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  • Electronic Resource  (17)
  • Inorganic Chemistry  (17)
  • Bicyclo[3.2.1]octanes, stereoselective syntheses of  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 112 (1979), S. 1751-1755 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Planar Threefold Coordination of Sulfur(VI): Crystal and Molecular Structures of (R3SiN)3S and (R3CN)3S (R=CH3) at -130°CThe crystal structures of the title compounds were determined from single crystal X-ray data (measured at -130°C) and refined to unweighted R-values of 0.034 for (R3SiN)3S (1) and 0.047 for (R3CN)3S(2). 2 crystallizes in the triclinic space group P1 and 1 in the hexagonal space group P63/m. Both structures exhibit a planar threefold nitrogen coordination of the sulfur but the large coefficients of the temperature factors perpendicular to the SN3 planes in 1 and 2 might indicate a disorder due to small deviations from planarity. The S—N bond lengths were found to be 150.4 (1) and 151.5 pm (2, mean).
    Notes: Die Strukturen der Titelverbindungen wurden aus Diffraktometer-Einkristalldaten (gemessen bei -130°C) bestimmt und zu ungewichteten R-Werten von 0.034 für (R3SiN)3S )(1) und 0.047 für (R3CN)3S (2)verfeinert. 2 kristallisiert triklin, P1. Und 1 hexagonal, P63/m. In beiden Strukturen wird eine trigonal planare Koordination des zentralen Schwefelatoms beobachtet, doch deuten die relativ großen Koeffizienten der anisotropen Temperaturfaktoren senkrecht zu den SN3-Ebenen in 1 und 2 auf eine Fehlordnung als Folge geringer Abweichungen von der Planarität in den einzelnen Molekülen hin. Die S—N-Abstände betragen 150.4 pm (1) und 151.5 pm (2, Mittelwert).
    Additional Material: 1 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 226-232 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Crystal and Molecular Structures of the S3N2+ Radical Cation in S3N2+SO3CF3- · 1/2 CH3CN and of S3N2(NSO2F)The molecular and crystal structures of S3N2+SO3CF3- · 1/2 CH3CN (1) and S3N2NSO2F (2) were determined from single crystal X-ray diffraction data. The S3N2+ radical cation in 1 is planar, two cations being connected through weak S—S bonding interactions to form dimers with a chair configuration. The S3N2 ring of 2, in which the NSO2F group is covalently bonded to one of the S atoms of the S — S group, is not planar; the S — S bond is weaker than in 1.
    Notes: Die Röntgenstrukturanalysen von S3N2+SO3CF3- - 1/2 CH3CN (1) und S3N2NSO2F (2) zeigen in 1 ein planares S3N2+-Radikalkation, wobei zwei Kationen über schwache S-S-Wechselwirkungen zu sesselförmigen Dimeren assoziiert sind. Der an einem S-Atom der S — S-Gruppe substituierte S3N2-Ring in 2 ist nicht planar; die S — S-Bindung ist schwächer als in 1.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation of trans-[Mo6Cl8]Cl4Br22- Starting from Crystalline [Mo6Cl8]Cl4(H2O)2 and Crystal Structure of [(C6H5)4As]2[Mo6Cl8]Cl4Br2The synthesis of the title compound is successful if the crystallized [(Mo6Cl8)Cl4(H2O)2] containing the H2O molecules in trans-position reacts with HBr + [(C6H5)4As]Br in ethanol in a heterogeneous reaction. The X-ray structure investigation confirms the existence of discrete trans-Br-substituted cluster anions of composition [(Mo6Cl8)Cl4Br2]2- in the crystal. The reaction in homogeneous solutions proceeds to Br-enriched compounds. [(C6H5)4As]2[(Mo6Cl8)Cl4Br2] crystallizes in the triclinic space group P¯1 with a = 11.071(2), b = 11.418(2), c = 12.813(2) Å, α = 116.10(2), β = 95.27(2) and γ = 94.41(2)° (-133°C). The crystal structure at -133°C was determined from single crystal X-ray diffraction data (R1 = 0.026). The [(Mo6Cl8)Cl4Br2]2--anions are not completely ordered but distributed statistically among the three positions which are possible within the limits of the ordered [Mo6Cl8]-cores (ratio 11:5:4). The frameworks of the anions consist of Mo6 cluster units with (slightly distorted) octahedral arrangement of the metal atoms (d(Mo—Mo): 2.600(1) up to 2.614(1) Å), which are coordinated by the halogeno ligands in a square-pyramidal manner. The details of the structure will be discussed and compared with similar [(Mo6X8)Y4] cluster units (X, Y = Cl, Br).
