1,721,063 research outputs found

    Organometallic-pi-complexes of the f-Elements

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    Handbook on the Physics and Chemistry of rare Earths, K.A. Gschneidner, Jr. and L. Eyring, Eds.

    Synthesis and characterization of N,N'-diarylformamidido complexes of palladium(II)

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    Trans-Pd(PPh3)2Cl2 reacts with Li(p-RC6H4N{A figure is presented}NC6H4R-p) (R = CH3O, CH3, H and Cl) in THF yielding the deeply colored complexes Pd(PPh3)2 (p-RC6H4NCH=NC6H4R-p)Cl (I), stable in the solid state. The main decomposition products in EtOH were identified when R = CH3, as trans-Pd(PPh3)2Cl2 and [Pd(p-CH3C6H4N{A figure is presented}NC6H4CH3-p)2]2(II). Dimeric complexes of type (II) can be synthesized also by reacting Li(p-CH3C6H4N{A figure is presented}NC6H4CH3-p) with Pd(NCCH3)2Cl2 in THF. The structures of all the new complexes are proposed on the basis of u. v., i.r. and n.m.r. data. © 1975

    Crystal structure of bis(triphenylphosphine)chloro-1,3-di-p-tolyltriazenidopalladium(II)

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    The crystal and mol. structures of the title compd. were detd. by x-ray diffraction. The structure was solved by Patterson methods and refined by least-squares calcns. to an R of 0.06. The crystals are triclinic, space group P1, with a 18.954(2), b 11.850(1), c 11.143(1) Å, 114.97(1), 94.75(1), and 97.51(1)°; d.(exptl.) = 1.36 and d.(calcd.) = 1.33 for Z = 2. The compd. has square-planar coordination with the phosphine groups trans to each other and the triazenido group acting as a monodentate ligand. The plane of the triazene N atoms contains the Pd atom. The interaction of the N -electrons appears to be absent. A possible mechanism for the fluxional behavior of the mol. is suggested

    The molecular and crystal structure of trans-hydridobis(triphenylphosphine)(1,3-di-p-tolyltriazenido)platinum(II)[PtH(PPh3)2(p-CH3C6H4NNNC6H4CH3-p)]

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    The structure of the title compd. was detd. at room temp. from 3-dimensional x-ray data collected by counter methods.\ud The compd. crystd. in the triclinic space group P1 with a 14.649(2), b 15.082(2), c 10.929(1) Å, 110.99(5)°, \ud 102.40(5)°, 84.54(5)°, and Z = 2. Full-matrix least-squares treatment of 4673 obsd. intensities gave an unweighted R of\ud 0.069. The Pt atom has square-planar coordination with Pt-P(1) 2.268(5), Pt-P(2) 2.267(5), and Pt-N(1) 2.09(2) Å. The\ud presence of the H atom is inferred from ir and 1H NMR data. The triazenido ligand, bonded to the metal through N(1),\ud lies perpendicular to the coordination plane

    Structure of cis-chlorobis(triphenylphosphine)-(1,3-di-p-tolyltriazenido)platinum(II)-chloroform, PtCl(PPh3)2(p-MeC6H4NNNC6H4Me-p).CHCl3

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    The structure of the title compd. was detd. at room temp. from 3-dimensional x-ray data collected by counter methods and refined by least-squares techniques to a final R of 0.059 based on 3897 observations above background. The compd. crystd. in the monoclinic space group P21/a with a 19.725(4), b 16.247(2), c 15.321(2) Å and 105.85(2)°, Z = 4. The Pt atom has square-planar coordination with Pt-P(1) = 2.289(6), Pt-P(2) = 2.251(7), Pt-Cl = 2.353(7), and Pt-N(1) = 2.11(2) Å. The aryldiazene moiety lies in a plane roughly perpendicular to the coordination plane and its Ph groups are twisted to relieve steric interactions with the adjacent phosphine Ph groups

    A worldwide perspective on large carnivore attacks on humans

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    VP was financially supported by the Project PID2020-114181GB-I00 financed by the Spanish Ministry of Science and Innovation, the Agencia Estatal de Investigacioón (AEI), and the Fondo Europeo de Desarrollo Regional (FEDER, EU).Bombieri G., Penteriani V., Almasieh K., Ambarlı H., Ashrafzadeh M.R., Das C.S., Dharaiya N., Hoogesteijn R., Hoogesteijn A., Ikanda D., Jędrzejewski W., Kaboli M., Kirilyuk A., Jangid A.K., Sharma R.K., Kushnir H., Lamichhane B.R., Mohammadi A., Monroy-Vilchis O., Mukeka J.M., Nikolaev I., Ohrens O., Packer C., Pedrini P., Ratnayeke S., Seryodkin I., Sharp T., Palei H.S., Smith T., Subedi A., Tortato F., Yamazaki K., del Mar Delgado M

    A novel synthesis and X-ray structure of a new aryldiazene complex: trans-(phenylacetylide)bis(triphenylphosphine)(p-fluorophenyldiazene)platinum(II) tetrafluoroborate

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    The title compound [Pt(CCPh)(HNNC6H4F-p)(PPh3)2](BF4) has been synthesized from Pt(HCCPh)(PPh3)2 and p-FC6H4N2BF4, and a mechanism for its formation is proposed; X-ray diffraction studies show that the acetylide ligand is σ-bonded and that the PCCC system is essentially linear, while the diazene ligand has a trans configuration around the NN bond, and the hydrogen-bearing nitrogen atom is coordinated to the platinum. © 1975

    Bonding and fluxional behavior of N,N'-di-p-tolylformamidino and 1,3-di-p-tolyltriazenido complexes of palladium(II)and platinum(II)

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    The fluxionality of M(PPh3)2Cl(ArNXNAr) and trans-Pt(PPh3)2H(ArNNNAr) (M = Pd(II), Pt(II); Ar = p-MeC6H4; X = CH,\ud N), is discussed on the basis of 1H NMR, x-ray, and ir studies. The stereochem. non-rigid process is proposed to occur\ud via a pseudo-pentacoordinate intermediate having both N atoms facing the metal through 2 electron lone pairs. A\ud different mechanism via a -bonding component in the M-(N ligand) bond is also discussed
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