5 years ago

Ligand-Induced Tuning of the Oxidase Activity of μ-Hydroxidodimanganese(III) Complexes Using 3,5-Di-tert-butylcatechol as the Substrate: Isolation and Characterization of Products Involving an Oxidized Dioxolene Moiety

Ligand-Induced Tuning of the Oxidase Activity of μ-Hydroxidodimanganese(III) Complexes Using 3,5-Di-tert-butylcatechol as the Substrate: Isolation and Characterization of Products Involving an Oxidized Dioxolene Moiety
Akira Endo, Dhrubajyoti Mondal, Atanu Rana, Muktimoy Chaudhury, Mithun Chandra Majee, Sanchita Kundu
Two-electron versus four-electron reduction of dioxygen by a series of monohydroxido-bridged dimanganese(III) complexes (A) in the presence of 3,5-di-tert-butylcatecholate (H2DBC) as an electron source is fine-tuned by the secondary coordination environment around the metal center, leading to semiquinonato (B) and quinonato (C) complexes, respectively. The latter undergoes a Michael-type nucleophilic 1,4-addition reaction with the solvent methanol to generate an unusual type of oxidized dioxolene moiety.

Publisher URL: http://dx.doi.org/10.1021/acs.inorgchem.7b00147

DOI: 10.1021/acs.inorgchem.7b00147

You might also like
Discover & Discuss Important Research

Keeping up-to-date with research can feel impossible, with papers being published faster than you'll ever be able to read them. That's where Researcher comes in: we're simplifying discovery and making important discussions happen. With over 19,000 sources, including peer-reviewed journals, preprints, blogs, universities, podcasts and Live events across 10 research areas, you'll never miss what's important to you. It's like social media, but better. Oh, and we should mention - it's free.

  • Download from Google Play
  • Download from App Store
  • Download from AppInChina

Researcher displays publicly available abstracts and doesn’t host any full article content. If the content is open access, we will direct clicks from the abstracts to the publisher website and display the PDF copy on our platform. Clicks to view the full text will be directed to the publisher website, where only users with subscriptions or access through their institution are able to view the full article.