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Synthesis of iron(II) dioximates with phosphine derivatives and their investigation by Moessbauer and IR spectroscopy

Journal Article · · Sov. J. Coordinat. Chem.; (United States)
OSTI ID:7007554

Newly synthesized compounds with the general formula (Fe/sup II/(dioxH)/sub 2/L/sub 2/), where dioxH stands for the monodeprotonated anions of dimethylglyoxime (dmgH) diphenylglyoxime (dpgH), 1,2-cyclohexanedione dioxime (nioxH), and ..cap alpha..-furildioxime (furgH), and L stands for n-butyldiphenylphosphine (PBuPh/sub 2/) and di-n-butylphenylphosphine (PBu/sub 2/Ph), have been investigated by Moessbauer and IR spectroscopy. The Moessbauer spectra of all the compounds at 80 and 300/sup 0/K consist of doublets, whose parameters correspond to the low-spin state of iron(II). The replacement of an axial ligand of PPh/sub 3/ by PBuPh/sub 2/ or PBu/sub 2/Ph results in a decreasing the magnitude of the quadrupole splitting by approx. 30%. It has been found that PBuPh/sub 2/ and PBu/sub 2/Ph have stronger sigma-donor and ..pi..-acceptor properties in comparison to PPH/sub 3/. The data from the IR and Moessbauer spectra confirm the existence of cis influence of the ligands in the complexes investigated.

OSTI ID:
7007554
Journal Information:
Sov. J. Coordinat. Chem.; (United States), Journal Name: Sov. J. Coordinat. Chem.; (United States) Vol. 13:5; ISSN SJCCD
Country of Publication:
United States
Language:
English

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