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  • 1
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 1466-1468 
    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
    ISSN: 1573-8779
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Crystal structures of (Et4N)2[Mo3S7Br6] (I) and (Et4N)(H9O4)[Mo3S7Cl6] (II) clusters belonging to the class of Mo3S 7 4+ were determined by X-ray diffraction analysis. Crystals I are orthorhombic a=19.106(3), b=12.930(2), c=29.887(5) Å, V=7383(2) Å3, space group Pbca, Z=8, dcalc=2.253 g/cm3, R(F)=0.0402, wR(F2)=0.0587 for 2493 Fhkl〉4σ. Crystals II are monoclinic, a=17.106(3), b=18.882(4), c=11.006(2), Å, β=126.13(3)°, V=2871.2(9) Å3, space group Cc, Z=4, dcalc=2.147 g/cm3, R(F)=0.0181, wR(F2)=0.0445 for 2307 Fhkl〉4σ. Structure I has an anion dimer with 3Sax…Cl=3.258(4)–3.404(4) Å; the dimer is similar to that observed in the structures of A2[M3X7Hal6], A=Ph4P+, Ph3EtP+, and PPN+. In structure II, infinite chains of anions bonded by 3Sax…Cl contacts of 3.183(3)–3.394(3) Å were found. A similar phenomenon was established earlier for the structure of (Et4N)(H9O4)[Mo3S7Br6] (III), which is not isostructural to II. Compounds II and III also differ in the structure of the H9O4 + cation: infinite helix in II and pyramid in III.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 623 (1997), S. 316-323 
    ISSN: 0044-2313
    Keywords: Urocanic Acid ; Cobalt ; Zinc Complexes ; Crystal Structures ; IR and Raman Spectra ; Thermal Behavior ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Crystal Structure, Vibrational Spectra, and Thermal Behavior of the Cobalt(II) and Zinc(II) Complexes of Urocanic AcidThe crystal structures of [Co(Urocan)2(H2O)4] and [Zn(Urocan)2(H2O)4] (urocan = anion of 4-imidazoleacrylic acid = urocanic acid) have been solved by single-crystal X-ray diffractometry. They are isostructural and crystallize in the monoclinic space group P21/c with Z = 2. A general assignment of their vibrational (IR and Raman) spectra, compatible with the structural characteristics, is proposed. The thermal behavior of both complexes was investigated by means of TG and DTA methods.
    Notes: Die Kristallstrukturen von [Co(Urocan)2(H2O)4] und [Zn(Urocan)2(H2O)4] (Urocan = Anion der Imidazol-4-acrylsäure = Urocaninsäure) wurden röntgenographisch an Einkristallen bestimmt. Sie sind isostrukturell und kristallisieren in der monoklinen Raumgruppe P21/c mit Z = 2. Eine Zuordnung ihrer Schwingungsspektren (IR und Raman), die mit den strukturellen Eigenschaften im Einklang steht, wird vorgeschlagen. Das thermische Verhalten beider Komplexe wurde an Hand von TG- und DTA-Messungen untersucht.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0044-2313
    Keywords: Chromium, molybdenum, tungsten chelate complexes ; IR, NMR, MS ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Alternative Ligands. XXVI. M(CO)4 L-Complexes (M = Cr, Mo, W) of the Chelating Ligands Me2ESiMe2(CH2)2E′ Me2 (Me = CH3; E = P, As; E′ = N, P, As)The reaction of M(CO)4NBD (NBD = norbornadiene; M = Cr, Mo, W) with the ligands Me2ESiMe2(CH2)2E′ Me2 yields the chelate complexes (CO)4M[Me2ESiMe2]) for E,E′ = P, As, but not for E and /or E′ = N. The NSi group is not suited for coordination because of strong (p-d)π-interaction. In the case of the ligands with E = P or As and E′ = N chelate complexes can be detected in the reaction mixture, but isolable products are complexes with two ligands coordinated via the E donor group. The new compounds are characterized by analytical and spectroscopic (IR, NMR, MS) investigations. The spectroscopic data are also used to deduce the coordinating properties of the ligands. X-ray diffraction studies of the molybdenum complexes (CO)4Mo[Me2ESiMe2(CH2)2AsMe 2] (E = P, As) in accord with the observed coordination effects show only small differences between SiE and CE donor functions. Attempts to use the ligands Me2ESiMe2(CH2)2AsMe2 (E = P, As) for the preparation of Fe(CO)3L complexes result in the fission of the SiE bonds and the formation of the binuclear systems Fe2(CO)6(EMe2)2 (E = P, As) together with the disilane derivative [Me2Si(CH2)2AsMe2]2.
