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  • 1
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 36 (1980), S. 678-680 
    ISSN: 1600-5740
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 36 (1980), S. 1196-1198 
    ISSN: 1600-5740
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 37 (1981), S. 688-690 
    ISSN: 1600-5740
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 39 (1983), S. 981-982 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 40 (1984), S. 600-602 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 38 (1982), S. 1290-1292 
    ISSN: 1600-5740
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Summary A method is described for immobilizing 2,3-dihydroxybenzoyl and 3,4,5-trihydroxybenzoylamide functional groups on the surface of silica. These bonded phases exhibit significant affinity for Cu(II), U(VI), Fe(III), Ce(IV), Ti(IV), V(V), Mo(VI), Cr(VI) and no or less affinity for Ni, Co, Zn, Mg, Ca, K and Na ions. Exchange capacities and other parameters such as effect of pH and time on the extraction efficiency of metal ions using these phases are evaluated. The capacities for the phase based on dihydroxybenzoylamide proceed as follows: Cr(VI)〉V(V)〉 Ti(IV) ∼ Sb(III)〉U(VI) ∼ Mo(VI)〉Cu(II)〉Fe(III). The distribution coefficients determined in presence of 0.5 M NaCl show large K d values for U(VI) (5.3) at pH 6 and Cr(VI) (4.3) at pH 1. The mode of bonding is studied by FT-IR spectra of the bound complexes of Cu(II), Cr(VI) and Rh(I) with the above phase.
    Notes: Zusammenfassung Eine Methode zur Herstellung der immobilisierten Chelatbildner 2,3-Dihydroxybenzoyl und 3,4,5-Trihydroxybenzoylamid an Silicagel wird beschrieben. Solche Phasen besitzen eine ausgeprägte Affinität für Cu(II), U(VI), Fe(III), Ce(IV), Ti(IV), V(V), Mo(VI) und Cr(VI), während eine geringe oder keine für M(II)- (M=Ni, Co, Zn, Mg, Ca) und M(I)-Ionen (M=Na, K) gegeben ist. Die Austauschkapazität und andere Parameter von Einfluß wie pH und Zeit für die Wirksamkeit dieser Phasen bei Metallionen-Extraktionen werden genannt. Für die Austauschkapazität der auf Dihydroxybenzoylamid beruhenden Phase gilt die Metallionen-Reihenfolge: Cr(VI)〉V(V)〉Ti(IV) ∼ Sb(III)〉U(VI) ∼ Mo(VI)〉Cu(II)〉Fe(III). Die Verteilungskoeffizienten K d für die beiden M(VI)-Ionen (M=U, Cr) in 0,5 M NaCl betragen 5,3 (M=U, pH 6) und 4,3 (M=Cr, pH 1). FT-IR-Spektren zur Charakterisierung der gebundenen Komplexe von Cu(II), Cr(VI) und Rh(I) mit der oben genannten Phase liegen vor.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 304 (1980), S. 286-286 
    ISSN: 1618-2650
    Keywords: Rhenium-Gallium-Carbonyl-Komplex ; Kristall-strukturanalyse, Röntgenbeugung, Gitterenergieberechnung
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 485 (1982), S. 234-240 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Gallium-, Indium-Manganese-, and Thallium-Rhenium Carbonyl CompoundsCompounds of type Na{Cl4-nM[Mn(CO)5]n} (M = Ga, In; n = 1, 2, 3) were prepared by reaction of the Lewis acids MCl3 and NaMn(CO)5. Instead of the sodium salts were obtained the compounds (C3H7CO2)2InMn(CO)4L (Indium atom with the coordination number 5) from Indium(III) butyrate with two carboxylate groups bonded as chelate ligands and NaMn(CO)4L [L = CO, P(C6H5)3] in the molar ratio 1:1. By reacting TlCl with NaRe(CO)5 i.r. spectroscopic measurements of the solution pointed out the intermediate product TlRe(CO)5, which was unstable against a disproportionation reaction into Tl and Tl[Re(CO)5]3. The last named compound delivered as a thermal decomposition product Re2(CO)8[μ-TlRe(CO)5]2. I.r. bands of the new compounds were assigned.
    Notes: Verbindungen des Typs Na{Cl4-nM[Mn(CO)5]n} (M = Ga, In; n = 1, 2, 3) wurden durch Umsetzungen der Lewissäuren MCl3 mit NaMn(CO)5 hergestellt. An Stelle der Natriumsalze entstanden die beiden Produkte (C3H7CO2)2InMn(CO)4L (Indiumatom mit Koordinationszahl 5) bei Umsetzungen zwischen Indium(III)-butyrat mit zwei chelatartig gebundenen Carboxylatgruppen und NaMn(CO)4L [L = CO, P(C6H5)3] im Molverhältnis 1:1. Bei der Reaktion von TlCl mit NaRe(CO)5 zeigten infrarotspektroskopische Lösungsuntersuchungen das Zwischenprodukt TlRe(CO)5, welches instabil gegenüber einer Disproportionierungsreaktion in Thalliummetall und Tl[Re(CO)5]3 war. Die letztgenannte Verbindung lieferte als ein thermisches Zersetzungsprodukt Re2(CO)8[μ-TlRe(CO)5]2. Es wurden den neuen Verbindungen IR-Banden zugeordnet.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 471 (1980), S. 175-186 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation of C6H5M(CO5 (M = Mn, Re) and Ortho-Metallated Ketones with a Manganese or Rhenium Ring MemberC6H5Mn(CO)5 and C6H5Re(CO)5 were obtained by a new preparation method by a photochemical reaction between M2(CO)10 (M = Mn, Re) and (C6H5)2Hg. The reaction of C6H5Mn(CO)5 with (CH3)2Hg at different reaction conditions yielded the o-metallated benzophenone or the acetophenone; such known o-metallated derivates were prepared as yet by a reaction between the ketones and CH3Mn(CO)5. The ortho-metallated ketones and or were reaction products between Mn2(CO)10 and R2Hg (R=C6H5 or p-(CH3)2NC6H4). On the contrary Re2(CO)10 and (C6H5)2Hg were capable to form the analogous ortho-metallated benzophenone derivatives only by an addition of benzophenone. A substitution reaction of a CO ligand by P(C6H5)3, a fission of the five-membered heterocyclic ring and a phenylation was carried out for some of such o-metallated ketones. The products were characterized by infrared spectroscopic measurements.
    Notes: C6H5Mn(CO)5 und C6H5Re(CO)5 wurden nach einem neuen Darstellungsverfahren durch eine photochemische Umsetzung zwischen M2(CO)10 und (C6H5)2Hg erhalten. Die Reaktion von C6H5Mn(CO)5 mit (CH3)2Hg ergab bei verschiedenen Reaktionsbedingungen das o-metallierte Benzophenon oder das Acetophenon; solche bekannten o-metallierten Derivate wurden bisher durch eine Umsetzung zwischen den jeweiligen Ketonen und CH3Mn(CO)5 hergestellt. Die o-metallierten Ketone und oder sind Reaktionsprodukte zwischen Mn2(CO)10 und R2Hg (R=C6H5) oder o-(CH3)2NC6H4). Demgegenüber reagierte Re2(CO)10 und (C6H5)2Hg nur bei einem Zusatz von Benzophenon zu den analogen ortho-metallierten Benzophenon-Derivaten. Eine CO-Ligandensubstitutionsreaktion gegen P(C6H5)3, eine Spaltung des heterozyklischen Fünfrings und eine Phenylierung wurden für einige solcher o-metallierter Ketone durchgeführt. Die Produkte wurden durch infrarotspektroskopische Messungen charakterisiert.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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