阅读说明：本技术 一种席夫碱聚集诱导荧光分子探针及其制备方法和应用 (Schiff base aggregation-induced fluorescent molecular probe and preparation method and application thereof ) 是由 胡小刚 刘锦辉 于 2019-08-30 设计创作，主要内容包括：本发明涉及一种席夫碱聚集诱导荧光分子探针及其制备方法和应用,所述荧光分子探针为席夫碱类化合物,利用一步简单反应合成具有聚集诱导发光性能的席夫碱,以二苯甲酮腙和5-氯水杨醛作为原料,通过氨基和醛基之间的专一反应将二苯甲酮腙和5-氯水杨醛键合,形成具有聚集诱导荧光性能的席夫碱化合物分子,该化合物分子能够通过配位作用特异性识别Cu<Sup>2+</Sup>,并通过其荧光信号的变化实现对Cu<Sup>2+</Sup>的定性和定量检测。本发明的荧光分子探针具有快速检测、灵敏度高、特异性强等优点,可以用来高灵敏度、高选择性、快速准确地检测水中的Cu<Sup>2+</Sup>。(The invention relates to a Schiff base aggregation-induced fluorescence molecular probe and a preparation method and application thereof, wherein the fluorescence molecular probe is a Schiff base compound, Schiff base with aggregation-induced emission performance is synthesized by utilizing one-step simple reaction, benzophenone hydrazone and 5-chlorosalicylaldehyde are used as raw materials, the benzophenone hydrazone and the 5-chlorosalicylaldehyde are bonded through the specific reaction between amino and aldehyde groups to form Schiff base compound molecules with aggregation-induced fluorescence performance, and the compound molecules can specifically recognize Cu through coordination 2+ And the change of the fluorescence signal of the Cu-doped copper alloy is used for realizing the effect on the Cu 2+ Qualitative and quantitative detection. The fluorescent molecular probe of the invention has the advantages of rapid detection,High sensitivity, strong specificity and the like, and can be used for quickly and accurately detecting Cu in water with high sensitivity and high selectivity 2+ 。)

1. A Schiff base aggregation-induced fluorescent molecular probe is characterized in that: the fluorescent molecular probe is a Schiff base compound, and has a specific structural formula as follows:

2. a method for preparing the schiff base aggregation-induced fluorescence molecular probe according to claim 1, comprising the steps of:

s1: adding benzophenone hydrazone, 5-chlorosalicylaldehyde and absolute ethyl alcohol into a reaction vessel, and stirring at room temperature; (ii) a

S2: after the reaction is finished, evaporating the solvent absolute ethyl alcohol to dryness, and re-dispersing the solvent absolute ethyl alcohol by using a small amount of absolute ethyl alcohol to obtain a suspension;

s3: suction-filtering the suspension obtained in S2 and washing the product with a large amount of absolute ethyl alcohol;

s4: and collecting the reaction product obtained in the step S3, and drying in vacuum at room temperature to obtain the Schiff base polymerization induced fluorescent molecular probe.

3. The method for preparing Schiff base aggregation-induced fluorescence molecular probe according to claim 2, wherein the method comprises the following steps: in the step S1, benzophenone hydrazone, 5-chlorosalicylaldehyde and absolute ethyl alcohol are added into a reaction vessel, nitrogen is introduced to remove oxygen, the solution is placed in a dark environment, and stirred with a magnetic stirrer at 700rpm at room temperature.

4. The method for preparing Schiff base aggregation-induced fluorescence molecular probe according to claim 2, wherein the method comprises the following steps: in the step S1, the molar ratio of the benzophenone hydrazone to the 5-chlorosalicylaldehyde is as follows: (0.5-1.5) 1; the volume of the reaction solvent absolute ethyl alcohol is 15-50 mL, and the stirring reaction time is 5-20 h.

5. The method for preparing Schiff base aggregation-induced fluorescence molecular probe according to claim 2, wherein the method comprises the following steps: in the step S2, the volume of the redispersing solvent absolute ethyl alcohol is 2-10 mL.

