Search results for "Rhodium"
showing 10 items of 244 documents
CCDC 762079: Experimental Crystal Structure Determination
2010
Related Article: Duc Hanh Nguyen, H.Laureano, S.Juge, P.Kalck, J.-C.Daran, Y.Coppel, M.Urrutigoity, M.Gouygou|2009|Organometallics|28|6288|doi:10.1021/om900684w
CCDC 804806: Experimental Crystal Structure Determination
2013
Related Article: D.H.Nguyen, J.Bayardon, C.Salomon-Bertrand, S.Juge, P.Kalck, J.-C.Daran, M.Urrutigoity, M.Gouygou|2012|Organometallics|31|857|doi:10.1021/om2008265
CCDC 194089: Experimental Crystal Structure Determination
2003
Related Article: M.Poyatos, E.Mas-Marza, J.A.Mata, M.Sanau, E.Peris|2003|Eur.J.Inorg.Chem.||1215|doi:10.1002/ejic.200390157
CCDC 814708: Experimental Crystal Structure Determination
2011
Related Article: N.Khiri, E.Bertrand, M.-J.Ondel-Eymin, Y.Rousselin, J.Bayardon, P.D.Harvey, S.Juge|2010|Organometallics|29|3622|doi:10.1021/om100520u
CCDC 1426906: Experimental Crystal Structure Determination
2016
Related Article: Erik Ekengard, Kamlesh Kumar, Thibault Fogeron, Carmen de Kock, Peter J. Smith, Matti Haukka, Magda Monari, Ebbe Nordlander|2016|Dalton Trans.|45|3905|doi:10.1039/C5DT03739E
A versatile rigid binucleating ligand for Rh2(μ-Cl)2 moieties: its application as a catalyst in hydrogenation and cyclopropanation
2003
A rigid non-deforming "MCl 2 M" binucleating ligand [7,8-μ-S(4'-C 6 H 3 (CH 3 ))S-C 2 B 9 H 1 0 ] - able to held the two rhodium atoms in a cooperative distance has been synthesized. The original two bridging chlorides are retained in [Rh 2 (C 5 Me 5 ) 2 Cl 2 {7,8-μ-S(4'-C 6 H 3 (CH 3 ))S-C 2 B 9 H 1 0 }] + . Hydrogenation of 1-hexene is 10 times faster with [Rh 2 (C 5 Me 5 ) 2 Cl 2 {7,8-μ-S(4'-C 6 H 3 (CH 3 ))S-C 2 B 9 H 1 0 }] + than with [Rh 2 (C 5 Me 5 ) 2 Cl 4 ]. A hydrogenation mechanism has been proposed which assumes that [Rh 2 (C 5 Me 5 ) 2 (Cl)(H){7,8-μ-S(4'-C 6 H 3 (CH 3 ))S-C 2 B 9 H 1 0 }] + is the first generated species in the process.
Access to α-Aminophosphonic Acid Derivatives and Phosphonopeptides by [Rh(P–OP)]-Catalyzed Stereoselective Hydrogenation
2020
The hydrogenation of N-substituted vinylphosphonates using rhodium complexes derived from P–OP ligands L1, ent-L1, or (R,R)-Me-DuPHOS as catalysts has been successfully accomplished, achieving very high levels of stereoselectivity (up to 99% ee or de). The described synthetic strategy allowed for the efficient preparation of α-aminophosphonic acid derivatives and phosphonopeptides, which are valuable building blocks for the preparation of biologically relevant molecules.
Voltammetric Analysis of Platinum in Environmental Matrices
2014
This article will summarize measurement data for Pt in different environmental samples obtained by the authors using a recently developed approach by voltammetric analysis. A fast accumulation of platinum and rhodium in the environmental and biological matrices has been observed in the last few years and concern has arisen about potential environmental and health risks. Voltammetry was used for the determination of Pt and Rh in airborne particulate collected in Palermo, Italy. Possible interferences by other environmental metals have also been evaluated. All samples show concentrations of Pt and Rh above average upper crust values. The Pt and Rh concentrations in particulate samples collect…
Input of P, N-(phosphanyl, amino)-ferrocene hybrid derivatives in late transition metals catalysis
2018
International audience; Unequally functionalized ferrocenes give access to valuable hemilabile reactivity in catalytic reaction. We address the synthesis of hybrid (P, N)-ferrocenyl compounds for which recent catalytic breakthrough applications have been reported, transversely in late transition metals chemistry. Palladium, nickel, rhodium, iridium, and emerging iron and gold catalysis are illustrated from selected examples, which include CC bond formation from cross-coupling and polymerization, allylic substitution, cyanation, hydroformylation, CH arylation and silylation and hydrogenation reactions.
Amino-phosphanes in RhI-Catalyzed Hydroformylation: Hemilabile Behavior of P,N Ligands under High CO Pressure and Catalytic Properties
2005
International audience; The catalytic properties of rhodium complexes containing the α-, β-, or γ-amino-phosphane ligands Ph2PCH2NEt2 (α-P,N-1), Ph2PCH(Ar)NHPh [α-P,N-2; Ar = η6(o-C6H4Cl)Cr(CO)3], Ph2PCH2NPh2 (α-P,N-3), Ph2PCH2CH(Ph)NHPh (β-P,N), Ph2PCH2(o-C6H4–NMe2) (γ-P,N-1), Ph2PCH(o-C6H4–CH2NHPh) (γ-P,N-2), and the α,β-diamino-phosphane ligand Et2NCH2P(Ph)CH2CH(Ph)NHPh (α,β-N,P,N), in styrene hydroformylation have been examined. The results show that the activity increases when the number of backbone carbon atoms linking P and N decreases from 3 to 1. IR and 31P HPNMR studies in solution show that all P,N ligands adopt exclusively a κ1-P coordination mode in rhodium chloride carbonyl co…