Literature DB >> 28734083

Highly Selective and Efficient Ring Hydroxylation of Alkylbenzenes with Hydrogen Peroxide and an Osmium(VI) Nitrido Catalyst.

Hoi-Ki Kwong1, Po-Kam Lo1, Shek-Man Yiu1, Hajime Hirao1,2, Kai-Chung Lau1, Tai-Chu Lau1.   

Abstract

The OsVI nitrido complex, OsVI (N)(quin)2 (OTs) (1, quin=2-quinaldinate, OTs=tosylate), is a highly selective and efficient catalyst for the ring hydroxylation of alkylbenzenes with H2 O2 at room temperature. Oxidation of various alkylbenzenes occurs with ring/chain oxidation ratios ranging from 96.7/3.3 to 99.9/0.1, and total product yields from 93 % to 98 %. Moreover, turnover numbers up to 6360, 5670, and 3880 can be achieved for the oxidation of p-xylene, ethylbenzene, and mesitylene, respectively. Density functional theory calculations suggest that the active intermediate is an OsVIII nitrido oxo species.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  alkylbenzenes; hydrogen peroxide; hydroxylation; nitrido; osmium complexes

Year:  2017        PMID: 28734083     DOI: 10.1002/anie.201705986

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  1 in total

1.  Immediate hydroxylation of arenes to phenols via V-containing all-silica ZSM-22 zeolite triggered non-radical mechanism.

Authors:  Yu Zhou; Zhipan Ma; Junjie Tang; Ning Yan; Yonghua Du; Shibo Xi; Kai Wang; Wei Zhang; Haimeng Wen; Jun Wang
Journal:  Nat Commun       Date:  2018-07-26       Impact factor: 14.919

  1 in total

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