Mild and Regioselective Hydroxylation of Methyl Group in Neocuproine: Approach to an N,O-Ligated Cu6 Cage Phenylsilsesquioxane
Alexey N Bilyachenko
1, 2
,
Mikhail M Levitsky
2
,
Lidia S Shulpina
2
,
Elena S. Shubina
2
,
Georgiy B. Shul'pin
4, 5
1
Тип публикации: Journal Article
Дата публикации: 2018-01-08
scimago Q2
wos Q1
БС1
SJR: 0.676
CiteScore: 5.1
Impact factor: 2.9
ISSN: 02767333, 15206041
Organic Chemistry
Inorganic Chemistry
Physical and Theoretical Chemistry
Краткое описание
The self-assembly synthesis of Cu(II)-silsesquioxane involving 2,9-dimethyl-1,10-phenanthroline (neocuproine) as an additional N ligand at copper atoms was performed. The reaction revealed an unprecedented aerobic hydroxylation of only one of the two methyl groups in neocuproine to afford the corresponding geminal diol. The produced derivative of oxidized neocuproine acts as a two-centered N,O ligand in the assembly of the hexacopper cage product [Cu6(Ph5Si5O10)2·(C14H11N2O2)2] (1), coordinating two of the six copper centers in the product. Two siloxanolate ligands [PhSi(O)O]5 in the cis configuration coordinate to the rest of the copper(II) ions. Compound 1 is a highly efficient homogeneous precatalyst in the oxidation of alkanes and alcohols with peroxides.
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Bilyachenko A. N. et al. Mild and Regioselective Hydroxylation of Methyl Group in Neocuproine: Approach to an N,O-Ligated Cu6 Cage Phenylsilsesquioxane // Organometallics. 2018. Vol. 37. No. 2. pp. 168-171.
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Bilyachenko A. N., Levitsky M. M., Khrustalev V. N., Zubavichus Y. V., Shulpina L. S., Shubina E. S., Shul'pin G. B. Mild and Regioselective Hydroxylation of Methyl Group in Neocuproine: Approach to an N,O-Ligated Cu6 Cage Phenylsilsesquioxane // Organometallics. 2018. Vol. 37. No. 2. pp. 168-171.
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TY - JOUR
DO - 10.1021/acs.organomet.7b00845
UR - https://pubs.acs.org/doi/10.1021/acs.organomet.7b00845
TI - Mild and Regioselective Hydroxylation of Methyl Group in Neocuproine: Approach to an N,O-Ligated Cu6 Cage Phenylsilsesquioxane
T2 - Organometallics
AU - Bilyachenko, Alexey N
AU - Levitsky, Mikhail M
AU - Khrustalev, Victor N.
AU - Zubavichus, Yan V.
AU - Shulpina, Lidia S
AU - Shubina, Elena S.
AU - Shul'pin, Georgiy B.
PY - 2018
DA - 2018/01/08
PB - American Chemical Society (ACS)
SP - 168-171
IS - 2
VL - 37
SN - 0276-7333
SN - 1520-6041
ER -
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BibTex (до 50 авторов)
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@article{2018_Bilyachenko,
author = {Alexey N Bilyachenko and Mikhail M Levitsky and Victor N. Khrustalev and Yan V. Zubavichus and Lidia S Shulpina and Elena S. Shubina and Georgiy B. Shul'pin},
title = {Mild and Regioselective Hydroxylation of Methyl Group in Neocuproine: Approach to an N,O-Ligated Cu6 Cage Phenylsilsesquioxane},
journal = {Organometallics},
year = {2018},
volume = {37},
publisher = {American Chemical Society (ACS)},
month = {jan},
url = {https://pubs.acs.org/doi/10.1021/acs.organomet.7b00845},
number = {2},
pages = {168--171},
doi = {10.1021/acs.organomet.7b00845}
}
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MLA
Скопировать
Bilyachenko, Alexey N., et al. “Mild and Regioselective Hydroxylation of Methyl Group in Neocuproine: Approach to an N,O-Ligated Cu6 Cage Phenylsilsesquioxane.” Organometallics, vol. 37, no. 2, Jan. 2018, pp. 168-171. https://pubs.acs.org/doi/10.1021/acs.organomet.7b00845.