Structure and intramolecular mobility of N-(thio)phosphoryl(thio)amides: IX. Structure of N-(diisopropoxyphosphoryl)methylthioamide in solutions by H-1, C-13 and P-31 NMR spectroscopy
Fk. Karataeva, Structure and intramolecular mobility of N-(thio)phosphoryl(thio)amides: IX. Structure of N-(diisopropoxyphosphoryl)methylthioamide in solutions by H-1, C-13 and P-31 NMR spectroscopy, RUSS J G CH, 70(7), 2000, pp. 1062-1067
The structure of N-(diisopropoxyphosphoryl)methylthioamide in CCl4, CD3CN,
CD2Cl2, C6D5CD3, and (CD3)(2)SO solutions was studied by H-1, C-13, and P-3
1 NMR spectroscopy. A tautomeric equilibrium that includes the amide (with
trans and cis arrangement of the substituents), thioimide, acylotropic, and
phosphorylotropic forms is found.