Abstract: Optically sensitized binders which are energetic polyphosphazenes tailored at the molecular level to achieve enhanced absorption of electromagnetic radiation by having attached thereto a chromophore to absorb light and therefore ignite the binder in use.

Abstract: Substituted poly(phosphazene) compounds comprising a combination of units having one or more of the structures (i) to (iii) wherein: the combination comprises R1 and R2; each R1, is independently an optionally substituted alkyl- or alkyl ether-based side chain containing an isocyanate-reactive moiety, an epoxide-reactive moiety, an amine-reactive moiety, a supramolecular noncovalent bonding moiety, or combinations thereof; and each R2 is independently an optionally substituted alkyl- or alkyl ether-based side chain containing nitro, nitramine, nitrate ester, azide, an ammonium compound moiety with energetic counter-ion, or combinations thereof. Methods of making the compounds are also described.

Abstract: Optically sensitised binders which are energetic polyphosphazenes tailored at the molecular level to achieve enhanced absorption of electromagnetic radiation by having attached thereto a chromophore to absorb light and therefore ignite the binder in use.

Abstract: Substituted poly(phosphazene) compounds comprising a combination of units having one or more of the structures (i) to (iii) wherein: the combination comprises R1 and R2; each R1, is independently an optionally substituted alkyl- or alkyl ether-based side chain containing an isocyanate-reactive moiety, an epoxide-reactive moiety, an amine-reactive moiety, a supramolecular noncovalent bonding moiety, or combinations thereof; and each R2 is independently an optionally substituted alkyl- or alkyl ether-based side chain containing nitro, nitramine, nitrate ester, azide, an ammonium compound moiety with energetic counter-ion, or combinations thereof. Methods of making the compounds are also described.

Abstract: The invention describes the synthesis of novel mono-amine and di-amine derivatives of hexa-nitro-hexaazaisohex-awurtzitane (CL-20). The synthesis is effected by the novel use of fluoroacylating compounds to protect the secondary amine groups of acylated precursors to CL-20 against nitrolysis. In so doing the mono-amine and di-amine derivatives of CL-20 are rendered and which in turn may be subsequently utilised as intermediates to generate further novel derivatives with differing physical and chemical properties to the parent compound. Formula (I), wherein:— X?H, and Y?H or NO2.

Abstract: The invention describes the synthesis of novel mono-amine and di-amine derivatives of hexa-nitro-hexaazaisohexawurtzitane (CL-20). The synthesis is affected by the novel use of fluoroacylating compounds to protect the secondary amine groups of acylated precursors to CL-20 against nitrolysis. In so doing the mono-amine and di-amine derivatives of CL-20 are rendered and which in turn may be subsequently utilized as intermediates to generate further novel derivatives with differing physical and chemical properties to the parent compound. Formula (I), wherein: —X?H, and Y?H or NO2.