Related Experiment Video
Updated: Aug 17, 2026

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
One-electron oxidation of [CCOCC]-* in the gas phase forms stable and decomposing forms of CCCCO
Mark Fitzgerald1, Suresh Dua, John H Bowie
1Department of Chemistry, The University of Adelaide, South Australia 5005.
Abstract:
The radical anion [CCOCC]-* may be made in the source of a VG ZAB 2HF mass spectrometer by the reaction between F-(from SF6) and (CH3)3SiC[triple bond]COC[triple bond]CSi(CH3)3. Vertical (Franck-Condon) one-electron oxidation of [CCOCC]-* in the first collision cell produces both singlet and triplet CCOCC. A combination of experiment and molecular modelling (at the CCSD(T)/aug-cc-pVDZ//B3LYP/6-31G* level of theory) gives data which are consistent with the CCOCC neutrals rearranging over small barriers to form singlet and triplet CCCCO in exothermic reactions. Both singlet and triplet CCCCO formed in this way have excess energy. Singlet CCCCO has sufficient excess energy to effect decomposition exclusively to CCC and CO. In contrast, some of the triplet CCCCO neutrals are stable, while others decompose to CCC and CO.
Related Concept Videos
Carbocations
Alkynes to Carboxylic Acids: Oxidative Cleavage
Oxidation of Alcohols
The process of oxidation in a chemical reaction is observed in any of the three forms:
Radical Formation: Elimination
Phase I Reactions: Oxidation of Carbon-Heteroatom and Miscellaneous Systems
In carbon-nitrogen systems, aliphatic and aromatic amines can undergo oxidative reactions. Secondary and tertiary amines, like those found in tricyclic antidepressants, can undergo N-dealkylation, a process that involves the oxidation of the alkyl group. In addition, oxidative...
Oxidative Cleavage of Alkenes: Ozonolysis
Ozone is a symmetrical bent molecule stabilized by a resonance structure.

