L
Luis A. Oro
Researcher at University of Zaragoza
Publications - 764
Citations - 18487
Luis A. Oro is an academic researcher from University of Zaragoza. The author has contributed to research in topics: Catalysis & Rhodium. The author has an hindex of 57, co-authored 764 publications receiving 17692 citations. Previous affiliations of Luis A. Oro include Spanish National Research Council & Complutense University of Madrid.
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Rhodium tetraflurobenzobarrelene or trimethyltetrafluorobenzobarrelene complexes with arene ligands. Crystal structures of [Rh(diolefin)(arene)]ClO4, (diolefin = TFB, arene = 1,2,4-C6H3Me3; diolefin = Me3TFB, arene = 1,2,4-C6H3Me3, C6Me6)
TL;DR: In this paper, the lattice constants are (i) a = b = 25.8460(8), c = 16.4439(6) A, γ = 120°, α = β = 90°, β = 98.241(2)°.
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Kinetic and spectroscopic study of the hydrogen-transfer reaction from 2-propanol to cyclohexanone catalyzed by [IrH2(pz)(Hpz)(PPh3)2] (Hpzpyrazole)
TL;DR: In this article, a rate expression of the form r = a [Ir] Tot / b [Hpz] 2 + 1 was derived for the hydrogen transfer reaction from 2-propanol to cyclohexanone.
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Iridium catalysts featuring amine-containing ligands for the dehydrogenation of formic acid
Ana Luque,Amaia Iturmendi,Laura Rubio-Pérez,Julen Munarriz,Julen Munarriz,Victor Polo,Vincenzo Passarelli,Manuel Iglesias,Luis A. Oro +8 more
TL;DR: The use of protic ligands to generate metal-ligand bifunctional catalysts has proved an excellent strategy to enhance the catalytic activity in formic acid dehydrogenation.
Comprar Iridium Complexes in Organic Synthesis | Luis A. Oro | 9783527319961 | Wiley
Luis A. Oro,Carmen Claver +1 more
TL;DR: Claver et al. as mentioned in this paper describe the process of combining Iridium Complexes in organic synthesis and their precio is 172,37 €. http://www.tiendas de libros de medicina.org.
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Postsynthetic modifications of [2,2,2-(H)(PPh3)2-closo-2,1-RhSB8H8] with Lewis bases: cluster modular tuning.
Susana Luaces,Vincenzo Passarelli,María José Artigas,Fernando J. Lahoz,Luis A. Oro,Ramón Macías +5 more
TL;DR: Variable temperature NMR studies of the reaction between and PPh3 or 2-Mepy demonstrated that at low temperatures there is formation of the 9,6-species that subsequently isomerizes to the 6,5-regioisomer, indicating that for the more sterically hindered Lewis bases, P Ph3, 2- Mepy and PCy3, the latter isomer is more stable and accessible through an intramolecular {Rh(PPh3)2}