Reactions of 1,1,3,3-tetrakis(dimethylamino)-1λ5,3λ5-diphosphete with diphenylchlorophosphane and methyl iodide
✍ Scribed by Fred Rosche; Gernot Heckmann; Ekkehard Fluck; Bernhard Neumüller
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 618 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1042-7163
No coin nor oath required. For personal study only.
✦ Synopsis
1, I , 3,3-Tetrakis (dimethylamino)-I k5,3k5-diphosphete, 1, reacts with diphenylchlorophosphane to yield I , I , 33tetrakis (dimethylamino)-4-diphenylphos-phany1-I,2-dihydro-3k5-[1,3]diphosphetium chloride, 2, or, depending on the reaction conditions, the isomer compound 3. The cation of 2 is deprotonated by LiN[Si(CH.JJ2 to give the diphenylphosphanyl-substituted derivative of 1, i.e., compound 4. Methyl iodide adds to 1 to form I , 1,3,3]diphosphetium iodide, 6. Deprotonation of 6 with n-butyllithium leads to the monomethyl derivative of 1, i.e., compound 7. Physical properties, N M R spectra, and mass spectra of compounds 2-4, 6, and 7 are described. The results of the X-ray structural analysis of 6 are reported and discussed.
📜 SIMILAR VOLUMES
I ,I ,3,3 -Tetrakis(dimethylamin0) -1 h5,3h5diphosphete, 1, reacts with cyanoformic acid methyl ester to form two isomers of the title compound 2. Properties, NMR, mass, and IR spectra of 2, as well as the molecular and crystal structure of the E isomer of 2, are described and discussed.
From 2-Phosphino-2H-phosphirene to 1-Phosphino-1H-phosphirene, 1λ 5 ,2λ 3 -Diphosphete, and 1,2-Dihydro-1λ 3 ,2λ 3 -diphosphete: An Experimental and Theoretical Study. -The formation of the title compounds from diazomethane derivative (I) and t-butylphosphaalkyne (II) via title intermediate (III) i