    Notes: Die Darstellung der in der Überschrift genannten Verbindung gelingt, wenn das kristallisierte [(Mo6Cl8)Cl4(H2O)2], das die H2O-Molekeln in trans-Stellung enthält, in Ethanol mit HBr + [(C6H5)4As]Br in heterogener Reaktion umgesetzt wird. Die röntgenographische Untersuchung bestätigt, daß im Kristall das isolierte trans-Br-substituierte Clusteranion [(Mo6Cl8)Cl4Br2]2- vorliegt. In homogener Lösung läft die Reaktion weiter zu Br-reicheren Produkten. [(C6H5)4As]2[(Mo6Cl8)Cl4Br2] kristallisiert in der triklinen Raumgruppe P¯1 mit a = 11,071(2), b = 11,418(2), c = 12,813(2) Å, α = 116,10(2), β = 95,27(2) und γ = 94,41(2)° (-133°C). Die Kristallstruktur bei -133°C wurde aus Einkristalldiffraktometerdaten bestimmt (R1 = 0,026). Die [(Mo6Cl8)Cl4Br2]2--Anionen sind im Kristall nicht vollständig geordnet, sondern verteilen sich statistisch im Verhältnis 11:5:4 auf die bei definiertem [Mo6Cl8]-Gerüst möglichen drei Positionen mit trans-ständiger Anordnung der Br-Liganden. Die Gerüste der Anionen bestehen aus Mo6-Clustern mit (leicht verzerrter) oktaedrischer Anordnung der Metallatome (d(Mo—Mo): 2,600(1) bis 2,614(1) Å), die quadratischpyramidal von Halogenatomen koordiniert sind. Die Einzelheiten der Struktur werden im Vergleich mit analog gebauten [(Mo6X8)Y6]-Clustern (X, Y = Cl, Br) diskutiert.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 524 (1985), S. 95-100 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 18C6 Crown Complex of Amidosulfuric AcidThe title compound (3) has been obtained from reaction of the crown ether 18C6 (1) with amidosulfuric acid (2) in water, methanol, and ethanol. The structure of the substance was elucidated with X-ray diffraction and IR data. The two constituents of 3 are connected through three oxygen-hydrogen bridges. 3 is ideally suited for the isolation and recovery of 1 from aqueous solutions.
    Notes: Durch Umsetzung des Kronenethers 18C6 (1) mit Amidoschwefelsäure (2) in Wasser, Methanol und Ethanol konnte die Titelverbindung (3) dargestellt werden. Die Struktur der Substanz wurde durch Röntgenstrukturanalyse und durch ihr IR-Spektrum aufgeklärt. Die beiden Komponenten von 3 sind durch drei Sauerstoff-Wasserstoff-Brücken miteinander verknüpft. 3 eignet sich hervorragend für die Isolierung und die Rückgewinnung von 1 aus wäßrigen Lösungen.
    Additional Material: 2 Ill.
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  • 5
    ISSN: 0009-2940
    Keywords: Thiolato ligands ; Nickel complexes ; Hydrogenase models ; Bioinorganic chemistry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mononuclear Nickel Thiolate Complexes Containing Nickel Sites in Different Oxidation States: Molecular Definition of [Ni(SC6H4O)2]2- and [Ni(SC6H4O)2]Herrn Professor Dietrich Mootz zum 60. Geburtstag gewidmet.A solution of NiCl2·6 H2O in EtOH/H2O reacts with nBu3N and o1-mercaptophenol to form [nBu3NH]2[Ni(SC6H4O)2]·EtOH (2) containing the nickel(II) complex [Ni(SC6H4O)2]2- (1). The molecular structures of 1 and its oxidation product, [Ni(SC6H4O)2]- (3), have been determined by X-ray diffraction. With respect to the chemical as well as electrochemical properties of the nickel sites of various hydrogenases, 3 is the first relevant model complex of coordination number four whose structural properties have been determined in different oxidation states.
