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Carbon nanotubes (CNTs) were covalently modified by fluorescence ligand (glycine-N-8-quinolylamide) and formed a hybrid material which could be used as a selective probe for metal ions detection. The anchoring to the surface of the CNTs was carried out by the reaction between the precursor and the carboxyl groups available on the surface of the support. Fourier transform infrared spectroscopy (FTIR) and Thermogravimetric analysis (TGA) unambiguously proved the existence of covalent bonds between CNTs and functional ligands. Fluorescence characterization shows that the obtained organic–inorganic hybrid composite is highly selective and sensitive (0.2 μM) to Zn(II) detection.
There has been growing interest during the last decade in the development of fluorescent molecular sensors for cations and anions in solution [1-8]. Especially, fabricating fluorescent materials for the detection of Zinc cation has drawn much more attention [9-13], as Zinc not only plays important roles in human bodies [14,15], but also closely relates to severe pathological diseases such as Alzheimer’s and Parkinson’s diseases . So far, much study has been done for the detection and real-time localization of Zn(II). Yasuhiro Shiraishi’s group has synthesized a quinoline–polyamine conjugate as a fluorescent chemosensor for quantitative detection of Zn(II) in water . Maarten Merkx et al. used chelating fluorescent protein chimeras for ratiometric detection of Zn(II) in living cells and the detection range was from 10 nM to 1 mM . Jinshi Ma and coworkers have synthesized several bis(pyrrol-2-yl-methyleneamine) ligands as fluorescent sensor for Zn(II) , and their results revealed that the ligands exhibit excellent fluorescent properties. However, much of the work was just based on organic molecules as fluorescent chemosensors. For a few practical applications the attachment of the fluorescent units to a solid support has advantages like the possibility of recovering the materials for their repetitive use. For this point, scientists chose silica nanoparticles , nanosized boehmite particles  and silicon nanowires  to support fluoresence ligands as fluorescence sensors. And these materials exhibit excellent selectivity and sensitivity to sense metal ions.
In this study, we chose multi-walled carbon nanotubes (MWNTs) as fluorescent support. Since its discovery, surface modification of MWNTs has received considerable attention [20-24]. The fluorophore in this study is glycine-N-8-quinolylamide (GNQ) molecule, in light of the fact that the 8-aminoquinoline derivatives could effectively coordinate with specific metal ions . The quinoline group has been covalently grafted to the surface of the MWNTs that can behave as recognition center for metal ions depending on its actual protonation state. We find that this new material (MWNTs-GNQ) has high selectivity and sensitivity to detect Zn(II), and the sensitivity is down to 0.2 μM., which is about the same as the silica nanoparticles-supported fluorescence sensors . For other sensing materials [26,27], the fluorescence enhancement selectivity is not only for Zn(II) but also for Cd(II), which may reduce selectivity when they are used just for Zn(II) detection. On the other hand, the fluorescence enhancement of MWNTs-GNQ is only for Zn(II).
As the use of organic–inorganic hybrid materials for bio-application has become a hot subject in the research field currently [28-31], MWNTs-GNQ may be used to build nanosensor devices to sense directly in intracellular environment, because carbon nanotubes (CNTs) can penetrate into cells and almost have no toxicity to organism [32,33].
The multi-walled carbon nanotubes (MWNTs, diameters: 20–40 nm, purity: 95–98%) prepared by the catalytic decomposition of CH4 were provided by Shengzhen Nanotech Port Ltd. Co (China). Methanol and Tetrahydrofuran were used after distillation. Other reagents were analytical and used without purification. Glycine-N-8-quinolylamide (GNQ) was synthesized according to the known method .
In a typical experiment, 300 mg pristine-MWNTs were added to a 180 mL 3:1 mixture of concentrated H2SO4and HNO3. The mixture was treated in an ultrasonic bath (40 kHz) for 20 min and stirred at 60 °C for 4 h under reflux. Then, the mixture was vacuum-filtered through a 0.22 μm Millipore polytetrafluoroethylene membrane and washed with distilled water until pH of the filtrate was 7. The filter cake was dried under vacuum at 40 °C for 24 h to obtain MWNTs-COOH.
