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A new β‐ketoimine ligand was prepared through traditional condensation of 2‐acetylcyclohexanone with 1‐naphthylamine. Consequently, the new moisture‐ and air‐stable bis(β‐ketoamino)nickel(II) complex Ni[2‐CH3C(O)C6H8(NAr)]2 (Ar = naphthyl) was synthesized and characterized. The solid‐state structures of the ligand and complex have been determined by single‐crystal X‐ray diffraction. Additionally, the new complex is a highly active catalyst precursor for polymerization of norbornene in combination with methylaluminoxane. Copyright © 2005 John Wiley & Sons, Ltd. 相似文献
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The applicability of silica gels for the application in solid-phase extraction was tested. Silica was modified with ketoimine
groups. Surface characteristics of the modified silica were determined by elemental analysis, NMR spectra of solid phases
(29Si CP MAS NMR), analysis of pore size distribution of the silica support, and nitrogen adsorption-desorption. Newly proposed
sorbents with ketoimine groups were applied in the preconcentration of trace amounts of the Cu (II) ions from lake water,
post-industrial water, and demineralized water unburdened back to the lake.
Presented at the 34th International Conference of the Slovak Society of Chemical Engineering, Tatranské Matliare, 21–25 May
2007. 相似文献
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《Journal of Coordination Chemistry》2012,65(1-3):197-207
Bimetallic and trimetallic complexes of stoichiometry [M(acacen)M′Y2], [M(sacacen)M′Y2], and {[M(acacen)]2M′Y2} have been prepared by reaction of the appropriate square-planar Schiff base metal complex with various secondary metal salts in toluene and/or absolute ethanol. Systems which are reported here include those where M = Cu(II); M′ = Cu(II), Ni(II), Co(II), Mn(lI) and Zn(II); Y? = Cl?, Br?, and NO3 ?. Trinuclear complexes have been isolated only for {[Cu(acacen)]2M′(NO3)2} where M′ = Cu(lI) or Mn(II); binuclear complexes result from all other combinations. The geometry of the chelated Cu(II) ion is square-planar in the bimetallic complexes and possibly square-pyramidal in the trimetallic compounds, while that of the secondary metal ion depends on the coordination preference of M′, the nature of Y? and whether the bridging donor atoms are oxygen or sulfur. Probable structures of the new polynuclear complexes have been deduced from spectral, conductivity and magnetic measurements. 相似文献
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1-Phenyl-1,3-butandione benzidine diketoimine 2a (C32H28N2O2,Mr=472.56) was synthesized in high yield by the reaction of 1-phenyl-1,3-butandione with benzidine in absolute ethanol,and determined by X-ray structure analysis. It crystallizes in the orthorhombic system,space group P21/c with a=7.9839(16),b=12.910(3),c=12.358(3),α=90.00,β=93.71(3),γ= 90.00°,V=1271.1(4)3,Z=2,Dc=1.235 g/cm3,μ=0.077 mm-1,F(000)=500,the final R= 0.0717 and wR=0.1187. It presents a linear centrosymmetric framework constituted by a linkage of benzidine as a bridge and two terminal 1-phenyl-1,3-butanedione moieties. 相似文献
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Sean H. Majer Joseph M. Tanski 《Acta Crystallographica. Section C, Structural Chemistry》2015,71(3):181-184
A novel activated prochiral ketoimine, (E)‐acetophenone O‐diphenylphosphoryl oxime, C20H18NO2P, with an electron‐withdrawing substituent on the imine N atom similar to other prochiral ketoimines, has been synthesized and the X‐ray crystal stucture determined. The molecules pack together in the solid state via weak intermolecular C—H...O interactions and both face‐to‐face and edge‐to‐face π‐stacking interactions. 相似文献
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