Zobrazeno 1 - 10
of 264
pro vyhledávání: '"Jesús J. Pérez-Torrente"'
Autor:
M. Victoria Jiménez, Ana I. Ojeda-Amador, Raquel Puerta-Oteo, Joaquín Martínez-Sal, Vincenzo Passarelli, Jesús J. Pérez-Torrente
Publikováno v:
Molecules, Vol 27, Iss 22, p 7666 (2022)
Iridium(I) compounds featuring bridge-functionalized bis-NHC ligands (NHC = N-heterocyclic carbene), [Ir(cod)(bis-NHC)] and [Ir(CO)2(bis-NHC)], have been prepared from the appropriate carboxylate- or hydroxy-functionalized bis-imidazolium salts. The
Externí odkaz:
https://doaj.org/article/ac0df0faced948d9852c36881cff75c7
Autor:
Ramón Azpíroz, Mert Olgun Karataş, Vincenzo Passarelli, Ismail Özdemir, Jesús J. Pérez-Torrente, Ricardo Castarlenas
Publikováno v:
Molecules, Vol 27, Iss 20, p 7002 (2022)
A series of mixed bis-NHC rhodium(I) complexes of type RhCl(η2-olefin)(NHC)(NHC’) have been synthesized by a stepwise reaction of [Rh(μ-Cl)(η2-olefin)2]2 with two different NHCs (NHC = N-heterocyclic carbene), in which the steric hindrance of bo
Externí odkaz:
https://doaj.org/article/bef86c2378404080886b5db34c46fc06
Autor:
Miguel González-Lainez, Miguel Gallegos, Julen Munarriz, Ramón Azpiroz, Vincenzo Passarelli, M. Victoria Jiménez, Jesús J. Pérez-Torrente
Publikováno v:
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
Scopus
instname
Scopus
Copper(I) [Cu2(μ-Br)2(tBuImCH2pyCH2L)]n (L = OMe, NEt2, NHtBu) compounds supported by flexible functionalized NHC-based polydentate ligands have been prepared in a one-pot procedure by reacting the corresponding imidazolium salt with an excess of co
Autor:
Miguel González-Lainez, M. Victoria Jiménez, Ramón Azpiroz, Vincenzo Passarelli, F. Javier Modrego, Jesús J. Pérez-Torrente
Publikováno v:
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
instname
A set of neutral [IrBr(L2)(κC-tBuImCH2PyCH2OMe)] and cationic [Ir(L2)(κ2C,N-tBuImCH2PyCH2OMe)]PF6 (L2 = cod, (CO)2) Ir(I) compounds featuring a flexible lutidine-derived polydentate ligand having NHC and −OMe as donor functions have been evaluate
Publikováno v:
Dalton Transactions. 51:12334-12351
Monodentate aminophosphanes HNP [NH(4-tolyl)PPh2] and SiMe3NP [SiMe3N(4-tolyl)PPh2] react with [Ir(μ-Cl)(cod)]2 affording tetra- or pentacoordinate complexes of formula [IrCl(L)n(cod)] (L = HNP, n = 1, 2; L = SiMe3NP, n = 1). The reaction of [IrCl(S
Publikováno v:
Polymer Chemistry. 13:1411-1421
A series of neutral [RhX(nbd)(κC-MeIm∩Z)] and cationic [Rh(nbd)(κ2C,N-MeIm∩Z)]+ (X = Cl, Br; MeIm = 3-methylimidazol-2-yliden-1-yl; ∩Z = N-functionalized wingtip; nbd = 2,5-norbornadiene) complexes featuring NHC ligands functionalized with a
Autor:
Pablo Hermosilla, Daniel Funes-Hernando, Ricardo Castarlenas, Andrea Di Giuseppe, Ramón Azpíroz, Eugenio Vispe, Jesús J. Pérez-Torrente
Publikováno v:
European Polymer Journal. 194:112117
The [Rh(μ-Cl)(IPr)(η2-coe)]2/pyridine system efficiently catalyzes the polyhydrothiolation of a series of dialkynes with dithiols, producing sulfur-rich poly(vinylidene sulfide)s with a typical Mw in the range 20.000–124.000 and vinylidene conten
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 51(18)
The iridium(III) hydride compound [IrH{κ3C,P,P′-(SiNP–H)}(CNtBu)2][PF6] (1PF6) was obtained by reaction of [Ir(SiNP)(cod)][PF6] with CNtBu as the result of the intramolecular oxidative addition of the SiCH2–H bond to iridium(I) [SiNP = Si(CH3)
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Compound [IrBr(CO)2(κC-tBuImCH2PyCH2OMe)] featuring a flexible pyridine/OMe functionalized NHC ligand κ1C coordinated efficiently catalyzes the selective N-monomethylation of nitroarenes using methanol as both the reducing agent and the C1 source.
Autor:
María Galiana‐Cameo, Raúl Romeo, Asier Urriolabeitia, Vincenzo Passarelli, Jesús J. Pérez‐Torrente, Victor Polo, Ricardo Castarlenas
Publikováno v:
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
instname
The dinuclear complex [Rh(μ-Cl)(η2-coe)(IPr)]2 is an efficient catalyst for the O-selective Markovnikov-type addition of 2-pyridones to terminal alkynes. DFT calculations support a hydride-free pathway entailing intramolecular oxidative protonation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60eaafecc92dc8121310fb80e5a46b76
http://hdl.handle.net/10261/284676
http://hdl.handle.net/10261/284676