about
UV-Induced Unimolecular Photochemistry of Diketene Isolated in Cryogenic Inert MatricesMatrix-isolation study and ab initio calculations of the structure and spectra of hydroxyacetone.Photochemistry of 5-allyloxy-tetrazoles: steady-state and laser flash photolysis study.Conformational switching induced by near-infrared laser irradiation.Conformational behavior and tautomer selective photochemistry in low temperature matrices: the case of 5-(1H-tetrazol-1-yl)-1,2,4-triazole.Infrared spectra and ultraviolet-tunable laser induced photochemistry of matrix-isolated phenol and phenol-d5.Conformers, infrared spectrum and UV-induced photochemistry of matrix-isolated furfuryl alcohol.Ultraviolet-tunable laser induced phototransformations of matrix isolated isoeugenol and eugenol.UV-laser photochemistry of isoxazole isolated in a low-temperature matrix.Influence of cage confinement on the photochemistry of matrix-isolated E-β-ionone: FT-IR and DFT study.Near-IR laser generation of a high-energy conformer of L-alanine and the mechanism of its decay in a low-temperature nitrogen matrix.Capture of an elusive nitrile ylide as an intermediate in isoxazole-oxazole photoisomerization.Near-IR-induced, UV-induced, and spontaneous isomerizations in 5-methylcytosine and 5-fluorocytosine.Near-infrared laser-induced generation of three rare conformers of glycolic acid.Three conformers of 2-furoic acid: structure changes induced with near-IR laser light.Conformational Changes in Thiazole-2-carboxylic Acid Selectively Induced by Excitation with Narrowband Near-IR and UV Light.Conformers of Kojic Acid and Their Near-IR-Induced Conversions: Long-Range Intramolecular Vibrational Energy Transfer.Conformational preferences of 3,4-dihydroxyphenylacetic acid (DOPAC).Photoisomerization and photochemistry of matrix-isolated 3-furaldehyde.Thermal and photoinduced control of relative populations of 4-methoxybenzaldehyde (p-anisaldehyde) conformers.Conformational space and photochemistry of alpha-terpinene.Positive identification of UV-generated, non-hydrogen-bonded isomers of o-hydroxybenzaldehyde and o-hydroxyacetophenone.Infrared spectra and photochemistry of matrix-isolated pyrrole-2-carbaldehyde.Stepwise conformational cooling towards a single isomeric state in the four internal rotors system 1,2-butanediol.A correlation between the proton stretching vibration red shift and the hydrogen bond length in polycrystalline amino acids and peptides.Structural and spectroscopic characterization of E- and Z-isomers of azobenzene.Conformational space and photochemistry of tyramine isolated in argon and xenon cryomatrixes.Photoisomerization of saccharin.Low-temperature Fourier transform infrared spectra and hydrogen bonding in polycrystalline L-alanine.Conformational study of monomeric 2,3-butanediols by matrix-isolation infrared spectroscopy and DFT calculations.Low temperature FTIR spectroscopy and hydrogen bonding in cytosine polycrystals.Matrix isolation infrared spectroscopic and theoretical study of 1,1,1-trifluoro-2-chloroethane (HCFC-133a).Low-temperature FTIR spectroscopic and theoretical study on an energetic nitroimine: dinitroammeline (DNAM).Low temperature Fourier transform infrared spectra and hydrogen bonding in polycrystalline uracil and thymine.Conformational cooling dynamics in matrix-isolated 1,3-butanediol.Matrix isolation FTIR spectroscopic and theoretical study of 3,3-dichloro-1,1,1-trifluoropropane (HCFC-243).Matrix-isolated diglycolic anhydride: vibrational spectra and photochemical reactivity.UV-induced hydrogen-atom transfer and hydrogen-atom detachment in monomeric 7-azaindole isolated in Ar and n-H2 matrices.Photochemical alpha-cleavage in pyran-2-thione: generation of aldehydethioketene and thioaldehydeketene photoproducts.Crystal and molecular structure of DL-serine hydrochloride studied by X-ray diffraction, low-temperature Fourier transform infrared spectroscopy and DFT(B3LYP) calculations.
