Paper

Photolytic reactions of bis(trimethylsilyl)mercury and bis(trimethylgermyl)mercury with benzene, toluene, and anisole. Free-radical aromatic silylation and germylation

Published Apr 1, 1971 · S. W. Bennett, C. Eaborn, R. A. Jackson

Journal of Organometallic Chemistry

Citations

Influential Citations

Abstract

Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.

Study Snapshot

Photolysis of bis(trimethylsilyl)mercury produces aromatic substitution products, with better yields from naphthalene and phenanthrene, while anisole produces other products.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Photolytic reactions of bis(trimethylsilyl)mercury and bis(trimethylgermyl)mercury with benzene, toluene, and anisole. Free-radical aromatic silylation and germylation

References

Citations