作者: Stephan Enthaler , Chika I. Someya , Elisabeth Irran
DOI: 10.1016/J.INOCHE.2014.12.017
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摘要: Abstract The coordination chemistry of the ligand precursor 1-benzoyl-4,5-dihydro-3,5-bis(trifluoromethyl)-1H-pyrazol-5-ol (1a) to iron(II) acetate was studied. In dependence added co-ligand different complex geometries were observed. case 4-dimethylaminopyridine (DMAP) as an octahedral found with O,N,O′-coordination tridentate (1a-2H), in which is planar, oxygen donors are trans each other, and nitrogen donor a cis position. other sites on iron center occupied by DMAP ligands. contrast that, triphenylphosphane oxidation process took place, revealed iron(III) comparable geometry for (O,N,O′-coordination, 1a-2H) demonstrating usefulness 1a-2H stabilize states. additional one oxide ethoxide Interestingly, ligands act bridging form bimetallic complex.