dc.contributor |
Казанский федеральный университет |
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dc.contributor.author |
Gafurov Zufar Nafigullovich |
|
dc.contributor.author |
Bekmuhamedov Giyaz Eduardovich |
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dc.contributor.author |
Kagilev Aleksey Aleksandrovich |
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dc.contributor.author |
Kantyukov Artyom Olegovich |
|
dc.contributor.author |
Sakhapov Ilyas Faridovich |
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dc.contributor.author |
Mikhaylov Ilya Konstantinovich |
|
dc.contributor.author |
Khayarov Khasan Rafaelevich |
|
dc.contributor.author |
Zaripov Ruslan Bulatovich |
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dc.contributor.author |
Islamov Daut Rinatovich |
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dc.contributor.author |
Usachev Konstantin Sergeevich |
|
dc.contributor.author |
Luconi Lapo |
|
dc.contributor.author |
Rossin Andrea |
|
dc.contributor.author |
Dzhambastiani Dzhuliano |
|
dc.contributor.author |
Yakhvarov Dmitry Grigorevich |
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dc.date.accessioned |
2020-03-16T11:16:13Z |
|
dc.date.available |
2020-03-16T11:16:13Z |
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dc.date.issued |
2020 |
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dc.identifier.citation |
Gafurov Z.N. Unsymmetrical pyrazole-based PCN pincer NiII halides: Reactivity and catalytic activity in ethylene oligomerization / Z.N. Gafurov, G.E. Bekmukhamedov, A.A. Kagilev, A.O. Kantyukov, I.F. Sakhapov, I.K. Mikhailov, K.R. Khayarov, R.B. Zaripov, D.R. Islamov, K.S. Usachev, L. Luconi, A. Rossin, G. Giambastiani, D.G. Yakhvarov // Journal of Organometallic Chemistry. - 2020. - V. 912. - P. 121163. https://doi.org/10.1016/j.jorganchem.2020.121163. |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/158217 |
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dc.description.abstract |
The reactivity of unsymmetrical pyrazole-based PCN pincer Ni(II) halides has been tested in the presence of copper(II) halides as an oxidizing agent as well as with NaBH4 and LiAlH4 as a hydride source. While the reaction with CuX2 resulted into the generation of metastable PCN pincer Ni(III) species, the treatment of (tBuPCN)NiCl with NaBH4 led to the preparation and isolation of the borohydride complex (tBuPCN)Ni(BH4). Attempts to isolate nickel-hydride species upon treatment of (tBuPCN)NiCl with either NaBH4 or LiAlH4 invariably led to the formation of free PCN(H) ligand and metallic Ni(0) nanoparticles after an in situ reductive elimination from the (metastable) hydride derivative (tBuPCN)NiH. Finally, the halide complexes (pre-activated by MMAO) have been tested as homogeneous catalysts in ethylene oligomerization showing moderate activity (~ 14 103 molC2H4,molNi 1,h1) with the formation of evennumbered olefins (mainly C4eC10 fractions) as products. |
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dc.language.iso |
en |
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dc.relation.ispartofseries |
JOURNAL OF ORGANOMETALLIC CHEMISTRY |
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dc.rights |
открытый доступ |
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dc.subject |
Unsymmetrical ligands; PCN pincer ligands; Nickel complexes; Nickel borohydrides; Ethylene oligomerization |
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dc.subject.other |
Химия |
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dc.title |
Unsymmetrical pyrazole-based PCN pincer NiII halides: Reactivity and catalytic activity in ethylene oligomerization |
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dc.type |
Article |
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dc.contributor.org |
Химический институт им. А.М. Бутлерова |
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dc.description.pages |
121163-121163 |
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dc.relation.ispartofseries-volume |
912 |
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dc.pub-id |
226252 |
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dc.identifier.doi |
10.1016/j.jorganchem.2020.121163 |
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