PHOTORCA

Photoregulated organocatalysis - From caged catalysts to photoswitchable catalytic systems

 Coordinatore UNIVERSITAET REGENSBURG 

 Organization address address: UNIVERSITAETSSTRASSE 31
city: REGENSBURG
postcode: 93053

contact info
Titolo: Dr.
Nome: Christian
Cognome: Blomeyer
Email: send email
Telefono: -9433201
Fax: -9432437

 Nazionalità Coordinatore Germany [DE]
 Totale costo 0 €
 EC contributo 160˙996 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-IEF-2008
 Funding Scheme MC-IEF
 Anno di inizio 2009
 Periodo (anno-mese-giorno) 2009-04-01   -   2011-03-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITAET REGENSBURG

 Organization address address: UNIVERSITAETSSTRASSE 31
city: REGENSBURG
postcode: 93053

contact info
Titolo: Dr.
Nome: Christian
Cognome: Blomeyer
Email: send email
Telefono: -9433201
Fax: -9432437

DE (REGENSBURG) coordinator 160˙996.90

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

organocatalysis    light    efficient   

 Obiettivo del progetto (Objective)

'The project combines the two recent and versatile methodologies of organocatalysis and photoregulation with the objective to develop photoregulated organocatalytic systems. Together with the proposed immobilization in order to recycle these innovative catalysts such systems are expected to be of great value in the context of sustainable chemistry as control of reactions should allow for minimizing the formation of byproducts and therefore should create more efficient synthetic processes. If compared to highly efficient and selective enzymatic transformations, organocatalysis as their “biomimetic counterpart” misses a regulating control as frequently found in natural systems. In this regard light can be considered as an almost ideal trigger, because of its non-invasive interaction with matter, but also because of the disitinct advantage to provide very good temporal and spatial resolution. As first proof of principle we want to modify the activity and control the selectivity of organocatalysts in situ by the use of light.'

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