Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Eduardo H. Staricco"'
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 123:1-5
The photolysis of perfluoropropyl fluoride and perfluoropropyl chloride vapour was studied in the 12.9–79.0 Torr and 6.1–40.7 Torr pressure ranges, using light of 232–240 and 254 nm, respectively. The products found were CF 3 CF 2 COF: CO, C 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27f674ddae2a22a99d6f71e6fbd080c0
https://doi.org/10.1016/s1010-6030(99)00032-5
https://doi.org/10.1016/s1010-6030(99)00032-5
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 117:163-169
Photolysis of CF3COCl in the presence of O2 yields the radical CF3O, which then reacts in the presence of CO and O2 to yield a variety of CF3-containing species initiated by the following reactions: CF 3 O+CO→CF 3 OCO CF 3 OCO+O 2 →CF 3 OC(O)O 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7718ea46741c64a085a0f6f28d4fbbcb
https://doi.org/10.1016/s1010-6030(98)00322-0
https://doi.org/10.1016/s1010-6030(98)00322-0
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 115:199-206
The quenching rate constant kq of the excited states *Cr(bpy)33+ and *Cr(phen)33+ by several substituted phenols was investigated as a function of temperature using the time resolved luminescence quenching technique. The activation parameters showed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b5b20a274f59ff34d9ec1638137b3fb
https://doi.org/10.1016/s1010-6030(98)00262-7
https://doi.org/10.1016/s1010-6030(98)00262-7
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 103:19-25
The photolysis at 254 nm of perfluoroacetyl chloride (CF3COCl) in the gas phase and with O2 in excess yielded CO2, CF2O, CF3OOOCF3, CF3COF and Cl2 as products. It was observed that the ratio of CF3COCl consumed to Cl2 formed was 2:1 and that the rate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0dbd5893a0423005ec4bfeaee2a2ab55
https://doi.org/10.1016/s1010-6030(96)04531-5
https://doi.org/10.1016/s1010-6030(96)04531-5
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 86:27-31
The photolysis of perfluoroacetyl chloride vapour was studied in the pressure range 4.6–59.9 Torr and with addition of inert gas up to 535.2 Torr using light of 254 and 280 nm. The quantum yield for the decomposition of CF 3 COCl taken as Φ [CF 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4bfa058bc377dc8de3ba58893855ee6
https://doi.org/10.1016/1010-6030(94)03920-p
https://doi.org/10.1016/1010-6030(94)03920-p
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c5be87db423493f087aee9039c690cd
https://doi.org/10.1002/chin.199105072
https://doi.org/10.1002/chin.199105072
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9c0777cd4e9f061a13f7d560ebae6f5
https://doi.org/10.1002/chin.199115078
https://doi.org/10.1002/chin.199115078
Publikováno v:
ChemInform. 22
CF3 radicals were generated by the photolysis of perfluoroacetic anhydride. In the presence of pentafluorobenzene, the CF3 radicals react according to the following mechanism: It was found that the addition reaction (3) becomes reversible above ca. 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8441329e091ee70929c8e4b3f730b91
https://doi.org/10.1002/chin.199132097
https://doi.org/10.1002/chin.199132097
Publikováno v:
ChemInform. 23
The reaction of CH2(1A1) with 1,1,2,2-tetrafluorocyclopropane was studied at 300 K and at pressures between 9.0 and 365.0 torr. Chemically activated 1-methyl-2,2,3,3-tetrafluorocyclopropane was formed and two competitive reaction paths, namely decomp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39f4788206e5277b8957e644a12d13f4
https://doi.org/10.1002/chin.199237073
https://doi.org/10.1002/chin.199237073
Publikováno v:
International Journal of Chemical Kinetics. 24:619-629
The reaction of CH2(1A1) with 1,1,2,2-tetrafluorocyclopropane was studied at 300 K and at pressures between 9.0 and 365.0 torr. Chemically activated 1-methyl-2,2,3,3-tetrafluorocyclopropane was formed and two competitive reaction paths, namely decomp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac2ed23c59fc546a5eeaa3272f918562
https://doi.org/10.1002/kin.550240702
https://doi.org/10.1002/kin.550240702