The acid-treated MWNTs-COOH of 200 mg was reacted with 20 mL SOCl2for 24 h under reflux, and then the residual SOCl2was removed by the reduced pressure distillation, the solid was washed with anhydrous THF several times until the brown-colored supernatant became to colorless. The remaining solid acyl chloride-functionalized MWNTs (MWNTs-COCl) was dried under vacuum at 20 °C for 24 h.
MWNTs-COCl of 100 mg was dispersed in 10 mL anhydrous chloroform and the mixture was sonicated for 20 min to create a homogeneous suspension. The mixture was added with 50 mg GNQ under a nitrogen atmosphere, and then immersed in an oil bath at 70 °C accompained by mechanical stirring for 24 h. The resulting reaction medium was vacuum-filtered through a 0.22 μm polycarbonate membrane three times to yield MWNTs-GNQ.
All the reactions in the experimental procedure were carried out under a nitrogen atmosphere.
Fourier transform infrared (FTIR) spectrometer (Bruker IFS66/S), Dupont-1090 Thermal gravimetric analysis (TGA) instrument and Gmbh Varioel Elementar Analysensyteme were used to characterize the materials. Perkin Elmer LS 55 spectrofluorimeter was used to obtain the fluorescence spectra of the fluorescence material.
Figure Figure1shows1shows the infrared spectra of a GNQ and b MWNTs-GNQ. In the FTIR spectrum of GNQ, the absorption peaks at 3383.64 cm−1, 3290.48 cm−1(–NH2), 2890.5 cm−1(C–H), 1658.27 cm−1(C=O), 1593.29 cm−1(N–H), 1523.3 cm−1(C–C), and 1059.01 cm−1(C–N) are found. Comparing with the FTIR spectrum of GNQ, the characteristic peaks of amino groups in the spectrum of MWNTs-GNQ disappeared, demonstrating that the amino groups on GNQ have reacted with acyl chloride groups on the surface of MWNTs. A new peak that appeared around 1686 cm−1is attributed to the amide carbonyl (C=O) stretch. Another new peak at 1629.87 cm−1is attributed to secondary amide band which accompanies the absorption at 1686 cm−1. Another peak at 1082.47 cm−1attributed to (C–N) has also been found, and it has obviously been enhanced. The results indicate that GNQ has been grafted to the surface of MWNTs.
The TGA curves of MWNTs-COOH and MWNTs-GNQ were recorded on a Dupont-1090 thermogravimeter in Ar atmosphere at the heating rate 10 °C/min from 20 °C to 500 °C (Fig. (Fig.2).2). According to Fig. Fig.2a,2a, there is a continuous weight lose of the MWNTs-COOH, and the amount of the weight loss is about 10% typical for acid-functionalized MWNTs. The weight loss curves in Fig. Fig.2b,2b, the major weight loss happened in the temperature range from 200 °C to 450 °C due to the degradation of the GNQ grafted to the MWNTs. The content of the GNQ grafted to the MWNTs is about 12 wt%, which is similar to the calculation result of the elemental microanalysis (Table (Table11).
The fluorescence spectra of GNQ and MWNTs-GNQ are shown in Fig. Fig.3.3. It can be seen that the fluorescence peak is red-shifted after modification. Compared with GNQ, the fluorescence intensity of MWNTs-GNQ is decreased. It may be affected by the black background of CNTs.
GNQ is expected to be a stronger coordinating agent because it is a tridentate ligand. When GNQ is selectively coordinated with metal ions, the fluorescence from GNQ is modified appropriately by the metal ions. This phenomenon can be utilized to construct a material for the detection of metal ions based on MWNTs (Scheme (Scheme2).2). Accordingly, titration of various metal ions in the presence of MWNTs-GNQ in methanol solution was performed, and the results are summarized in Fig. Fig.4.4. After titration of various metal ions, it is observed that the intensity of fluorescence from MWNTs-GNQ containing Zn(II) is much higher than that of other metal ions. This is very nice because under many conditions (e.g., physiological conditions) various metal ions may exist at certain concentrations compared to Zn(II).
