1964
DOI: 10.1021/ja01069a013
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Isotropic Proton Magnetic Resonance Shifts in π-Bonding Ligands Coordinated to Paramagnetic Nickel(II) and Cobalt(II) Acetylacetonates

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Cited by 66 publications
(11 citation statements)
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“…Nickel(0) species are typically unreactive toward Cl 2 [43], although both Ni(CO) 2 [8]. The wellresolved 1 H spectra result from the favorable electron relaxation time of paramagnetic octahedral Ni II complexes [43,49]. The formulations of 9a-c were confirmed by elemental analysis.…”
Section: Reactivity Of the Ni 0 Complexesmentioning
confidence: 99%
“…Nickel(0) species are typically unreactive toward Cl 2 [43], although both Ni(CO) 2 [8]. The wellresolved 1 H spectra result from the favorable electron relaxation time of paramagnetic octahedral Ni II complexes [43,49]. The formulations of 9a-c were confirmed by elemental analysis.…”
Section: Reactivity Of the Ni 0 Complexesmentioning
confidence: 99%
“…However, a n-spin transfer mechanism was reported to predominate in the 'H nmr isotropic shifts of some octahedral Schiff base Ni(I1) complexes (26)(27)(28)(29). The charge transfer from metal to ligand via a n-mechanism in the divalent tris(2,2'-bipyridine) metal complexes of the first transition metals was also confirmed by Torii and co-workers (30), by Felix et al (31), and by Nakamoto and co-workers (32).…”
mentioning
confidence: 99%
“…A number of reports have been published on the 'H n.m.r. spectra of the complexes Co(acac),L, and Ni(acac),L, where L is pyridine (13), piperidine (13), a-, P-, and y-picolines (13), aryl phosphines, arsines, amines, sulfides, halides, and isonitriles (14), substituted anilines (15), substituted pyridine N-oxides (16,17) and quinoline N-oxides (18). No contact shifts were observed with bromobenzene, tris-otolylphosphine, triphenylarsine, triphenylamine, benzonitrile, and diphenyl sulfide (13).…”
Section: Discussionmentioning
confidence: 99%