LINEAR BORON-DIPYRROMETHENE ELECTRON DONOR HAVING 180º COORDINATION INCLUDED ANGLE AND SUPRAMOLECULAR METAL MACRO-RING, AND SYNTHESIS PROCESSES THEREFOR AND APPLICATIONS THEREOF

Abstract

Disclosed are a linear boron-dipyrromethene electron donor having a 180 coordination included angle and a supramolecular metallacycle, and synthesis processes therefor and applications thereof. The invention provides a linear boron-dipyrromethene electron donor as shown in formula 3 or formula 4, and a boron-dipyrromethene ligand-based supramolecular coordination compound having a 180 coordination included angle which is prepared by the metal coordination of the linear boron-dipyrromethene electron donor. Compared with a prepolymer, the boron-dipyrromethene ligand-based supramolecular coordination compound has better cell passive uptake capacity, cell fluorescence imaging capacity and photosensitive (singlet oxygen generation) capability.

Claims

1. A linear boron-dipyrromethene electron donor having a 180 coordination included angle, wherein a chemical structural formula thereof is formula 3 or formula 4: ##STR00008##

2. The linear boron-dipyrromethene electron donor having the 180 coordination included angle according to claim 1, wherein, when the structural formula of the linear boron-dipyrromethene electron donor is formula 3, the following synthetic route is adopted: ##STR00009## specifically: (1) a compound 6, phenol and potassium carbonate are added into acetonitrile, stirred and refluxed at 50 C. to 85 C. to react for 1 hour to 3 hours, and post-processed to obtain a compound 7; and (2) the compound 7, 4-(4-pyridyl)phenylboronic acid, potassium carbonate and tetrakis(triphenylphosphine)palladium are added into a mixed solvent of tetrahydrofuran and water to react at 65 C. to 85 C. under the protection of nitrogen for 6 hours to 12 hours, and post-processed to obtain the linear boron-dipyrromethene electron donor of formula 3.

3. The linear boron-dipyrromethene electron donor having the 180 coordination included angle according to claim 2, wherein a molar ratio of the compound 6 to the phenol and the potassium carbonate in the step (1) is 1:2.5 to 3:3; and a molar ratio of the compound 7 to the 4-(4-pyridyl)phenylboronic acid, the potassium carbonate and the tetrakis(triphenylphosphine)palladium in the step (2) is 1:2.5 to 4.5:6 to 12:0.05 to 0.1.

4. The linear boron-dipyrromethene electron donor having the 180 coordination included angle according to claim 1, wherein, when the structural formula of the linear boron-dipyrromethene electron donor is formula 4, the following synthetic route is adopted: ##STR00010## specifically: (1) diphenyl disulfide and sodium borohydride are added into tetrahydrofuran and heated to 50 C. to 80 C., then added with methanol, and refluxed for 0.5 hour to 1 hour; and then cooled, added with a dichloromethane solution of a compound 6, continuously stirred for 5 minutes to 10 minutes, and post-processed after reaction to obtain a compound 8; and (2) the compound 8, 4-(4-pyridyl)phenylboronic acid, potassium carbonate and tetrakis(triphenylphosphine)palladium are added into tetrahydrofuran and water to react at 65 C. to 85 C. under the protection of nitrogen for 6 hours to 12 hours, and post-processed to obtain the linear boron-dipyrromethene electron donor of formula 4.

5. The linear boron-dipyrromethene electron donor having the 180 coordination included angle according to claim 4, wherein a molar ratio of the compound 6 to the diphenyl disulfide and the sodium borohydride in the step (1) is 1:2 to 2.5; 4 to 5; and a molar ratio of the compound 8 to the 4-(4-pyridyl)phenylboronic acid, the potassium carbonate and the tetrakis(triphenylphosphine)palladium in the step (2) is 1:2.5 to 4.5:6 to 12:0.05 to 0.1.

