INTRAMOLECULAR O-H...O-NI AND N-H...O-NI HYDROGEN-BONDING IN NICKEL DIPHENYLPHOSPHINOENOLATE PHENYL COMPLEXES - ROLE IN CATALYTIC ETHENE OLIGOMERIZATION - CRYSTAL-STRUCTURE OF [NIPH(PH2PHC...C(...O)(O-C6H4NHPH))(PPH3)]
P. Braunstein et al., INTRAMOLECULAR O-H...O-NI AND N-H...O-NI HYDROGEN-BONDING IN NICKEL DIPHENYLPHOSPHINOENOLATE PHENYL COMPLEXES - ROLE IN CATALYTIC ETHENE OLIGOMERIZATION - CRYSTAL-STRUCTURE OF [NIPH(PH2PHC...C(...O)(O-C6H4NHPH))(PPH3)], Journal of the Chemical Society, Chemical Communications, (19), 1994, pp. 2203-2204
Nickel diphenylphosphinoenolate complexes are prepared from ortho-HX-s
ubstituted phenacylidenetriphenylphosphoranes (X = 0, NMe, NPh) which
display strong intramolecular hydrogen bonding between the enolate oxy
gen and the H-X function; this feature dramatically influences the mol
ecular mass distribution of the oligomers obtained by catalytic oligom
erisation of ethene.