1959
DOI: 10.1021/ba-1959-0023.ch009
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Preparation of Alkyl Mercurials with Tetraethyllead

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Cited by 6 publications
(3 citation statements)
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“…The product was then added to 800 ml of 1% HCl and ether-distilled, and then the residue was filtered and dried. Whelen 19 synthesized C 2 H 5 HgCl from mercuric chloride and tetraethyllead. The ethanolic solution of (C 2 H 5 ) 4 Pb was added gradually to a suspension of HgCl 2 in ethanol and the whole mixture was heated for 4 h at 65…”
Section: Speciation Analysis and Environmentmentioning
confidence: 99%
“…The product was then added to 800 ml of 1% HCl and ether-distilled, and then the residue was filtered and dried. Whelen 19 synthesized C 2 H 5 HgCl from mercuric chloride and tetraethyllead. The ethanolic solution of (C 2 H 5 ) 4 Pb was added gradually to a suspension of HgCl 2 in ethanol and the whole mixture was heated for 4 h at 65…”
Section: Speciation Analysis and Environmentmentioning
confidence: 99%
“…One former application of tetraethyllead was based on the facile electrophilic cleavage of its Pb−C bond. Reaction of tetraethyllead with mercuric acetate resulted in the formation of ethylmercuric acetate (eq 28), which is a water-soluble fungicide but is no longer used as such. Ethylation of group 15 trihalides occurs readily (eq 29) …”
Section: Reactions and Other Uses Of Tetraethylleadmentioning
confidence: 99%
“…of metal, were used to make pesticides in 1958 (Anderson, 1960). Whelen (1959) stated that the overafl yearly value of the alkylmercurials is the order of $100,000,000, and that they have contributed measurably to our agricultural abundance. The organomercurial compounds are firmly established as highly effective industrial and agricultural fungicides which are finding ever increasing use.…”
mentioning
confidence: 99%