DOI:
10.1039/C8RA03591A
(Paper)
RSC Adv., 2018,
8, 19701-19706
A highly selective TPE-based AIE fluorescent probe is developed for the detection of Ag+ †
Received
26th April 2018
, Accepted 22nd May 2018
First published on 30th May 2018
Abstract
The detection of Ag+ in the environment is very important to determine the level of pollution from silver complexes, which have caused various human health problems. Herein, an aggregation-induced emission (AIE) chromophore (tetraphenylethane, TPE) attached to a benzimidazole group (tetra-benzimidazole, TBI–TPE) is synthesized and utilized to detect Ag+ in the environment. The strong chelating effect between the benzimidazole group and Ag+ leads to the formation of aggregates, and strong yellow fluorescence signals were observed after adding Ag+ into a TBI–TPE solution. The stoichiometry of the complex of TBI–TPE and Ag+ was established to be 1
:
2 using photochemical and mass spectra measurements. The detection limit of the Ag+ assay is 90 nM with a linear range from 100 nM to 6 μM. This study provides a facile method to determine Ag+ in real environmental samples with satisfactory results.
1. Introduction
Silver is an important basic metal and has many applications, including pharmaceuticals, the chemical industry, accessories, electronics, photography and so on.1–4 Metal pollution resulting from industrial processes including leather tanning, cement production, and metal plating is a serious environmental problem.5–8 In the pharmaceutical industry low concentrations of silver complexes are used for their strong antibacterial effect. However, at high concentrations silver is harmful to human health and can cause brain damage, skin oxidation and have negative impacts on the immune system.9–13 So it is imperative to establish a highly selective and sensitive method for detecting Ag+ in the environment.
Conventional methods for the detection of Ag+ include atomic absorption spectrometry, atomic emission spectrometry, potentiometric titration, inductively coupled plasma-mass spectrometry (ICP-MS), electrochemistry, molecular imprinting biosensors and colorimetry etc.14–20 Although these methods can be used to detect lower concentrations of Ag+, they require complex instrumentation, tedious operations and time-consuming sample pretreatment. Compared to these methods, fluorescence spectroscopy has many advantages, such as low cost, high sensitivity, easy operation and simple sample preparation.20–24 Nevertheless, it is well known that Ag+ is commonly used as a fluorescent quencher, and most reports on Ag+ detection are based on quenching effects due to a charge transfer process between Ag+ and a probe. Fluorescent probes for Ag+ with “turn on” type signals are rarely reported.25–30
The emergence of aggregation-induced emission (AIE) fluorophores have provided many chances to build “signal on” probes, where fluorescence is weak when dissolved, but becomes significantly more emissive in the aggregate state. Restriction of intramolecular rotation is the main AIE mechanism, in which the intramolecular rotations are greatly hampered due to limited space when aggregated. The non-radiation decay channels are inhibited, and the excited states can only go back to the ground state by radiation decay, thus enhancing the fluorescence significantly.31–36 In recent years, fluorescent materials with AIE properties have drawn extensive attention because they have a wide range of applications in many fields, including fluorescent cell imaging, organic light-emitting diodes, sensor materials, protein conformation studies, chiral recognition and so on.37–46 Among these AIE molecules, TPE is one of the most widely studied and used materials owing to its excellent optical properties, high quantum yield and photostability.47–51
It has been reported that Ag(I) possesses high affinity for benzimidazole leading to stable coordination complexes.51–57 With these considerations in mind, we designed and synthesized a novel fluorophore containing TPE and a benzimidazole group for the first time. The TBI–TPE is rich in N atoms, which offers good coupling ability with Ag+. Based on the strong coordination, Ag+ and TBI–TPE formed an AIE aggregate inducing significant fluorescence enhancement, hence a new fluorescence “turn on” sensor for the detection of Ag+ is developed. This AIE probe exhibits high chemical selectivity and a fast response time and has been successfully utilized in the determination of Ag+ in real environmental samples.
