Affiliation:
1. Department of Chemistry and Chemical Biology, McMaster University, 1280 Main Street West, Hamilton, ON L8S 4M1, Canada.
Abstract
The reactions of dimethyl- and diphenylgermylene (GeMe2 and GePh2, respectively) with cyclohexene oxide (CHO) and propylene sulfide (PrS) have been studied in hydrocarbon solvents at 25 °C by laser flash and steady-state photolysis methods using appropriately substituted germacyclopent-3-ene derivatives as germylene precursors. GeMe2 reacts with CHO and PrS with rate constants in the range of 1.2–1.7 × 1010 M−1 s−1 in hexanes at 25 °C to form new transient products that are assigned to the corresponding Lewis acid-base complexes of the germylene with the substrates. The complexation reactions were found to be reversible and are characterized by equilibrium constants of KC = (3.7 ± 0.8) × 103 M−1 and (3 ± 1) × 104 M−1 for complexation of GeMe2 with CHO and PrS, respectively. The complexes decay over approximately 10 μs with the concomitant formation of tetramethyldigermene (Ge2Me4), identifiable by its characteristic UV-vis spectrum centered at λmax = 370 nm. Diphenylgermylene behaves analogously, reacting rapidly and reversibly with the two substrates to form the corresponding Lewis acid-base complexes (λmax ≈ 355 nm) that decay over several tens of microseconds with the concomitant growth of the characteristic UV-vis spectrum of tetraphenyldigermene (Ge2Ph4) (λmax = 440 nm). Steady-state photolysis of the germylene precursors in the presence of CHO afforded germanium-containing oligomers but showed no evidence of oxygen abstraction or the formation of substrate-derived product(s). Similar photolyses in the presence of PrS also afforded germanium-containing oligomers, but as well yielded propene in 20%–30% yield and (in the case of the GePh2 precursor) minor amounts of low molecular weight compounds that appear to be derived from the corresponding germanethione. Density functional theory calculations of the chalcogen abstraction reactions of GeMe2 with oxirane and thiirane in the gas phase have been carried out at the B3LYP/6-311+G(d,p) level of theory and are in good qualitative agreement with the experimental data.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
5 articles.
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