6. A triangular supramolecular complex of a boron-dipyrromethene ligand having a 180 coordination included angle, wherein a chemical structural formula thereof is formula 1 or formula 2: ##STR00011##

7. The triangular supramolecular complex of the boron-dipyrromethene ligand having the 180 coordination included angle according to claim 6, wherein a synthetic route of the triangular supramolecular complex is as follows: ##STR00012## specifically: the linear boron-dipyrromethene electron donor having the 180 coordination included angle according to claim 1 and an organic platinum electron acceptor 5 having a 60 coordination included angle are dissolved in dimethyl sulfoxide to react at 30 C. to 50 C. for 6 hours to 12 hours, and post-processed to obtain the triangular supramolecular complex of the boron-dipyrromethene ligand having the 180 coordination included angle.

8. The triangular supramolecular complex of the boron-dipyrromethene ligand having the 180 coordination included angle according to claim 7, wherein a mass ratio of the linear boron-dipyrromethene electron donor having the 180 coordination included angle to the organic platinum electron acceptor 5 having the 60 coordination included angle is 1:1.

Description

DESCRIPTION OF THE DRAWINGS

[0035] FIG. 1 is an .sup.1H-NMR spectrum of a compound 6 synthesized in First Embodiment (with deuterated chloroform as a solvent);

[0036] FIG. 2 is an .sup.1H-NMR spectrum of a compound 7 synthesized in First Embodiment (with deuterated chloroform as a solvent);

[0037] FIG. 3 is a .sup.13C-NMR spectrum of the compound 7 synthesized in First Embodiment (with deuterated chloroform as a solvent);

[0038] FIG. 4 is a high resolution mass spectrum of the compound 7 synthesized in First Embodiment;

[0039] FIG. 5 is an .sup.1H-NMR spectrum of a pyridine ligand 3 synthesized in First Embodiment (with deuterated chloroform as a solvent);

[0040] FIG. 6 is a .sup.13C-NMR spectrum of the pyridine ligand 3 synthesized in First Embodiment (with deuterated chloroform as a solvent);

[0041] FIG. 7 is a high resolution mass spectrum of the pyridine ligand 3 synthesized in First Embodiment;

[0042] FIG. 8 is an .sup.1H-NMR spectrum of a compound 8 synthesized in First Embodiment (with deuterated chloroform as a solvent);

[0043] FIG. 9 is a .sup.13C-NMR spectrum of the compound 8 synthesized in First Embodiment (with deuterated chloroform as a solvent);

[0044] FIG. 10 is a high resolution mass spectrum of the compound 8 synthesized in First Embodiment;

[0045] FIG. 11 is an .sup.1H-NMR spectrum of a pyridine ligand 4 synthesized in First Embodiment (with deuterated chloroform as a solvent);

[0046] FIG. 12 is a .sup.13C-NMR spectrum of the pyridine ligand 4 synthesized in First Embodiment (with deuterated chloroform as a solvent);

[0047] FIG. 13 is a high resolution mass spectrum of the pyridine ligand 4 synthesized in First Embodiment;

[0048] FIG. 14 is an .sup.1H-NMR spectrum of an organic platinum electron acceptor 5 synthesized in Second Embodiment (with deuterated chloroform as a solvent);

[0049] FIG. 15 is an .sup.1H-NMR spectrum of a compound 1 synthesized in Second Embodiment (with deuterated dimethyl sulfoxide as a solvent);

[0050] FIG. 16 is a .sup.31P-NMR spectrum of the compound 1 synthesized in Second Embodiment (with deuterated dimethyl sulfoxide as a solvent);

[0051] FIG. 17 is a mass spectrum of a platinum acceptor 1 synthesized in Second Embodiment;

[0052] FIG. 18 is an .sup.1H-NMR spectrum of a metallacycle 2 synthesized in Second Embodiment (with deuterated dimethyl sulfoxide as a solvent);

[0053] FIG. 19 is a .sup.31P-NMR spectrum of the metallacycle 2 synthesized in Second Embodiment (with deuterated dimethyl sulfoxide as a solvent);