6. The method for preparing Schiff base aggregation-induced fluorescence molecular probe according to claim 2, wherein the method comprises the following steps: in the step S3, the volume of the washing solvent, namely absolute ethyl alcohol, is 20-50 mL.

7. The Schiff base aggregation-induced fluorescence molecular probe used for Cu according to claim 1²⁺And (5) carrying out analysis and detection.

Technical Field

The invention relates to the technical field of material preparation and detection, in particular to a Schiff base aggregation-induced fluorescent molecular probe and a preparation method and application thereof. Is suitable for detecting Cu in trace amount in various water samples²⁺The rapid detection of (2).

Background

Copper ions are one of trace elements necessary for the human body and are the third most abundant transition metal element in the body. It is involved in the formation of many proteins and enzyme catalytic factors, such as cytochrome C oxidase and long oxide dismutase; however, when the copper content in the body is too high, the kidney and the liver are damaged, so that diseases such as cirrhosis and hepatic ascites may occur, and alzheimer's disease, parkinson's disease, and melks disease may also occur. For plants, too high a copper ion concentration may affect the absorption of other essential ions by plants, and thus the normal growth and development of the plants. Therefore, it is very important to realize the high-sensitivity detection of copper ions.

The traditional method for detecting copper ions comprises an atomic absorption spectrometry, an ultraviolet-visible spectrophotometry, an ion chromatography, a colorimetric method and the like, and although the traditional detection method has the characteristics of high accuracy, wide linear range, strong specificity and the like, the pretreatment process is complex, the detection cost is high, and the rapid detection on site is difficult to realize. Compared with the traditional detection methods, the fluorescence spectrometry has the advantages of high sensitivity, small sample consumption, simple instrument and equipment, simple and convenient operation, capability of realizing in-situ real-time online and nondestructive detection and the like, and shows wider and wider application prospect.

After being excited by light with a certain range of wavelength, a common fluorescent molecular probe can emit fluorescence longer than incident wavelength, and when the incident light disappears, the emitted light also disappears; however, when the concentration of the fluorescent molecules in the solution is increased, the fluorescence of the solution is quenched due to Aggregation of the fluorescent molecules, which causes the conjugated structures between the fluorescent molecules to stack up and return to the ground state from the excited state, which is a common Aggregation-Quenching effect (ACQ) of the fluorescent molecules. Due to the ACQ phenomenon, the application of the traditional organic molecular fluorescent material in high concentration and solid state is greatly limited. Therefore, how to overcome the ACQ property in the organic fluorescent material is an urgent problem to be solved in the realization of wider application of the organic fluorescent material.

In 2001, Tang et al found that silacyclopentadiene derivative hardly generates fluorescence in a good solvent, but the fluorescence signal in a poor solvent and a solid state is greatly enhanced, and the fluorescence signal is continuously enhanced with the increase of the aggregation degree; this is in contrast to the conventional Aggregation of organic fluorescent molecules to produce quenching phenomena (ACQ), which is defined as Aggregation-Induced Emission (AIE). The organic fluorescent molecule with AIE property fundamentally solves the problem of aggregation induced quenching, so that the organic fluorescent material can be applied in more aspects. With the continuous and deep research on the organic fluorescent molecules with AIE properties, more and more organic fluorescent molecules with AIE properties are synthesized and applied to the fields of ion detection, biological small molecule detection, cell imaging and the like, so that the organic fluorescent molecules are rapidly developed in the aspect of detection and tracing. The aggregation-induced emission material fundamentally overcomes the problem of ACQ caused by the traditional organic fluorescent molecules, and can generate strong fluorescence even if the concentration of the material is low in an aqueous solution. In recent years, many studies have been made on AIE fluorescent probes, and various AIE probes have been developed. However, these AIE probes generally have problems of complicated synthesis steps, low yield, long time consumption, and the like. Therefore, it is desired to achieve rapid and efficient synthesis of an AIE probe by a simple reaction in one step, and to easily obtain an ideal functionalized AIE probe by changing a functional group carried by a reactant.

