Syntheses of tris(t-butylisocyanide)bis(tri-p-dimethyl- aminophenylphosphine)cobalt(I) and cobalt(II) perchlorates: a reversal of the usual stabilities of cobalt oxidation states
The complexes [Co(CNCMe 3 ) 3 {P(C 6 H 4 NMe 2 -p) 3 } 2 ](ClO 4 ) 2 and [Co(CNCMe 3 ) 3 {P(C 6 H 4 NMe 2 -p) 3 } 2 ]ClO 4 are reported. The Co(II) complex, formed by reaction of excess triarylphos-phine with the alkylisocyanide Co(II) complex, is stable and the favoured product. The Co(I) complex,...
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Published in | Journal of coordination chemistry Vol. 59; no. 12; pp. 1407 - 1411 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
Taylor & Francis Group
05.08.2006
|
Subjects | |
Online Access | Get full text |
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Summary: | The complexes [Co(CNCMe
3
)
3
{P(C
6
H
4
NMe
2
-p)
3
}
2
](ClO
4
)
2
and [Co(CNCMe
3
)
3
{P(C
6
H
4
NMe
2
-p)
3
}
2
]ClO
4
are reported. The Co(II) complex, formed by reaction of excess triarylphos-phine with the alkylisocyanide Co(II) complex, is stable and the favoured product. The Co(I) complex, formed by hydrazine reduction of the Co(II) complex, has limited stability in solution, readily oxidizing to the Co(II) species. Upon prolonged irradiation of the Co(II) complex in acetone, [Co{OP(C
6
H
4
NMe
2
-p)
3
}
4
](ClO
4
)
2
is produced. |
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ISSN: | 0095-8972 1029-0389 |
DOI: | 10.1080/00958970500512708 |