64487-59-8Relevant articles and documents
On the scent of asymmetrical dandelion dendrimers Part I. Starting materials from the regiospecific aminolysis of N3P3Cl6 by amino-alcohols
Sournies, Francois,Zai, Karine,Vercruysse, Karine,Marie-Christine Labarre,Labarre, Jean-Francois
, p. 19 - 26 (1997)
Starting materials for the design of asymmetrical dandelion dendrimers were synthesized upon the preliminary fixation of suitable amino-alcohols on hexachlorocyclotriphosphazene, N3P3Cl6, as 'blockers'. Further linkage of diamines on solid supports leads to the expected asymmetrical moieties.
New organofunctional cyclophosphazene derivatives
Allen, Christopher W.,Hayes, Robert F.,Myer, Charles N.,Freund, Amy S.,Kearney, Marie E.
, p. 79 - 82 (2007/10/03)
The rational design, synthesis and polymerization of the methacrylphosphazenes N3P3Cl5O(CHR)x(CHR′) yOC(O)CMe=CH2 (x=y=1,2, R=R′=H; x=1, R=Me, y=1, R′=H; x=1, R=H, y=1, R′=Me) is reported. Another new type of alkenyloxy derivative is prepared from 5-nonbornene-2-methoxide and N3P3Cl5. The preparation of spirocyclic derivatives with methacrylate or protected hydroxyl groups is reported Various functionalized ferrocene derivatives of the cyclophosphazenes have been prepared with particular attention being paid to the synthesis and electrochemical characterization of the N3P3Cl6-n(NMeCH2C5H 4FeC5H5)n(n=1,2,3,4) series.
