The photosubstitution of 2-fluoro-4-nitroanisole with n-hexylamine. Evidence of two different triplet excited states in a dual mechanistic pathway.

doi:10.1016/S0040-4020(01)86698-9

Paper

DOI: 10.1016/S0040-4020(01)86698-9

The photosubstitution of 2-fluoro-4-nitroanisole with n-hexylamine. Evidence of two different triplet excited states in a dual mechanistic pathway.

Published 1990 · R. Pleixats, J. Marquet

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The photoreaction of 2-fluoro-4-nitroanisole with n-hexylamine leads to fluoride (major) and methoxy (minor) substitution, with two different triplet excited states in a dual mechanistic pathway.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

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Photochemistry of nitro and nitroso compounds reveals diverse reactions and reactions involving nitrosamines, nitroso compounds, and nitroso compounds.

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Recent Advances in the Photochemistry of the Carbon–Halogen Bond

Carbon-halogen bond photochemistry has advanced significantly, with new methods for analyzing and understanding the photoreduction of aromatic halides in non-polar solvents.

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Photochemical cleavage reactions of 8-quinolinyl sulfonates in aqueous solution.

Photolysis of 8-quinolinyl benzenesulfonate derivatives in aqueous solutions mainly occurs via homolytic cleavage of S-O bonds in the excited triplet state, with minimal byproduct production.

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Tetrahedron