阅读说明：本技术 一种具有aie效应的双bodipy类近红外荧光染料及其制备方法 (double-BODIPY near-infrared fluorescent dye with AIE effect and preparation method thereof ) 是由 徐海军 王怡 李鹏飞 宗轩莱 于 2021-08-06 设计创作，主要内容包括：本发明涉及一种具有AIE效应的双BODIPY类近红外荧光染料及其制备方法,使用BODIPY衍生物(I)先后与对苯二甲醛和4-(二苯氨基)苯甲醛发生两步Knoevenagel缩合反应得到化合物(III)。通过引入具有AIE效应的强给/受体基团,将传统的BODIPY类荧光染料从ACQ分子转变为AIE分子,在近红外区域表现出良好的聚集诱导发光效应。且该荧光染料具有大的斯托克斯位移(70nm),作为一种新型近红外AIE荧光染料,在发光材料、生物荧光成像、化学传感器、光动力治疗等众多领域均具有广阔的应用前景。该制备方法反应条件温和、选择性较好、分离提纯较为简便。(The invention relates to a double-BODIPY near-infrared fluorescent dye with AIE effect and a preparation method thereof, wherein a BODIPY derivative (I) is subjected to two-step Knoevenagel condensation reaction with terephthalaldehyde and 4- (diphenylamino) benzaldehyde in sequence to obtain a compound (III). By introducing a strong donor/acceptor group with AIE effect, the traditional BODIPY fluorescent dye is converted from ACQ molecules into AIE molecules, and the good aggregation-induced emission effect is shown in a near infrared region. And the fluorescent dye has large Stokes shift (70nm), and has wide application prospect in a plurality of fields such as luminescent materials, biological fluorescence imaging, chemical sensors, photodynamic therapy and the like as a novel near-infrared AIE fluorescent dye. The preparation method has the advantages of mild reaction conditions, good selectivity and simple and convenient separation and purification.)

1. A double BODIPY near infrared fluorescent dye (III) with AIE effect is characterized in that the structural formula is shown as the formula (III):

2. the preparation method of the double BODIPY near infrared fluorescent dye (III) with the AIE effect, which is claimed in claim 1, is characterized in that the preparation method comprises the following steps: firstly, carrying out Knoevenagel condensation reaction on a BODIPY derivative (I) and terephthalaldehyde to obtain a compound (II), and then carrying out Knoevenagel condensation reaction on the compound (II) and 4- (diphenylamino) benzaldehyde to obtain a double BODIPY near-infrared fluorescent dye (III) with an AIE effect, wherein the reaction formula of the preparation process is as follows:

3. the method for preparing the double BODIPY near infrared fluorescent dye (III) with the AIE effect according to claim 2, which is characterized by comprising the following steps:

1) dissolving terephthalaldehyde and a BODIPY derivative (I) in a mixed solution of methanol and dichloromethane in a certain proportion under an anhydrous condition, dropwise adding 1M methanol solution of sodium methoxide into the mixed solution, and reacting at room temperature for 6-8 hours after dropwise adding. Adding water to quench the reaction, extracting with dichloromethane, drying the organic layer with anhydrous sodium sulfate, evaporating under reduced pressure to remove the solvent, and separating and purifying by silica gel column chromatography, wherein the eluent is dichloromethane-petroleum ether (v: v ═ 9: 1), to obtain a compound (II);

2) under anhydrous conditions, compound (II), 4- (diphenylamino) benzaldehyde and freshly dried p-toluenesulfonic acid were added to a 100mL two-necked reaction flask equipped with a Dean-Stark apparatus, followed by the addition of 10mL of toluene to dissolve, and 0.2mL of piperidine was added as a catalyst, stirred and heated to reflux for 4-6 hours. And after the reaction is finished, cooling to room temperature, extracting with dichloromethane, washing with water, drying, evaporating the solvent under reduced pressure, and separating and purifying by silica gel column chromatography, wherein an eluent is dichloromethane-petroleum ether (v: v ═ 2: 3), so that the double BODIPY near-infrared fluorescent dye (III) with the AIE effect is obtained.

4. The method according to claim 3, wherein in step 1), the ratio of the amounts of terephthalaldehyde, BODIPY derivative (I) and sodium methoxide is 1: 2.2-2.5: 8-10, and the volume ratio of methanol to dichloromethane is 2: 1.

5. The method according to claim 3, wherein in step 2), the ratio of the compound (II), p-toluenesulfonic acid and 4- (diphenylamino) benzaldehyde is 1: 0.5: 4.0-6.0, and the ratio of the volume of toluene, piperidine and compound (II) to the amount of the substance is 50mL and 1 mL: 1 mmol.

