Grant: Discovery Grants Program - Individual
Acadia University
$37,000.00
Design and synthesis of new photocaging chromophores and phototchemical carbanion progenitors
FY 2007-08
Summary
Protecting groups are molecular entities that can be attached to a variety of molecules of interest in order to deactivate a certain feature of that molecule, such as its chemical reactivity or its biological function. 'Photocages' are protecting groups that detach from the molecule of interest when they absorb light (usually in the UVA wavelength range), thereby reactivating the molecule. Exposure of a 'caged' molecule to brief pulses of light can cause a sudden increase in the concentration of the molecule of interest in its active form. Photocages are used extensively in this way to suddenly introduce a variety of molecules into biological systems. Biochemists are then able to study very fast biological events that are triggered by this sudden concentration increase, such as the movements of muscle tissues and communication between nerve cells. Unfortunately, all currently available photocages suffer from one or more serious drawbacks which limits their utility. For example, the most popular photocage exhibits poor solubility in water, slow release rate, and leads to formation of interfering by-products. This research plan is devoted to developing new photocages primarily for use in biological studies and in synthetic applications, that remedy the drawbacks associated with those currently available. The proposed photocages are of two main types: 1) 'carbocation-mediated' photocages that release the protected molecule by formation of a carbocation reactive intermediate, and 2) 'carbanion-mediated' photocages that release the protected molecules from a first formed carbanion reactive intermediate. All proposed photocages are expected to show excellent release rates, high efficiency, good aqueous solubility, good absorption in the UVA wavelength range, and formation of benign photoproducts. This research also seeks to broaden the range of light absorbing molecules that can be used to generate carbanion reactive intermediates. This will enable the creation of new photocages with tunable properties such as reactivity and water solubility.
Program
Discovery Grants Program - Individual
Recipient
Location
Nova Scotia, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
326969-2006
Name nom
Lukeman, Matthew
Department département
Chemistry
Organization id
78
Institution établissement
Acadia University
Province en
Nova Scotia
Province fr
Nouvelle-Écosse
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2007
Competition year année de concours
2006
Award amount
37000
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
1201
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Life sciences (including biotechnology)
Area of application fr
Sciences de la vie (y compris biotechnologie)
Research subject code
3706
Research subject group en
Organic chemistry
Research subject group fr
Chimie organique
Research subject en
Organic photochemistry
Research subject fr
Photochimie organique
Partie
2
Nb partie
3
Application title
Design and synthesis of new photocaging chromophores and phototchemical carbanion progenitors
Keyword
NA
Application summary
Protecting groups are molecular entities that can be attached to a variety of molecules of interest in order to deactivate a certain feature of that molecule, such as its chemical reactivity or its biological function. 'Photocages' are protecting groups that detach from the molecule of interest when they absorb light (usually in the UVA wavelength range), thereby reactivating the molecule. Exposure of a 'caged' molecule to brief pulses of light can cause a sudden increase in the concentration of the molecule of interest in its active form. Photocages are used extensively in this way to suddenly introduce a variety of molecules into biological systems. Biochemists are then able to study very fast biological events that are triggered by this sudden concentration increase, such as the movements of muscle tissues and communication between nerve cells. Unfortunately, all currently available photocages suffer from one or more serious drawbacks which limits their utility. For example, the most popular photocage exhibits poor solubility in water, slow release rate, and leads to formation of interfering by-products. This research plan is devoted to developing new photocages primarily for use in biological studies and in synthetic applications, that remedy the drawbacks associated with those currently available. The proposed photocages are of two main types: 1) 'carbocation-mediated' photocages that release the protected molecule by formation of a carbocation reactive intermediate, and 2) 'carbanion-mediated' photocages that release the protected molecules from a first formed carbanion reactive intermediate. All proposed photocages are expected to show excellent release rates, high efficiency, good aqueous solubility, good absorption in the UVA wavelength range, and formation of benign photoproducts. This research also seeks to broaden the range of light absorbing molecules that can be used to generate carbanion reactive intermediates. This will enable the creation of new photocages with tunable properties such as reactivity and water solubility.