Mass spectrometric study of 4,4-disubstituted 1-alkylidene-2,5-cyclohexadienes and their ion-molecule reactions with transition metal ions in the gas phase
The most general pathway for the decomposition of the molecular ions of 4,4-disubstituted 1-alkylidene-2,5-cyclohexadienes is the loss of the substituent at the geminal unit. The facility of this process is a function of the stability of the group eliminated. The formation of cationic rhodium complexes containing alkylidenecyclohexadiene and alkylidenecyclohexadienyl ligands is possible in the gas phase as a result of intramolecular dissociation and ion-molecule reactions. The formation of cationic complexes also occurs as a result of the reaction of benzene derivatives with acacRh(CO)/sup +//sub n/ ions. The donor capacity of 4,4-disubstituted 1-alkylidene-2,5-cyclohexadienes in reactions with acacRh(CO)/sup +//sub n/ ions is comparable with the donor capacity of their aromatic isomers.
- Research Organization:
- A.N. Nesmeyanov Institute of Heteroorganic Compounds, Moscow, USSR
- OSTI ID:
- 6417207
- Journal Information:
- Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States), Journal Name: Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States) Vol. 35:5; ISSN BACCA
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
400201* -- Chemical & Physicochemical Properties
ANIONS
BINDING ENERGY
CARBONYLS
CATALYTIC EFFECTS
CATIONS
CHARGED PARTICLES
CHEMICAL BONDS
COLLISIONS
COMPLEXES
COMPLEXOMETRY
DIENES
DISSOCIATION
ELECTRONS
ELEMENTARY PARTICLES
ENERGY
EVAPORATION
FERMIONS
HYDROCARBONS
ION COLLISIONS
ION-MOLECULE COLLISIONS
IONIZATION
IONS
ISOMERS
LEPTONS
LIGANDS
MASS SPECTRA
MOLECULAR IONS
MOLECULE COLLISIONS
ORGANIC COMPOUNDS
PHASE TRANSFORMATIONS
POLYENES
RHODIUM COMPLEXES
SPECTRA
SYNTHESIS
TRANSITION ELEMENT COMPLEXES
VALENCE