6. The dual BODIPY-based near infrared fluorescent dye (III) having an AIE effect according to claim 1, wherein the dual BODIPY-based near infrared fluorescent dye (III) exhibits a good AIE effect during the increase of the volume fraction of water in the DMSO/water mixed solvent from 0 to 90%. Wherein, when the proportion of water is increased to 90%, the fluorescence intensity is maximized and enhanced by 12.5 times.

7. Use of a double BODIPY near infrared fluorescent dye (III) with AIE effect prepared according to the preparation method of claim 1 or any one of claims 2 to 5 in the fields of luminescent materials, bioluminescence imaging, chemical sensors, photodynamic therapy.

Technical Field

The invention belongs to the technical fields of organic compound synthesis, functional fluorescent dyes and fine chemical engineering, and particularly relates to a double-BODIPY near-infrared fluorescent dye with an AIE effect and a preparation method thereof.

Background

The space structure of the traditional fluorescent molecule is not three-dimensional due to the pi conjugated system of the traditional fluorescent molecule, and energy loss is caused by mutual collision of molecules in an aggregation state, so that fluorescence quenching (ACQ) caused by aggregation occurs. This phenomenon greatly restricts the range of applications of fluorescent materials. In 2001, the subject group of Tang-loyal courier reported an organic fluorescent molecule with the phenomenon of "Aggregation Induced Emission (AIE)". In contrast to ACQ molecules, AIE molecules are restricted in molecular motion in the aggregation state, and inhibit non-radiative transition processes to promote radiative transition processes, resulting in significant enhancement of luminescence. The problem of fluorescence quenching due to aggregation is fundamentally solved by the discovery of the properties of AIE. With the intensive research on this phenomenon in the scientific community, luminescent materials with AIE effect have achieved tremendous success in the application fields of chemical sensors, biological imaging, photodynamic therapy, stimulus responsive materials, and the like.

In the process of researching and expanding an AIE molecular system, compared with fluorescent molecules in a visible light region, the molecules with near infrared fluorescence emission can effectively reduce the interference of tissue autofluorescence and enhance the sensing and imaging depth. Particularly, the near-infrared fluorescent material with AIE performance can well solve the problem of fluorescence quenching caused by aggregation of the traditional fluorescent material in organisms. When the fluorescent dye exists in an aggregation state, the fluorescent dye avoids scattered light of organisms, simultaneously shows excellent photobleaching resistance, and can realize fluorescence imaging with high resolution and high signal-to-noise ratio. Therefore, some functional near-infrared AIE fluorescent dyes have great potential in the life science fields of molecular diagnosis, targeted therapy and the like.

In a plurality of organic fluorescent dyes, BODIPY is used as a basic fluorescent group, and has the characteristics of good photo-thermal stability, difficult external influence on a fluorescent signal, narrow spectral absorption/emission peak, high sensitivity, easy modification of a parent structure and the like. The Cyanostyrylbenzene (CS) molecule is a typical electron acceptor, and has characteristics of a highly stable energy level, high solubility due to "distortion elasticity" characteristics, and the like. In addition, the distorted spatial conformation can ensure the AIE performance of the molecule, and is beneficial to the design of AIE functional molecules. Triphenylamine (TPA) is an electron donor with excellent performance, and in an aggregation state, a space twisted structure of a triphenylamine unit can prevent pi-pi stacking interaction between molecules, so that fluorescence quenching is effectively avoided, and the luminous intensity of the molecules in the aggregation state is enhanced. Generally, an electron donor can increase the HOMO energy level, and an electron acceptor can reduce the LUMO energy level, so that the molecular energy gap is obviously reduced to realize spectral red shift. However, the AIE effect near infrared fluorescent dye molecules still have the problems of more synthesis steps, low yield and small quantity. Therefore, the near-infrared fluorescent dye with good AIE effect is obtained by introducing a strong electron donor triphenylamine and a strong electron acceptor cyanostyryl benzene to modify and expand the conjugated structure of the BODIPY through Knoevenagel condensation reaction. Has important significance for developing AIE molecular system and expanding the application field of AIE materials.

Disclosure of Invention

The purpose of the invention is as follows: aiming at the defects in the prior art, the invention aims to provide a double BODIPY near infrared fluorescent dye with AIE effect and a preparation method thereof.

The technical scheme is as follows: in order to achieve the purpose of the invention, the invention adopts the technical scheme that:

the invention relates to a double BODIPY near infrared fluorescent dye with AIE effect and a preparation method thereof, which is characterized in that the near infrared fluorescent dye has a structural formula shown in formula (III):

a double BODIPY near infrared fluorescent dye with AIE effect and a preparation method thereof comprise the following steps:

1) dissolving terephthalaldehyde and a BODIPY derivative (I) in a mixed solution of methanol and dichloromethane in a certain proportion under an anhydrous condition, dropwise adding 1M methanol solution of sodium methoxide into the mixed solution, and reacting at room temperature for 6-8 hours after dropwise adding. The reaction was quenched with water, extracted with dichloromethane, the organic layer was dried over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure, and then separated and purified by silica gel column chromatography, eluent dichloromethane-petroleum ether (v: v ═ 9: 1) to give compound (II).

