Search results for "PHOTODISSOCIATION"
showing 10 items of 90 documents
Photoiodocarboxylation of Activated C═C Double Bonds with CO2 and Lithium Iodide
2018
The photolysis at 254 nm of lithium iodide and olefins 1 carrying an electron-withdrawing Z-substituent in CO2-saturated (1 bar) anhydrous acetonitrile at room temperature produces the atom efficient and transition metal-free photoiodocarboxylation of the C═C double bond. The reaction proceeds well for terminal olefins 1 to form the new C-I and C-C σ-bonds at the α and β-positions of the Z-substituent, respectively, and is strongly inhibited by polar protic solvents or additives. The experimental results suggest that the reaction channels through the radical anion [CO2•-] in acetonitrile, yet involves different intermediates in aqueous medium. The stabilizing ion-quadrupole and electron don…
Iodine and mercury resonance lamps for kinetics experiments and their spectra in the far ultraviolet
2000
Electrodeless iodine and mercury iodide radio-frequency discharge lamps have been made to provide intense sources of resonance radiation of iodine and mercury in the 183-253 nm region. Production technology and emission spectra in the ultraviolet and vacuum ultraviolet regions are described. Both lamps (iodine and mercury iodide) are designed and used for monitoring the iodine 2P1/2 (206.163 nm) and 2P3/2 (183.038 nm) level population kinetics after flash photolysis of I2 or other precursor molecules in laboratory experiments. The technique is suitable for the investigation of the gas phase reaction kinetics following the photolysis of I2 in the presence of O3.
Subsurface chemistry of mantles of interstellar dust grains in dark molecular cores
2010
Context. The abundances of many observed compounds in interstellar molecular clouds still lack an explanation, despite extensive research that includes both gas and solid (dust-grain surface) phase reactions. Aims. We aim to qualitatively prove the idea that a hydrogen-poor subsurface chemistry on interstellar grains is responsible for at least some of these chemical "anomalies". This chemistry develops in the icy mantles when photodissociation reactions in the mantle release free hydrogen, which escapes the mantle via diffusion. This results in serious alterations of the chemical composition of the mantle because pores in the mantle provide surfaces for reactions in the new, hydrogen-poor …
Eine einfache Darstellung von 8-Azidoadenosin-5′-triphosphat; ein Agens zur Photoaffinitätsmarkierung von ATP-bindenden Proteinen
1978
Eine vereinfachte Synthese von 8-Azido-ATP (3) wird beschrieben. Die neue Methode ist kurzer und fuhrt zu wesentlich besseren Ausbeuten als die bekannte Methode. Neben 3 entstehen dabei 8-Azido-ADP und 8-Azido-AMP. Es wurden mit einem Reaktionsansatz alle drei 8-Azidonucleotide gleichzeitig erhalten. 8-Azido-ATP (3) wurde durch Elementaranalyse, Dunnschichtchromatographie, Infrarotspektroskopie und UV-Absorptionsspektroskopie charakterisiert. Die Photolyse bei verschiedenen pH-Werten wurde untersucht. Durch F1ATPase wird 3 umgesetzt. A Facile Synthesis of 8-Azidoadenosine 5′-Triphosphate; a Photoaffinity Label for ATP-Binding Proteins A simple procedure for the synthesis of 8-azido-ATP (3) …
Transformation of monuron photosensitized by soil extracted humic substances: energy or hydrogen transfer mechanism?
1997
The humic and fulvic acids extracted from a Ranker type soil sensitize the transformation of monuron. When monuron is irradiated at 365 nm in the presence of the fulvic acid, its degradation is faster in deoxygenated medium than in air-saturated solution. Chloride ions are released, and the para-hydroxylated derivative is formed as upon direct photolysis. It is deduced that the consumption of monuron observed in the absence of oxygen is due to an energy transfer from reactive triplet states of the fulvic acid to monuron. Energy transfer reactions also take place when hydroquinone or acetophenone are used as sensitizers, showing that the energy level of the triplet state of monuron is lower …
Photolysis of Adsorbed Phases: Ethanoic Acid-Insulators and Semiconductors Systems. Influence of Acid-Base Properties.
