluore-scence intensity change of dye 1 is nearly insensitive to added salt in the concentration range studied.

Fig.4 pH value-dependent emission spectra of dye 1 in the absence/presence of other ions in CH3CNH2O(1∶1,V/V)solution(λem=540 nm,λex=490 nm)

However,addition of H+into CH3CN-H2O(1∶1, V/V)solution of 2 did not bring about any significant changes in the fluorescence emission spectra,with only a slight bathochromic shift (Fig.5).This insensitive behavior of 2 to H+is due to the weaker electron donating ability of its p-alkoxy-substituted phenyl moiety than p-alkylamino-substituted moiety of 1, which leads to the immunity of 2 against the activation of an electron-transfer(ET)process even in more polar solvents,and therefore it is difficult to accurately assess its binding constant with H+.Obviously,2 is not suitable for fluorescent pH indicator based on the design principle of PET while 1 can be served as a very sensitive fluore-scent off/on probe for detecting traces of free(solvated)protons in polar solvents considering its high cation induced fluorescence enhancement factor Fmax/Fmin.

Fig.5 Fluorescence spectra of dye 2 in the absence (dashed line)and presence of 40 eqiv of H+in CH3CN-H2O(solid line)

2.3 Electrochemical properties

The redox properties of 1,2 and 3 were examined by cyclic voltammetry in 0.1 mol·L-1TBAP in acetonitrile.Each of dyes 1,2 and 3 displays a oneelectron reversible reduction wave at-1696 mV(vs Fc+/Fc)and a one-electron reversible oxidation wave at 565 mV,which are close to those of the conventional BDP dyes.This may be due to reduction and oxidation only centering at the BDP core,independent of the substituted groups at meso-position of the BDP core.

The thermodynamic driving force (ΔGET)for the excited state electron transfer in polar media can be described by the Rehm-Weller equation[20](Eq.(2)) where E1/2(D+/D)and E1/2(A/A-)are the ground-state oxidation potential of the receptor and the reduction potential of the electron-deficient fluorophore, respectively,E00is the zero-zero transition energy of the excited state donor-acceptor pair (D-A*),Ecis the Coulomb stabilization energy of the radical ion pair D·+-A·-.

Here,a second oxidation wave appearing at 228 mV for 1 is assigned to the oxidation of the attached dimethylamino substituted phenyl moiety at mesoposition of the BDP core while the oxidation potential of p-methoxy-substituted phenyl moiety for 2 is much larger and can not be detected under this experimental conditions.To assess the feasibility of PET within the dyes,we took the value of dimethoxybenzene(1150 mV vs Fc+/Fc)as a model for 1 and 2.Ecis taken as 0.1 eV[21].As can be seen from the calculated values of ΔGETfor these compounds summarized in Table 2, light-induced electron transfer within 1 is thermodynamically favorable while the opposite result is obtained for 2.All these findings are in good agreement with the experimental observations that only compound 1 shows a significant PET fluorescence quenching.

Table 2 Redox potentials and electron-transfer parameters of 1,2 and 3 in acetonile(potentials in mV vs Fc+/Fc)

3 Conclusion

Three new exocyclic ring-fused boron-dipyrromethene (BDP)dyeswith N,N-dimethylaniline,pmethoxyphenyl or phenyl subunit at meso-position were synthesized by a one-pot,three-step procedure,and their spectroscopic and electrochemical properties were also investigated.Their longest wavelength absorption or emission band is red shifted 15～20 nm compared to that of the classic BDP dyes.Dye 2 displays a strong fluorescence emission with poor response to H+, irrespective ofthe solvent polarity,whereas dye 1 exhibits very weak residual fluorescence in CH3CN-H2O solution,and its fluorescence intensity considerably enhanced upon adding of H+.BDP 1 can be used as a fluorescent probe for H+in the acidic pH range excited with visible light.

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檢測(cè)氫離子的熒光探針：含稠合外環(huán)的硼-二吡咯亞甲基染料的合成、光譜和電化學(xué)性質(zhì)研究

徐海云1,2沈 珍＊,1

(1南京大學(xué)配位化學(xué)國(guó)家重點(diǎn)實(shí)驗(yàn)室，化學(xué)化工學(xué)院，南京 210093)
(2商丘師范學(xué)院化學(xué)系，商丘 476000)

本文合成了3個(gè)新型中位分別為N，N-二甲基苯胺、對(duì)-甲氧基苯基或苯基取代的含稠合外環(huán)的硼-二吡咯亞甲基染料。研究了它們的吸收光譜、穩(wěn)態(tài)熒光光譜和電化學(xué)性質(zhì)；采用熒光光譜滴定方法研究了它們?cè)趶?qiáng)極性溶劑中對(duì)氫離子的響應(yīng)；將氫離子滴加到N，N-二甲基苯胺取代的硼-二吡咯亞甲基染料(1)的CH3CN-H2O(1∶1，V/V)溶液中，其溶液的熒光顯著增強(qiáng)；染料1在可見光激發(fā)下，可以作為酸性pH范圍內(nèi)檢測(cè)氫離子的熒光探針。

硼-二吡咯亞甲基染料；稠合外環(huán)；氫離子識(shí)別；電子轉(zhuǎn)移；熒光探針

O613.2；O613.8+1

A

1001-4861(2011)06-1177-08

2010-12-24。收修改稿日期：2011-02-25。

國(guó)家自然科學(xué)基金(No.20401009)，霍英東教育基金會(huì)(No.104013)，河南省科技廳科技攻關(guān)(No.082102210050)，河南省教育廳自然科學(xué)研究資助計(jì)劃(No.2011A150023)，商丘師院重大項(xiàng)目培育計(jì)劃立項(xiàng)(No.2011ZDPY02)，2010年商丘師范學(xué)院青年骨干教師資助計(jì)劃資助項(xiàng)目。＊

。E-mail：zshen@nju.edu.cn，xuhyun@163.com