1988
DOI: 10.1002/chin.198848228
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ChemInform Abstract: Reaction of Bisdithiophosphonates with p‐Quinones.

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Cited by 3 publications
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“…These compounds seem to be secondary products formed from arylbisdithiophosphonic acid as an initial product via the elimination of hydrogen sulfide and monomeric unit of dithiadiphosphetanes 1 by the effect of acetonitrile as a sulfur acceptor. Indeed, we have previously shown that bisalkyldithiophosphonic acids react with acetonitrile to form cyclic alkyltrithiopyrophosphonates and thioacetamide . On the other hand, anhydrous benzene seems to be the most appropriate inert solvent for successful synthesis of stable bisaryldithiophosphonic acids .…”
Section: Resultsmentioning
confidence: 99%
“…These compounds seem to be secondary products formed from arylbisdithiophosphonic acid as an initial product via the elimination of hydrogen sulfide and monomeric unit of dithiadiphosphetanes 1 by the effect of acetonitrile as a sulfur acceptor. Indeed, we have previously shown that bisalkyldithiophosphonic acids react with acetonitrile to form cyclic alkyltrithiopyrophosphonates and thioacetamide . On the other hand, anhydrous benzene seems to be the most appropriate inert solvent for successful synthesis of stable bisaryldithiophosphonic acids .…”
Section: Resultsmentioning
confidence: 99%
“…[161][162][163][164] The reaction of bis(dithiophosphonic acids) with RCN gives a 1:1 adduct which decomposes to RC(S)-NH2 and cyclic trithiopyrophosphonates 112. The stability of 112 decreases as n increases (Scheme 59). 165 Lithium salts of polyfluorinated alcohols treated with «s-l,3-di-fert-butyl-2,4-dichloro-l,3,2,4-diazadiphosphetidine give rise to the corresponding polyfluoro bis-(alkoxy-bridged) diazadiphosphetidine species 113 (Scheme 60).166…”
Section: Phosphonium Saltsmentioning
confidence: 99%
“…[3][4][5][6][7][8][9]. The reactions of 2,4-dialkyl-or diaryl-1,3-dithia-2,4-diphosphetane-2,4-disulfides with glycols are used to obtain bisdithiophosphonic acids [1][2][3][4][5][6][7][8]. At the same time the reaction of catechol with 2,4-diferrocenyl-1,3-dithia-2,4-diphosphetane-2,4-disulfide results in 1,3,2-dioxaphospholane derivative [10], which is a secondary product formed during the desulfurization of the intermediate phenylene bisdithiophosphonic acid.…”
mentioning
confidence: 99%
“…Bisdithiophosphonic acids containing two α,ω-dithiophosphoryl groups [1,2] are of interest as the podand-like compounds in substitution, intercalation, addition, and complexation reactions to create on their basis antioxidants for polymers, antioxidant additives for lubricating oils, corrosion inhibitors, extractants of metal ions, etc. [3][4][5][6][7][8][9].…”
mentioning
confidence: 99%