2. Experimental section
2.1 Materials
4,4′-Dimethylbenzophenone, titanium tetrachloride (TiCl4), pyridine, N-bromobutanimide (NBS), dibenzoyl peroxide (BPO), and 1,2-diaminobenzene were purchased from Aladdin. Anhydrous tetrahydrofuran, silver nitrate, sodium acetate trihydrate, and chloroform-d, 99.8 atom% D were purchased from Energy Chemical. Dimethyl sulfoxide-d6 was purchased from Sigma-Aldrich. All other reagents were of analytical grade and used as received. Ultrapure water was prepared using a Milli-Q water purification system.
2.2 Apparatus
Fluorescence spectra were recorded on a Hitachi High-Technologies Corporation Tokyo Japan 5J2-0004 model F-7000 FL spectrofluorometer. UV-vis absorption was characterized by a UV-vis/NIR spectrophotometer (Shimadzu, Japan). The NMR spectra were recorded with a AVANCEDRX400 NMR spectrometer (Bruker, Germany) operated at 400/600 MHz. Electrospray ionization mass spectra were obtained with a High Performance 1100 Liquid Chromatography-Mass Spectrometer (Agilent Technologies, USA). The morphology and size of aggregates were characterized with Scanning Electron Microscopy (SEM) (Quanta, FEI) and a JEM 2100 high resolution transmission electron microscope (HRTEM, JEOL, Japan).
2.3 Synthesis
The synthetic strategies adopted are outlined in Scheme 1.
![image file: c8ra03591a-s1.tif](/image/article/2018/RA/c8ra03591a/c8ra03591a-s1.gif) |
| Scheme 1 Synthetic route to new 1,1,2,2-tetrakis(4-(1H-benzo[d]imidazole-2-yl)phenyl)ethene molecules, TBI–TPE. | |
2.3.1 Compound 1 (1,1,2,2-tetra-p-tolylethene). Compound 1 was synthesized as previously reported.58 Zinc powder (1.0 g, 15.3 mmol) was added into a 100 mL double-neck flask. Under an N2 atmosphere, 25 mL anhydrous THF was added, cooled to −5 °C, and then TiCl4 (1.1 mL, 10 mmol) and pyridine (0.05 mL, 0.6 mmol) were added dropwise. The mixture was refluxed at 75 °C for 2 h and 20 mL THF solution of 4,4′-dimethylbenzophenone (1.05 g, 5 mmol) was added. The solution was further refluxed at 75 °C for 12 h. Upon completion of the reaction, the solution was cooled to room temperature and poured into a 40 mL 30% water solution of K2CO3, which was stirred for 5 min and then filtered. The filtrate was extracted with ethyl acetate, successively washed with water, brine, and dried with Na2SO4. A light-yellow solid was obtained by rotary evaporation, and purified by column chromatography (silica gel, petroleum ether) to result in a white product 1 (yield, 85%). The 1H NMR and 13C NMR spectra of product 1 (400 MHz, CDCl3, 25 °C), δ (TMS, ppm) are shown in Fig. S1 and S2,† respectively. High resolution MS of product 1 is shown in Fig. S3,† (m/z): calculated for C30H28 [M + H]+ 389.2225, found 389.2228, [M + Na]+ 411.2083, found 411.2080, [M + K]+ 427.1822, found 427.1825 (high resolution).
2.3.2 Compound 2 (1,1,2,2-tetrakis(4-(bromomethyl)phenyl)-ethene). 1,1,2,2-Tetra-p-tolylethene 770 mg (2 mmol) obtained in the previous step was added into a 100 mL round bottom flask, and then NBS (1424 mg, 8 mmol), BPO (64 mg) and CCl4 (30 mL) were added. Under an N2 atmosphere, the mixture reacted at 80 °C for 2 h. Then, adding in NBS (1424 mg, 8 mmol) and BPO (64 mg), the mixture reacted at 80 °C for a further 2 h. After 2 h, NBS (1424 mg, 8 mmol), and BPO (64 mg) were added, and the mixture was left for 24 h. It was then filtered quickly while the solution was hot, and the solid was washed with ethyl acetate, and the filtrate collected. The organic phase is obtained by rotary evaporation of the yellow solid, without further purification we then proceeded directly to the next step.
