Zobrazeno 1 - 10
of 18
pro vyhledávání: '"L. F. R. CAFFERATA"'
Publikováno v:
Molecules, Vol 5, Iss 3, Pp 362-364 (2000)
The kinetics of the thermal decomposition reaction of cis-6-phenyl-5,6-(2-phenyl-propilydene)-3,3-tetramethylene-1,2,4-trioxacyclohexane (I) was investigated in the temperature range of 100-130°C in selected solvents of different physicochemi
Externí odkaz:
https://doaj.org/article/14565565440a4176914e30af85a1f30a
Autor:
Gladys Nora Eyler, L. F. R. Cafferata, Carmen M. Mateo, Elida Ester Álvarez, Adriana I. Cañizo
Publikováno v:
The Journal of Organic Chemistry. 64:8457-8460
The kinetic data of the thermal decomposition reaction of trans-3,3-dimethyl-5,6-tetramethylene-1,2,4-trioxacyclohexane has been measured in different solvents (benzene, toluene, 2-propanol, 2-methoxyethanol, and p-dioxane) at 0.02 mol kg-1 initial c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01c6d5d5eab641b8ea8441ed924b8d5b
https://doi.org/10.1021/jo980658j
https://doi.org/10.1021/jo980658j
Publikováno v:
ChemInform. 24
Diethyl ketone triperoxide is obtained in a simple and efficient one-step procedure using the acid-catalysed oxidation reaction of diethyl ketone by hydrogen peroxide. Its thermolysis in toluene solution is initiated by a rate determining peroxidic b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b19ed003700d2c504cb26ec6577c270
https://doi.org/10.1002/chin.199330203
https://doi.org/10.1002/chin.199330203
Autor:
L. F. R. Cafferata, J. J. Furlong
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee6545cb8111de8246614efc2c472d17
https://doi.org/10.1002/chin.199629256
https://doi.org/10.1002/chin.199629256
Autor:
L. F. R. Cafferata
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4251636698e622397b3ad05e93490f68
https://doi.org/10.1002/chin.199642278
https://doi.org/10.1002/chin.199642278
Autor:
Gladys Nora Eyler, E. L. Svartman, L. F. R. Cafferata, Elida Ester Álvarez, Adriana I. Cañizo
Publikováno v:
The Journal of Organic Chemistry. 56:411-414
The kinetics of the thermal decomposition reactions of acetone, pinacolone, and cyclohexanone cyclic diperoxides were investigated in variaous solvents at different temperatures. Linear relationships were observed between the enthalpy and entropy of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d94d421fe114d175db1bf5e493692555
https://doi.org/10.1021/jo00001a074
https://doi.org/10.1021/jo00001a074
Publikováno v:
The Journal of Organic Chemistry. 55:1058-1061
The kinetics and mechanism of the thermal decomposition reactions of three substituted tetraoxanes (benzophenone diperoxide, cyclohexanone diperoxide, and pinacolone diperoxide in benzene solution were investigated in the temperature range 108-165°C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d2b831351a02fa7ecf597307d9c27f6
https://doi.org/10.1021/jo00290a045
https://doi.org/10.1021/jo00290a045
Publikováno v:
Tetrahedron Letters. 34:1745-1746
Diethyl ketone triperoxide is obtained in a simple and efficient one-step procedure using the acid-catalysed oxidation reaction of diethyl ketone by hydrogen peroxide. Its thermolysis in toluene solution is initiated by a rate determining peroxidic b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17b578d6e096cc7aa93e8d2b5d7b5fea
https://doi.org/10.1016/s0040-4039(00)60767-0
https://doi.org/10.1016/s0040-4039(00)60767-0
Publikováno v:
The Journal of Organic Chemistry. 49:2107-2111
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8caff920fc6a4330d9cfed337c33d2de
https://doi.org/10.1021/jo00186a005
https://doi.org/10.1021/jo00186a005
Publikováno v:
Zeitschrift für Physikalische Chemie. 29:188-200
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb1dee84c045559446e7904c060bdd3f
https://doi.org/10.1524/zpch.1961.29.3_4.188
https://doi.org/10.1524/zpch.1961.29.3_4.188