[0054] FIG. 20 is a mass spectrum of the metallacycle 2 synthesized in Second Embodiment;

[0055] FIG. 21A is a confocal laser scanning microscope cell image of metallacycles 1 and 2 in Third Embodiment (the cell is a U87 cell), wherein, the first row corresponding to the U87 cell incubated with pyridine ligand 4, the second row corresponding to the U87 cell incubated with metallacycle 2, and the first column is DAPI channel, the second column is BODIPY channel, and the third column is merged DAPI channel and BODIPY channel; and

[0056] FIG. 21B is a line scan image of the U87 cell incubated with pyridine ligand 4 (left) and metallacycle 2 (right) in Third Embodiment 3 and stained with DAPI;

[0057] FIG. 22 is a cell singlet oxygen detection graph of the metallacycles 1 and 2 in Third Embodiment (the cell is a U87 cell).

DETAILED DESCRIPTION

[0058] The present invention is further described hereinafter with reference to specific embodiments, but the scope of protection of the present invention is not limited to this.

[0059] To make the objects, technical solutions, and advantages of the present invention clearer, the present invention is further described in detail hereinafter with reference to the drawings and embodiments. It should be understood that specific embodiments described herein are only used for explaining the present invention and are not intended to limit the present invention. In addition, the technical features involved in the implementations of the present invention described hereinafter may be combined with each other as long as they do not conflict with each other.

First Embodiment

##STR00006##

Preparation of Compound 7:

[0060] A compound 6 (500 mg, 0.8 mmol), phenol (164 mg, 2.1 mmol) and potassium carbonate (289 mg, 2.5 mmol) were added into a 250 mL round-bottom flask, and added with 150 mL of acetonitrile as a solvent. The above reaction product was put into an oil bath pan at 85 C., and stirred and refluxed to react for 1 hour. After reaction, the product was cooled to room temperature, then poured into 200 mL of water, and extracted with ethyl acetate (50 mL) for three times, and the product was dried with anhydrous magnesium sulfate to remove the solvent. The product was separated and purified through silica gel column chromatography (petroleum ether/dichloromethane in a volume ratio of 2:1). The product was rinsed with n-hexane, and dried to obtain a red powdery solid (299 mg, 50%).

[0061] .sup.1H NMR (500 MHz, CDCl.sub.3, 298 K): 7.44 (d, J=7.9 Hz, 2H), 7.33 (q, 6H), 7.13 (t, J=7.4 Hz, 2H), 7.08 (m, 6H), 2.48 (s, 3H). .sup.13C NMR (126 MHz, CDCl.sub.3, 298 K): 160.2, 155.7, 141.6, 141.4, 138.1, 130.4, 129.8, 129.6, 129.4, 129.3, 124.3, 118.0, 61.9, 21.5. ESI-HR-MS: m/z 756.9491 [7+K].sup.+, calcd. for [C.sub.28H.sub.19BF.sub.2I.sub.2N.sub.2O.sub.2Na].sup.+, 756.9229.

Preparation of Compound 3:

[0062] A compound 7 (500 mg, 0.7 mmol), 4-(4-pyridyl)phenylboronic acid (346 mg, 1.7 mmol), potassium carbonate (577 mg, 4.2 mmol), tetrakis(triphenylphosphine)palladium (80 mg, 0.07 mmol), tetrahydrofuran (40 mL) and purified water (10 mL) were added into a 100 mL Shrek bottle to react at 65 C. under the protection of nitrogen for 12 hours, and cooled to room temperature. The product was extracted with dichloromethane (50 mL) for three times. The product was dried with anhydrous magnesium sulfate to remove the solvent, and the product was purified through a silica gel column (dichloromethane/methanol in a volume ratio of 20/1). Finally, the product was rinsed with cold n-hexane, and dried to obtain a purple powdery solid (250 mg, 46%).

