dc.contributor.author |
Ovcharenko V. |
|
dc.contributor.author |
Kuznetsova O. |
|
dc.contributor.author |
Fursova E. |
|
dc.contributor.author |
Romanenko G. |
|
dc.contributor.author |
Polushkin A. |
|
dc.contributor.author |
Sagdeev R. |
|
dc.date.accessioned |
2018-09-18T20:03:53Z |
|
dc.date.available |
2018-09-18T20:03:53Z |
|
dc.date.issued |
2014 |
|
dc.identifier.issn |
0020-1669 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/136154 |
|
dc.description.abstract |
© 2014 American Chemical Society. The reaction of cobalt(II) pivalate with a spin-labeled Schiff base (HL1) in organic solvents formed trinuclear complex [Co3(Piv)2L1 2L2 2]·Solv (Solv is Me2CO and/or C7H16 and CH3CN) containing both nitroxide L1 and the product of its single-electron reduction, nitrone L2. The formation of [Co3(Piv)2L1 2L2 2] was a consequence of an unusual phenomenon, which we called "redox-induced change in the ligand coordination mode". A reduction of L1 to L2 led to a change in the set of donor atoms and even in the size of the metallocycle. This phenomenon was also found for mononuclear [CrL1 2L2] and [FeL1 2L2]·Me2CO. |
|
dc.relation.ispartofseries |
Inorganic Chemistry |
|
dc.title |
Redox-induced change in the ligand coordination mode |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
19 |
|
dc.relation.ispartofseries-volume |
53 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
10033 |
|
dc.source.id |
SCOPUS00201669-2014-53-19-SID84907831086 |
|