Disclosure of Invention

Based on this, the invention aims to overcome the defect of detecting Cu in the prior art²⁺The method has the advantages of overcoming the defects of complex operation, long time consumption, poor selectivity and the like, simultaneously solving the problem of aggregation-induced quenching caused by overhigh concentration of the traditional fluorescent probe, improving the biological application of the traditional fluorescent probe, and providing the Schiff base aggregation-induced fluorescent molecular probe and the preparation method thereof.

In order to achieve the purpose, the invention adopts the following technical scheme:

a Schiff base aggregation-induced fluorescent molecular probe is a Schiff base compound and has a specific structural formula as follows:

compared with the prior art, the fluorescent molecular probe compound has an intramolecular conjugated structure, so that a fluorescent signal can be generated at 420nm under the irradiation of incident light. Meanwhile, intramolecular hydrogen bonds can be formed between the intramolecular hydroxyl groups and nitrogen atoms, intramolecular proton transfer can occur when the intramolecular hydroxyl groups are excited by incident light, so that molecules are converted from an alcohol structure to a ketone structure, and a stronger fluorescence signal can be emitted at 560nm due to the increase of the conjugation degree in the molecules under the ketone structure. In addition, the molecule is not in a planar structure, does not form H-aggregate to cause fluorescence quenching when forming aggregate in poor solvent, and can promote the proton transfer process in excited state molecule in aqueous solution, thereby exhibiting the performance of aggregation-induced fluorescence enhancement. The fluorescent molecular probe has the advantages of good photostability, high sensitivity, high detection speed, high fluorescence intensity, low detection limit and the like.

The invention also aims to provide a preparation method of the Schiff base aggregation-induced fluorescent molecular probe, which comprises the following steps: the method comprises the following steps:

s1: adding benzophenone hydrazone, 5-chlorosalicylaldehyde and absolute ethyl alcohol into a reaction vessel, and stirring at room temperature; (ii) a

S2: after the reaction is finished, evaporating the solvent absolute ethyl alcohol to dryness, and re-dispersing the solvent absolute ethyl alcohol by using a small amount of absolute ethyl alcohol to obtain a suspension;

s3: suction-filtering the suspension obtained in S2 and washing the product with a large amount of absolute ethyl alcohol;

s4: and collecting the reaction product obtained in the step S3, and drying in vacuum at room temperature to obtain the Schiff base polymerization induced fluorescent molecular probe.

Compared with the prior art, the invention adopts benzophenone hydrazone to react with salicylaldehyde modified with other functional groups to generate the Schiff base with AIE performance. The reaction condition is mild and efficient, and the reaction can be completed only in several hours at room temperature. The Schiff base aggregation-induced fluorescent molecular probe capable of being detected qualitatively and quantitatively is synthesized simply and efficiently by adopting a one-step method. The method utilizes the specific reaction between aldehyde group and amino group to form a nitrile group, bonds benzophenone hydrazone and 5-chlorosalicylaldehyde together, has mild and rapid reaction conditions, and can be carried out at room temperature. Meanwhile, the product has poor solubility in absolute ethyl alcohol, and the benzophenone hydrazone and 5-chlorosalicylaldehyde have good solubility in absolute ethyl alcohol, so that the product can be purified only by washing the product with absolute ethyl alcohol.

Further, in the step S1, benzophenone hydrazone, 5-chlorosalicylaldehyde and absolute ethyl alcohol are added into the reaction vessel, nitrogen is introduced to remove oxygen, the solution is placed in a dark environment, and a magnetic stirrer is used to stir at 700rpm at room temperature.

Further, in step S1, the molar ratio of the benzophenone hydrazone to the 5-chlorosalicylaldehyde is: (0.5-1.5) 1; the volume of the reaction solvent absolute ethyl alcohol is 15-50 mL, and the stirring reaction time is 5-20 h.

