Publications by authors named "Jeanette A Adjei"

Article Synopsis
  • Dimethyl 2-vinylcyclopropane-1,1-dicarboxylate was reacted with primary or secondary phosphines using light (photolytic conditions), without needing a radical initiator.
  • The process produced moisture and air-stable tertiary phosphines that were then modified, yielding oils with a 27%-73% yield.
  • Control experiments suggest that the hydrophosphination likely occurs via a radical mechanism activated by UV light.
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The coordination chemistry of the title ligands with Mo metal centers was investigated. Thus, the synthesis and characterization (NMR, X-ray diffraction) of four mononuclear formally Mo(6+) complexes of ()-1--2-(4',4'-dimethyl-2'-oxazolin-2'-yl)-eth-1-en-1-ates (L: R = -Ph, -Ph--NO, -Ph--OMe and --Bu), derived from the part enols (LH), is described. The resulting air-stable MoOL complexes (-) exist, as shown by single-crystal X-ray diffraction experiments, in the -dioxido--κ-,-L conformation in the solid state for all four examples.

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The synthesis and characterisation (UV-Vis, IR, X-ray diffraction, ) of a series of Ni(ii) complexes derived from both known and novel 2-acylmethyl-2-oxazolines (2a-g: , ()-1-R-2-(4,4'-dimethyl-2'-oxazolin-2'-yl)eth-1-en-1-ol; R = -Ph, -2-furanyl, --NO-Ph, --Bu, -2-thiofuranyl, -NC-Ph, -CF) is reported. These Ni materials (3a-g) represent the first group 10 metal complexes of this ligand class. All derivatives reported are paramagnetic ( = 1) compounds of formulae Ni(κ-,-L) where L represents an enolate of structure ()-1-R-2-(4',4'-dimethyl-2'-oxazolin-2'-yl)eth-1-en-1-ate formed proton loss from 2.

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