Cyclodiphosphazane

From Wikipedia, the free encyclopedia

Cyclodiphosphazanes are saturated four membered P2N2 ring systems and one of the major classes of cyclic phosphazene compounds.[1] Bis(chloro)cyclodiphosphazanes, (cis-[ClP(μ-NR)]2) are important starting compounds for synthesizing a variety of cyclodiphosphazane derivatives by nucleophilic substitution reactions; are prepared by reaction of phosphorus trichloride (PCl3) with a primary amine (RNH2) or amine hydrochlorides (RNH3Cl).[2]

Organic substituents on nitrogen play an important role in formation of cyclic phosphazane compounds.[3] The cyclic tetramers and trimer are formed with methyl and ethyl substituents on nitrogen, whereas formation of cyclic dimers (cis-[ClP(μ-NR)]2) have been observed exclusively with more sterically demanding primary amines such as tert-butylamine and aniline.[4]

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