Further, the volume of the redispersing solvent absolute ethyl alcohol in the step S2 is 2-10 mL.

Further, the volume of the washing solvent, namely absolute ethyl alcohol, in the step S3 is 20-50 mL.

The Schiff base aggregation-induced fluorescent molecular probe can be used for Cu in a water sample²⁺And (5) carrying out analysis and detection.

When copper ions exist in the solution, oxygen atoms and nitrogen atoms in molecules of the fluorescent molecular probe compound can form coordinate bonds with the copper ions, so that intramolecular hydrogen bonds and proton transfer processes in excited-state molecules are destroyed, the molecules cannot be converted into ketone structures from alcohol type, and fluorescence at 560nm is quenched, while fluorescence at 420nm is basically unaffected.

The Schiff base aggregation-induced fluorescence molecular probe is an organic fluorescence molecule taking aggregation-induced emission molecules as a light source, and compared with the traditional organic fluorescence molecule, the fluorescence molecular probe has many excellent characteristics: 1. the defect of aggregation induced quenching caused by overhigh concentration is overcome, and the organic fluorescent molecule has excellent fluorescence performance in aqueous solution, while the traditional organic fluorescent molecule generally has poor water solubility and is difficult to increase the concentration and the fluorescence intensity of the organic fluorescent molecule in the aqueous solution; 2. the preparation is simple and efficient, the synthesis reaction can be completed in a short time only under the condition of room temperature, and the reaction is safe and has high yield.

For a better understanding and practice, the invention is described in detail below with reference to the accompanying drawings.

Drawings

FIG. 1 is a Fourier transform infrared spectrum of a Schiff base aggregation-induced fluorescent molecular probe (SYB-Cl) according to the present invention;

FIG. 2 shows Schiff base aggregation-induced fluorescence molecular probe (SYB-Cl) and Cu with different concentrations²⁺Hydrogen nuclear magnetic resonance spectrum of (A, B, C represents Cu, respectively)²⁺The concentration is 0 mu mol/L, 5 mu mol/L and 10 mu mol/L);

FIG. 3 is a fluorescence intensity spectrum of Schiff base aggregation-induced fluorescence molecular probe (SYB-Cl) solution of the present invention after adding 16 kinds of metal ions;

FIG. 4 shows Cu in Schiff base aggregation-induced fluorescence molecular probe (SYB-Cl) solution²⁺Fluorescence intensity spectra of competitive binding with other 15 metal ions;

FIG. 5 shows Cu in Schiff base aggregation-induced fluorescence molecular probe (SYB-Cl) solution²⁺Fluorescence intensity spectra of competitive binding to 16 anions;

FIG. 6 shows that Cu with different concentrations is added into a Schiff base aggregation-induced fluorescence molecular probe (SYB-Cl) solution²⁺The subsequent fluorescence spectrogram;

FIGS. 7 and 8 show the fluorescence intensity of Schiff base aggregation-induced fluorescence molecular probe (SYB-Cl) and Cu in accordance with the present invention²⁺A graph of concentration dependence;

FIG. 9 is a diagram showing the solvent ratio optimization results of Schiff base aggregation-induced fluorescence molecular probe (SYB-Cl) according to the present invention;

FIG. 10 is a graph showing the pH optimization results of Schiff base aggregation-induced fluorescent molecular probe (SYB-Cl) according to the present invention;

FIG. 11 is a graph showing the optimization results of the binding time of the Schiff base aggregation-induced fluorescent molecular probe (SYB-Cl) of the present invention.

Detailed Description

The present invention is described in further detail below.

The invention takes the synthesized aggregation-induced fluorescent molecule as a luminous source and Cu²⁺The probe molecule is synthesized by a one-step method, the condition is mild, the reaction is rapid, the problem of aggregation-induced quenching of the traditional fluorescent organic molecule is fundamentally solved, and the probe molecule has the advantages of good photostability, high sensitivity, high detection rate, low detection limit, low cost and the like. The technical solution of the present invention will be described in detail below with reference to specific examples.