[0063] .sup.1H NMR (500 MHz, CDCl.sub.3, 297 K): 8.61 (d, J=5.4 Hz, 4H), 7.58 (d, J=7.7 Hz, 2H), 7.46 (m, 14H), 7.13 (q, 6H), 7.02 (d, J=8.1 Hz, 4H), 6.95 (t, J=7.3 Hz, 2H), 2.53 (s, 3H). .sup.13C NMR (126 MHz, CDCl.sub.3, 297 K): 158.5, 156.5, 150.2, 147.5, 143.1, 141.2, 136.6, 132.1, 130.6, 130.0, 129.5, 129.5, 128.4, 127.8, 127.4, 126.9, 123.7, 121.9, 121.3, 116.6, 21.6. ESI-HR-MS: m/z 772.2929 [3+H].sup.+, calcd. for [C.sub.50H.sub.36BF.sub.2N.sub.4O.sub.2].sup.+, 772.2930.

##STR00007##

Preparation of Compound 8:

[0064] Diphenyl disulfide (362 mg, 1.7 mmol), sodium borohydride (126 mg, 3.3 mmol) and 30 mL of tetrahydrofuran were added into a 100 mL flask, and heated to 80 C. The mixture was added with 5 mL of methanol, refluxed for 1 hour, and cooled to room temperature, a dichloromethane solution (10 mL) of a compound 6 (500 mg, 0.8 mmol) was added into the above solution, and continuously stirred for 5 minutes, and the reaction was ended. The product was extracted with dichloromethane and ethyl acetate twice respectively, with 50 mL each time. Water was removed with anhydrous magnesium sulfate to remove the solvent. The product was purified through a silica gel column (petroleum ether/dichloromethane in a volume ratio of 2:1). Finally, the product was rinsed with cold n-hexane, and dried to obtain a blue powdery solid (530 mg, 85%).

[0065] .sup.1H NMR (500 MHz, CDCl.sub.3, 297 K): 7.43 (d, 6H), 7.35 (d, J=7.7 Hz, 2H), 7.30 (m, 6H), 7.12 (s, 2H), 2.47 (s, 3H). .sup.13C NMR (126 MHz, CDCl.sub.3, 297 K): 153.3, 141.9, 141.7, 138.6, 137.1, 133.5, 131.2, 130.6, 129.8, 129.5, 129.2, 127.6, 84.1, 21.5. ESI-HR-MS: m/z 750.6026 [8+H].sup.+, calcd. for [C.sub.28H.sub.20BF.sub.2I.sub.2N.sub.2S.sub.2].sup.+, 750.9213.

Preparation of Compound 4:

[0066] A compound 8 (1000 mg, 1.3 mmol), 4-(4-pyridyl)phenylboronic acid (633 mg, 3.3 mmol), potassium carbonate (1105 mg, 8.0 mmol) and tetrakis(triphenylphosphine)palladium (154 mg, 0.13 mmol) were added into a 250 mL Shrek bottle, and added with tetrahydrofuran (100 mL) and water (25 mL) as a solvent. After reaction at 65 C. under the protection of nitrogen for 12 hours, the product was cooled to room temperature, the mixed solution obtained from the reaction was poured into 100 mL of water, and the product was extracted with dichloromethane (50 mL) for three times. The solvent was removed, the product was purified through silica gel column chromatography (dichloromethane/methanol in a volume ratio of 20:1), and finally the product was rinsed with cold n-hexane, and dried to obtain a black powdery solid (100 mg, 9%).

[0067] .sup.1H NMR (500 MHz, CDCl.sub.3, 297 K): 8.64 (d, J=5.37 Hz, 4H), 7.53 (d, J=7.9 Hz, 2H), 7.43 (s, 12H), 7.36 (d, J=7.9 Hz, 2H), 7.21 (d, 4H), 7.02 (t, 8H), 2.50 (s, 3H). .sup.13C NMR (126 MHz, CDCl.sub.3, 297 K): 150.3, 150.0, 147.8, 142.0, 141.3, 136.9, 136.78, 136.8, 135.6, 134.0, 133.8, 130.6, 130.6, 129.4, 129.2, 129.0, 128.8, 127.1, 126.5, 121.4, 21.5. ESI-HR-MS: m/z 805.2430 [4+H].sup.+, calcd. for [C.sub.50H.sub.36BF.sub.2N.sub.4S.sub.2].sup.+, 805.2437.

