Abstract
The reaction of the crowned 1,3-dithiole-2-thiones 1 and 2 with triethyl phosphite leads to the tetrathiafulvalenes 3 and 4, as well as 1,3-dithiole-2-yl phosphonate esters 5 and 6. The structure of the phosphonate 6 was confirmed by a single-crystal X-ray structure analysis. Using deuterated triethylphosphites (P(OCH2CD3)3 7, P(OCD2CH3)3, 8) the intramolecular proton transfer yielding the phosphonates was studied.
Synthese der Phosphonsäureester wird gezeigt, daß das zu deren Bildung notwendige Proton von einer CH2-Gruppe des P(OCH2CH3)3 geliefert wird.
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