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Grant: Discovery Grants Program - Individual

University of Windsor

$54,000.00

Base-Metal Complexes for Challenging Organometallic Transformations

FY 2017-18

Summary
This proposal describes approaches to render sustainable 1st-row transition metals, such as nickel and cobalt, as catalysts for applications such as the functionalization of C-H, C-F and C-O bonds. The short term goals of the projects involve identification of new ways to render these metals reactive towards traditionally inert bonds. Approaches to this include using ligand design or identifying new mechanisms for bond activation. The long term goal of each project is the commercial application of these catalytic technologies in fields such as pharmaceutical synthesis and biomass conversion. The atom-economic relatively green conversion of traditionally inert C-H bonds to functional groups has been achieved by a number of metal-catalyzed systems in the past decades. Complexes of the expensive 3rd-row late transition metals, such as iridium and platinum, are commonly used in these conversions, due to the strong bonds these elements form to both carbon and hydrogen, which aids in cleaving strong C-H bonds. Comparatively, complexes of nickel are at an extreme thermodynamic disadvantage in these reactions, but nickel has the distinct advantage of being on the order of 10000 times cheaper, due to its relative abundance. Our research suggests that not only can nickel complexes also activate strong C-H bonds, they can also perform catalytic C-H bond transformations that are unprecedented and perhaps unique to these systems. Our current goals are to fully understand the mechanism and scope of these reactions. Similar to C-H bond activation, the activation of C-F and C-O bonds are also problematic for both kinetic and thermodynamic reasons. We hope to do a thorough study of C-F bond activation by nickel complexes to gain insight into how the mechanism and thermodynamic parameters of these reactions are influenced by ancillary ligand choices. The end goal is a rational approach to both C-F bond activation and catalytic C-F bond formation for pharmaceuticals or radionuclide use. The activation of C-O bonds is related to C-F bond activation, and has application in both synthesis and biomass conversion to fuels or fine chemicals.
Program
Discovery Grants Program - Individual
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
261742-2013
Name nom
Johnson, Samuel
Department département
Chemistry and Biochemistry
Organization id
37
Institution établissement
University of Windsor
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2017
Competition year année de concours
2013
Award amount
54000
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
1504
Committee name en
Chemistry
Committee name fr
Chimie
Area of application code
1200
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Advancement of knowledge
Area of application fr
Avancement des connaissances
Research subject code
3600
Research subject group en
Inorganic chemistry
Research subject group fr
Chimie inorganique
Research subject en
Inorganic chemistry
Research subject fr
Chimie inorganique
Partie
5
Nb partie
6
Application title
Base-Metal Complexes for Challenging Organometallic Transformations
Keyword
NSERC
Application summary
This proposal describes approaches to render sustainable 1st-row transition metals, such as nickel and cobalt, as catalysts for applications such as the functionalization of C-H, C-F and C-O bonds. The short term goals of the projects involve identification of new ways to render these metals reactive towards traditionally inert bonds. Approaches to this include using ligand design or identifying new mechanisms for bond activation. The long term goal of each project is the commercial application of these catalytic technologies in fields such as pharmaceutical synthesis and biomass conversion. The atom-economic relatively green conversion of traditionally inert C-H bonds to functional groups has been achieved by a number of metal-catalyzed systems in the past decades. Complexes of the expensive 3rd-row late transition metals, such as iridium and platinum, are commonly used in these conversions, due to the strong bonds these elements form to both carbon and hydrogen, which aids in cleaving strong C-H bonds. Comparatively, complexes of nickel are at an extreme thermodynamic disadvantage in these reactions, but nickel has the distinct advantage of being on the order of 10000 times cheaper, due to its relative abundance. Our research suggests that not only can nickel complexes also activate strong C-H bonds, they can also perform catalytic C-H bond transformations that are unprecedented and perhaps unique to these systems. Our current goals are to fully understand the mechanism and scope of these reactions. Similar to C-H bond activation, the activation of C-F and C-O bonds are also problematic for both kinetic and thermodynamic reasons. We hope to do a thorough study of C-F bond activation by nickel complexes to gain insight into how the mechanism and thermodynamic parameters of these reactions are influenced by ancillary ligand choices. The end goal is a rational approach to both C-F bond activation and catalytic C-F bond formation for pharmaceuticals or radionuclide use. The activation of C-O bonds is related to C-F bond activation, and has application in both synthesis and biomass conversion to fuels or fine chemicals.
University of Windsor - $54,000 Grant (2017-18) | Canada Spends