It was reported that most of the previous Zn(II) sensors do not exhibit good selectivity to these metal cations [26,27] (for instance, the selectivity in many cases is close to 1:1 for Zn(II):Cd(II)). This may bring trouble to certain applications where Co(II), Ni(II), Cu(II), or Cd(II) may interfere (e.g., in environmental science). Herein, MWNTs-GNQ shows 2.8-fold fluorescence enhancement for Zn(II) versus just minimal fluorescence enhancement for Cd(II) and Ni(II). From these results, it is evident that MWNTs-GNQ have a high selectivity to Zn(II).
As for selectivity of MWNTs-GNQ to metal ions, when Zn(II) forms a complex with MWNTs-GNQ with a suitable radius and an electronic structure 3d104 s0, the electron-transfer process of MWNTs-GNQ is forbidden , and an extended π–electron conjugation system is formed synchronously. This conjugation system is involved in an internal charge transfer process from the ligand donor to the Zn(II) acceptor, and simultaneously inhibits the excited-state proton transfer and photo-induced electron transfer that strongly suppress the fluorescence of MWNTs-GNQ. Thus Zn(II) considerably enhances the fluorescence of MWNTs-GNQ.
To further characterize the performance of the sensing material for Zn(II), a series of comparison experiments were carried out with MWNTs-GNQ. Because Zn(II) always coexists with Cu(II) or Cd(II), titration addition of 1 × 10−5 M Cu(II) and Cd(II) to MWNTs-GNQ solution containing Zn(II) led to contrary results (Fig. (Fig.5).5). When Cu(II) was added to the solution, it led to about 97.5% quenching of the total fluorescence intensity, probably because Cu(II) formed some complex with GNQ group, resulting in quenching of fluorescence as reported . But Cd(II) almost had no influence on the fluorescence intensity of the MWNTs-GNQ solution containing Zn(II), because the electronic structure of Cd(II) is fairly similar to that of Zn(II). To resolve the problem of fluorescence quenching by Cu(II), a masking agent of Na2S2O3 was chosen. As is well known that S2O32− can form a very stable complex with Cu(II), the coordination number is three, and Na(I) almost has no influence to fluorescence intensity of MWNTs-GNQ. The results are shown in Fig. Fig.5,5, from which we can see that the masking agent almost does not affect the experimental results except in the case when the system contains Zn(II) and Cu(II). When three stoichiometry S2O32− were added to the Zn(II) and Cu(II) solution, the fluorescence intensity was greatly enhanced. Although, compared to the solution only containing Zn(II), the intensity was a little weaker, Na2S2O3 is still a good masking agent to mask Cu(II). We thus conclude that the presence of Cd(II) does not affect the sensitivity of MWNTs-GNQ for Zn(II) detection, and Na2S2O3 could be used as a masking agent when Cu(II) coexists in the system.
The sensitivity of fluorescence enhancing from MWNTs-GNQ by Zn(II) was further investigated, and the results are shown in Fig. Fig.6a.6a. The fluorescence intensity of MWNTs-GNQ gradually increased with increasing Zn(II) concentration. When more than 1 eq. Zn(II) was added, only a marginal increase was observed (Fig. (Fig.6b),6b), which suggested the 1:1 stoichiometry of the ligand to the zinc ions. Because Zn(II) desires a square planar geometry when coordinated, while the three nitrogen on MWNTs-GNQ can only provide a tridentate ligand, the fourth coordination can come from the solvent methanol oxygen. It can be seen from Fig. Fig.6b6b that when the concentration of Zn(II) is lower than 0.2 μM, the relative fluorescence intensity is about 1. But when the concentration of Zn(II) is higher than 0.2 μM, the relative fluorescence intensity is also increased. It can be expressed by the following formula:
Wherein,Ais the value of the fluorescence intensity,Cis the concentration of Zn(II), and the range ofCis from 0.2 μM to 10 μM in this study. So, it is evident that the detection limit for Zn(II) is established at 0.2 μM under the experimental conditions in our study.
We have prepared a new organic–inorganic hybrid sensing material based on CNTs as support and glycine-N-8-quinolylamide as fluorescent center. The results of the fluorescence characterization show that the composite has a highly selective and sensitive (0.2 μM) detection for Zn(II), and reveal that ratiometric Zn(II) sensing is possible with fluorophore chemically modified carbon nanotubes. This novel fluorescent material may be used as a fluorescent device in intracellular environment for the detection of Zn(II).