CHEMCATSUSDE

ChemCatSusDe: Chemical Catalysis towards a Sustainable Development: Transformation of Bio-Resources and Atom-Efficient Reactions Catalyzed by Bio-Metals

 Coordinatore UNIVERSITE DE RENNES I 

 Organization address address: RUE DU THABOR 2
city: RENNES CEDEX
postcode: 35065

contact info
Titolo: Ms.
Nome: Yolaine
Cognome: Bompays
Email: send email
Telefono: 33223233723

 Nazionalità Coordinatore France [FR]
 Totale costo 147˙298 €
 EC contributo 147˙298 €
 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-2010-IIF
 Funding Scheme MC-IIF
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-09-01   -   2013-02-28

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITE DE RENNES I

 Organization address address: RUE DU THABOR 2
city: RENNES CEDEX
postcode: 35065

contact info
Titolo: Ms.
Nome: Yolaine
Cognome: Bompays
Email: send email
Telefono: 33223233723

FR (RENNES CEDEX) coordinator 147˙298.00

Mappa

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 Word cloud

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efficient    metals    earth    cyclic    stability    calculations    magnesium    catalysts    complexes    excellent    heteroleptic    monomers    polymerisation    hydroelementation    display    chemistry    host    renewable    zinc    catalytic    alkaline    atom   

 Obiettivo del progetto (Objective)

'ChemCatSusDe addresses some of the industrial and economical issues of our society: fossil fuel depletion, use of renewable resources derived from the biomass, environmentally friendly chemistry for a sustainable future. At its core lies the versatility of complexes of zinc, magnesium, calcium, strontium and barium (the so-called bio-metals): green catalysts able to perform both the polymerisation of cyclic esters and highly atom-efficient hydroelementation reactions will be designed. The objectives defined by the researcher and the host institution in Rennes are: - Synthesis of well-defined complexes of the large alkaline-earth (Ca, Sr, Ba). The coordination chemistry of these metals in the presence of chelating, mono-anionic ligands will be studied. Owing to the extreme oxophilic nature of these elements, these catalytic precursors are expected to display excellent activities. The same synthetic strategies will also be extended to the preparation of complexes of the smaller zinc and magnesium, which display an excellent compromise between stability and catalytic activity - Use of these complexes for the catalytic immortal ring-opening polymerisation of cyclic monomers derived from renewable bioresources for the production of biocompatible and/or biodegradable polymers. All catalysts will be used for the polymerisation of lactide and monomers such as morpholinediones and b- or g-valerolactones - Hydroelementation of terminal alkenes catalyzed by heteroleptic amido-alkaline-earth complexes. Catalysts for the 100% atom-efficient hydrosilylation, -phophination and -amination of unsaturated substrates will be prepared - Study of the stability and reactivity of the targeted heteroleptic complexes by theoretical calculations: the design of catalytic systems will be elaborated and/or optimized according to preliminary calculations or those based on experimental structural data. - Development of long-term collaborations between the host and return institutions'

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