| Abstract
| - Synthetically useful dichlorotriphosphazanes, e.g., I and II, form as three diastereomers; however, in polar solvents such as acetonitrile, association with solvent occurs which leads to novel “averaging” of the three diastereomers as shown by 31P NMR spectral data.
- The new skeletally stabilized dichlorotriphosphazanes C6H4N2(PhPCl)2PPh (5) and C6H4N2(MePCl)2PMe (6) havebeen prepared from reactions between PhPCl2 or MePCl2 and 1,2-(NH2)2C6H4 or 1,2-(Me3SiNH)2C6H4, respectively.Reaction of PhPCl2 with the phosphadiazole C2H4(Me3SiN)2PPh yields triphosphazane C2H4N2(PhPCl)2PPh (8).Compounds 5, 6, and 8 form as mixtures of three diastereomers; characterization is based on spectral data andderivatization of 5 and 8 to the amino and thio(amino) triphosphazanes C6H4N2[PhP(NHiPr)]2PPh (7) andC2H4N2[PhP(S)NEt2]2PPh (10). The 31P NMR spectra of 5 and 6 in solution have been measured as a functionof temperature and solvent donor and dielectric strength. The solution properties of the dichlorotriphosphazanesand the implications of these on subsequent reaction chemistry are discussed.
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