Mécanisme de formation et de transformation des spirophosphoranes—II
作者:R. Burgada、H. Germa、M. Willson
DOI:10.1016/0040-4020(73)80085-7
日期:1973.1
The rearrangement reactions of compounds (X and Y = 0 or Me) during synthesis or during thermolysis are described. They are discussed in terms of relative stabilities of the patterns QX Y— in phospholanes rings or as chains between two phosphorus atoms and in terms of thermodynamically or kinetically controlled processes.
Scherer,O.J.; Wokulat,J., Zeitschrift fur Naturforschung. Teil B. Anorganische Chemie, organische Chemie, Biochemie, Biophysik, Biologie, 1967, vol. 22, p. 474 - 477
作者:Scherer,O.J.、Wokulat,J.
DOI:——
日期:——
Synthesis, structure and relative hydrolytic stability of cis-[PtCl2L] and cis-[W(CO)4L] where L is the bidentate triaminophosphine ligand [MeNCH2CH2N(Me)PN(Me)CH2]2
作者:John Powell、Alan Lough、Michael Raso
DOI:10.1039/dt9940001571
日期:——
trans-[PtCl2-(µ-L)}2] and with [W(CO)4(nbd)](nbd = norbornadiene) to give cis-[W(CO)4L] and [W(CO)4(µ-L)}n](n= 2–4). The ligand L and [W(CO)4L] are readily hydrolysed to give HPO32–, 2MeNHCH2CH2NH2Me+ and MeNHCH2CH2NHMe. In contrast the complex [PtCl2L] is considerably more resistant to ligand hydrolysis. The molecularstructures of cis-[PtCl2L], cis-[W(CO)4L] and [W(CO)4(MeNHCH2CH2NHMe)]a hydrolysis