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Grant: Discovery Grants Program - Individual

Queen's University

$90,000.00

Organic synthesis and materials chemistry via catalytic organoborane chemistry

FY 2012-13

Summary
The ability to prepare complex organic molecules efficiently has been critical in the development of the pharmaceutical industry. Recently, similar abilities have become important in areas such as liquid crystals and organic electronics. In this case, the molecules employed must be free of isomers and other contaminants that may impact performance. Thus, state-of-the-art synthetic techniques to prepare molecules for materials applications is critical. In the case of pharmaceutical applications of organic molecules, the most urgent need is for new structures that have not been made previously and may have unique physiological activities. For these reasons, we propose to examine the synthesis of two novel classes of molecules with applications in the pharmaceutical and materials areas. Chiral 1,1-diaryl alkanes are molecules that are exceedingly difficult to make by existing routes, yet these provide novel chiral scaffolds that are of interest to the pharmaceutical industry and materials chemistry. Likewise, the chiral 1,1,1-triarylmethanes and alkanes are virtually unknown in their enantiomerically pure state. We have proposed routes to prepare these important classes of compounds based on recent chemistry from our lab. The routes provide compounds of >95% optical and isomeric purity. In our second area of research, we propose to employ frustrated Lewis pair (FLP) chemistry for the activation of alkane C-H bonds. When an acidic and a basic molecule are present in solution but are inhibited (usually by sterics) from reacting with each other they are said to be a Frustrated Lewis Pair. In this case, the molecules can cooperate to split relatively unreactive bonds such as H-H, H-Si and H-B. We plan to employ this method for the activation of C-H bonds, which is a critical goal in terms of synthesis and energy since effective C-H activation strategies could better utilize petroleum feedstocks. Initially we will use organic structures that are biased towards the desired reaction in order to demonstrate feasibility, but we plan to move toward organic molecules with less and less functionality. HQP involved in this chemistry will gain a wide range of expertise in the area of organic synthesis, catalysis, air sensitive techniques and materials chemistry.
Program
Discovery Grants Program - Individual
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
194284-2010
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
2012
Competition year année de concours
2010
Award amount
90000
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
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
3
Nb partie
5
Application title
Organic synthesis and materials chemistry via catalytic organoborane chemistry
Keyword
NSERC
Application summary
The ability to prepare complex organic molecules efficiently has been critical in the development of the pharmaceutical industry. Recently, similar abilities have become important in areas such as liquid crystals and organic electronics. In this case, the molecules employed must be free of isomers and other contaminants that may impact performance. Thus, state-of-the-art synthetic techniques to prepare molecules for materials applications is critical. In the case of pharmaceutical applications of organic molecules, the most urgent need is for new structures that have not been made previously and may have unique physiological activities. For these reasons, we propose to examine the synthesis of two novel classes of molecules with applications in the pharmaceutical and materials areas. Chiral 1,1-diaryl alkanes are molecules that are exceedingly difficult to make by existing routes, yet these provide novel chiral scaffolds that are of interest to the pharmaceutical industry and materials chemistry. Likewise, the chiral 1,1,1-triarylmethanes and alkanes are virtually unknown in their enantiomerically pure state. We have proposed routes to prepare these important classes of compounds based on recent chemistry from our lab. The routes provide compounds of >95% optical and isomeric purity. In our second area of research, we propose to employ frustrated Lewis pair (FLP) chemistry for the activation of alkane C-H bonds. When an acidic and a basic molecule are present in solution but are inhibited (usually by sterics) from reacting with each other they are said to be a Frustrated Lewis Pair. In this case, the molecules can cooperate to split relatively unreactive bonds such as H-H, H-Si and H-B. We plan to employ this method for the activation of C-H bonds, which is a critical goal in terms of synthesis and energy since effective C-H activation strategies could better utilize petroleum feedstocks. Initially we will use organic structures that are biased towards the desired reaction in order to demonstrate feasibility, but we plan to move toward organic molecules with less and less functionality. HQP involved in this chemistry will gain a wide range of expertise in the area of organic synthesis, catalysis, air sensitive techniques and materials chemistry.