Isolable cyclic (alkyl)(amino)carbene–phosphonyl radical adducts

2020 ◽  
Vol 56 (9) ◽  
pp. 1341-1344
Author(s):  
Yulia Livshits-Kritsman ◽  
Boris Tumanskii ◽  
Gabriel Ménard ◽  
Roman Dobrovetsky
Keyword(s):  
Uv Irradiation ◽  
Radical Reactivity ◽  
Phosphonyl Radical

Isolable cAAC–phosphonyl radical adducts were prepared; interestingly, some of them show typical phosphorus-centered radical reactivity under UV irradiation.

Wavelength-specific Activation of MAP Kinase Family Proteins by Monochromatic UV Irradiation¶

2001 ◽  
Vol 73 (2) ◽  
pp. 147 ◽  
Author(s):  
Yukihito Kabuyama ◽  
Miwako K. Homma ◽  
Masayuki Sekimata ◽  
Yoshimi Homma
Keyword(s):  
Map Kinase ◽  
Uv Irradiation ◽  
Kinase Family

The Study of Photoreversibility, Photopolimerization and Photocleavage Properties of Polyurethane Coumarin by Means of Electronic Spectrometry and AFM Methods

2017 ◽  
Vol 68 (7) ◽  
pp. 1632-1635
Author(s):  
Silviu Gurlui ◽  
Emil Buruiana ◽  
Ioan Gabriel Sandu ◽  
Mitachi Strat
Keyword(s):  
Uv Irradiation ◽  
Room Temperature ◽  
Dimethyl Formamide ◽  
Photon Excitation ◽  
Photochemical Properties ◽  
Film State

The spectroscopic and photochemical properties of polyurethane coumarin (PUC) in dimethyl sulf-oxide (DMSO), thetra hydro furan (THF), dimethyl formamide (DMF) and film state were investigated at room temperature under one photon excitation. The results show that under irradiation of l ] 310 nm photodimerization process are increased and under UV irradiation with l[ 260 nm, photocleavage of polymer have been evidenced, too.

The Influence of Some Factors on Spirolactone Stability in Solution

2008 ◽  
Vol 59 (7) ◽  
Author(s):  
Daniela Lucia Muntean ◽  
Silvia Imre ◽  
Cosmina Voda
Keyword(s):  
High Performance Liquid Chromatography ◽  
Liquid Chromatography ◽  
Uv Irradiation ◽  
High Performance ◽  
Degradation Products ◽  
Simultaneous Action ◽  
Ethanolic Solution ◽  
Degradation Processes ◽  
Stable Solutions ◽  
Preformulation Study

The influence of some factors on spironolactone stability in solution was studied, by applying high-performance liquid chromatography, as a part of a pharmaceutical preformulation study in order to obtain a spironolactone solution for alopecia treatment. Solutions of 1 mg/ml spironolactone in aqueous ethanolic solution 1 : 1 and in 20 mM cyclodextrines solutions (b-, hydroxi-b- and methyl-b-cyclodextrine) was used, maintained at 8 and 22 �C, protected from light and after UV irradiation at 254 nm. The main degradation products were 7a-thiospirolactone and canrenone. The most stable solutions were the alcoholic ones and with methyl-beta-cyclodextrine, but the simultaneous action of temperature and UV irradiation allowed degradation processes after one hour of exposure, more aggressive in the presence of methyl-beta-cyclodextrine. In conclusion, for alopecia treatment with spironolactone a 1 mg/mL ethanolic solution could be used and it is recommendable the protection of treated zone.

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