[0068] FIG. 1 is an .sup.1H-NMR spectrum of the compound 6 synthesized in First Embodiment (with deuterated chloroform as a solvent);

[0069] FIG. 2 is an .sup.1H-NMR spectrum of the compound 7 synthesized in First Embodiment (with deuterated chloroform as a solvent);

[0070] FIG. 3 is a .sup.13C-NMR spectrum of the compound 7 synthesized in First Embodiment (with deuterated chloroform as a solvent);

[0071] FIG. 4 is a high resolution mass spectrum of the compound 7 synthesized in First Embodiment;

[0072] FIG. 5 is an .sup.1H-NMR spectrum of the pyridine ligand 3 synthesized in First Embodiment (with deuterated chloroform as a solvent);

[0073] FIG. 6 is a .sup.13C-NMR spectrum of the pyridine ligand 3 synthesized in First Embodiment (with deuterated chloroform as a solvent);

[0074] FIG. 7 is a high resolution mass spectrum of the pyridine ligand 3 synthesized in First Embodiment;

[0075] FIG. 8 is an .sup.1H-NMR spectrum of the compound 8 synthesized in First Embodiment (with deuterated chloroform as a solvent);

[0076] FIG. 9 is a .sup.13C-NMR spectrum of the compound 8 synthesized in First Embodiment (with deuterated chloroform as a solvent);

[0077] FIG. 10 is a high resolution mass spectrum of the compound 8 synthesized in First Embodiment;

[0078] FIG. 11 is an .sup.1H-NMR spectrum of the pyridine ligand 4 synthesized in First Embodiment (with deuterated chloroform as a solvent);

[0079] FIG. 12 is a .sup.13C-NMR spectrum of the pyridine ligand 4 synthesized in First Embodiment (with deuterated chloroform as a solvent); and

[0080] FIG. 13 is a high resolution mass spectrum of the pyridine ligand 4 synthesized in First Embodiment.

Second Embodiment

Preparation of Supramolecular Metallacycle 1 Based on BODIPY:

[0081] A BODIPY ligand 3 (20.0 mg, 0.026 mmol) and a platinum acceptor 5 (36.2 mg, 0.026 mmol) were dissolved in 0.5 mL of dimethyl sulfoxide (DMSO) to react at 50 C. for 12 hours. After reaction, the product was cooled to room temperature and filtered, and a filtrate was added with anhydrous ether to reduce the solubility of the product for precipitation. After centrifugation, an upper layer supernatant was poured out, and the remaining solid product was pumped by an oil pump to obtain a powdery solid (55 mg, 98%).

[0082] .sup.1H NMR (500 MHz, DMSO-d.sub.6, 297 K): 8.83 (t, 18H), 8.09 (s, 12H), 7.93 (m, 9H), 7.83 (m, 21H), 7.71 (m, 12H), 7.59 (m, 12H), 7.29 (m, 12H), 7.04 (m, 18H), 4.00 (s, 18H), 2.56 (s, 9H), 1.31 (s, 72H), 1.08 (m, 108H). .sup.31P NMR (202 MHz, DMSO-d.sub.6, 297 K): 13.70 ppm (s, .sup.195Pt satellites, .sup.1J.sub.Pt-P=2669.4 Hz). ESI-TOF-MS: m/z 1152.72 [1OTf].sup.5+, 1478.16 [1OTf].sup.4+.

