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Fragmentation of substituted 2-sila-1,3-dioxacycloalkanes under electron impact

Journal Article · · Chem. Heterocycl. Compd. (Engl. Transl.); (United States)
DOI:https://doi.org/10.1007/BF00519949· OSTI ID:6335268
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The mass spectrometric dissociation of 2-sila-1,3-dioxacycloalkanes takes place mainly with loss of the substituent from position 2 of the heterocycle. The fragment formed here eliminates the molecular of carbonyl compounds or alkenes.
Research Organization:
Ufa Petroleum Institute, USSR
OSTI ID:
6335268
Journal Information:
Chem. Heterocycl. Compd. (Engl. Transl.); (United States), Journal Name: Chem. Heterocycl. Compd. (Engl. Transl.); (United States) Vol. 22:2; ISSN CHCCA
Country of Publication:
United States
Language:
English

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Related Subjects

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
400201* -- Chemical & Physicochemical Properties
640304 -- Atomic
Molecular & Chemical Physics-- Collision Phenomena
74 ATOMIC AND MOLECULAR PHYSICS
ALKANES
ALKENES
CHARGED PARTICLES
CHEMICAL REACTION KINETICS
COLLISIONS
CYCLOALKANES
CYCLOALKENES
DISSOCIATION
DISSOCIATION ENERGY
ELECTRON COLLISIONS
ELECTRON-MOLECULE COLLISIONS
ELEMENTS
ENERGY
ENERGY LEVELS
EXCITED STATES
HETEROCYCLIC COMPOUNDS
HYDRIDES
HYDROCARBONS
HYDROGEN COMPOUNDS
IONIZATION
IONIZATION CHAMBERS
IONIZATION POTENTIAL
IONS
KINETICS
MASS SPECTRA
MEASURING INSTRUMENTS
METASTABLE STATES
MOLECULAR IONS
MOLECULAR STRUCTURE
MOLECULE COLLISIONS
ORGANIC COMPOUNDS
ORGANIC SILICON COMPOUNDS
ORGANOMETALLIC COMPOUNDS
RADIATION DETECTORS
REACTION KINETICS
SEMIMETALS
SILANES
SILICON
SILICON COMPOUNDS
SPECTRA