Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Guillaume Passard"'
Publikováno v:
ACS Catalysis. 8:8671-8679
The oxygen reduction reaction (ORR) is catalyzed by manganese(II) porphyrins in the presence of Bronsted acids (HAs). Analyses of the catalytic cyclic voltammetric profiles have permitted the ORR mechanism to be constructed and rate constants to be e
Autor:
Bryce L. Anderson, Guillaume Passard, Christopher J. Gagliardi, Dilek K. Dogutan, Robert L. Halbach, Daniel G. Nocera, Jonathan S. Lindsey, Masahiko Taniguchi, Andrew G. Maher
Publikováno v:
ACS Catalysis. 7:3597-3606
A sparsely substituted chlorin macrocycle containing a Co(II) center (1-Co) has been synthesized and structurally characterized. The Co(II) atom resides in a square planar coordination environment and induces significant out-of-plane distortion of th
Publikováno v:
Proceedings of the National Academy of Sciences. 111:14990-14994
Significance Conversion of CO 2 into liquid fuels is one of the most important contemporary energy and environmental challenges. As a first step in this direction, the electrochemical reduction of CO 2 to CO requires catalysts, usually derived from t
Publikováno v:
Journal of the American Chemical Society. 135:9023-9031
Most of the electrocatalytic processes of interest in the resolution of modern energy challenges are associated with proton transfer. In the cases where heavy atom bond cleavage occurs concomitantly, the question arises of the exact nature of its cou
Publikováno v:
Chem. Sci.. 4:819-823
The cleavage of metal–oxygen or metal–carbon bonds is an essential step in the activation by transition metal complex catalysis of small molecules involved in the resolution of modern energy challenges. Deciphering the role of proton transfer as
Publikováno v:
Journal of the American Chemical Society. 138(9)
The selective four electron, four proton, electrochemical reduction of O2 to H2O in the presence of a strong acid (TFA) is catalyzed at a dicobalt center. The faradaic efficiency of the oxygen reduction reaction (ORR) is furnished from a systematic e
Publikováno v:
ECS Meeting Abstracts. :960-960
The oxygen reduction reaction (ORR) is catalyzed by manganese(II) tetraphenyl porphyrin (Mn(II)TPP) in the presence of Brønsted acids (HAs). Analysis of the catalytic wave in the cyclic voltammogram of the ORR reaction leads to the proposal two equi
Publikováno v:
Journal of the American Chemical Society. 137(16)
In relation to contemporary energy challenges, a number of molecular catalysts for the activation of small molecules, mainly based on transition metal complexes, have been developed. The time has thus come to develop tools allowing the benchmarking o
Publikováno v:
Journal of the American Chemical Society. 136(33)
Two derivatives of iron tetraphenylporphyrin bearing prepositioned phenolic functionalities on two of the opposed phenyl groups prove to be remarkable catalysts for the reduction of CO2 to CO when generated electrochemically at the Fe(0) oxidation st
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2012, 18 (42), pp.13473-13479. ⟨10.1002/chem.201201884⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2012, 18 (42), pp.13473-13479. ⟨10.1002/chem.201201884⟩
International audience; The substituted iron–thiolate complex [Fe2(μ-bdt)(CO)4{P(OMe)3}2] (bdt=benzenedithiolate) is an active catalyst for electrochemical hydrogen production in aqueous sodium dodecyl sulfate solution, with a high apparent rate c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::287f572ca337f846d923b35dd6b0c29b
https://hal.univ-brest.fr/hal-01556797
https://hal.univ-brest.fr/hal-01556797