981 resultados para 1,1`-BIS(DIPHENYLPHOSPHINO)FERROCENE DPPF
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"Deutsch von Albert Zucker."
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"Gratis-beilage zur Tafel der viertel-quadrate. Napiertafel enthaltend die 8 vielfachen aller zahlen vermittels zusammensetzen der dazu erforderlichen stäbchen, zur bequemeren und rascheren ausführung von multiplicationen und divisionen vielstelliger zahlen laut gebrauchsanweisung, herausgegeben nach angabe des herren A. Steinhauser" (4 p. (23 cm.) and tab. (22 x 19 cm.) laid in.
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Mode of access: Internet.
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Vol. 1 index to vol. 1-10, 1848-1853; vol. 2, to vol. 11-20, 1853-1856; vol. 3 to vol. 21-30, 1856-1858; vol. 4, to vol. 31-42, 1858-1860; vol. 5, to vol. 43-50, 1861-1864; vol. 6, to vol. 51-60, 1865-1869; vol. 7, to vol. 61-64, 1870-1871; vol. 8, to vol. 65-75, 1872-1877; vol. 9, to vol. 76-80, 1878-1880; vol. 10, to vol. 81-85, 1880-1882; vol. 11, to vol. 86-90, 1882-1884; vol. 12, to vol. 91-96, 1885-1887; vol. 13, to vol. 97-100, 1888-1891; vol. 14, to vol. 101-105, 1892-1896; vol. 15, to vol. 106-110, 1897-1901; vol. 16 to vol. 111-115, 1902-1906.
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Mode of access: Internet.
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Available on demand as hard copy or computer file from Cornell University Library.
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Mode of access: Internet.
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Aus der Sammlung des Leo Baeck Institute, digitalisiert in Kooperation mit dem Center for Jewish History, NY
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von M.L. Michelup, geprüftem Hauptschullehrer
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Two oxorhenium(V) complexes with bidentate phosphine ligands were synthesized and isolated as [ReOCl3(dppm)] 1 and [ReOCl3(dppp)] 2 [where dppm = 1,1-bis(diphenylphosphino) methane and dppp = 1.3-bis(diphenylphosphino) propanel. Complex 2 was structurally characterized. Both the complexes were used as catalysts in the epoxidation of olefins using NaHCO3 as co-catalyst and H2O2 as terminal oxidant. (c) 2008 Elsevier B.V. All rights reserved.
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Bis(diphenylphosphino)methane dioxide compounds of uranyl nitrate and uranyl bis(beta-diketonates) have been synthesized and characterized by spectroscopic and X-ray diffraction methods. Monodentate, bidentate chelate and bridging bidentate modes of coordination for this ligand have been established from the single-crystal X-ray diffraction studies of its compounds, [UO2(DBM)(2)DPPMO], [UO2(NO3)(2)DPPNO] and [{UO2(DBM)(2)}(2)DPPMO], respectively. (C) 2004 Elsevier Ltd. All rights reserved.
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Extended-chain complexes containing multiple transition metal centres linked by conjugated mu-cyanodiazenido(1-) ligands [N= N-C N]-have been obtained by reaction of trans-[BrW(dppe)(2)(N2CN)], 1, [dppe = 1,2-bis(diphenylphosphino) ethane] with dirhodium(II) tetra-acetate, bis(benzonitrile) palladium(II) dichloride, and bis(aqua) M(II) bis(hexa. uoroacetylacetonate) (M = Mn, Ni, Cu, Zn): stronger Lewis acids such as tetrakis(acetonitrile) palladium(II) tetra. uoroborate and boron trifl. uoride promote hydrolysis of complex 1, leading to the isolation of a novel carbamoylhydrazido(2-) complex, trans-[BrW(dppe) 2(N2HC=ONH2)](+)[BF4](-).
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The 1,3-dipolar cycloaddition between azomethine ylides and alkenes is efficiently catalysed by [{(Sa)-Binap-Au(tfa)}2] (Binap=2,2′-bis(diphenylphosphino)-1,1′-binaphthyl; tfa=trifluoroacetyl). Maleimides, 1,2-bis(phenylsulfonyl)ethylene, chalcone and nitrostyrene were suitable dipolarophiles even when using sterically hindered 1,3-dipole precursors. The results obtained in these transformations improve the analogous ones obtained in the same reactions catalysed by [Binap–Ag(tfa)]. In addition, computational studies have also been carried out to demonstrate both the high enantioselectivity exhibited by the chiral gold(I) complex, and the non-linear effect observed in this transformation.
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