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Ruthenium-Catalyzed Aerobic Oxidation of Alcohols on Zeolite-Encapsulated Cobalt Salophen Catalyst
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
2002 Ingår i: Topics in catalysis, ISSN 1022-5528, Vol. 19, nr 1, s. 119-124Artikel i tidskrift (Refereegranskat) Published
Ort, förlag, år, upplaga, sidor
2002. Vol. 19, nr 1, s. 119-124
Identifikatorer
URN: urn:nbn:se:su:diva-24477OAI: oai:DiVA.org:su-24477DiVA, id: diva2:197626
Anmärkning
Part of urn:nbn:se:su:diva-71Tillgänglig från: 2004-03-11 Skapad: 2004-03-11Bibliografiskt granskad
Ingår i avhandling
1. Studies of Biomimtic Oxidations and Racemizations
Öppna denna publikation i ny flik eller fönster >>Studies of Biomimtic Oxidations and Racemizations
2004 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

This thesis deals with studies of ruthenium-catalyzed hydrogen transfer reactions for oxidations and racemization.

Through optimisation of the substrate-selective redox catalyst, the electron and proton transfer mediator (a benzoquinone derivative), and the oxygen-activating metal macrocycle a highly efficient biomimetic oxidation of secondary alcohols was obtained. Several alcohols were subjected to the new oxidation protocol and the corresponding ketones were isolated in high yield.

The deactivation of the oxygen-activating metal macrocycle retarded the aerobic oxidation of primary alcohols. Encapsulation of the metal macrocycle into zeolite, described in chapter 3, proved to be an efficient method to solve this problem and comparable conversion of alcohols was achieved. The immobilization of the oxygen-activating porphyrin to a surface can be an alternative approach to solve the deactivation problem. Therefore as the first step towards studies of immobilized porphyrins on a metal surface (of gold or silver), S-thioacetyl derivatized porphyrins were synthesized; two alternative syntheses are described in chapter 4.

A new and effecient ruthenium-catalyzed racemization protocol was established by proper ligand tuning. The racemization of the enantiomerically pure alcohols was increased significantly; this work is reported in chapter 5.

Ort, förlag, år, upplaga, sidor
Stockholm: Institutionen för organisk kemi, 2004. s. 52
Nyckelord
oxidation of alcohols, ruthenium, porphyrin, racemization
Nationell ämneskategori
Organisk kemi
Identifikatorer
urn:nbn:se:su:diva-71 (URN)91-7265-819-3 (ISBN)
Disputation
2004-04-01, Magnélisalen, Arrheniuslaboratoriet, Svante Arrhenius väg 12 A, Stockholm, 14:00
Opponent
Handledare
Tillgänglig från: 2004-03-11 Skapad: 2004-03-11 Senast uppdaterad: 2013-08-15Bibliografiskt granskad

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