Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Martin Albrecht"'
Autor:
Martin Albrecht, Peter Broekmann, Frédéric Gloaguen, Motiar Rahaman, Philippe Schollhammer, Alexander V. Rudnev, Abhijit Dutta, Simone Bertini
Publikováno v:
Green Chemistry
Green Chemistry, Royal Society of Chemistry, 2021, ⟨10.1039/D1GC00388G⟩
Bertini, Simone; Rahaman, Motiar; Dutta, Abhijit; Schollhammer, Philippe; Rudnev, Alexander V.; Gloaguen, Fredric; Broekmann, Peter; Albrecht, Martin (2021). Oxo-functionalised mesoionic NHC nickel complexes for selective electrocatalytic reduction of CO 2 to formate. Green chemistry, 23(9), pp. 3365-3373. Royal Society of Chemistry 10.1039/D1GC00388G
Green Chemistry, Royal Society of Chemistry, 2021, ⟨10.1039/D1GC00388G⟩
Bertini, Simone; Rahaman, Motiar; Dutta, Abhijit; Schollhammer, Philippe; Rudnev, Alexander V.; Gloaguen, Fredric; Broekmann, Peter; Albrecht, Martin (2021). Oxo-functionalised mesoionic NHC nickel complexes for selective electrocatalytic reduction of CO 2 to formate. Green chemistry, 23(9), pp. 3365-3373. Royal Society of Chemistry 10.1039/D1GC00388G
International audience; Strategies for the conversion of CO2 to valuable products are paramount for reducing the environmental risks associated with high levels of this greenhouse gas and offer unique opportunities for transforming waste into useful
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92ee44d2e1f20a8444dd745af8b11cff
http://hdl.handle.net/20.500.12278/38138
http://hdl.handle.net/20.500.12278/38138
Autor:
Martin Albrecht, Philippe Schollhammer, Catherine Elleouet, Simone Bertini, François Y. Pétillon, Andrea Mele
Publikováno v:
CHIMIA
CHIMIA, Schweizerische Chemische Gesellschaft, 2020, 74 (6), pp.499-503. ⟨10.2533/chimia.2020.499⟩
CHIMIA, Vol 74, Iss 6, Pp 499-503 (2020)
CHIMIA, 2020, 74 (6), pp.499-503. ⟨10.2533/chimia.2020.499⟩
CHIMIA, Schweizerische Chemische Gesellschaft, 2020, 74 (6), pp.499-503. ⟨10.2533/chimia.2020.499⟩
CHIMIA, Vol 74, Iss 6, Pp 499-503 (2020)
CHIMIA, 2020, 74 (6), pp.499-503. ⟨10.2533/chimia.2020.499⟩
A novel complex featuring a mesoionic carbene [Fe2(CO)5(trz)(?-pdt)] (1) (trz = 1-phenyl-l,3-methyl,4-butyl-1,2,3-triazol-5-ylidene), was synthesized and spectroscopically and structurally characterized. The reductive behaviour of this compound in th
Publikováno v:
Dalton Transactions. 47:74-82
We synthesized a set of triazolylidene iridium(iii) complexes [IrCp*(C^N)L]n+ (Cp* = pentamethylcyclopentadienyl, C^N = C,N-bidentate coordinating pyridyl-triazolylidene) containing different neutral or anionic ancillary ligands L and evaluated their
Autor:
Ángela Vivancos, Martin Albrecht
Publikováno v:
Organometallics. 36:1580-1590
A series of ditriazolylidene ligand precursors (2) containing alkyl or ether linkers of different lengths between the triazolium heterocycles (trzH–linker–trzH, with linkers (a) −, (b) CH2, (c) (CH2)2, (d) (CH2)3, and (e) CH2OCH2) have been pre
Publikováno v:
Organometallics. 36:1469-1478
The alkyne azide “click” reaction was successfully used to prepare new Bodipy-functionalized triazoles and triazolium salts. The Bodipy functionality was compatible with cyclometalation conditions as well as with transmetalation procedures involv
Publikováno v:
ACS Catalysis. 6:8192-8200
A set of nickel(II) Cp complexes with triazolylidenes containing various different wingtip groups (aryl, alkyl, pyridyl, CH2OH) have been synthesized by direct metalation of the corresponding triazolium salt with nickelocene. Distinct effects of the
Publikováno v:
Organometallics. 35:2980-2986
The first mixed normal/abnormal NHC ruthenium(II) complexes bearing triazole/imidazole-based ligands are presented. The ruthenium complexes show differing coordination geometries depending on the ligand sphere and the coordination of the triazole. Tw
Publikováno v:
Organometallics. 34:5723-5733
Different rhodium(III) complexes [Rh(C,C)(P,P)X2]+ bearing both a cis-chelating dicarbene and a diphosphine ligand were synthesized (C,C = methylene(4,4′-diimidazolylidene); P,P = 1,2-bis(diphenylphosphino)ethane (dppe), (R)-(+)-2,2′-bis(diphenyl
Publikováno v:
Chemical reviews. 118(19)
Mesoionic carbenes are a subclass of the family of N-heterocyclic carbenes that generally feature less heteroatom stabilization of the carbenic carbon and hence impart specific donor properties and reactivity schemes when coordinated to a transition
Autor:
Matteo Planchestainer, Nathalie Segaud, Muralidharan Shanmugam, Jonathan McMaster, Francesca Paradisi, Martin Albrecht
Publikováno v:
Angewandte Chemie International Edition
Planchestainer, M, Segaud, N, Shanmugam, M, Mcmaster, J, Paradisi, F & Albrecht, M 2018, ' Carbene in Cupredoxin Protein Scaffolds: Replacement of a Histidine Ligand in the Active Site Substantially Alters Copper Redox Properties ', Angewandte Chemie International Edition, vol. 57, no. 33, pp. 10677-10682 . https://doi.org/10.1002/anie.v57.33
Planchestainer, M, Segaud, N, Shanmugam, M, Mcmaster, J, Paradisi, F & Albrecht, M 2018, ' Carbene in Cupredoxin Protein Scaffolds: Replacement of a Histidine Ligand in the Active Site Substantially Alters Copper Redox Properties ', Angewandte Chemie International Edition, vol. 57, no. 33, pp. 10677-10682 . https://doi.org/10.1002/anie.v57.33
N-heterocyclic carbene (NHC) ligands have hada major impact in homogeneous catalysis, however, theirpotential role in biological systems is essentially unexplored.We replaced a copper-coordinating histidine (His) in the activesite of the redox enzyme