Fluorescent probe and preparation method thereof

The invention relates to a Schiff base aggregation-induced fluorescent molecular probe, which is a Schiff base compound and has the specific structural formula:

the above compounds may be abbreviated as SYB-Cl. The synthesis route of the Schiff base compound is as follows:

the preparation method of the fluorescent probe comprises the following steps:

s1: adding benzophenone hydrazone (EB), 5-chlorosalicylaldehyde (SY-5Cl) and absolute ethyl alcohol into a reaction vessel, and stirring at room temperature, wherein the molar ratio of the benzophenone hydrazone to the 5-chlorosalicylaldehyde is as follows: (0.5-1.5) 1.

Specifically, absolute ethyl alcohol, benzophenone hydrazone and 5-chlorosalicylaldehyde are added into a 100mL round-bottom flask, and nitrogen is introduced for 5min to remove oxygen; the solution was placed in a dark environment and stirred vigorously with a magnetic stirrer at 700rpm to obtain a mixed solution after the reaction was completed. The volume of the reaction solvent absolute ethyl alcohol is 15-50 mL, and the stirring reaction time is 5-20 h.

S2: after the reaction is finished, the solvent is evaporated to dryness by spinning and is redispersed by a small amount of absolute ethyl alcohol.

Specifically, the solvent of the mixed solution obtained in the step S1 is evaporated to dryness under reduced pressure at 30 ℃ to obtain a yellow powder; the solid was redispersed as a yellow powder with a small amount of absolute ethanol. The volume of the redispersion solvent absolute ethyl alcohol is 2-10 mL.

S3: the suspension obtained in step S2 was filtered with suction and the product was washed with a large amount of anhydrous ethanol.

Specifically, the yellow suspension obtained in the step S2 is slowly dropped onto an organic filter membrane, and the solvent is filtered to dryness; the yellow solid was rinsed several times with a large amount of absolute ethanol. The volume of the washing solvent absolute ethyl alcohol is 20-50 mL.

S4: and collecting the reaction product and drying in vacuum at room temperature to obtain the Schiff base polymerization induced fluorescent molecular probe.

Specifically, the reaction product is placed in a vacuum drying oven at a constant temperature of 25 ℃ for 24h, and after drying, the product is collected, sealed and protected from light and stored at 4 ℃ and marked as SYB-Cl.

The Schiff base aggregation-induced fluorescent molecular probe can be used for Cu in a water sample²⁺And (5) carrying out analysis and detection.

Characterization and test results

Referring to FIG. 1, FIG. 1 is a Fourier transform infrared spectrum of SYB-Cl, 5-chlorosalicylaldehyde (SY-5Cl) and benzophenone hydrazone (EB) according to the present invention. Wherein, for SY-5Cl, 3214cm^-1Is the stretching vibration peak of the phenolic hydroxyl O-H; 3049 to 2877cm^-1The peak is C (═ O) -H stretching vibration peak group of aldehyde group, 1914-1772 cm^-1The weak peak is the overtone peak of the benzene ring; 1682cm^-1A stretching vibration peak of C ═ O; 1474cm^-1The peak at the position is a characteristic peak of the vibration of the benzene ring framework. Combining with infrared spectrum of SYB-Cl, presuming that after the target compound is formed, the absorption peak of phenolic hydroxyl is converted into broad peak due to formation of intramolecular hydrogen bond, and carbonyl disappears at 3053cm^-1A stretching vibration peak of-C (═ N) -H appears; 1953-1731 cm^-1The weak peak is the overtone peak of the benzene ring; original C ═ O formed C ═ N, so that 1682cm^-1The frequency of the stretching vibration peak is shifted to 1605cm^-1；1472cm^-1The peak at the position is a characteristic peak of the vibration of the benzene ring framework. The disappearance of the infrared characteristic peak of the aldehyde group proves that 5-chlorosalicylaldehyde does not exist in the product, and benzophenone does not exist in the productThe hydrazone successfully bonds the 5-chlorosalicylaldehyde.

