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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 334 (1992), S. 179-180 
    ISSN: 0941-1216
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Lanthanide-Complexes with Rapid Z/E-Isomerisation of the 3-Acetyltetramic Acid Ligand
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0044-2313
    Keywords: Chelating agent: CuII and NiII complex ; complexation ; relaxation times ; 13C-n. m. r. ; magnetic properties ; X-ray analysis ; structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Isomerization at the Complexation of 3-Acetyltetramic Acid: Structure and Magnetic Properties of the CuII- and NiII-Complex of 2,7-Bis (1′, 5′, 5′ -trimethylpyrrolidin-2′,4′ -dion-3′ -yl)-3,6-diazaocta-2,6-dien2,7-Bis(1′, 5′, 5′ -trimethylpyrrolidin-2′, 4′ -dion-3′ -yl)-3,6-diazaoctadien formes CuII and NiII complexes with different constitutions (because of the Z/E isomerization). Results of X-ray analysis of N,N′ -ethylenbis(1′, 5′, 5′ -trimethylpyrrolidin-2′, 4′ -dion-3′ -acetiminato)nickel(II) 1 respectively -copper(II) 2 shows, that the complexing agent in 1 occurs in the E-form, whereas the ligand of the CuII complex forms the Z-form. Magnetic susceptibility and shift effects of the 13C-NMR signals point to a weak paramagnetism of the NiII complex. ESR-spectra are obtained from 2 only. Furthermore, the CuII complex reduces the relaxation times T1 and T2 of 1H and 17O nuclei spins from water. From the temperature dependence of the shortening of the relaxation times an activation energy is calculated which describes the reorientation of the copper complex in the “water matrix”.
    Notes: 2,7-Bis(1′, 5′, 5′ -trimethylpyrrolidin-2′, 4′ -dion-3′ -yl)-3,6-diazaocta-2,6-dien bildet aufgrund der Z/E-Isomerisierung als Ligand CuII- und NiII- Komplexe unterschiedlicher Konstitution. Die Ergebnisse der Röntgenstrukturanalyse von N,N′ -Ethylen-bis- (1′, 5′, 5′ -trimethylpyrrolidin-2′, 4′ -dion-3′ -acetimina-to)-Nickel-(II) 1 bzw. -Kupfer-(II) 2 zeigen, daß bei 1 der Ligand in der E-Form hingegen beim Kupferkomplex in der Z-Form vorliegt. Die magnetische Suszeptibilität und die Verschiebungseffekte der Ligandensignale in den 13C-NMR-Spektren deuten einen schwachen Paramagnetismus des Nickelkomplexes an. EPR-Spektren konnten nur vom Kupferkomplex 2 erhalten werden. Des weiteren verkürzt 2 die Relaxationszeiten T1 und T2 der Kernspinzustände von 1H und 17O des Wassers. Aus der Temperaturabhängigkeit der Relaxationszeitverkürzung wird eine Aktivierungsenergie berechnet, die zur Beschreibung der Reorientierung des Kupferkomplexes in der „Wassermatrix“ dient.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 13 (1986), S. 217-221 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The fragmentations of 2′-, 3′- and 5′-halogenated deoxyribonucleosides were studied using low-resolution mass spectrometry and deuteration experiments. The major reaction pathways provide ions which allow detection of halogen introduction and simple differentiation between the 3′- and 5′-derivatives with respect to the 2′-derivatives. Additionally, it has been shown that the 2′-derivatives from 2,2′-anhydrouridine during the process of evaporation, thus affecting the spectra obtained.
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 332 (1990), S. 319-324 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tautomeric 3-Acetyltetramic Acid Derivatives -1H/13C-n.m.r.-InvestigationThe molecular structure of 1,5,5-trimethyl-3-acetyltetramic acid (I) and its Schiffbases with ethylendiamin (II) and 1,3-diaminopropan-2-ol (III) is described by an equilibrium of four tautomers. The solvent dependence of the equilibrium is attributed to the strength of the intramolecular hydrogen bond. The higher proton affinity of the Schiff-bases (II and III) in comparison with the ketone (I) should be responsible for the faster equilibration of II and III.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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