2) Under anhydrous conditions, compound (II), 4- (diphenylamino) benzaldehyde and freshly dried p-toluenesulfonic acid were added to a 100mL two-necked reaction flask equipped with a Dean-Stark apparatus, followed by the addition of 10mL of toluene to dissolve, and 0.2mL of piperidine was added as a catalyst, stirred and heated to reflux for 4-6 hours. And after the reaction is finished, cooling to room temperature, extracting with dichloromethane, washing with water, drying, evaporating the solvent under reduced pressure, and separating and purifying by silica gel column chromatography, wherein an eluent is dichloromethane-petroleum ether (v: v ═ 2: 3), so that the double BODIPY near-infrared fluorescent dye (III) with the AIE effect is obtained. The specific chemical reaction formula is as follows:

in the step 1), the mass ratio of the terephthalaldehyde, the BODIPY derivative (I) and the sodium methoxide is 1: 2.2-2.5: 8-10, and the volume ratio of the methanol to the dichloromethane is 2: 1.

In the step 2), the ratio of the compound (II), p-toluenesulfonic acid and 4- (diphenylamino) benzaldehyde substance is 1: 0.5: 4.0-6.0, and the ratio of the volume of toluene, piperidine and compound (II) to the substance amount is 50 mL: 1 mmol.

The invention has the advantages of

Compared with the prior art, the double BODIPY near infrared fluorescent dye with the AIE effect and the preparation method thereof have the advantages that: (1) the preparation method has mature reaction, selectively introduces strong electron donor/acceptor, reduces molecular energy gap to enable the spectrum to generate obvious red shift, the maximum electron absorption spectrum of the fluorescent dye is 697nm, and the maximum fluorescence emission wavelength is 767 nm; (2) has high molar extinction coefficient (greater than 2.19 × 10)⁵cm^-1mol^-1L), large Stokes shift (70nm) and good light stability, and can effectively solve the defects in biological application caused by fluorescence self-absorption; (3) introducing an electron donor/acceptor group with AIE characteristics on a BODIPY matrix to convert a traditional near infrared molecule from an ACQ molecule into an AIE molecule; the maximum fluorescence intensity of the fluorescent dye in an aggregation state can be enhanced by 12.5 times, and a superior Aggregation Induced Emission (AIE) effect is shown in a near infrared region; the method has wide application in fields of luminescent materials, biological fluorescence imaging, chemical sensors, photodynamic therapy and the likeHas wide application prospect.

Drawings

FIG. 1 is a diagram of the UV-VIS absorption spectrum of a dual BODIPY near infrared fluorescent dye (III) having AIE effect;

FIG. 2 is a fluorescence emission spectrum of a dual BODIPY near infrared fluorescent dye (III) having AIE effect;

FIG. 3 is a fluorescence emission spectrum of a double BODIPY near infrared fluorescent dye (III) with AIE effect in DMSO/water mixed solutions with different ratios;

FIG. 4 shows the enhancement factor of fluorescence intensity of dual BODIPY near infrared fluorescent dye (III) with AIE effect in DMSO/water mixed solution with different ratio (as the emission intensity I of fluorescent dye in pure DMSO solution)₀For comparison).

Detailed Description

The invention is further described below with reference to the specific drawings.

By using¹H-NMR and MALDI-TOF-MS characterize and confirm the structure of the double BODIPY near infrared fluorescent dye with AIE effect. The detection instrument is as follows: bruker ARX400 NMR Spectrometer, Bruker ARX600 NMR Spectrometer (all using deuterated chloroform as solvent), Shimadzu UV-3100 UV-visible spectrophotometer (scan range 300-900 nm, light path slit 2nm), fluorescence spectrum was measured with American Amico Bowman Series 2 Luminescence Spectrometry.

