
TY  - JOUR
A1  - Brophy, JJ 
A1  - Gallagher, MJ 
T1  - Phosphonium salts. I. The alkaline hydrolysis of some bis-phosphonium salts
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1969
VL  - 22
IS  - 7
SP  - 1385
EP  - 1398
KW  - 
UR  - https://doi.org/10.1071/CH9691385 
N2  - Ethane- and ethene-1,2-bisphosphonium salts are cleaved by alkali into a phosphine and a phosphine oxide with loss of the two-carbon bridge. When the phosphorus atom carries benzyl substituents, loss of the benzyl groups is competitive with loss of the bridge.     Based on a kinetic study, a synchronous mechanism, analogous to the alkaline hydrolysis of acyclic monophosphonium salts, is proposed to account for the fragmentation.     With 6-membered 1,4-diphosphonio heterocyclic salts the nature of the products is dependent on whether alkali or phosphonium salt is present in excess. With an excess of alkali a synchronous mechanism again appears to operate, while with an excess of salt the reaction proceeds stepwise and without loss of the bridge. A partial explanation of these facts is advanced in terms of non-bonded interactions in the intermediate phosphoranes.     The synchronous reaction appears to be favoured by coplanarity of the P-C-C-P system. 
ER  -

