SYNMICS

Exploiting Synergistic Properties of Mesoionic Carbene Complexes: Teaching Rusty Metals Challenging Catalysis

 Coordinatore UNIVERSITAET BERN 

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 Nazionalità Coordinatore Switzerland [CH]
 Totale costo 2˙111˙111 €
 EC contributo 2˙111˙111 €
 Programma FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call ERC-2013-CoG
 Funding Scheme ERC-CG
 Anno di inizio 2015
 Periodo (anno-mese-giorno) 2015-02-01   -   2020-01-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITY COLLEGE DUBLIN, NATIONAL UNIVERSITY OF IRELAND, DUBLIN

 Organization address address: BELFIELD
city: DUBLIN
postcode: 4

contact info
Titolo: Mr.
Nome: Donal
Cognome: Doolan
Email: send email
Telefono: +353 17161656
Fax: +353 17161216

IE (DUBLIN) beneficiary 0.00
2    UNIVERSITAET BERN

 Organization address address: Hochschulstrasse 4
city: BERN
postcode: 3012

contact info
Titolo: Ms.
Nome: Maddalena
Cognome: Tognola
Email: send email
Telefono: +41 31 6314809

CH (BERN) hostInstitution 2˙111˙111.00
3    UNIVERSITAET BERN

 Organization address address: Hochschulstrasse 4
city: BERN
postcode: 3012

contact info
Titolo: Prof.
Nome: Martin
Cognome: Albrecht
Email: send email
Telefono: +41 31 6314243
Fax: +41 31 6313995

CH (BERN) hostInstitution 2˙111˙111.00

Mappa


 Word cloud

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

ni    transition    transformations    fe    energy    mesoionic    ligand    metal    mdash    synthetic    catalytic    catalyst    cooperativity    carbenes    metals    ligands    conversion   

 Obiettivo del progetto (Objective)

'The non-innocence of specific ligands in transition metal complexes is well-documented. For example, mesoionic carbenes engage in bond activation processes via reversible hydrogen capture. Such cooperativity between the metal center and the ligand flattens the potential energy surface of a catalytic reaction and hence rises the competence of the catalyst, thus entailing higher turnover numbers as well as the conversion of more challenging substrates. Likewise, such cooperativity is expected to enhance the catalytic activity of metal centers that are typically not considered to be catalytically very active, such as the ‘rusty’ first row transition metals (Mn, Fe, Ni). Surprisingly, however, this concept has largely been overlooked when designing catalytic transformations based on these earth-abundant and low-cost transition metals. This project will exploit the synergistic potential of mesoionic carbenes as synthetically highly versatile and actively supporting ligands to access a new generation of sustainable high-performance catalysts based on Me, Fe, and Ni for challenging redox transformations such as dehydrogenative oxidations. Specificlly, 1,2,3-triazolylidenes, which support ligand-metal cooperativity through their mesoionic character, will be utilized for (transient) storage/release of protons and electrons. Apart from enabling challenging transformations — with obvious impact on synthetic methodology, energy conversion, and molecular electronics — this project will break into new grounds in catalyst design that will be widely applicable as a new paradigm. Furthermore, this project will capitalize on the unique synthetic versatility of triazolylidene precursors and the opportunity to combine different functional entities such as carbohydrates, surfactants, or dyes with an organometallic entity, thus providing a straightforward approach to new classes of multifunctional materials for application in therapeutics and diagnostics, or as smart surfaces.'

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WASSR (2009)

Water anomalies in the stretched and supercooled regions

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QSOX1BIOFUNC (2012)

Frontiers of Oxidative Protein Folding and Assembly: Catalysis of Disulfide Formation Downstream of the Endoplasmic Reticulum

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MOLBIL (2013)

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