    Notes: Die Umsetzung von M(CO)4NBD (NBD = Norbornadien; M = Cr, Mo, W) mit den Liganden Me2ESiMe2(CH2)2E′Me2 liefert für E,E′ = P, As die Chelatkomplexe (CO)4M[Me2ESiMe2(CH2)2E′Me 2], nicht jedoch für E und/oder E′ = N. Die NSi-Gruppierung ist wegen der starken (p-d)π-Rückbindung nicht zur Koordination befähigt; im Fall der Liganden mit E = P oder As und E′ = N sind im Reaktionsgemisch zwar Chelatkomplexe nachweisbar, bei den isolierbaren Produkten handelt es sich jedoch um Komplexe mit zwei E-koordinierten Liganden. Die neuen Verbindungen werden durch analytische und spektroskopische (IR, NMR, MS) Untersuchungen charakterisiert. Die spektroskopischen Daten dienen auch der Beurteilung der Koordinations-eigenschaften der Liganden. Die Röntgenbeugungsanalyse der Molybdänkomplexe (CO)4Mo[Me2ESiMe2(CH2) 2AsMe2] (E = P, As) ergibt in Übereinstimmung mit den Koordinationseffekten nur geringe Unterschiede zwischen SiE und CE-Donorfunktionen. - Bei Versuchen, die Liganden Me2ESiMe2(CH2)2AsMe2 (E = P, As zur Synthese von Fe(CO)3L-Komplexen zu nutzen, werden unter Spaltung der SiE-Bindung die Zweikernsysteme Fe2(CO)6(EMe2)2(E = P, As) und das Disilanderivat [Me2Si(CH2)2AsMe2]2 erhalten.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0044-2313
    Keywords: Nickelcarbonyl Complexes ; Tripod Ligands ; Basic Complex Fragments ; Cage Structures ; IR ; MS ; NMR ; X-Ray ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Alternative Ligands. XXXI. Nickelcarbonyl Complexes of Tripod Ligands of the Type XM′(OCH2PMe2)n(CH2CH2PR2)3-n (M′ = Si, Ge; n = 0-3)The coordinating properties of the tripod ligands RM′(OCH2PMe2)n(CH2CH2PMe2)3-n (M′ = Si, Ge) (1-7), MeSi(OCH2PMe2)2CH2CH2P(CF3)2 (8), MeSi(OCH2PMe2)2CH2CH2NMe2(10) as well as of the tetradentate representative Si(OCH2PMe2)4 (9) have been investigated by the preparation of the novel nickel carbonyl complexes LNiCO (11-18), Si(OCH2PMe2)4[Ni(CO)2]2 (19) and (HOCH2PMe2)2Ni(CO)2 (20). They are obtained in moderate to good yields by the reaction of Ni(CO)4 with the corresponding ligands in toluene (20-111°C) (see Table 1). The new compounds have been characterized by analytical (C, H) and spectroscopic investigations (IR; 1H-, 13C-, 19F, 31P-NMR, MS). The ligand properties are discussed on the basis of spectroscopic data [in particular coordination shifts Δδ = δ(complex) - δ(ligand)] leading to the conclusion that the high electron density on Ni gives rise to a weak, but significant Ni→Si interaction. An important indication comes from the large low field shift ΔδF = 34.5 ppm for the SiF acceptor bridge in 17. This result is supported by an X-ray diffraction study of 11 giving an NiSi distance of 3.941(2) Å. With the exception of O2…P3 (Abb. 7) all other O…P through-cage contacts are longer than the NiSi distance. An additional release from the high charge density on Ni is obtained via π-backbonding to the neighbouring groups OCPMe2, CCPMe2 and CO.