2.3.3 Compound 3 (4,4′,4′′,4′′′-(ethene-1,1,2,2-tetrayl)tetrabenzaldehyde). The solid from the previous step (2.0 g), sodium acetate trihydrate (1500 mg, 18 mmol), silver nitrate (3400 mg, 20 mmol), THF (25 mL) and H2O (5 mL) were mixed and further refluxed at 75 °C for 24 h, the solution was cooled to room temperature and filtered. The filtrate was extracted with ethyl acetate, washed successively with water, brine, and dried with Na2SO4. A light yellow viscous liquid was obtained by rotary evaporation, and purified by column chromatography (silica gel, petroleum ether/ethyl acetate = 5
:
1) to result in a yellow-green product 3 (yield: 25%).59–61 1H NMR and 13C NMR spectra of product 3 (400 MHz, CDCl3, 25 °C), δ (TMS, ppm) are shown in Fig. S4 and S5,† respectively. As shown in Fig. S6,† high resolution MS (m/z) of product 3: calculated for C30H20O4 [M + H]+ 445.1434, found 445.1433, [M + Na]+ 467.1253, found 467.1259 (high resolution).
2.3.4 Compound 4 (1,1,2,2-tetrakis(4-(1H-benzo[d]imidazol-2-yl)phenyl)ethene) TBI–TPE. 4,4′,4′′,4′′′-(Ethene-1,1,2,2-tetrayl)tetrabenzaldehyde (46 mg, 0.1 mmol), 1,2-diaminobenzene (130 mg, 1.2 mmol), ammonium acetate (92 mg, 1.2 mmol), EtOH (2 mL) were further refluxed at 75 °C for 5 h. The precipitate was collected by centrifugation and washed with ethanol. The product was dried in vacuum at 60 °C overnight to give a yellow solid (yield, 70%).61–64 1H NMR and 13C NMR spectra (600 MHz, DMSO-d6, 25 °C), δ (TMS, ppm) of compound 4 are shown in Fig. S7 and S8,† respectively. As shown in Fig. S9,† high resolution MS (m/z) of compound 4: calculated for C54H36N8 [M + 2H]2+ 399.1612, found 399.1604 (high resolution).
2.4 Analysis of real sample
A waste liquor sample was taken from a factory in Kunming city. The sample was filtered through a 0.22 μm membrane (Millipore) prior to detection. One hundred microliters of the above waste sample was added to 900 μL of methyl alcohol solution containing TBI–TPE (2 μM) and then analyzed using the developed detection method.
3. Results and discussion
3.1 Design and synthesis of (1,1,2,2-tetrakis(4-(1H-benzo[d]imidazol-2-yl)phenyl)ethene) TBI–TPE
The four-step synthesis adopted for preparing TBI–TPE is shown in Scheme 1. Compound 1 (1,1,2,2-tetra-p-tolylethene) was prepared from 4,4′-dimethylbenzophenone by McMurry coupling. Compound 2 was obtained by NBS under the induction of a free radical initiator (BPO) in CCl4 at 80 °C. Compound 2 is oxidized to compound 3 using silver as the catalyst. TBI–TPE is produced by refluxing 3 at 75 °C.
To verify the results of our synthesis, these compounds were checked by NMR and MS (Fig. S1–S9†).
3.2 AIE properties
After structure confirmation, the AIE properties of TBI–TPE were investigated. To further illustrate the AIE feature, the study of the emission characteristics of TBI–TPE in mixtures of CH3OH and water with different water fractions was conducted. As shown in Fig. 1 and S10,† the fluorescence of TBI–TPE is a yellowish green emission at 525 nm and is strongest at fw = 90%, which is 13 times stronger than the one at fw = 0%. The compound is almost non-emissive when it is dissolved in pure organic solution (fw = 0%) and it gradually becomes emissive as water is added, proving its prominent AIE activity. The increase in fluorescence intensity indicated TBI–TPE tended to aggregate when the fw value increased. Upon aggregation, the free intramolecular rotations of the excited molecules are restricted. This blocks the non-radiative relaxation pathway and favors the radiative decay.
