122888-83-9Relevant academic research and scientific papers
Photochemistry of Functionalized Diphosphiranes
Gouygou, Maryse,Tachon, Christine,Koenig, Max,Dubourg, Antoine,Declercq, Jean-Paul,et al.
, p. 5750 - 5756 (2007/10/02)
The structure of the functionalized trans-diphosphiranes 1a-e, obtained by reaction of halogenocarbenes with the trans-diphosphene is confirmed by X-ray diffraction.The photolysis of 1a-e lead to the functionalized cis- and trans-1,3-diphosphapropenes 2a-e as major products, via the diphosphiranyl 7 and the diphosphapropenyl 8 radical intermediates.The latter are characterized by ESR spectroscopy using the spin-trap method.The trans configuration of 2a is also confirmed by X-ray diffraction.The mechanism of the ring-opening, involving P-P bond rupture, is discussed.
THE CARBENIC INSERTION INTO THE P-P BOND
Koenig, M.,Gouygou, M.,Tachon, C.,Ouatib, R. El,Etemad-Moghadam, G.
, p. 305 - 308 (2007/10/02)
The cycloaddition reactions on Phosphorus Chemistry has allowed a new development of the three membered ring organophosphorus compounds.Starting from functionalized diphosphiranes obtained by action of carbenes on diphosphenes, we have studied their ring opening reactions leading to carbon insertion into P-P bond.
RING-OPENING OF DIPHOSPHIRANES LEADING TO 1,3-DIPHOSPHAALLENE
Gouygou, M.,Tachon, C.,El Quatib, R.,Ramarijaona, O.,Etemad-Moghadam, G.,Koenig, M.
, p. 177 - 178 (2007/10/02)
The 3,3-dihalogeno-1,2-diphosphiranes 1(a-b) and its photochemical isomers, the 2,3-dihalogeno-diphosphapropenes 8(a-b) lead to the 1,3-diphosphaallene 4 by action the methyllithium.The anionic ring opening mechanism appears most likely.
