Abstract
GRAPHICAL ABSTRACTPhospholenes containing one or two methyl groups at the 3 and 4 positions on the heterocyclic ring and bis(trimethylsilyl)amino groups on phosphorus were prepared by treating 1-bromo or 1-chlorophospholenes with lithium bis(trimethylsilyl)amide. Several P(V) derivatives of these 2-and 3-phospholenes were prepared by oxidation with hexachloroethane. The chloro groups in the resulting P-chloro-N-trimethylsilyl derivatives were subsequently replaced by phenoxy groups to afford P-phenoxy-N-trimethylsilyl substituted ring compounds. The P-phenoxy-N-trimethylsilyl derivative was hydrolyzed to the corresponding P-amino phosphine oxide; treated with trifluoroethanol to form a new trispirocyclic phosphazene; and copolymerized with Me2P(OPh) = NSiMe3 to give a new phosphazene copolymer containing the phospholene ring (Mw = 3.8 × 104 Da). These new compounds were characterized by 1H, 13C, and 31P NMR spectroscopy. The spirocyclic phosphazene was also characterized by X-ray crystallography.
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