Search results for "Palladium"
showing 10 items of 956 documents
CCDC 133153: Experimental Crystal Structure Determination
2000
Related Article: F.Estevan, A.Garcia-Bernabe, P.Lahuerta, M.Sanau, M.A.Ubeda, J.R.Galan-Mascaros|2000|J.Organomet.Chem.|596|248|doi:10.1016/S0022-328X(99)00673-7
CCDC 142834: Experimental Crystal Structure Determination
2001
Related Article: R.Broussier, E.Bentabet, M.Laly, P.Richard, L.G.Kuz'mina, P.Serp, N.Wheatley, P.Kalck, B.Gautheron|2000|J.Organomet.Chem.|613|77|doi:10.1016/S0022-328X(00)00501-5
CCDC 193057: Experimental Crystal Structure Determination
2003
Related Article: L.Escriche, J.A.Munoz, R.Kivekas, R.Sillampaa, J.Casabo|2002|Eur.J.Inorg.Chem.||3258|doi:10.1002/1099-0682(200212)2002:12<3258::AID-EJIC3258>3.0.CO;2-P
CCDC 834838: Experimental Crystal Structure Determination
2013
Related Article: A.Massard, V.Rampazzi, A.Perrier, E.Bodio, M.Picquet, P.Richard, J.-C.Hierso, P.Le Gendre|2012|Organometallics|31|947|doi:10.1021/om200999n
Isomerism in [MCl2(ERR‘)2] (M = Pd, Pt; E = S, Se; R, R‘ = Me, Ph)
2006
A series of thioether and selenoether complexes [MCl2(EPh2)2] and [MCl2(SMePh)2] (M = Pt, Pd; E = S, Se) have been prepared and characterized to explore the isomerism of the complexes in solution and in the solid state. The NMR spectroscopic information indicates that only one isomer is present in solution in case of the palladium complexes, while two isomers are formed in the case of most platinum complexes. Single-crystal X-ray structures of trans-[PdCl2(SPh2)2] (1t), trans-[PdCl2(SePh2)2] (2t), cis-[PtCl2(SePh2)2] (4c), trans-[PdCl2(SMePh)2] (5t), and trans-[PtCl2(SMePh)2] (7t) are reported and have been used as starting points for the X-ray powder diffraction structure determinations us…
STACKING-FAULTS IN VERY FINE PALLADIUM PARTICLES SUPPORTED ON PUMICE
1990
By means of an X-ray diffraction study, carried out with best-fitting procedures, of the asymmetry and peak maximum shifts of some reflections, stacking-faults in the FCC lattice of very fine palladium particles supported on pumice were detected using the Warren-Wagner-Cohen theoretical approach.
Migration of bidentate anionic ligands in binuclear compounds derived from 1,2-bis(imino)propyl-palladium(II) complexes
1983
Abstract The complexes [Pd(AB){C(NR)CMeNR}(PPh3)] (I; AB = 2,4-pentanedionate, N-methylsalicylaldiminate, pyrrole-2-N-methylaldiminate; R = p-C6H4OMe) react with ‘MCl2’ (‘MCl2’ = CoCl2, NiCl2, CuCl2, ZnCl2, [PdCl2(NCMe)2], K[PtCl3(CH2CH2)]) to give either the binuclear adducts [(PPh3)(AB)Pd{C(NR)CMeNR}MCl2] (II) or the zwitterionic isomers [(PPh3)Cl2Pd{C( NR)CMeNR}M (AB)] (III) depending on the nature of the metal M and of the anionic ligand AB. The formation of products III is accounted for in terms of an intramolecular migration of ligands between the two metal centers Pd and M of the initially formed MCl2 adducts II.
Electrochemical reduction properties of A-frame compounds and crystal structure of Pd2(dppm)2(Me)2(Br)+ dimer
2006
Abstract Two series of A-frame complexes, [Pd2(dppm)2(R)2(μ-X)]+ (R = Me and X = Cl, Br, I, H; R = Mes and X = Br, I), were investigated by cyclic voltammetry (CV). The 2-electron reduction potentials for the first series increase from I (−1.10), Br (−1.17), Cl (−1.25) to H (−1.65 V versus SCE, in CHCl3), as well as in the second series; Br (−1.35) and I (−1.38 V versus SCE, in THF). The nature of the LUMO where the electron reduction takes place is qualitatively addressed by DFT on the corresponding model complexes [Pd2(H2PCH2PH2)2(R)2(μ-X)]+. The LUMO and (LUMO + 1) of the halide derivatives exhibit the presence of Pd d x 2 - y 2 atomic orbitals interacting in an anti-bonding fashion with…
Reactions of pyridine-2-carbaldimines with chloro-bridged palladium(II) and platinum(II) 2-methylallyl dimers. Solution behaviour of the cationic com…
1987
Abstract The reactions of pyridine-2-carbaldimines, py-2- CHNR (R = C6H4OMe-p, Me), with allylic dimers [MCl(n3-2-MeC3H4)]2 give rise to stoichiometry, concentration, solvent and temperature dependent equilibria, in which the cationic complexes [M(n3- 2-MeC3H4)(py-2-CHNR)]+ and the anion [MCl2(n3- 2-MeC3H4)]- or Cl- are involved. In general, the ligand/dimer reaction (1/1 molar ratio) yields the ionic products [M(n3-2-MeC3H4)(py-2-CHNR)]- [MCl2(n3-2-MeC3H4)], which can be isolated as solids, whereas the same reaction in a 1/0.5 molar ratio yields the species [M(n3-2-MeC3H4 )(py-2-CH NR)] Cl, which can be studied only in solution, but are easily converted into [M(n3-2-MeC3H4)(py-2-CH NR…
A Next‐Generation Air‐Stable Palladium(I) Dimer Enables Olefin Migration and Selective C−C Coupling in Air
2020
Abstract We report a new air‐stable PdI dimer, [Pd(μ‐I)(PCy2 tBu)]2, which triggers E‐selective olefin migration to enamides and styrene derivatives in the presence of multiple functional groups and with complete tolerance of air. The same dimer also triggers extremely rapid C−C coupling (alkylation and arylation) at room temperature in a modular and triply selective fashion of aromatic C−Br, C−OTf/OFs, and C−Cl bonds in poly(pseudo)halogenated arenes, displaying superior activity over previous PdI dimer generations for substrates that bear substituents ortho to C−OTf.