Photochemical reaction of 1- and 2-naphthalenecarbonitrile with some methylbenzenes

doi:10.1016/S0040-4020(01)91311-0

Paper

Photochemical reaction of 1- and 2-naphthalenecarbonitrile with some methylbenzenes

Published 1984 · A. Albini, Silvia Spreti

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Abstract

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1- and 2-naphthalenecarbonitriles photochemically react with 1,2,4,5,-tetramethylbenzene to produce 1,1'-(1,2-ethane-diyl)bis-(2,4,5-trimethylbenzene) and 1,2-dihydro-2-na

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

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Paper

Photochemical reaction of 1- and 2-naphthalenecarbonitrile with some methylbenzenes

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References

Photoreactions of 1- and 2-naphthonitriles with tetramethylethylene in various solvents

Photoreactions of 1- and 2-naphthonitriles with tetramethylethylene in various solvents produce unique cyclobutanes and photoreduction products, with deuterium incorporation observed in CH3OD.

Emission from aromatic hydrocarbon-diene and -olefin exciplexes

Luminescence from aromatic hydrocarbon-diene and -olefin exciplexes suggests their role in singlet quenching processes, with charge-resonance contributing to their formation.

Chemistry of exciplexes. Photocycloadditions of anthracenes to conjugated polyenes

Photocycloadditions of anthracenes to conjugated polyenes can yield novel adducts, with the concerted pathway being favored by polar solvents, due to surface crossing from exciplex intermediates.

Kinetics of Fluorescence Quenching by Electron and H‐Atom Transfer

Fluorescence quenching rate constants in de-oxygenated acetonitrile can be correlated with electron transfer rate constants, but hydrogen-atom transfer may be the quenching mechanism in some systems.

Citations