Two-photon fluorescent dye taking isoquinolinone as parent, preparation method thereof and application
A two-photon fluorescence, isoquinolinone technology, applied in luminescent materials, chemical instruments and methods, naphthalene dicarboxamide dyes/phthalimide dyes, etc., can solve the problem of reducing the application value of RNA dyes, poor photostability, and responsiveness Long time and other problems, to achieve the effect of high-efficiency two-photon absorption capacity, increase absorption cross-section, and increase π-electron conjugated system
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[0042] 8. taking isoquinolinone as claimed in claim 1 is the preparation method of the two-photon fluorescent dye of parent, comprises the steps:
[0043] 1) 4-bromo-1,8-naphthalene anhydride reacts with the compound of formula i according to the molar ratio of 1:1-1:5 to prepare compound B:
[0044]
[0045] The reaction temperature is 70-150°C, the reaction time is 1-12 hours, and the reaction solvent is selected from dichloromethane, ethanol, ethyl acetate, acetic acid or a mixture thereof;
[0046] In a preferred embodiment, the reaction temperature is 80-140°C, the reaction time is 2-10 hours, the reaction solvent is selected from ethanol, ethyl acetate, acetic acid or a mixture thereof, 4-bromo-1,8-naphthalene anhydride and formula i Mole is 1:1-1:4;
[0047] In a further preferred embodiment, the reaction temperature is 90-120°C, the reaction time is 3-10 hours, the reaction solvent is selected from ethyl acetate, acetic acid or a mixture thereof, 4-bromo-1,8-naphth...
Embodiment 1
[0064] Embodiment 1. Preparation of dye compound A 1
[0065]
[0066] (1) Synthesis of Intermediate 1
[0067] Add 20mmol of 4-bromo-1,8-naphthalene anhydride and 35mmol of 4-nitro-o-phenylenediamine into a round bottom flask containing 20ml of acetic acid solution under nitrogen protection. The reaction was heated to reflux at 105°C for 3 hours and then stopped. The mixture was poured into ice water, precipitated out, and suction filtered to obtain the crude product of yellow solid powder, intermediate product 1, with a yield of 84%.
[0068] (2) Dye A 1 Synthesis
[0069] Add 20 mmol of crude product 1 and 25 mmol of ethanolamine from the previous step into a round-bottomed flask containing 20 ml of ethylene glycol monomethyl ether solution, under nitrogen protection. The reaction was heated to reflux at 125°C for 4 hours and then stopped. The mixture was poured into ice water, an orange-red precipitate was precipitated, and the crude product was obtained by suctio...
Embodiment 2
[0070] Example 2. Dye Compound A 1 Labeling assay on cellular RNA
[0071] Compound A synthesized using Example 1 1 , at a concentration of 5 μM A 1 - Add 4 μL of DMSO solution to the Hela cells at 37°C, 5% CO 2 dye A 1 Hela cells were incubated in culture medium for 30 minutes. Then, shake and rinse with PBS for 5min×3, then add cell culture medium, and conduct two-photon laser confocal imaging. Select a representative area, observe with an oil lens (60×), and repeat three times. Experimental results such as figure 2 As shown, the imaging shows that there is a strong fluorescent signal in the cellular RNA of Hela cells, while there is no fluorescent signal in other regions of the cell. figure 2 For adding dye A 1 Focused image of posterior HeLa cells. The excitation wavelength is 800nm, and the collection wavelength range is 520-570nm. The scale bar in the figure is 20 μm.
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