10602-62-7Relevant academic research and scientific papers
MASS SPECTROMETRY OF 1-PHENYL-1,2-DIBROMOPROPYLPHOSPHONIC ACID AND ITS METHYL ESTERS
Meyerson, Seymour,Kuhn, Eugene S.,Ramirez, Fausto,Yemul, Shrishailam S.,Marecek, James F.
, p. 2633 - 2642 (2007/10/02)
erythro-1-Phenyl-1,2-dibromopropylphosphonic acid is known to decompose rapidly into the monomeric metaphosphate anion(PO3(1-)), 1-phenyl-1-bromopropene, and bromide ion in protic or aprotic solvents in the presence of a hindered tertiary amine.The present study compares the behavior of this phosphonic acid in solution and in the gas phase.The gas-phase thermolysis of the acid involves mainly the loss of bromine and of the phosphoryl group, -P(O)(OR)(OR') (R=R'=H).The same type of pathway is followed in the ionization/excitation processes ("cationic reactions") that follow from electron impact in mass spectrometry.The thermal and cationic reactions of the monomethyl and dimethyl esters of the phosphoric acids (R=H, R'=CH3 and R=R'=CH3, respectively, in -P(O)(OR)(OR')) are entirely analogous to those of the free dibasic acid.
Reactions of the Monomeric Metaphosphate Anion Generated from Different Sources
Ramirez, Fausto,Marecek, James F.,Yemul, Shrishailam S.
, p. 1345 - 1349 (2007/10/02)
The reactions of 0.2 M acetonitrile solutions of 2,4-dinitrophenyl dihydrogen phosphate and erythro-1-phenyl-1,2-dibromopropylphosphonic acid containing 2 molar equiv of diisopropylethylamine have been studied at 25 deg C by means of 31P NMR spectrometry
