作者:Sylvie L. Tardif、Andrzej Z. Rys、Charles B. Abrams、Imad A. Abu-Yousef、Pierre B.F. Lesté-Lasserre、Erwin K.V. Schultz、David N. Harpp
DOI:10.1016/s0040-4020(97)00555-3
日期:1997.8
The chemistry of the generation and trapping of diatomicsulfur (S2) and sulfur monoxide (SO) are reviewed with special emphasis on recent work, including initial efforts to detect and trap diatomic selenium (Se2).
Reduction of α,α′-diketo selenides with a low-valenttitaniumreagent usually affords 3,4-dihydroxyselenolanes, from which the corresponding selenophenes are obtained by acid-catalyzed dehydration. A surprising exception is the formation of 2,4-dihydroxy- 2,4-di--butylselenolane from bis(2--butyl-2-oxoethyl) selenide, the former being converted to 2,4-di--butylselenophene by acid treatment.
作者:Andrzej Z. Rys、Erwin K.V. Schultz、David N. Harpp
DOI:10.1080/17415993.2010.513440
日期:2010.10.1
Metallocene pentaselenides and elemental selenium were employed in an effort to generate diatomic selenium (Se2) under thermal conditions. Trapping experiments were carried out with six dienes. A successful formation of a diselenium adduct was observed in the case of 5,6-dimethylene-cyclohexa-1,3-diene (1a). The other dienes produced the corresponding dihydroselenophenes. The in-depth study of the limitations of our method to generate Se2 is described; a plausible mechanism rationalizing the observed results is proposed.