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Synthesis and Structural Studies of Two New Base Adducts of Bis(2,4‐pentanedionato)cobalt( II )
Author(s) -
Tanase Stefania,
Bouwman Elisabeth,
Reedijk Jan,
Driessen Willem L.,
Ferbinteanu Marilena,
Huber Martina,
Mills Allison M.,
Spek Anthony L.
Publication year - 2004
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.200300708
Subject(s) - chemistry , adduct , crystallography , lone pair , hydrogen bond , cobalt , octahedron , denticity , ligand (biochemistry) , crystal structure , electron paramagnetic resonance , monomer , stereochemistry , inorganic chemistry , molecule , organic chemistry , nuclear magnetic resonance , biochemistry , physics , receptor , polymer
The syntheses, spectroscopic properties and crystal structures of two new base adducts of bis(2,4‐pentanedionato)cobalt( II ) with 3,5‐dimethylpyrazole (Hdmpz) ( 1 ) and dimethylethanolamine (Hdmea) ( 2 ) are described. The crystal structures of both compounds contain monomeric Co II complexes with cis ‐distorted octahedral environments, even for the monodentate Hdmpz ligand which is quite unique. These mononuclear complexes are linked by hydrogen bonds between the anionic 2,4‐pentanedionato groups and the neutral Hdmpz or Hdmea ligands. The low‐temperature polycrystalline‐powder EPR spectra display unresolved metal hyperfine coupling. The g values are anisotropic in both cases; the anisotropy is larger for the Hdmea adduct. Interesting insights into the coordination effects were gained with the help of electron‐density descriptors (Laplacian of density and Natural Bond Orbitals). This revealed a slight deviation of the coordinating lone pairs of the pentanedionato ligands from the Co−O axis, as well as a nonstandard hybrid composition. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)

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