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  • 1
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 47 (1991), S. 2041-2043 
    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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  • 2
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 42 (1986), S. 1602-1604 
    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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  • 3
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 43 (1987), S. 41-43 
    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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  • 4
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 41 (1985), S. 1591-1592 
    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 49 (1993), S. 1307-1309 
    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
    ISSN: 0020-1693
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 575 (1989), S. 165-170 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The New Intercalation Compound TaS2 · 0.5 C4NH5. Preparation and Physical PropertiesThe new intercalation compound TaS2 · 0.5 C4NH5 is obtained by reaction of 2H-TaS2 with surplus pyrrol in a closed system at 473 K. The powder diffraction pattern can be indexed based on a hexagonal unit cell with lattice parameters a = 3.315(1) and c = 22.256(7) Å. The temperature induced deintercalation has been studied from 293 to 1073 K. From 677 to 725 K there is a plateau in the TG curve which is attributed to the staging compound TaS2 · 0.33 C4NH5. Up to 1073 K a total mass of 10% has been squeezed out.From 300 to 50 K there is a nearly linear decrease of the resistivity of TaS2 · 0.5 C4NH5 while below 40 K a pronounced ascent has been observed followed by a transition to superconductivity at T ≤ 7,5 K. The degree of polymerized pyrrol in the host structure has been studied using XPS and a N1s signal, 5 eV broad, was monitored which indicates the existence of several sites of differently bonded N atoms.
    Notes: Die neue Intercalationsverbindung TaS2 · 0,5 C4NH5 entsteht bei der direkten Reaktion von 2H-TaS2 mit überschüssigem Pyrrol in geschlossener Ampulle bei einer Temperatur von 473 K. Das Pulverdiagramm der Titelverbindung ist auf Basis einer hexagonalen Zelle indizierbar mit a = 3,315(1) und c = 22,256(7) Å. Die thermische Deintercalation wurde im Temperaturbereich von 293 bis 1073 K untersucht. Zwischen 677 und 725 K deutet ein Plateau im TG-Diagramm auf die Existenz einer Phase der Zusammensetzung TaS2 · 0,33 C4NH5. Bis 1073 K wurde ein Massenverlust von 10% registriert.Im Temperaturbereich von 300 bis 50 K nimmt der Widerstand von TaS2 · 0,5 C4NH5 nahezu linear ab, unterhalb von T = 40 K ist ein ausgeprägter Anstieg zu verzeichnen. Ab T ≤ 7,5 K treten Übergänge in den supraleitenden Zustand auf. Im ESCA Spektrum deutet ein 5 eV breites N1s Signal auf die Existenz von Stickstoffatomen in unterschiedlicher Umgebung.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 537 (1986), S. 79-87 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Electrochemical Investigation of 1,1-Dicyanoethylene-2,2-dithiolate and Structure of the Anion 1,1-Dicyanoethylene-2,2-thiolatodisulfide, (—S(S)CC(CN)2)22-The anion 1,1-dicyanoethylene-2,2-dithiolate (S2C4N2)2- exhibits two anodic maxima in the cv-diagram. The reaction product of the first oxidation step is the dimer [(NC)2C=C(S)S—S(S)C=C(CN)2]2-. An x-ray crystal structure determination shows that the anion consists of two planar (S2C4N2) units which are oriented perpendicular within the anion.