1986
The paper reports the results of experiments in which the photodecomposition of adsorbed ethanoic acid (and in few cases of adsorbed acetone and ethanol) was carried out by using several silica gel samples, whose properties were modified by adding oxidic dopants as γ-Al2O3, which is acidic in character, and MgO, which is mainly basic. Also the related system MgO-Al2O3 was investigated. Few IR spectra on selected pure specimens and on specimens containing adsorbed ethanoic acid were recorded with the aim of following the variation of the surfaces-adsorbate interaction with the variation of the acid-base properties. It was also of interest to compare the photoreactivity of insulators and semi…
Photoinduced molecular rearrangements. Some comments on the ring-photoisomerization of 1,2,4-oxadiazoles into 1,3,4-oxadiazoles
2001
The ring-photoisomerization of 3-amino- and 3-methylamino-5-phenyl-1,2,4-oxadiazoles into the corresponding 2-amino- and 2-methylamino-5-phenyl-1,3,4-oxadiazoles has been reinvestigated by examining the effect of a base on the photoreaction. On irradiating at λ = 254 nm in methanol, yields of the ring-photoisomers were found to be significantly enhanced by the addition of triethylamine (TEA) in the photoreaction medium. By contrast, irradiation of the 3-amino-5-phenyloxadiazole in acetonitrile containing TEA gave an almost complete photoreduction into benzoylguanidine, while few percent of the ring photoisomer were detected. Furthermore, the pyrene-sensitized photolysis of 3-amino-5-phenylo…
ChemInform Abstract: Photoinduced Molecular Rearrangements. Some Comments on the Ring-Photoisomerization of 1,2,4-Oxadiazoles into 1,3,4-Oxadiazoles.
2010
The ring-photoisomerization of 3-amino- and 3-methylamino-5-phenyl-1,2,4-oxadiazoles into the corresponding 2-amino- and 2-methylamino-5-phenyl-1,3,4-oxadiazoles has been reinvestigated by examining the effect of a base on the photoreaction. On irradiating at λ = 254 nm in methanol, yields of the ring-photoisomers were found to be significantly enhanced by the addition of triethylamine (TEA) in the photoreaction medium. By contrast, irradiation of the 3-amino-5-phenyloxadiazole in acetonitrile containing TEA gave an almost complete photoreduction into benzoylguanidine, while few percent of the ring photoisomer were detected. Furthermore, the pyrene-sensitized photolysis of 3-amino-5-phenylo…
Fluoro heterocycles. A photochemical methodology for the synthesis of 3-amino- and 3-(N-alkylamino)-5-perfluoroalkyl-1,2,4-oxadiazoles
2000
Abstract A photochemical methodology for the synthesis of perfluoroalkyl-1,2,4-oxadiazoles has been described. 3-Amino- and 3-( N -alkylamino)-5-perfluoroalkyl-1,2,4-oxadiazoles have been prepared by irradiation of 3-perfluoroalkanoylamino-4-phenyl-1,2,5-oxadiazoles (furazans) at λ =313 nm in methanol and in the presence of ammonia or primary aliphatic amines.
Photodissociation of Formyl Fluoride in Rare Gas Matrixes
2006
Photodissociation of formyl fluoride (HCOF) is studied in Ar, Kr, and Xe matrixes at 248 and 193 nm excitation by following spectral changes in the infrared absorption spectra. In all matrixes, the main photodissociation products are CO/HF species, including CO-HF and OC-HF complexes and thermally unstable CO/HF species (a distorted CO/HF complex or a reaction intermediate), which indicate negligible cage exit of atoms produced via the C-F and C-H bond cleavage channels. However, the observation of traces of H, F, CO, CO(2), F(2)CO, FCO, and HRg(2)(+) (Rg = Kr or Xe) in Kr and Xe matrixes would imply some importance of other reaction channels too. The analysis of the decay curves of the pre…