Reactions of activated organonickel σ-complexes with elemental (white) phosphorus
作者:D. G. Yakhvarov、S. V. Kvashennikova、O. G. Sinyashin
DOI:10.1007/s11172-013-0358-9
日期:2013.11
toward elemental (white) phosphorus was studied. For the reaction to occur, the complexes must be activated by removal of the bromide anion from the coordination sphere of nickel. This can be achieved either in the presence of halogen scavengers or by electrochemical reduction. The arylphosphinic acids ArP(O)(OH)H formed by hydrolysis of organic nickel phosphides are the major reaction products of the
[Ar = Ph, 2,4,6-trimethylphenyl (Mes), 9-anthryl (Ant)] leads to the formation of binuclear nickel(II) complexes with bridging ArP(H)O2− ligands. Crystal structures of the binuclear complexes [Ni2(μ-O2P(H)Ar)2(bpy)4]Br2 (Ar = Ph, Mes, Ant) have been determined. In each structure, the metal ions have distorted octahedral coordination and are doubly bridged by two arylphosphinato ligands. Magnetic susceptibility
ACTIVE ENERGY RADIATION HARDENABLE WATER BASE INK COMPOSITION AND UTILIZING THE SAME, METHOD OF INKJET RECORDING, INK CARTRIDGE, RECORDING UNIT AND INKJET RECORDING APPARATUS
申请人:CANON KABUSHIKI KAISHA
公开号:EP1734088A1
公开(公告)日:2006-12-20
To provide an active energy ray curable aqueous ink composition exhibiting excellent curing performance by including a water-soluble polymerizable substance with high reactivity and a water-soluble polymerization initiator having high initiation efficiency; and an inkjet recording method, ink cartridge, recording unit, and inkjet recording apparatus all using the active energy ray curable aqueous ink composition. The active energy ray curable aqueous ink composition includes at least water; a polymerizable substance which undergoes radical polymerization by active energy rays; and a polymerization initiator which generates radicals by active energy rays, in which the polymerizable substance is a water-soluble compound having 2 to 6 (meth)acrylic groups; and the polymerization initiator is a water-soluble acylphosphine oxide compound.
P–C bond formation via P–H addition of a fluoroaryl phosphinic acid to ketones
作者:Andreas Orthaber、Jörg H. Albering、Ferdinand Belaj、Rudolf Pietschnig
DOI:10.1016/j.jfluchem.2010.07.008
日期:2010.10
The synthesis, structure and reactivity of the fluoroaryl phosphinic acid HF(4)C(6)-P(O)HOH is reported and compared to a sterically comparable yet non-fluorinated analog with similar size. The fluoroaryl phosphinic acid undergoes reversible P-H addition to the carbonyl functionality of ketones under formation of a P-C bond which is retained in the resulting alpha-hydroxy phosphinic acid. The latter shows an extended 2D hydrogen bonded network in the solid state. (C) 2010 Elsevier B.V. All rights reserved.
Tracking of the formation of binuclear nickel complexes of [Ni2(µ-O2PR1R2)2(bpy)4]Br2 type by ESI and MALDI mass spectrometry
作者:Aliya F. Khusnuriyalova、Vasily M. Babaev、Ildar Kh. Rizvanov、Kirill E. Metlushka、Vladimir A. Alfonsov、Oleg G. Sinyashin、Dmitry G. Yakhvarov
DOI:10.1016/j.poly.2017.02.005
日期:2017.5
The formation of binuclear nickel complexes of type [Ni-2(mu-(O2PRR2)-R-1)(2)(bpy)(4)]Br-2, where R-1 = H, R-2 = phenyl (Ph), 2,4,6-trimethylphenyl (Mes), 2,4,6-triisopropylphenyl (Tipp) or (RR2)-R-1 = -OCH2CH(Et) NHCH(Ph)-; bpy = 2,2'-bipyridine, in solution and their fragmentation behavior have been investigated by ESI and MALDI mass spectrometry. It was found that binuclear cationic fragments [Ni-2(mu-(O2PRR2)-R-1)(2)(bpy)(2)Br](+) are characteristic ions displaying the formation of binuclear nickel(II) complexes in solution. (C) 2017 Elsevier Ltd. All rights reserved.