2006
DOI: 10.1080/00958970500537788
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Reaction of 1-benzoylethylpyridinium-4-aldoxime chloride with aquapentacyanoferrate(II)

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Cited by 9 publications
(22 citation statements)
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“…The enhanced interest in the low-spin aquapentacyanoruthenate(II) ion, i.e., [Ru(CN) 5 H 2 O] 3− , lies in the fact that it represent models for biological systems and has been used for investigation of specific binding groups in amino acids [15] and peptides. It can also coordinate typically with only one additional incoming or substituting ligand, easily losing a coordinated water molecule and subsequently forming highly stable nitrogen heterocyclic substituted complexes.…”
Section: H 2 O]mentioning
confidence: 99%
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“…The enhanced interest in the low-spin aquapentacyanoruthenate(II) ion, i.e., [Ru(CN) 5 H 2 O] 3− , lies in the fact that it represent models for biological systems and has been used for investigation of specific binding groups in amino acids [15] and peptides. It can also coordinate typically with only one additional incoming or substituting ligand, easily losing a coordinated water molecule and subsequently forming highly stable nitrogen heterocyclic substituted complexes.…”
Section: H 2 O]mentioning
confidence: 99%
“…The rates of substitution for the low-spin [Ru(CN) 5 3− ion with two naphthalenesubstituted ligands, viz. nitroso-R-salt and α-nitroso-β-naphthol (further designated as NRS and αNβN, respectively, throughout the text), and the results are compared with previously reported systems on Ru(II) [13].…”
Section: H 2 O]mentioning
confidence: 99%
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