Radical and Ionic Reactions of Tetraethylthiuram Disulfide
Keyword(s):
Abstract 1. Investigation of the process of radical dissociation of TETD in carbon tetrachloride indicates that at 145° thiuram radicals are formed which react with the carbon tetrachloride to form (C2H5)2N—C‖S—SCl and CS2. 2. A quantitative determination of the products of the base-influenced dissociation of TETD was carried out. A kinetic investigation of this reaction, in which initiator (K2S2O3) and inhibitor (PBNA) were shown to have no velocity effect whatever, indicates that the process is an ionic one. 3. It is shown that in the reaction of TETD with diethylamine, one of the reaction products appears to be diethylammonium diethyldithiocarbamate.
1953 ◽
Vol 26
(1)
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pp. 251-256
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2010 ◽
Vol 78
(8)
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pp. 631-643
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2002 ◽
Vol 50
(3)
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pp. 401-405
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1936 ◽
Vol 8
(4)
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pp. 260-263
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1992 ◽
Vol 206
(2)
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pp. 353-358
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1945 ◽
Vol 17
(9)
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pp. 563-564
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2008 ◽
Vol 26
(1)
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pp. 78-82
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