1961
DOI: 10.1021/ja01484a002
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The Electronic Structures of Tetrahedral Cobalt(II) Complexes

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Cited by 505 publications
(138 citation statements)
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“…Thus, in the presence of a large excess of base (Co:Si: OH = 2.5:4:50), the Co(OH)2 initially present reacted further to produce, in part, deep blue solutions of [Co(OH)4] 2-, whose electronic spectrum [Umax = 535(sh), 590, 620 nm] was close to that published by Cotton et al (1961). A second product was deep blue Na2CoSiO4; no NaCo-smectite was formed.…”
Section: Clay Synthesis In the Presence Of Sodiumsupporting
confidence: 72%
“…Thus, in the presence of a large excess of base (Co:Si: OH = 2.5:4:50), the Co(OH)2 initially present reacted further to produce, in part, deep blue solutions of [Co(OH)4] 2-, whose electronic spectrum [Umax = 535(sh), 590, 620 nm] was close to that published by Cotton et al (1961). A second product was deep blue Na2CoSiO4; no NaCo-smectite was formed.…”
Section: Clay Synthesis In the Presence Of Sodiumsupporting
confidence: 72%
“…The spectrum of the N,N'dimethylurea example is similar to those of (N-methylurea),]CI, to be isostructural with the oxygen bonded cobalt compound. Slight differences in the spectrum of a given complex with change of anion may be attributed to solid state effects (21,22). Unfortunately, the infrared spectra of these organic ligands have not yet been ass~gned to permit bands other than the carbonyl stretching and N-H stretching frequencies to be considered unambiguously.…”
Section: Table 11mentioning
confidence: 99%
“…(Mn+) + En+ (13) The O.S.S.E. term varies, of course, from ion to ion depending on the el~c tronic configuration and Dq of the particular ion.…”
Section: Summary Remarksmentioning
confidence: 99%