Grant: Discovery Grants Program - Individual
Queen's University
$60,000.00
Organic synthesis using homogeneous and heterogeneous transition metal catalysts
EF 2006-07
Résumé
Transition metal catalysts such as those composed of rhodium, platinum and palladium are employed in a variety of processes, inculding catalytic converters in cars. These same metals are often used in molecular catalysts for the conversion of simple organic molecules into more complex ones. Metal catalysts in the molecular state are prepared by introducing ligands on the metal which prevent decomposition to the bulk metal. These ligands can even make a metal like palladium soluble in organic solvents. The ligands are also employed to adjust the reactivity of the metal. Chiral ligands can even be used to generate chiral products from achiral starting materials. This is one of the most efficient methods for the synthesis of chiral products, since only catalytic amounts of the initial chiral material (the chiral ligand) is required. We have proposed to study three important catalytic processes, the hydroboration of olefins, the oxidation of alcohols and the preparation of carbon-carbon bonds in Suzuki coupling reactions. Our study of these reactions will focus on the following key points: understanding the mechanism; expanding the scope of the reaction; introducing chirality; recovering the catalyst. This latter point is often overlooked since metal catalysts are usually cheaper than the products they are used to produce. However, not only is it more efficient to be able to recover the catalyst, it is also critical for the purity of the product. This has become a significant problem in both the pharmaceutical and electronic materials industries where trace amounts of metals can cause significant problems. In the case of pharmaceutical products, the presence of metals such as Pd and Rh may cause significant toxicity. In the case of materials, metal contamination can cause shorts in electronic devices, or limit the ability of a material to act as an insulator. Thus we will also address different strategies to remove metals from reaction mixtures as well as ways to immobilize the complexes so that they do not contaminate the prodcut to begin with.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
194284-2006
Name nom
Crudden, Cathleen
Department département
Chemistry
Organization id
29
Institution établissement
Queen's University
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2006
Competition year année de concours
2006
Award amount
60000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
24
Committee name en
Inorganic & Organic Chemistry
Committee name fr
Chimie inorg. et org.
Area of application code
1202
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Physical sciences
Area of application fr
Sciences physiques
Research subject code
3704
Research subject group en
Organic chemistry
Research subject group fr
Chimie organique
Research subject en
Synthetic methodology
Research subject fr
Méthodologie en synthèse
Partie
1
Nb partie
5
Application title
Organic synthesis using homogeneous and heterogeneous transition metal catalysts
Keyword
NA
Application summary
Transition metal catalysts such as those composed of rhodium, platinum and palladium are employed in a variety of processes, inculding catalytic converters in cars. These same metals are often used in molecular catalysts for the conversion of simple organic molecules into more complex ones. Metal catalysts in the molecular state are prepared by introducing ligands on the metal which prevent decomposition to the bulk metal. These ligands can even make a metal like palladium soluble in organic solvents. The ligands are also employed to adjust the reactivity of the metal. Chiral ligands can even be used to generate chiral products from achiral starting materials. This is one of the most efficient methods for the synthesis of chiral products, since only catalytic amounts of the initial chiral material (the chiral ligand) is required. We have proposed to study three important catalytic processes, the hydroboration of olefins, the oxidation of alcohols and the preparation of carbon-carbon bonds in Suzuki coupling reactions. Our study of these reactions will focus on the following key points: understanding the mechanism; expanding the scope of the reaction; introducing chirality; recovering the catalyst. This latter point is often overlooked since metal catalysts are usually cheaper than the products they are used to produce. However, not only is it more efficient to be able to recover the catalyst, it is also critical for the purity of the product. This has become a significant problem in both the pharmaceutical and electronic materials industries where trace amounts of metals can cause significant problems. In the case of pharmaceutical products, the presence of metals such as Pd and Rh may cause significant toxicity. In the case of materials, metal contamination can cause shorts in electronic devices, or limit the ability of a material to act as an insulator. Thus we will also address different strategies to remove metals from reaction mixtures as well as ways to immobilize the complexes so that they do not contaminate the prodcut to begin with.