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  • 1
    Electronic Resource
    Electronic Resource
    Synthese und Eigenschaften von molekularen Leitern auf der Basis von dmit-isologen Chelaten Kristall- und Molekülstruktur des Tetramethylammonium-bis-[bis-(1,3-dithiol-2-selon-4,5-diselenolato)nickelat]; [(CH3)4N][Ni(dsise)2]2 (1994)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 90-100 
    Details
    ISSN: 0044-2313
    Keywords: Dichalcogenolenchelates ; conducting materials ; x-ray ; EPR ; dmit isologues ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Syntheses and Properties of Molecular Conductors based on dmit isologous Chelates. Crystal and Molecular Structure of Tetramethylammonium-bis-[bis(1,3-dithiole-2-selone-4,5-diselenolato)nickelate]; [(CH3)4N] [Ni(dsise)2]2Syntheses and properties of dichalcogenolate chelates of the general type [(CH3)4N]n[ML2] (n ≤ 2; M = Ni, Pd, Pt); L = dmit (1,3-dithiole-2-thione-4,5-dithiolate), dmise (1, 3-dithiole-2-selone-4,5-dithiolate), dsit (1, 3-dithiole-2-thione-4,5-diselenolate), dsise (1, 3-dithiole-2-selone-4,5-diselenolate), dsis (1, 3-diselenole-2-selone-4,5-diselenolate) are reported. The effects of the chalcogen atom variation in these chelates are discussed by using UV/VIS, IR, EPR, cyclovoltammetric and conductivity data. The x-ray structure of [(CH3)4N][Ni(dsise)2]2 (space group Pccn, a = 7.427(1), b = 39.144(5), c = 11.836(1) Å) and the conductivity of the crystal (12 S cm-1 at room temperature) are given.
    Notes: Synthese und Eigenschaften von Dichalkogenolat-Chelaten vom Typ [(CH3)4N]n[ML2] mit n ≤ 2; M = Ni, Pd, Pt und L = dmit (1, 3-Dithiol-2-thion-4,5-dithiolat), dmise (1,3-Dithiol-2-selon-4,5-dithiolat), dsit (1,3-Dithiol-2-thion-4,5-diselenolat), dsise (1,3-Dithiol-2-selon-4,5-diselenolat) und dsis (1, 3-Diselenol-2-selon-4, 5-diselenolat) werden beschrieben. Anhand von UV/VIS-, IR-, EPR-, cyclovoltammetrischen und Leitfähigkeitsuntersuchungen werden die Auswirkungen der Chalkogenvariation in den Chelaten diskutiert. Die röntgenkristallographischen Daten von [(CH3)4N] [Ni(dsise)2]2 (Raumgruppe Pccn, a = 7,427(1), b = 39,144(5), c = 11,836(1) Å) und die Kristalleitfähigkeit (12 S cm-1, Raum-temperatur) werden vorgestellt.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19946200115
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  • 2
    Electronic Resource
    Electronic Resource
    Die Chelatbildung von N-Tris(2-aminoethyl)amin-N′,N′,N″,N″,N‴,N‴-hexaessigsäure (H6TTAHA) und N-(Pyrid-2-yl-methyl)ethylendiamin-N,N′,N′-triessigsäure (H3PEDTA) mit Gadolinium(III) - Synthesen, Komplexstabilität und NMR-RelaxivitätProfessor Egon Uhlig zum 65. Geburtstag gewidmet (1995)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 621 (1995), S. 807-811 
    Details
    ISSN: 0044-2313
    Keywords: Chelates, Gadolinium(III) ; Stability Constants ; 1H-NMR Relaxivity ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Chelate Formation of N-Tris(2-aminoethyl)amine-N′,N′,N″,N″,N‴,N‴-hexaacetic Acid (H6TTAHA) and N-(Pyrid-2-yl-methyl)ethylenediamine-N,N′,N′-triacetic Acid (H3PEDTA) with Gadolinium(III) - Syntheses, Stability Constants, and NMR-RelaxivitiesThe chelate formation of N-tris(2-aminoethyl)amine-N′,N′,N″,N″,N‴,N‴-hexaacetic acid (H6TTAHA) and N-(pyrid-2-yl-methyl)ethylenediamine-N,N′,N′-triacetic acid (H3PEDTA) with gadolinium(III) has been studied potentiometrically in aqueous solution at 25°C and μ = 0.1 (KCl). [Gd(TTAHA)]3-: 1gβM/ML = 19.0; {H[Gd(TTAHA)]}2-: 1gKH/MHL = 8.30; [Gd(PEDTA)]: 1gβM/ML = 15.56. Both 1 : 1 gadolinium(III) complexes were isolated as Na2H[Gd(C18H24N4O12)] · 3.5 H2O and [Gd(C14H16N3O6)] · 3 H2O, respectively. Their 1H-NMR relaxivities [1 · mmol-1 · s-1] ({H[Gd(TTAHA)]}2-: 9.5; [Gd(PEDTA)]: 8.8) offer promising applications for 1H-NMR imaging.
    Notes: Die Komplexbildung von N-Tris(2-aminoethyl)amin-N′,N′,N″,N″,N‴,N‴-hexaessigsäure (H6TTAHA) und N-(Pyrid-2-yl-methyl)ethylendiamin-N,N′,N′-triessigsäure (H3PEDTA) mit Gadolinium(III) wurde in wässeriger Lösung bei 25°C und μ = 0,1 (KCl) potentiometrisch untersucht. [Gd(TTAHA)]3-: 1gβM/ML = 19,0; {H[Gd(TTAHA)]}2-: 1gKH/MHL = 8,30; [Gd(PEDTA)]: 1gβM/ML = 15,56. Die 1 : 1-Gadolinium(III)-Komplexe wurden im Fall der H6TTAHA als Dinatriumsalz Na2H[Gd(C18H24N4O12)] · 3,5 H2O, bei der H3PEDTA als Neutralkomplex [Gd(C14H16N3O6)] · 3 H2O erhalten. Ihre NMR-Protonenrelaxivitäten [1 · mmol-1 · s-1] ({H[Gd(TTAHA)]}2-; 9,5; [Gd(PEDTA)]: 8,8) eröffnen Anwendungen als Kontrastmittel für die Kernspintomographie.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19956210518
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    Paper (German National Licenses)
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