P50
Q29037596-1C2F95D3-4E3C-4FC0-A742-DBED4D942EBAQ31158271-8BA7F2BA-EF43-4689-8628-9DA0860578C6Q33323045-74907232-A6A1-481E-B866-1363C8AE2121Q33452723-565B8719-82AE-4805-8C61-5322B5062A4BQ33895652-5100EB33-0138-4A85-9EBD-BD7B3CC8FBA5Q34133338-8DC94A23-2A00-4EC0-A0E4-1D7576A0656DQ34155093-C264CD2A-94BF-4DE0-B4BA-E96525893C64Q34349651-E73156B2-ABB8-41FD-995D-6657D0BA2C06Q34407261-BC51E5E7-60B9-418C-BF3A-5583BD4720C9Q34543758-62C1F62F-1233-4680-97EB-A0B27114BD34Q34654708-E659C3E1-BA94-4B68-B76C-C35884E9281AQ35001036-9D8D1D54-7E61-42B3-A24F-9DA6AEE2D00AQ35100025-623D9BD1-1899-46C7-BDB3-67276C101E42Q35202834-39BA7BD2-4869-4183-87C7-476E3C50D07CQ35542674-F9AAADA2-2EEC-4AC3-B628-D0519F0156F2Q35960771-AB438593-710E-426C-A91B-C419DE1F7416Q35987104-1DABEB01-99AA-4810-B749-09F2416F1AFBQ41582117-96C7C4FA-F60A-415D-9234-A7B89DC05BD0Q42836720-2FAACD51-E531-44BE-A770-ECCA9E89246DQ42996011-90A4C3E7-3A62-4A4E-B5BD-3FBBEF4442DAQ43101542-3D2B285B-3A15-4053-84C6-B5E26130DB9AQ43106176-85CBB87D-557B-43DF-935C-48921A32C092Q43182006-CFB43609-4175-43E9-8EE2-3146332F60FEQ43265729-0593E0B0-9FCB-460A-AA85-92E9D8CA0349Q43270360-8B07C1D6-573B-4A12-9BEA-CD3515CC6C85Q43483590-8DFAE693-F69A-42A5-AD99-AA8284A2B056Q43687934-C063DE87-D22C-4615-ACB2-B885F2D42053Q43873081-FECF9316-DE64-4C8A-B3B6-7E9796207FCFQ44648460-072E047C-0F97-498C-B85A-42EC4B28E094Q44678840-88134C14-F3A9-4846-9B3F-E7C6318C02EBQ44689718-5878BF0A-1E6A-4496-BA2B-32D8A79AD152Q44803296-F6673041-BF6C-4C78-93D2-30672162D5D0Q44862113-26BD6703-5282-42E1-A957-A853A8007498Q44974701-15E5D370-4431-40FF-BC89-ED43C225D805Q46039431-312EB82B-18A0-4CFE-8A9F-87E873DA7B33Q46286638-326A37BC-F1C9-4E3C-BA49-9C6B8E06FC5CQ46319443-4F028C51-57DE-4034-84BD-1B3594072D44Q46380356-5A94F3AC-6178-4DB2-B530-EC294928736EQ46479706-B88E3A3D-C377-4F52-889B-EE3A35519F55Q46536285-328B3585-816D-46D5-8D90-360F823CF73D
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Igor Reva
@ast
Igor Reva
@en
Igor Reva
@es
Igor Reva
@nl
Igor Reva
@sl
type
label
Igor Reva
@ast
Igor Reva
@en
Igor Reva
@es
Igor Reva
@nl
Igor Reva
@sl
prefLabel
Igor Reva
@ast
Igor Reva
@en
Igor Reva
@es
Igor Reva
@nl
Igor Reva
@sl
P1053
B-2866-2008
P106
P1153
6701755059
P21
P31
P3829
P496
0000-0001-5983-7743