EXAMPLE 1 preparation of Compound (II)

Terephthalaldehyde (80mg, 0.6mmol) and BODIPY derivative (I) (672mg, 1.4mmol) were dissolved in a mixed solution of methanol and dichloromethane (v/v, 16mL/8mL) under anhydrous conditions, and a methanol solution (1M, 6mL) of sodium methoxide was added dropwise thereto, followed by reaction at room temperature for 6 hours after completion of the addition. The reaction was quenched with water, extracted with dichloromethane, the organic layer was dried over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure and purified by silica gel column chromatography using dichloromethane-petroleum ether (v: v ═ 9: 1) as eluent to give compound (II) (244mg, 38%).¹H NMR(400MHz，CDCl₃)：δ7.91(s，4H)，7.38-7.39(d，J＝3.6Hz，2H)，7.28(s，2H)，6.97(s，4H)，6.83-6.84(d，J＝3.6Hz，2H)，6.04(s，2H)，2.64(s，6H)，2.60(s，6H)，2.34(s，6H)，2.13(s，12H)，1.44(s，6H)，1.41(s，6H)。

Example 2 preparation of a bis-BODIPY near Infrared fluorescent dye (III) having AIE Effect

Compound (II) (214mg, 0.2mmol), 4- (diphenylamino) benzaldehyde (328mg, 1.2mmol) and freshly dried p-toluenesulfonic acid (17mg, 0.1mmol) were charged under anhydrous conditions to a 100mL two-necked reaction flask equipped with a Dean-Stark apparatus, then 10mL toluene and 0.2mL piperidine were added, stirred and heated to reflux for 5 hours; after the reaction is finished, the reaction product is cooled to room temperature, extracted by dichloromethane, washed by water, dried, decompressed and evaporated to dryness, and then separated and purified by silica gel column chromatography, and the eluent is dichloromethane-petroleum ether (v: v ═ 2: 3), so that the double BODIPY near infrared fluorescent dye (III) with the AIE effect (200mg, 48%) is obtained.¹H NMR(600MHz，CDCl₃): δ 7.91(s, 4H), 7.55-7.63(m, 4H), 7.47-7.48(d, J ═ 8.4Hz, 4H), 7.42(d, J ═ 3.6Hz, 2H), 7.27-7.30(t, J ═ 7.8Hz, 12H), 7.26(s, 4H), 7.23-7.24(d, J ═ 7.8Hz, 8H), 7.13-7.14(d, J ═ 7.8Hz, 8H), 7.07-7.09(t, J ═ 8.4Hz, 12H), 7.02-7.04(m, 8H), 6.97(s, 8H), 6.93(d, J ═ 3.6Hz, 2H), 6.78-6.80(m, 2H), 6.67(s, 2H), 6.34 (s, 6.46H), 1.46(s, 6H), 1H), 16.8H, 16H, 1H, and 7.9H. UV-vis: 354nm, 427nm, 506nm, 697nm (FIG. 1); emission wavelet: 767nm (FIG. 2); MALDI-TOF-MS: calculated for C₁₄₀H₁₁₀B₂F₄N₁₀S₂：2092.848，found：2093.269[M+H]⁺。

Example 3 ultraviolet-visible absorption Spectroscopy of solution of Dual BODIPY near Infrared fluorescent dye (III) having AIE Effect

Dissolving double BODIPY near infrared fluorescent dye (III) with AIE effect in dichloromethane, and configuring to concentration of 1 × 10^-5The ultraviolet-visible absorption spectrum of the methylene chloride solution was measured. FIG. 1 shows the UV-VIS absorption spectrum of a fluorescent dye (III) solution prepared in example 2 of the present invention.

Example 4 fluorescence emission Spectroscopy of solution of bis-BODIPY near Infrared fluorochrome (III) with AIE Effect

Dissolving double BODIPY near infrared fluorescent dye (III) with AIE effect in dichloromethane, and configuring to concentration of 1 × 10^-5And measuring the fluorescence emission spectrum of the dichloromethane solution with mol/L. FIG. 2 shows the fluorescence spectrum of a fluorescent dye (III) solution prepared in example 2 of the present invention.

Example 5 AIE Effect of Dual BODIPY-based near Infrared fluorescent dyes (III)

Dissolving double BODIPY near infrared fluorescent dye (III) in DMSO to obtain a solution with a concentration of 1 × 10^-3mol/L stock solution. 10 parts of stock solution are respectively added with DMSO/water solution with different proportions to be diluted to 3 mL. Wherein the content of distilled water is respectively 90%, 80%, 70%, 60%, 50%, 40%, 30%, 20%, 10% and 0%; the change process of the fluorescence emission spectrum is measured at the excitation wavelength of 710 nm. As can be seen from fig. 3, the fluorescence intensity of the solution with 10% water volume fraction is slightly lower than that of the pure DMSO solution, and when the water volume fraction of the system is further increased, the fluorescence intensity is significantly increased. When the proportion of water was increased to 90%, the fluorescence intensity reached a maximum, increasing by a factor of 12.5. FIG. 4 shows the fluorescence intensity enhancement factor (I) of the fluorescent dye (III) prepared in example 2 of the present invention in solution systems with different water contents₀Indicating the fluorescence intensity in pure DMSO).