Oxidation Reactivity of Bis(μ-oxo) Dinickel(III) Complexes: Arene Hydroxylation of the Supporting Ligand

In the nick(el) of time: Bis(μ-oxo) dinickel(III) complexes 2 (see scheme), generated in the reaction of 1 with H₂O₂, are capable of hydroxylating the xylyl linker of the supporting ligand to give 3. Kinetic studies reveal that hydroxylation proceeds by electrophilic aromatic substitution. The lower...

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Veröffentlicht in:Angewandte Chemie (International ed.) 2009-01, Vol.48 (18), p.3304-3307
Hauptverfasser: Honda, Kaoru, Cho, Jaeheung, Matsumoto, Takahiro, Roh, Jungyun, Furutachi, Hideki, Tosha, Takehiko, Kubo, Minoru, Fujinami, Shuhei, Ogura, Takashi, Kitagawa, Teizo, Suzuki, Masatatsu
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container_end_page 3307
container_issue 18
container_start_page 3304
container_title Angewandte Chemie (International ed.)
container_volume 48
creator Honda, Kaoru
Cho, Jaeheung
Matsumoto, Takahiro
Roh, Jungyun
Furutachi, Hideki
Tosha, Takehiko
Kubo, Minoru
Fujinami, Shuhei
Ogura, Takashi
Kitagawa, Teizo
Suzuki, Masatatsu
description In the nick(el) of time: Bis(μ-oxo) dinickel(III) complexes 2 (see scheme), generated in the reaction of 1 with H₂O₂, are capable of hydroxylating the xylyl linker of the supporting ligand to give 3. Kinetic studies reveal that hydroxylation proceeds by electrophilic aromatic substitution. The lower reactivity than the corresponding μ-η²:η²-peroxo dicopper(II) complexes can be attributed to unfavorable entropy effects.
doi_str_mv 10.1002/anie.200900222
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subjects Hydroxylation
kinetics
Ligands
nickel
Nickel - chemistry
Organometallic Compounds - chemistry
oxidation
Oxidation-Reduction
reaction mechanisms
title Oxidation Reactivity of Bis(μ-oxo) Dinickel(III) Complexes: Arene Hydroxylation of the Supporting Ligand
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