![image file: c8ra03591a-f1.tif](/image/article/2018/RA/c8ra03591a/c8ra03591a-f1.gif) |
| Fig. 1 (A) Fluorescence intensity spectra. (B) Plots of fluorescence intensity versus water fraction of TBI–TPE in mixtures of CH3OH/water with different water fractions (from 0 to 95%). (C) Images of TBI–TPE in CH3OH with the increasing water fraction taken under daily light (top), and UV light illumination (bottom) (λex = 365 nm). TBI–TPE concentration = 10 μM, Ex = 335 nm. | |
3.3 Silver ion sensing studies
3.3.1 The action and mechanism of TBI–TPE and Ag+. To examine the fluorescence response of TBI–TPE towards Ag+, we added Ag+ into a CH3OH solution of TBI–TPE. As shown in Fig. 2A, S11,† the fluorescence spectra indicated that the addition of Ag+ obviously increased the fluorescence intensity of composites at 525 nm (Fig. 2A, S11†). Whereas, the UV absorption spectra of TBI–TPE in CH3OH in the presence of Ag+ did not change (Fig. 2B).
![image file: c8ra03591a-f2.tif](/image/article/2018/RA/c8ra03591a/c8ra03591a-f2.gif) |
| Fig. 2 (A) Fluorescence spectra. (B) UV absorption spectra of TBI–TPE (4 μM) in CH3OH in the presence of Ag+ (4 μM), Ex = 370 nm. | |
In Fig. 3A the Tyndall effect can be observed in a Ag–TBI–TPE solution by laser irradiation, indicating the formation of aggregates. The formation of Ag–TBI–TPE aggregates was further confirmed by HRTEM and SEM measurements (Fig. 3B, S12†). Nanoparticles with diameter of 20 nm were observed in these images. The above results reveal that aggregates of Ag–TBI–TPE were formed in CH3OH solution, resulting in enhanced fluorescence, which is similar to the AIE mechanism of assay.
![image file: c8ra03591a-f3.tif](/image/article/2018/RA/c8ra03591a/c8ra03591a-f3.gif) |
| Fig. 3 (A) Photographs of TBI–TPE (100 μM) in CH3OH exposed to daylight (left), and TBI–TPE in the presence of Ag+ (300 μM) exposed to a laser pen (right). (B) TEM image of the aggregates. (C) Job’s plot showing 1 : 2 binding of TBI–TPE with Ag+. (D) Illustration of the self-assembly aggregation. | |
Next, we studied the stoichiometric coordination of TBI–TPE with Ag+. As shown in Fig. 3C, Job’s plot established that the stoichiometry ratio of the TBI–TPE and Ag+ strongly fluorescent complex is 1
:
2. Furthermore, the mass of Ag–TBI–TPE complex was determined using MALDI-TOF MS. A peak at 2021.398 was obtained (Fig. 4A), suggesting the Ag–TBI–TPE complex formed is (TBI–TPE)2Ag4, which corresponds to the theoretical calculation (2021.312, Fig. 4B). These results are consistent with the Job’s plot. According to these results, we speculate that the N atoms of imidazole are good electron donors, which display good ability to coordinate positive Ag+, forming a stable and strong fluorescent complex. The schematic diagram of this phenomenon is shown in Fig. 3D.
![image file: c8ra03591a-f4.tif](/image/article/2018/RA/c8ra03591a/c8ra03591a-f4.gif) |
| Fig. 4 Experimental (A), and calculated (B), MALDI-TOF of the Ag–TBI–TPE complex. | |
Furthermore, it is well known that pH changes according to the concentration of Ag+, which will greatly effect the interaction between Ag+ and the probe. The effect of pH on the interaction between Ag+ and the probe were investigated by fluorescence measurement. As shown in Fig. S13,† the fluorescence intensity at 525 nm increased with increasing pH from 4.0 to 7.0, and the fluorescence signal decreased with increasing pH value. This tendency revealed that the interaction between the probe and Ag+ would be effected by the deprotonation process. The best fluorescent performance of Ag–TBI–TPE at neutral pH is beneficial for the detection of Ag+ in environmental samples.
3.3.2 Selectivity of assay. The N atoms of the imidazole moiety have a unique chelating ability to transition metal ions. So to verify the fluorescence response of TBI–TPE towards other metal ions, we examined the emission characteristics of TBI–TPE in the presence of various metal ions in CH3OH solution. As shown in the inset of Fig. S14,† the fluorescence emission of TBI–TPE in the presence of other metal ions is weak. The corresponding fluorescence spectra (Fig. 5A) indicates that the addition of other metal ions (Cu2+, Ca2+, Cd2+, Co2+, Cr2+, Mg2+, Er3+, Eu3+, Fe2+, Fe3+, K+, Zn2+, Na+, Ni2+, Pd2+, Sn2+, Tb3+ and Zr4+) into TBI–TPE solution causes no change, weak fluorescence is retained. This result indicates that the fluorescence response of TBI–TPE is highly selective towards Ag+ over other metal ions.
