A new x-ray source capable of operating at up to 80
watts has been designed and developed, and put to use with
the Oregon State University Cylindrical Electrostatic
Analyzer. The new source produces over four times the
photoelectron intensity of its predecessor, from gaseous
samples, and accommodates a wider selection...
Dihalocarbenes have been generated mainly by thermal decomposition
of sodium trihaloacetate and phenyl (trihalomethyl)mercury,
and give gem-dihalocyclopropyl adducts with various steroid olefins.
A new procedure involving the use of sealed tubes makes possible the
addition of dihalocarbenes to sterically hindered olefins. In this manner,
7-cholestenyl benzoate when treated with PhHgCC1₃...
The photochemical reaction between O⁻ ions and F centers
was investigated. The activation energy was determined by the
Arrhenius law to be 0.10 + 0.04 eV for temperature below 180°K.
The diffusion of alpha centers towards the oxide ion was eliminated
as the rate limiting step and the low trapping...
An examination was made of some reactions involving a transfer
of carbon from boron to carbon. In the case of the reaction of
a C[subscript n] alkylorganoborane with dichlorocarbene the intermediate was
a C[subscript n]₊₁ chloroalkylorganoborane. Oxidation of this intermediate
yielded an homologous acid (33%) and the usual alcohol (66%)....
The photoelectron spectra of a series of halogenated
molecules have been investigated in the gas phase. Both
core-ionization energies and Auger kinetic energies were
measured to probe the nature of the interaction that holds
a core electron to the molecule.
It was found that satellite structure (shake) could be
used...
Cyclopropylcyclobutene was prepared via the intermediate
dicyclopropylcarbinyl carbene which was generated by the thermal
decomposition of the sodium salt of dicyclopropylketone p-toluenesulfonylhydrazone.
The successive thermal isomerization of cyclopropylcyclobutene
to 2-cyclopropyl-1, 3-butadiene and to vinylcyclopentene
was studied. Kinetic data were obtained for the cyclopropylcyclobutene
to 2-cyclopropyl-1, 3-butadiene isomerization in the gas...
Examination of a proposed reaction scheme to prepare bicyclo-(2.2.0)hexan-1-ol produced the first known condensation of an
enamine with its carbonyl precursor. Hydrolysis of the resulting
dienamine gave an unusual conjugated cyclobutenone in which the
double bond is exocyclic. Characterization and reactions of the
cyclobutenone were successfully carried out.