2,4-N,N′-Bis(dialkylamido)-2,4-dithioxo-1,3,2λ5,4λ5-dithiadiphosphetanes
Dialkylamide derivatives of the monometadithioxaphosphoric acid stabilised by pyridine as a donor, i.e. [(C5H5N)PS2NR2], readily react with AlCl3. The elimination of the donor and formation of the adduct C5H5N·AlCl3 liberates the unstable σ3λ5‐phosphoranes (PS2NR2). The latter are stabilised by [2+2...
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Published in | European journal of inorganic chemistry Vol. 2004; no. 19; pp. 3842 - 3845 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY-VCH Verlag
01.10.2004
WILEY‐VCH Verlag |
Subjects | |
Online Access | Get full text |
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Summary: | Dialkylamide derivatives of the monometadithioxaphosphoric acid stabilised by pyridine as a donor, i.e. [(C5H5N)PS2NR2], readily react with AlCl3. The elimination of the donor and formation of the adduct C5H5N·AlCl3 liberates the unstable σ3λ5‐phosphoranes (PS2NR2). The latter are stabilised by [2+2] “cycloaddition‐dimerization” leading to the title compounds [PS2NR2]2 in nearly quantitative yields. The synthesis and characterisation of two compounds possessing NR2 substituents of very different basicities clearly demonstrate the generalisation of such a procedure as an easy way of accessing further derivatives in this class. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004) |
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Bibliography: | istex:15231A054F78AFB61F015A2505591E0B798CEFD7 ArticleID:EJIC200400343 ark:/67375/WNG-HF8TMD3H-M |
ISSN: | 1434-1948 1099-0682 |
DOI: | 10.1002/ejic.200400343 |