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Showing 1 to 3 of 3 for “"Radical Clocks"”.

  1. Radical rearrangement in the spiro(cyclopropane-1,1'-indan) and 3',4'-dihydrospiro(cyclopropane-1,1'(2H)-naphthalene) systems. An investigation of fast radical clocks

    … opening rearrangements of cyclopropylcarbinyl radicals incorporated in rigid indanyl and tetrahydronaphthyl frameworks were investigated by the competitive tin hydride method. At 75$\sp\circ$C, the spiro (cyclopropane-1,1$\sp\prime$-indan) -2$\sp\prime$-yl and …

    uiuc Repository record for Radical rearrangement in the spiro(cyclopropane-1,1'-indan) and 3',4'-dihydrospiro(cyclopropane-1,1'(2H)-naphthalene) systems. An investigation of fast radical clocks (opens in a new tab)

  2. Towards Water-Soluble Peroxyl Radial Clocks

    … conditions, forming an alkoxyl and acyloxyl radical, the latter of which rapidly decarboxylates to form a carbon centered radical. While peroxyesters are generally decomposed under anaerobic conditions to serve as sources of carbon-centered radicals to initiate radical reactions, it has been …

    queens Repository record for Towards Water-Soluble Peroxyl Radial Clocks (opens in a new tab)

  3. Electrochemical oxidation of aliphatic carboxylates: Kinetics, thermodynamics, and evidence for a shift from a concerted to a stepwise mechanism in the presence of water

    … the series which is expected trend based on radical stabilization energies of the alkyl groups on the aliphatic carboxylates. Hydrogen bonding was investigated as a possible source for the discrepancy between our results and the reported mechanism of the dissociative electron transfer. …

    vt Repository record for Electrochemical oxidation of aliphatic carboxylates: Kinetics, thermodynamics, and evidence for a shift from a concerted to a stepwise mechanism in the presence of water (opens in a new tab)