    Notes: Das Anion 1,1-Dicyanoethylen-2,2-dithiolat (S2C4N2)2- zeigt im CV-Diagramm zwei anodische Maxima. Als Folgeprodukt der Primäroxydation entsteht das Dimere [(NC)2C=C(S)S—S(S)C=C(CN)2]2-, dessen Struktur röntgenographisch aufgeklärt wurde. Im Dimeren sind die (S2C4N2)-Einheiten planar und relativ zueinander senkrecht angeordnet.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Protonation and Methylation of 1, 1-Dicyanoethylene-2, 2-dithiolate Dianion. Preparative and Structural InvestigationsProtonation of alkaline metal salts of [S2C = C(CN)2]2- (I) in water yields a product of composition H2S2C4N2 (II). The species has to be formulated as dimere and crystallizes with two moles DMSO from DMSO solution with space group C2/c and a = 20.611(3), b = 4.800(1), c = 20.638(3) Å, β = 103.3(1)°, Z = 4. The X-ray structural analysis shows II to be a centrosymmetric 1, 3-Dithiacyclobutane system.On methylation of I with CH3I in the molar ratio 1:1, the monomethylated anion III can be isolated as AsPh4 salt. The compound crystallizes in the monoclinic space group P21/c, with a = 23.632(2), b = 14.304(1), c = 7.989(1) Å, β = 100.1(8)° and Z = 4. There are nearly planar anions [MeS(S)C=C(CN)2]- with an anti-conformation of the MeS group.
    Notes: Alkalimetallsalze des Dianions [S2C=C(CN)2]2- (I) liefern bei Protonierung in wässriger Lösung ein Produkt der Zusammensetzung H2S2C4N2 (II). II erweist sich als dimeres H4S4C8N4 und kristallisiert mit 2 mol DMSO in der Raumgruppe C2/c mit a = 20,611(3), b = 4,800(1), c = 20,638(3) Å, β = 103,3(1)° und Z = 4. Die Strukturanalyse steht in Einklang mit NMR- und IR-Daten und liefert für II ein zentrosymmetrisches Desaurin.Die Methylierung von I mit CH3I im Verhältnis 1:1 liefert das Mono-S-methylprodukt (III), das in From des Tetraphenylarsoniumsalzes strukturell charakterisiert wurde. Die Verbindung kristallisiert in der Raumgruppe P21/c mit a = 23,632(2), b = 14,304(1), c = 7,989(1) Å, β = 100,1(8)° und Z = 4. Die Anionen III sind nahezu planar und zeichnen sich durch eine anti-Konformation der CH3S-Gruppierung aus.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 543 (1986), S. 207-216 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Methylation and Oxidation of 1,1-Dicyanoethylene-2,2-oxo-thiolate Dianion: Preparative and Structural InvestigationsThe reaction of K2[S(O)C=C(CN)2] with CH3I yields the mono-S-methylproduct. The potassium salt crystallizes in the space group P21/c with a = 3.951(1), b = 15.623(3), c = 11.916(2) Å, β = 93.46(3)° and Z = 4. The methyl group is directed towards the oxygen atom.Potassium has a monocapped trigonal prismatic coordination: 5 N and 2 O atoms.The oxidation of 1,1-Dicyanoethylene-2,2-oxo-thiolate yields the dimere [(NC)2C=C(O)—S—S—(O)C=C(CN)2]2- in the first oxidation step. An X-ray crystal structure determination shows that the anion consists of two planar [S(O)C=C(CN)2] units which are oriented perpendicular within the anion.
    Notes: Die Reaktion Von K2[S(O)C=C(CN)2] mit CH3I liefert das Mono-S-methylprodukt, das in Form des Kaliumsalzes strukturell charakterisiert wurde. Die Verbindung kristallisiert in der Raumgruppe P21/c mit a = 3,951(1), b = 15,623(3), c = 11,916(2) Å, β = 93,46(3)° und Z = 4. Die Methylgruppe zeigt zum Sauerstoffatom des Monoanions. Kalium ist siebenfach in Form eines monocapped trigonalen Prismas Von 5 N- und 2 O-Atomen umgeben.Die Oxydation Von 1,1-Dicyanoethylen-2,2-oxo-thiolat liefert im Primärschritt das Dimere [(NC)2C=C(O)—S—S—(O)C=C(CN)2]2-, dessen Konstitution röntgenographisch aufgeklärt wurde. Im Dimeren sind die [S(O)C=C(CN)2]-Einheiten planar und relative zueinander senkrecht angeordnet.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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