Zobrazeno 1 - 10
of 14
pro vyhledávání: '"A. W. Zwaard"'
Autor:
A. W. Zwaard, H. Kloosterziel
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 100:126-128
The reaction of some 7-substituted cycloheptatrienes with KNH2 in liquid ammonia is described. In several cases stable carbanions are formed. Their NMR spectra are consistent with a non-planar pentadienyl-like structure. A comparison of the 1H-NMR sp
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 103:174-176
In basic alcohol, 7-(methoxycarbonyl)-1,3,5-cycloheptatriene (7b) forms its 2-, 3- and 1-isomers (viz.2b, 3b and 1b) in successive reactions. All isomers show specific hydrogen exchange in CD3ONa/CD3OD. For 3- and 1-(methoxycarbonyl)-1,3,5-cyclohepta
Autor:
A. W. Zwaard, J. C. M. Mossink
Publikováno v:
SPIE Proceedings.
Classification schemes to identify laser hazards may give a quick insight into the hazards of radiation. However the most serious accidents involve exposure to high voltages. Besides toxic chemicals may present hazards in laser work stations. In this
Publikováno v:
Recueil des travaux chimiques des Pays-Bas = Journal of the Royal Netherlands Chemical Society, 101, 137-141. Royal Netherlands Chemical Society
Semi-empirical calculations (mostly MINDO/3) have been performed on singlet C7H7−. A preference for planar structures is evident from the calculations. Two different structures (an allylic structure and a pentadienylic structure, respectively) are
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 101:187-191
Coalescence phenomena have been observed in the NMR spectra of a variety of 7-substituted 1,3,5-cycloheptatrienes upon varying temperature and/or solvent. Using two different methods, the energy of activation of the process responsible for coalescenc
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 103:188-192
Under the influence of basic alcohol, 7-phenyl-1,3,5-cycloheptatriene (7c) forms its 1-, 2- and 3-isomers (viz.1c, 2c and 3c) in parallel reactions, contrary to suggestions made in the literature. The activation parameters for these reactions are giv
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 102:285-290
Modified Forsen-Hoffman experiments (in the FT mode) show that, in 7-substituted cyclohepta-1,3,5-trienes benzenesulphonyl groups migrate in a random way, while phenylthio substituents show a specific 1,2-migration. Activation parameters for the migr
Publikováno v:
Chemischer Informationsdienst. 14
Autor:
A. W. Zwaard, H. Kloosterziel
Publikováno v:
Chemischer Informationsdienst. 12
The reaction of some 7-substituted cycloheptatrienes with KNH2 in liquid ammonia is described. In several cases stable carbanions are formed. Their NMR spectra are consistent with a non-planar pentadienyl-like structure. A comparison of the 1H-NMR sp
Publikováno v:
Chemischer Informationsdienst. 13
Coalescence phenomena have been observed in the NMR spectra of a variety of 7-substituted 1,3,5-cycloheptatrienes upon varying temperature and/or solvent. Using two different methods, the energy of activation of the process responsible for coalescenc