» Articles » PMID: 31336013

Carbocatalytic Oxidative Dehydrogenative Couplings of (Hetero)Aryls by Oxidized Multi-Walled Carbon Nanotubes in Liquid Phase

Overview
Journal Chemistry
Specialty Chemistry
Date 2019 Jul 24
PMID 31336013
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

HNO -oxidized carbon nanotubes catalyze oxidative dehydrogenative (ODH) carbon-carbon bond formation between electron-rich (hetero)aryls with O as a terminal oxidant. The recyclable carbocatalytic method provides a convenient and an operationally easy synthetic protocol for accessing various benzofused homodimers, biaryls, triphenylenes, and related benzofused heteroaryls that are highly useful frameworks for material chemistry applications. Carbonyls/quinones are the catalytically active site of the carbocatalyst as indicated by model compounds and titration experiments. Further investigations of the reaction mechanism with a combination of experimental and DFT methods support the competing nature of acid-catalyzed and radical cationic ODHs, and indicate that both mechanisms operate with the current material.

Citing Articles

Dehydrogenative Coupling Reactions with Guanidino-Functionalized Aromatics.

Walter P, Schulz M, Hubner O, Poddelskii A, Kaifer E, Himmel H Chemistry. 2024; 30(71):e202402917.

PMID: 39370772 PMC: 11653247. DOI: 10.1002/chem.202402917.


Divergent Carbocatalytic Routes in Oxidative Coupling of Benzofused Heteroaryl Dimers: A Mechanistic Update.

Casadio D, Aikonen S, Lenarda A, Nieger M, Hu T, Taubert S Chemistry. 2021; 27(16):5283-5291.

PMID: 33427343 PMC: 8048508. DOI: 10.1002/chem.202005433.