Lactone-derived carbon-centered radicals: formation and reactivity with oxygen.

[reaction: see text] Several lactones were examined to test the reactivity of carbon-centered radicals toward oxygen. Notably, the radical derived from 2-coumaranone (4) is unreactive toward oxygen, while 2-cuomaranone itself shows enhanced reactivity toward hydrogen abstraction by alkoxyl radicals. We propose that five parameters influence diminished reactivity toward oxygen, i.e., (a) benzylic resonance stabilization, (b) unpaired spin delocalization on oxygen, (c) favorable stereoelectronic effects, (d) electron-withdrawing effects, and (e) steric effects.

Temperature-dependent photochemistry of 1,3-diphenylpropenes. The di-pi-methane reaction revisited.

The temperature-dependent photochemical behavior of 1,3-diphenylpropene and several of its 3-substituted derivatives has been investigated over a wide temperature range. The singlet state is found to decay via two unactivated processes, fluorescence and intersystem crossing, and two activated processes, trans,cis isomerization and phenyl-vinyl bridging. The latter activated process yields a diradical intermediate which partitions between ground-state reactant and formation of the di-pi-methane rearrangement product. Kinetic modeling of temperature-dependent singlet decay times and quantum yields of fluorescence, isomerization, di-pi-methane rearrangement, and nonradiative decay provides rate constants and activation parameters for each of the primary and secondary processes. Substituents at the 3-position are found to have little effect on the electronic spectra or unactivated fluorescence and intersystem crossing pathways. However, they do effect the activated primary and secondary processes. Thus, the product ratios are highly temperature dependent.

One- vs two-photon processes in the photochemistry of 1,n-dihaloalkanes.

1,n-Dihaloalkanes can be photochemical precursors of n-haloalkyl and -allyl radicals and cations, which are generated via one-photon processes. Time-resolved techniques have provided considerable information on the structures and reactivity of these intermediates. Low-temperature matrix isolation, two-laser two-color, laser-drop, and laser-jet photolysis techniques are powerful tools to photolyze haloalkyl radicals and to generate carbenes or biradicals via two-photon processes.

The 4,4'-(1,2-ethanediyl)bisbenzyl biradical: its generation, detection, and (photo)chemical behavior in solution.

The 4,4'-(1,2-ethanediyl)bisbenzyl biradical (2) is clearly and efficiently generated by photolysis of [3.2]paracyclophane-2-one (8) in cyclohexane solution. This intermediate is also formed via two-photon processes from [2.2]paracyclophane (3) and 1,2-bis(4-chloromethylphenyl)ethane (4). The products arising thermally from biradical 2 are [2.2]paracyclophane and [2.2.2.2]paracyclophane (11) (under high-intensity conditions). Furthermore, two-laser two-color flash photolysis shows that biradical 2 is photostable in solution at room temperature. Thus, formation of p-xylylene (1) from 2 occurs neither thermally nor photochemically.