Please refer to FIG. 2, which shows SYB-Cl (10. mu. mol/L) and different concentrations of Cu²⁺(A, B, C represents Cu, respectively)²⁺The concentrations of 0 mu mol/L, 5 mu mol/L and 10 mu mol/L) are shown, and the addition of Cu is obvious²⁺The Ha and Hb peak heights in the latter EBE NMR spectra were reduced due to Cu²⁺Respectively coordinate with oxygen atoms on hydroxyl groups and nitrogen atoms on-HC ═ N < - >, so that the height of a hydroxyl group peak Ha is reduced; furthermore, we have found that Cu is added²⁺The latter has a single peak at 8.78 and increases with increasing concentration, which is believed to be due to Cu²⁺Is introduced by water molecules. The water peak at 3.33 is seen to be higher and higher, while the increase of water molecules promotes intramolecular hydrogen bond formation and the progress of the ESIPT process, resulting in the splitting of the Hb peak, so it can be seen that the Hb peak height decreases while the peak height at 8.78 increases.

Referring to FIGS. 3, 4 and 5, the "Probe" group indicates the fluorescence intensity of the SYB-Cl solution without added ions; FIG. 3 shows the addition of 100. mu.L of 1.0mmol/L metal ion solution (Co) to 900. mu.L of 10. mu.M SYB-Cl solution²⁺、Ag⁺、Na⁺、Ca²⁺、K⁺、Zn²⁺、Fe²⁺、Hg²⁺、Al³⁺、Cr³⁺、Mn²⁺、Pb²⁺、Cu²⁺、Mg²⁺、Cd²⁺、Fe³⁺) And fully mixing the components uniformly and standing the mixture for 30min to obtain a fluorescence test result graph. FIG. 4 shows the addition of 100. mu.L of 10mmol/L metal ion solution (Co) to 800. mu.L of 5. mu.M SYB-Cl solution²⁺、Ag⁺、Na⁺、Ca²⁺、K⁺、Zn²⁺、Fe²⁺、Hg²⁺、Al³⁺、Cr³⁺、Mn²⁺、Pb²⁺、Mg²⁺、Cd²⁺、Fe³⁺) The experiments are divided into two groups; one group was added with 100. mu.L of deionized water, and the other group was added with 100. mu.L of 100. mu. mol/L Cu²⁺Shaking the solution sufficiently, and standing for 30min to test the obtained fluorescence image. FIG. 5 shows the addition of 100. mu.L of 1 to 900. mu.L of 10. mu.M SYB-Cl solution0mmol/L anion solution (HPO)₄ ^2-、NO₃ ^-、Ac^-、HSO₃ ^-、I^-、CO₃ ^2-、NO₂ ^-、SiO₃ ^2-、HCO₃ ^-、Citrate^3-、F^-、SO₄ ^2-、Cl^-、Br^-、S₂O₈ ^2-、SCN^-) And fully mixing the components uniformly and standing the mixture for 30min to obtain a fluorescence test result graph.

FIG. 3 reflects, Ca²⁺、Na⁺、K⁺Plasma had little effect on fluorescence intensity of SYB-Cl, Al³⁺、Ag⁺、Zn²⁺、Co²⁺、Pb²⁺、Mn²⁺、Mg²⁺、Hg²⁺、Fe²⁺、Fe³⁺、Cr³⁺、Cd²⁺The fluorescence intensity of SYB-Cl is respectively reduced by about 7 to 24 percent, and Cu is added²⁺The fluorescence intensity of the latter SYB-Cl was reduced by about 91%. As can be seen, Cu²⁺The fluorescence intensity of SYB-Cl has great influence, and the fluorescence quenching of SYB-Cl can be caused, and other metal ions have little or no influence on the fluorescence intensity of SYB-Cl, which indicates that SYB-Cl has little influence on Cu²⁺Has good selectivity.

