A kind of cyclometalated iridium-azo complex and its preparation method and application
A technology of cyclometalation and complexes, which is applied in the field of preparation of cyclometalated iridium complexes, can solve problems such as unfavorable for distinguishing self-quenching of endogenous fluorescent dyes, unfavorable imaging stability, affecting cell observation, etc., and achieves background fluorescence intensity Weak, simple and stable results, high dyeing sensitivity
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Embodiment 1
[0023] Example 1 Preparation of Ligand Selenium-5,6-dione-1,10-phenanthroline (phendione-Se)
[0024] (1) 2,2'-bipyridine-N-oxide
[0025] You can refer to the literature ( Chem.Comm. 2011, 47 , 11011-11013) method to prepare. Dissolve 7.8g of 2,2'-bipyridine in 40mL of trifluoroacetic acid, add 8.5mL of 30% hydrogen peroxide, stir at room temperature for 4h, neutralize with 6N sodium hydroxide solution, and then use 4'50cm 3 After extraction with chloroform, the organic phases were combined and washed with saturated sodium chloride solution, then dried over anhydrous sodium sulfate, filtered, and evaporated to remove chloroform to obtain a colorless oil, which was dried in vacuo overnight to obtain a white needle-like solid.
[0026] (2) 4-nitro-2,2'-bipyridine-N-oxide
[0027] Dissolve 3g of 2,2'-bipyridine-N-oxygen in 19mL of concentrated sulfuric acid with stirring in an ice bath, then add dropwise to the mixed acid of fuming nitric acid / concentrated sulfuric acid (...
Embodiment 2
[0036] Example 2 [Ir(pq) 2 (azobpy)Ir(pq) 2 ] 2+ In Vitro Response Experiments to Physiological Thiols
[0037] The complexes used below are the compounds prepared in Example 1.
[0038] Prepare a 5mM complex solution with acetonitrile / HEPES (10mM, pH7.5) buffer solution with a volume ratio of 1:1, add different concentrations of cysteine, homocysteine or glutathione dropwise, and stir well After standing at room temperature for 5 min, the fluorescence intensity was measured. The excitation wavelength and maximum emission wavelength of the complex are 430nm and 560nm respectively. See the experimental results image 3 . It can be seen from the figure that the original fluorescence of the complex is relatively weak, but after adding a small amount of physiological thiols, such as cysteine, homocysteine or glutathione, the fluorescence of the complex is greatly enhanced. Has a very sensitive fluorescence response.
Embodiment 3
[0039] Example 3 [Ir(pq) 2 (azobpy)Ir(pq) 2 ] 2+ Intracellular Response Experiments to Physiological Thiols
[0040] The complexes used below are the compounds prepared in Example 1.
[0041] Cell culture: Hela cells were cultured in DMEM medium containing 10% fetal bovine serum, cells (5′l0 8 / L) inoculated in a special glass bottom culture dish for confocal microscopy, the diameter of the culture dish is 35mm, the thickness of the cover glass is 0.085~0.13mm, the diameter of the micropore in the center of the dish is 10mm, and 5% CO 2 Incubate at 37°C under 95% air conditions, and after 24 hours of adherent growth, replace with serum-free medium and continue to incubate for 4 hours.
[0042] Confocal microscope-cell imaging: Hela cells were incubated with the complex (5 μM) for 30 minutes, the culture medium was aspirated, and then washed with PBS buffer for 3 to 4 times, imaged on a Leica TCSSP5 laser scanning confocal microscope, using a 63′ / 1.4 oil lens , use 405nm...
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