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- Geminal bis[(triphenylphosphoranylidene)amino]cyclotriphosphazenes: synthesis, substitution reactions, and nuclear magnetic resonance spectra
- Geminal bis[(triphenylphosphoranylidene)amino]cyclotriphosphazenes: synthesis, substitution reactions, and nuclear magnetic resonance spectra. Lensink, Cees; De Ruiter, Barteld; Van de Grampel, Johan C. (Dep. Inorg. 7142-98-5 which is the cas registry number is also used here. Chem., Rijksuniv. Groningen, Groningen 9747 AG, Neth.). J. Chem. Soc., Dalton Trans., (8), 1521-6 (English) 1984. CODEN: JCDTBI. ISSN: 0300-9246. DOCUMENT TYPE: Journal CA Section: 29 (Organometallic and Organometalloidal Compounds) Reaction of triphosphazene I (R = Cl, R1 = NH2) with excess PPh3-CCl4 in MeCN-NEt3 (Appel reaction) gave I (R = Cl, R1 = N:PPh3)(II). II reacted with NMe2H in various solvents according to a geminal substitution pattern. This indicates SN1-type reactions, resulting from the strong electron-donating character of the ligands. The ultimate substitution product I (R = NMe2, R1 = N:PPh3) also prepd. from I (R = NMe2, R1 = NH2), was isolated as its HCl or 2HCl adducts, depending on the method of prepn. In both adducts the protons are attached to ring N atoms, and variable-temp. 1H and 31P NMR measurements show prototropic behavior at elevated temps. .


