4431-24-7Relevant articles and documents
A practical method for the generation of organoarsenic nucleophiles towards the construction of a versatile arsenic library
Tanaka, Susumu,Imoto, Hiroaki,Kato, Takuji,Naka, Kensuke
supporting information, p. 7937 - 7940 (2016/06/09)
Nucleophilic arsenic reagents were prepared in situ from a nonvolatile cyclooligoarsine. As-As bond cleavage of the cyclooligoarsine readily proceeded with anion sources. Various kinds of organoarsenic compounds were easily constructed in high yields by selecting anion sources and electrophiles. In comparison with conventional methods of As-C bond formation, a wide variety of organoarsenic compounds were safely and easily synthesized by using this method.
Steric and electronic control of the Arbuzov reaction in transition-metal halides: A 1H and 31P NMR study of the reaction of [CpCo(L L)X]+ complexes (L L = N, P, as chelate ligands; X- = Cl-, Br-, I-, CN-) with P(OCH3)3
Landon, Shayne J.,Brill, Thomas B.
, p. 1266 - 1271 (2008/10/08)
Synthesis of a series of complexes, [CpCo(L L)X]+ (L L = N, P, As chelate ligands; X- = Cl-, Br-, I-, CN-), was undertaken with the goal of characterizing the Michaelis-Arbuzov reaction between these complexes and P(OCH3)3. 1H and 31P NMR results provide support for the previously postulated two-step mechanism involving an initial equilibrium reaction [CpCo(L L)X]+ + P(OCH3)3 ? {CpCo(L L)[P(OCH3)3]}2+ + X- followed by alkylation of X- to produce an organometal-phosphonate complex, {CpCo(L L)[P(OCH3)3]}2+ + X- → {CpCo(L L)[P(O)(OCH3)2]}+ + CH3X. Several of the intermediate phosphite dications were synthesized and characterized. They enable the above reactions to be qualitatively separated. The initial reaction was quenched by sterically bulky chelate ligands. The rate of the overall reaction parallels the electron donor power of the attacking nucleophile (CN- > I- > Br- > Cl-) and also depends on the donor atoms of L L (N > P). Chelate dissociation occurs when L L = As. The results for [CpCo(L L)X]+ and other transition metal-halide complexes are discussed in terms of why the Arbuzov reaction takes place in some of these complexes but not with others.