about
In search of excited-state proton transfer in the lumichrome dimer in the solid state: theoretical and experimental approach.Direct characterization of hydrogen peroxide bleached thermomechanical pulp using spectroscopic methods.Color and luminescence stability of selected dental materials in vitro.Near and mid infrared spectroscopy and multivariate data analysis in studies of oxidation of edible oils.Riboflavin interactions with oxygen-a survey from the photochemical perspective.Effect of substituents of alloxazine derivatives on the selectivity and affinity for adenine in AP-site-containing DNA duplexes.Electron ionization and electrospray ionization mass spectrometric study of a series of isomeric N-chloro(or bromo)benzyl-substituted (E)-2'(3'- or 4')-hydroxy-4-stilbazole halides.Spectroscopy and Photophysics of Monomethyl-Substituted Derivatives of 5-Deazaalloxazine and 10-Ethyl-5-Deaza-Isoalloxazine.Characterization of edible oils using total luminescence spectroscopy.Electron ionization mass spectrometric study of substituted alloxazine-5-oxides and iso-alloxazine-5-oxide.Electron ionisation and electrospray ionisation mass spectrometric study of a series of isomeric methyl-, dimethyl- and trimethylalloxazines.Ground- and excited-state double proton transfer in lumichrome/acetic acid system: theoretical and experimental approach.Luminescence of selected dental composites in vitro.Influence of water on photophysical properties of N-bromobenzyl- or nitrobenzyl derivatives of substituted 4-hydroxystilbazolium hemicyanines.Influence of pH on photophysical properties of (E)-1-(4-chlorobenzyl)-4-(4-hydroxystyryl)pyridinium chloride.Photophysical properties of izomeric N-chlorobenzyl substituted (E)-2' (3'-or 4')-hydroxy-4-stilbazolium chlorides in alcohols.Chemical quenching of singlet oxygen by betanin.Study of photophysical properties of 5-deazaalloxazine and 1,3-dimethyl-5-deazaalloxazine in dependence of pH using different spectral techniques.Time-resolved spectroscopy of the singlet excited state of betanin in aqueous and alcoholic solutions.Sulfanyl porphyrazines: Molecular barrel-like self-assembly in crystals, optical properties and in vitro photodynamic activity towards cancer cellsSynthesis, characterization and photophysical properties of novel 5,7-disubstituted-1,4-diazepine-2,3-dicarbonitrilesPorphyrazines with peripheral isophthaloxyalkylsulfanyl substituents and their optical propertiesPhotostability and Photostabilization of Drugs and Drug ProductsUV–vis spectroscopy combined with azastilbene probe as a tool for testing basicity of mesoporous silica modified with nitrogen compoundsSpectroscopy and photophysics of flavin-related compounds: 3-benzyl-lumiflavinAcid–Base Equilibriums of Lumichrome and its 1-Methyl, 3-Methyl, and 1,3-Dimethyl DerivativesHydrogen-Bonded Complexes of LumichromeSynchronous Fluorescence Spectroscopy of Edible Vegetable Oils. Quantification of TocopherolsPhotochemistry of riboflavin derivatives in methanolic solutionsQuantification of 5-methyl-2'-deoxycytidine in the DNAPhotophysics, excited-state double-proton transfer and hydrogen-bonding properties of 5-deazaalloxazinesCombining Flavin Photocatalysis and Organocatalysis: Metal-Free Aerobic Oxidation of Unactivated Benzylic SubstratesAzodicarboxylate-free esterification with triphenylphosphine mediated by flavin and visible light: method development and stereoselectivity controlPhotodynamic inactivation of Enterococcus faecalis by non-peripherally substituted magnesium phthalocyanines entrapped in lipid vesicles
P50
Q30812390-992B95F4-162A-4152-A070-E395D6F83C67Q33301452-A6B6010B-B1EF-4D72-8C92-F2AEB4EF8ED3Q34180414-472159FD-4EB0-4F74-AC1F-CA527BAF288BQ35632449-358D133A-131D-469A-8566-F1AA5F8A76FAQ38258793-5F4E1B4E-023A-4714-8E32-F3D1FE2A057EQ42916009-8D47E40A-9140-4320-BBE5-56A05A6076BDQ43137593-B92E6B0E-539F-4F83-B092-FE65095A0CEAQ44153238-420A1125-A2B9-4DE7-9848-83EB05C9D6E9Q45204531-268D3FD3-461F-48ED-AC80-70D12E0E132BQ46150252-9FF7C758-A4FD-48BB-A99A-06B1987D5776Q46816555-F8649A0E-60CF-4245-B11F-CE0CACBA7F41Q46860390-0CAE4734-34A4-4FEE-AFCB-D14FDEA656B4Q48349349-6794FA4F-956D-4AA2-92B3-BDCA86FEAF65Q50436427-B5F972E0-2955-46FF-BB38-93707D4ABAA7Q50507766-BDFDAEA6-8286-4214-9EB2-DA9653ECB32BQ50542398-F697B236-862A-402F-AB9B-E8A49BF2CC6CQ51303455-2B1E28EB-5523-4CF4-BED8-5C107C905AD3Q53450041-DB144373-2593-488A-B39D-AA57817DE044Q53457238-4518A948-CC85-470E-9D31-AA3115376EAEQ58834216-A89EF430-74F9-4107-88A7-63801186C8D7Q58834225-3D9ADA1C-3354-4FF2-AF6D-A5363678AAD2Q58834232-1D1AF158-E37F-4EF4-B857-CE4574F23F3BQ59124786-21C3941B-8EAA-40D9-A1B2-45BE0D0E9A90Q60288656-505F1E34-9293-46BE-BA62-BA9A04AE69F0Q61352827-31853276-E7CA-46B4-86DA-B4D55FE64ED6Q61857239-3828D635-8E39-4FD5-9A41-E76584C55BD3Q61857263-58634178-35BB-47C9-B4A9-9E7752776E0BQ61857276-1B1B7B8E-3012-4F7B-BBB5-BE63C9441217Q83176499-5843E1FF-80D2-4EF3-94D9-F48B8F43A718Q85429622-8084A8C9-202A-4365-9549-C4E5EFE6E28BQ87850023-9A2EEB07-3EE8-41A0-B4ED-CB1A37C1E46AQ90738029-819C90E2-59AF-4427-AFDC-4987C8228DD7Q91379430-007EE0DB-3425-4F11-A26E-408713A1124BQ91628127-FF5A8723-3125-4FC5-8F4A-7FC0A5B5EC05
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Marek Sikorski
@ast
Marek Sikorski
@en
Marek Sikorski
@es
Marek Sikorski
@nl
Marek Sikorski
@sl
type
label
Marek Sikorski
@ast
Marek Sikorski
@en
Marek Sikorski
@es
Marek Sikorski
@nl
Marek Sikorski
@sl
prefLabel
Marek Sikorski
@ast
Marek Sikorski
@en
Marek Sikorski
@es
Marek Sikorski
@nl
Marek Sikorski
@sl
P1053
A-8102-2008
P106
P1153
7006300171
P21
P31
P3829
P496
0000-0002-9527-7322