The Reactions of 3,6-Di-tert-butyl-1,2-benzoquinone and 3,6-Ditert-butylcatechol with tert-Butyl Hydroperoxide. -The reaction of the title quinone (I) as well as its corresponding catechol with tert-butyl hydroperoxide in aprotic solvents results in ring oxidation accompanied by ring expansion furn
The Reaction of 3,6-di-tert-butyl-o-benzoquinone with tin amalgam: Synthesis and structure of tin catecholato complexes
✍ Scribed by Alexandr V. Piskunov; Aryna V. Lado; Georgy K. Fukin; Evgeny V. Baranov; Ludmila G. Abakumova; Vladimir K. Cherkasov; Gleb A. Abakumov
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 276 KB
- Volume
- 17
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.20271
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The reduction of 3,6‐di‐tert‐butyl‐o‐benzoquinone with tin amalgam gives the different tin catecholate complexes. The use of polar solvents for this reaction leads to the formation of Cat~2~Sn · L~2~ species (where Cat—dianion of 3,6‐di‐tert‐butylcatechol, L = Et~2~O, THF, Py). The reaction carried out in toluene produces the mixture of dicatecholate tin(IV) and catecholate tin(II) derivatives. The complex Cat~2~Sn · (Et~2~O)~2~ was shown to be a good starting reagent for the preparation of different tin(IV) catecholate complexes of the type Cat~2~Sn · L′ (L′ = 1,2‐dimethoxyethane, 1,4‐di‐tert‐butyldiazadiene‐1,3, o‐phenantrolyne, α,α′‐dipyridyl) using ligand exchange reactions. Compounds Cat~2~Sn · (Et~2~O)~2~, Cat~2~Sn · (THF)~2~, Cat~2~Sn · (Bu^t^NCHCHNBu^t^), and (CatSn)~3~ have been crystallographically characterized. © 2006 Wiley Periodicals, Inc. Heteroatom Chem 17:481–490, 2006; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20271
📜 SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.