FIG. 4 reflects, Co²⁺、Ag⁺、Na⁺、Ca²⁺、K⁺、Zn²⁺、Fe²⁺、Hg²⁺、Al³⁺、Cr³⁺、Mn²⁺、Pb²⁺、Mg²⁺、Cd²⁺、Fe³⁺The addition of plasma does not affect Cu²⁺Fluorescence quenching performance of SYB-Cl shows that other 15 metal ions are in SYB-Cl to Cu²⁺The identification process does not cause significant interference.

FIG. 5 reflects, HPO₄ ^2-、NO₃ ^-、Ac^-、I^-、CO₃ ^2-、NO₂ ^-、SiO₃ ^2-、HCO₃ ^-、F^-、SO₄ ^2-、Cl^-、Br^-、S₂O₈ ^2-、SCN^-The addition of the plasma does not substantially affect Cu²⁺Fluorescence quenching Properties on SYB-Cl, Citrate^3-And HSO₃ ^-Has 16 percent fluorescence enhancement effect on fluorescence, and shows that 16 anions are in SYB-Cl to Cu²⁺The identification process does not cause significant interference.

Please refer to fig. 6, which is a diagram of 5.0 × 10^-6Adding 1.0X 10 mol/L SYB-Cl solution^-7～1.0×10^{- 5}mol/L Cu²⁺Fluorescence spectra obtained after the solution. FIG. 6 reflects fluorescence intensity of SYB-Cl as a function of Cu²⁺The concentration increases and decreases regularly. Please refer to FIG. 7 and FIG. 8, and FIG. 7 and FIG. 8 are Cu²⁺Concentration versus fluorescence intensity of SYB-Cl. As can be seen from FIG. 7, the ratio is 1X 10^-7～1×10^-5mol/L of Cu²⁺SYB-Cl fluorescence intensity with Cu over a range of concentrations²⁺Decrease with increase in concentration, and SYB-Cl fluorescence intensity and Cu²⁺The concentration presents a good linear relation, and the linear regression equation is as follows: y 975.38967 × e^(-x/1.26252)+119.4456 with a linear correlation coefficient R of 0.9993, where y denotes the addition of Cu²⁺Fluorescence intensity of the post solution, x represents Cu²⁺And (4) concentration. As can be seen from FIG. 8, the ratio is 1X 10^-7～1×10^-5mol/L of Cu²⁺In the concentration range with Cu²⁺Ln (I-119.446) decreases linearly with concentration, the linear equation being: y-0.6654 x +6.76942, linear correlation coefficient R0.9998, and lowest detection limit of 4.9 × 10^-8mol/L, wherein y represents ln (I-119.446), and x represents Cu²⁺Concentration, I represents the fluorescence intensity of the solution. According to the above SYB-Cl fluorescence intensity and Cu²⁺The concentration relation can detect the Cu in the actual water sample²⁺And the concentration thereof is determined.

(4) Please refer to fig. 9, 10 and 11, which are graphs showing the solvent ratio optimization, pH optimization and binding time optimization results of schiff base aggregation-induced fluorescent molecular probe (SYB-Cl), respectively. As can be seen from fig. 9, the material has the best fluorescent properties when the solvent is pure water; similarly, as can be seen from figure 10,the material has the best quenching performance when the pH is the original solution (pH 5.6); it can be observed from FIG. 11 that the fluorescence intensity of the solution remained substantially unchanged after the binding time was greater than 35min, and therefore 40min was selected as SYB-Cl versus Cu²⁺Optimal binding time.

The above-mentioned embodiments only express several embodiments of the present invention, and the description thereof is more specific and detailed, but not construed as limiting the scope of the invention. It should be noted that, for a person skilled in the art, several variations and modifications can be made without departing from the inventive concept, which falls within the scope of the present invention.