dc.contributor.author |
Shtyrlin V. |
|
dc.contributor.author |
Serov N. |
|
dc.contributor.author |
Islamov D. |
|
dc.contributor.author |
Konkin A. |
|
dc.contributor.author |
Bukharov M. |
|
dc.contributor.author |
Gnezdilov O. |
|
dc.contributor.author |
Krivolapov D. |
|
dc.contributor.author |
Kataeva O. |
|
dc.contributor.author |
Nazmutdinova G. |
|
dc.contributor.author |
Wendler F. |
|
dc.date.accessioned |
2018-09-18T20:22:56Z |
|
dc.date.available |
2018-09-18T20:22:56Z |
|
dc.date.issued |
2014 |
|
dc.identifier.issn |
1477-9226 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/139296 |
|
dc.description.abstract |
Ionic liquid (1-ethyl-3-methylimidazolium acetate, [C2C 1im][AcO])-copper(ii) diacetate monohydrate-water-air (O2) systems have been investigated by 13C NMR, EPR, spectrophotometry, HPLC, and synthetic chemistry methods at different temperatures. The C-H bond activation of [C2C1im]+ with the formation of the unusual dication 1,1′-diethyl-3,3′-dimethyl-2,2′- biimidazolium ([(C2C1im)2]2+) at 50°C and 1-ethyl-3-methyl-1H-imidazol-2(3H)-one (C2C 1imO) at 50-85°C was revealed. Two new complexes with the above compounds, [(C2C1im)2][Cu(AcO)4] and Cu2(AcO)4(C2C1imO)2, were isolated from the systems and characterized by X-ray structural analysis. Catalytic cycles with the participation of copper(ii) acetate and dioxygen and the production of [(C2C1im)2]2+ and C2C1imO have been proposed. The catalysis presumably includes the formation of the CuII(O2)CuII active centre with μ-η2:η2-peroxide bridging in analogy with tyrosinase and catechol oxidase activity. © 2014 The Royal Society of Chemistry. |
|
dc.relation.ispartofseries |
Dalton Transactions |
|
dc.title |
The C-H bond activation in 1-ethyl-3-methylimidazolium acetate-copper(ii) acetate-water-air (dioxygen) systems |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
2 |
|
dc.relation.ispartofseries-volume |
43 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
799 |
|
dc.source.id |
SCOPUS14779226-2014-43-2-SID84890013282 |
|