![image file: c8ra03591a-f5.tif](/image/article/2018/RA/c8ra03591a/c8ra03591a-f5.gif) |
| Fig. 5 (A) Bars denote the fluorescence intensity difference (F − F0)/F0 in the presence of a series of metal ions. F0 is the fluorescence intensity of TBI–TPE (10 μM) only, and F is the fluorescence intensity of TBI–TPE in the presence of metal ions (20 μM). (B) Time-dependent fluorescence response of the 2 μM TBI–TPE to 4 μM Ag+ in CH3OH. (C) Fluorescence spectra of TBI–TPE (2 μM) in CH3OH in the presence of increasing concentrations of Ag+ (from 0 to 6 μM); Ex = 370 nm. (D) Variation of the fluorescence intensity at 525 nm of TBI–TPE with a gradual increase in the concentration of Ag+. (E) Variation of the intensity ratio of TBI–TPE (2 μM) with an increase in the concentration of Ag+ for the determination of the detection limit, where F0 is the intensity at 525 nm when the metal ion concentration is 0, and F is the intensity at each metal ion concentration tested during titration. Ex = 370 nm. | |
3.3.3 Response time. Fig. 5B depicts the typical time-dependent fluorescent spectra of the CH3OH solution containing TBI–TPE after the addition of Ag+ into the TBI–TPE solution. Upon addition of Ag+, the fluorescent spectrum of TBI–TPE was recorded immediately and then every 30 s. The fluorescent intensity of TBI–TPE was increased significantly and reached a plateau after 1 min. Hence, this result indicates that TBI–TPE can serve as a fluorescent chemical probe for the detection of Ag+ with fast response.
3.3.4 Sensitivity of assay. The fluorescence response of TBI–TPE to Ag+ at different concentrations is shown in Fig. 5C and D. The fluorescence at 525 nm was increased gradually as Ag+ concentration increased 0 to 4 μM. When the concentration reaches 4 μM, the intensity of fluorescence remains constant. This indicates that TBI–TPE has a certain coordination relationship with Ag+ when the fluorescence intensity reaches a certain value and then reaches a plateau. Titration studies with TBI–TPE revealed good linearity between increasing level log[(F − F0)/F0] and log[Ag+] in the range from 0.1 to 4 μM (Fig. 5E) where, F0 is the fluorescence intensity of TBI–TPE (2 μM) only, and F is the fluorescence intensity of TBI–TPE in the presence of metal ions. The detection limit is 90 nM on the basis of a signal-to-noise ratio of 3
:
1.
3.4 Sample application
The practicability of TBI–TPE fluorescent probe was assessed by applying it to the analysis of Ag+ in waste liquor samples, provided by a factory in Kunming city. An average value of 0.112 ± 0.003 μM Ag+ was found for n = 3 determinations using our developed approach with good recovery (99 ± 2%), after subtraction of the intercept from the standard calibration curve (Fig. 5E), which is consistent with the ICP-MS measurement, 0.113 ± 0.008 μM. These results suggest that our fluorescence probe can be used for Ag+ determination in environmental samples.
4. Conclusions
In conclusion, we have designed and synthesized an AIE fluorescence probe containing benzimidazole group, which exhibited highly sensitive and selective “turn-on” fluorescence for the determination of Ag+ with a detection limit of 0.090 μM. The stoichiometry of TBI–TPE and Ag+ in the complex was established to be 1
:
2 using Job’s plot and MS studies. Thanks to the unique AIE property of TPE, a facile strategy for the construction of high performance “signal on” fluorescent probes has been presented and could be developed for other potential applications.
Conflicts of interest
There are no conflicts to declare.
Acknowledgements
This work was financially supported by the National Natural Science Foundation of China (NSFC, 21765024).
Notes and references
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Footnote |
† Electronic supplementary information (ESI) available. See DOI: 10.1039/c8ra03591a |
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