Preparation of Supramolecular Metallacycle 2 Based on BODIPY:

[0083] A BODIPY ligand 4 (20.0 mg, 0.025 mmol) and a platinum acceptor 5 (34.7 mg, 0.025 mmol) were dissolved in 0.5 mL of dimethyl sulfoxide (DMSO), and the solution reacted at 50 C. for 12 hours. After reaction, the product was cooled to room temperature and filtered to remove insoluble solid impurities, and a filtrate was added with anhydrous ether to reduce the solubility of the product for precipitation. After centrifugation, an upper layer supernatant was poured out, and the remaining solid product was pumped by an oil pump to obtain a powdery solid (54 mg, 98%).

[0084] .sup.1H NMR (500 MHz, DMSO-d.sub.6, 297 K): 8.88-8.81 (m, 18H), 8.10 (s, 12H), 8.89-8.80 (m, 32H), 7.72 (m, 6H), 7.53 (m, 6H), 7.37 (m, 6H), 7.21 (m, 24H), 7.13 (m, 9H), 4.01 (s, 18H), 2.50 (s, 9H), 1.34 (m, 72H), 1.11 (m, 108H). .sup.31P NMR (202 MHz, DMSO-d.sub.6, 297 K): 13.80 ppm (s, .sup.195Pt satellites, .sup.1J.sub.Pt-P=2674.9 Hz). ESI-TOF-MS: m/z 1171.89 [25OTf].sup.5+, 1502.13 [24OTf].sup.4+.

[0085] FIG. 14 is an .sup.1H-NMR spectrum of the organic platinum electron acceptor 5 synthesized in Second Embodiment (with deuterated chloroform as a solvent);

[0086] FIG. 15 is an .sup.1H-NMR spectrum of the compound 1 synthesized in Second Embodiment (with deuterated dimethyl sulfoxide as a solvent);

[0087] FIG. 16 is a .sup.31P-NMR spectrum of the compound 1 synthesized in Second Embodiment (with deuterated dimethyl sulfoxide as a solvent);

[0088] FIG. 17 is a mass spectrum of the platinum acceptor 1 synthesized in Second Embodiment;

[0089] FIG. 18 is an .sup.1H-NMR spectrum of the metallacycle 2 synthesized in Second Embodiment (with deuterated dimethyl sulfoxide as a solvent);

[0090] FIG. 19 is a .sup.31P-NMR spectrum of the metallacycle 2 synthesized in Second Embodiment (with deuterated dimethyl sulfoxide as a solvent); and

[0091] FIG. 20 is a mass spectrum of the metallacycle 2 synthesized in Second Embodiment.

Third Embodiment

Cell Uptake Experiment and Singlet Oxygen Experiment of Metallacycles 1 and 2:

[0092] U87 cells were inoculated in a 24-well plate and cultured for 12 hours. A medium was removed, and a DMEM (Dulbecco modified Eagle medium) solution of a monomer 4 and a metallacycle 2 was added to co-culture for 24 hours. The cells were washed with PBS (phosphate buffer saline), and fixed with 4% formaldehyde solution for 10 minutes. The cells were washed with PBS, and added with DAPI (4,6-diamidino-2-phenylindole) to co-culture for 10 minutes. The cells were washed with PBS twice, and finally observed by a CLSM (Confocal Laser Scanning Microscope).

[0093] U87 cells were inoculated in a 24-well plate and cultured for 12 hours. A medium was removed and a DMEM solution of a monomer 4 and a metallacycle 2 was added to co-incubate for 24 hours. The cells were washed with PBS, and added with a DCF-DA (reactive oxygen species fluorescent probe) solution to incubate for 30 minutes. The cells were washed with PBS, and added with a DMEM solution, the 24-well plate was exposed to an LED lamp with a wavelength of 600 nm to 605 nm for 1 minute, and then the fluorescence of each well was observed by a CLSM.

[0094] FIG. 21A is a confocal laser scanning microscope image of the U87 cells after co-incubation with the BODIPY monomer 4 and the metallacycle 2, and FIG. 21 (b) shows distribution of the cells at white lines (with a scale of 20 m); and

[0095] FIG. 22 is a CLSM image of the DCHF-DA probe in the U87 cells and shows an average fluorescence intensity of the probe.