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When is a radical not a radical?
1Inflammation Research Group, London Hospital Medical College, UK.
Free Radical Research
|July 1, 1996
Abstract:
It is not commonly realised that symmetrical Fe(III) complexes are expected to have EPR spectra dominated by a symmetrical narrow line close to the free-spin g-value. The aim of this note is to stress that such features can be mistakenly identified as the spectra for stable organic radicals. This situation is a particular problem in studies of animal or plant tissue samples.
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Radicals: Electronic Structure and Geometry
This lesson delves into the geometry of a radical, which is influenced by the electronic structure of the molecule. The principle is similar to that of a lone pair, where the unpaired electron influences the geometry at the radical center.
Accordingly, the structure of a trivalent radical lies between the geometries of carbocations and carbanions. An sp2-hybridized carbocation is trigonal planar, while an sp3-hybridized carbanion is trigonal pyramidal. Here, the difference in geometry is...
Accordingly, the structure of a trivalent radical lies between the geometries of carbocations and carbanions. An sp2-hybridized carbocation is trigonal planar, while an sp3-hybridized carbanion is trigonal pyramidal. Here, the difference in geometry is...
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Radicals can be formed by adding a radical to a spin-paired molecule. This is typically observed with unsaturated species, where the addition of a radical across the π bond leads to the production of a new radical by dissolving the π bond. For example, the addition of a Br radical to an alkene yields a carbon-centered radical.
Similar to charge conservation in chemical reactions, spin conservation is implicit for radical reactions. Accordingly, the product formed must possess an unpaired...
Similar to charge conservation in chemical reactions, spin conservation is implicit for radical reactions. Accordingly, the product formed must possess an unpaired...
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Radical Reactivity: Overview
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Radicals
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