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Bio Inspired Side-on Attachment of a Ruthenium Photo-sensitizer to an Iron Hydrogenase Active Site Model
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
Vise andre og tillknytning
2006 Inngår i: Dalton Transactions, ISSN 1477-9226, nr 38, s. 4599-4606Artikkel i tidsskrift (Fagfellevurdert) Published
sted, utgiver, år, opplag, sider
2006. nr 38, s. 4599-4606
Identifikatorer
URN: urn:nbn:se:su:diva-24565OAI: oai:DiVA.org:su-24565DiVA, id: diva2:197806
Merknad
Part of urn:nbn:se:su:diva-7187Tilgjengelig fra: 2007-11-22 Laget: 2007-11-14bibliografisk kontrollert
Inngår i avhandling
1. Transition Metal Hydrides: Biomimetic Studies and Catalytic Applications
Åpne denne publikasjonen i ny fane eller vindu >>Transition Metal Hydrides: Biomimetic Studies and Catalytic Applications
2007 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

In this thesis, studies of the nature of different transition metal-hydride complexes are described. The first part deals with the enantioswitchable behaviour of rhodium complexes derived from amino acids, applied in asymmetric transfer hydrogenation of ketones. We found that the use of amino acid thio amide ligands resulted in the formation of the R-configured product, whereas the use of the corresponding hydroxamic acid- or hydrazide ligands selectively gave the S-alcohol.

Structure/activity investigations revealed that the stereochemical outcome of the catalytic reaction depends on the ligand mode of coordination.

In the second part, an Fe hydrogenase active site model complex with a labile amine ligand has been synthesized and studied. The aim of this study was to find a complex that efficiently catalyzes the reduction of protons to molecular hydrogen under mild conditions. We found that the amine ligand functions as a mimic of the loosely bound ligand which is part of the active site in the hydrogenase.

Further, an Fe hydrogenase active site model complex has been coupled to a photosensitizer with the aim of achieving light induced hydrogen production. The redox properties of the produced complex are such that no electron transfer from the photosensitizer part to the Fe moiety occurs.

In the last part of this thesis, the development of a protocol for the transfer hydrogenation of ketones to secondary alcohols without the involvement of transition metal catalysts is described. A variety of ketones were efficiently reduced in 2-propanol using catalytic amounts of alkali alkoxide under microwave irradiation.

sted, utgiver, år, opplag, sider
Stockholm: Institutionen för organisk kemi, 2007
Emneord
transition metals, catalysis, bioinorganic chemistry, hydrides
HSV kategori
Forskningsprogram
organisk kemi
Identifikatorer
urn:nbn:se:su:diva-7187 (URN)978-91-7155-539-7 (ISBN)
Disputas
2007-12-14, Magnélisalen, Kemiska övningslaboratoriet, Svante Arrhenius väg 12 A, Stockholm, 10:00 (engelsk)
Opponent
Veileder
Tilgjengelig fra: 2007-11-22 Laget: 2007-11-14 Sist oppdatert: 2015-10-18bibliografisk kontrollert

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