    Notes: Die Koordinationseigenschaften der Tripod-Liganden RM′(OCH2PMe2)n(CH2CH2PMe2)3-n (M′ = Si, Ge) (1-7), MeSi(OCH2PMe2)2CH2CH2P(CF3)2 (8), MeSi(OCH2PMe2)2CH2CH2NMe2 (10) sowie des vierzähnigen Vertreters Si(OCH2PMe2)4 (9) wurden durch Darstellung der neuen Nickelcarbonylkomplexe LNiCO (11-18), Si(OCH2PMe2)4[Ni(CO)2]2 (19) und (HOCH2PMe2)2Ni(CO)2 (20) untersucht. Diese sind in mäßigen bis guten Ausbeuten durch Umsetzung von Ni(CO)4 mit den entsprechenden Liganden in Toluol (20 bis 111 °C) zugänglich (s. Tab. 1). Die neuen Verbindungen wurden durch analytische (C, H) und spektroskopische Untersuchung (IR; 1H-, 13C-, 19F-, 31P-NMR, MS) charakterisiert. Die Ligandeneigenschaften werden auf der Basis der spektroskopischen Daten [insbesondere der Koordinationsverschiebungen Δδ = δ(Komplex) - δ(Ligand)] diskutiert. Als Schlußfolgerung ergibt sich, daß die hohe Elektronendichte am Ni zu einer schwachen, aber signifikanten Ni → Si-Wechselwirkung führt. Darauf weist insbesondere die überraschend große Tieffeldverschiebung ΔδF = 34,5 ppm für die SiF-Akzeptorbrücke in 17 hin. Dieser Befund wird durch eine Röntgenstrukturanalyse an 11 gestützt, die einen NiSi-Abstand von 3,941(2) Å ergibt. Mit Ausnahme von O2…P3 (Abb. 7) sind alle übrigen O…P-Kontakte durch den Käfig länger als der NiSi-Abstand. Eine zusätzliche Entlastung des Ni von der hohen Ladungsdichte erfolgt durch π-Rückbindung zu den Nachbargruppen OCPMe2, CCPMe2 und CO.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0044-2313
    Keywords: Pentafluorophenyliodinetetrafluoride ; preparation ; crystal structure ; iodinepentafluoride ; tris(pentafluorophenyl)-bismuth ; pentafluorophenyliodinedifluoride, pentafluoroiodobenzene ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Pentafluorophenyliodine(V) Compounds. 2. Pentafluorophenyliodine Tetrafluoride C6F5IF4: Synthesis via Fluorine-Aryl-Substitution on IF5  -  Properties and Structure. Structural Analysis of the Monovalent Iodine Parent Compound C6F5IThe nucleophilic fluorine-aryl substitution reaction on IF5 with pentafluorophenyl, Bi(C6F5)3, leads to C6F5IF4 in good yields and high purity. The thermal stability of C6F5IF4 and its NMR spectrometric behaviour in solution will be described. The crystal structure of C6F5IF4 will be discussed in comparison to IF5. In addition data of the molecular and crystal structure of the monovalent iodine parent compound C6F5I will be given.
    Notes: Durch nukleophile Fluor-Aryl-Substitution an IF5 mit Pentafluorphenyl, Bi(C6F5)3, gelingt die Darstellung von C6F5IF4 in guten Ausbeuten und hoher Reinheit. Beschrieben wird die thermische Stabilität und das NMR-spektrometrische Verhalten in Lösung. Die Kristallstruktur von C6F5IF4 wird im Vergleich mit IF5 diskutiert. Ferner werden die Molekül- und Kristallstrukturdaten der monovalenten Iodstammverbindung C6F5I mitgeteilt.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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