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2041-2045 
    ISSN: 0009-2940
    Keywords: Imidazol-2-ylidene - Borane adducts ; Calculations, ab initio ; Borane - Imidazol-2-ylidene adducts ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Imidazole Derivatives, VI[1].  -  Stable Carbene BoranesStable imidazol-2-ylidene - borane adducts 8 and 9 are obtained from 1,3,4,5-tetraalkylimidazol-2-ylidenes 7 and Me2S BH3 or Et2O BF3. An X-ray structure analysis of 8b has been performed. An ab initio calculation [MP2(fu)/6-31G**] reveals a low energy difference between two rotamers. The bond orders of the cyclic bonds imply only a minor interaction between the N - C - N and the C - C fragment.
    Additional Material: 1 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2047-2049 
    ISSN: 0009-2940
    Keywords: 2-Telluroimidazolines ; 125Te NMR ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Imidazole Chemistry, III[1].  -  2-Telluroimidazolines  -  Stable Tellurocarbonyl Compounds2-Telluroimidazolines 6 are obtained as stable solids from the imidazol-2-ylidenes 4 and tellurium in good yields. The X-ray structure of 6c reveals the relevance of the mesomeric structure 5 [d(C1 - Te) = 2.087(4) Å] which is confirmed by the upfield shift in the 125Te NMR spectra (dL 〈  - 150).
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  • 8
    ISSN: 0009-2940
    Keywords: Silicon ; Germanium ; Tin ; Carbene homologues ; Digermene ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of the diaminosilylene :Si(tBuNCH2CH2NtBu) (5) with the diaminogermylene :Ge(tBuNCH2CH2NtBu) is thought to proceed via a germasilene → silylgermylene rearrangement and dimerisation to furnish the (Z)-1,2-diamino-1,2-disilyldigermene (Z)-9. The X-ray structure analysis of (Z)-9 reveals a long Ge—Ge bond length of 245 pm and a large trans-bent angle of 42°. Air-oxidation of (Z)-9 takes place with retention of configuration at the germanium atoms to provide the corresponding substituted (Z)-2,4-digerma-1,3-dioxetane (Z)-10. Treatment of 5 with the stannylene :Sn[N(SiMe3)2)2 gives, as a final product, the hydridodisilylstannane 12. The structures of (Z)-10 and 12 were also determined by X-ray crystallography.
    Additional Material: 1 Tab.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 849-851 
    ISSN: 0009-2940
    Keywords: Selenium iodides ; Imidazoles ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Imidazole Derivatives, IX.  -  Stabilisation of Selenium Diiodide by ComplexationHerrn Professor Helmut Werner zum 60. Geburtstag gewidmet.Stable selenium diiodide complexes 2 are obtained by the reaction of the 2-selenoxoimidazolines 1 with iodine. An X-ray structure analysis of 2c reveals its monomeric nature. In the trigonal bipyramid, the iodo substituents are situated in axial positions forming elongated iodine bonds [Se-I(1) 2.854(1), Se—I(2) 2.768(1) Å; I(1)—Se—I(2) 175.4(0)°].
    Additional Material: 1 Ill.
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  • 10
    ISSN: 0009-2940
    Keywords: Ring enlargement ; Phellandrene ; Carbonylation ; Bicyclo[3.2.1]octanes, stereoselective syntheses of ; Iron complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Carbonylating Ring Enlargement, 41). - Diastereoselective Syntheses of Bicyclo[3.2.l]oct-3-ene-2,8-diones by Double Carbonylation of (It)-(-)-α-PhellandreneIn order to clarify the stereochemistry of the carbonylating ring enlargement of cyclohexadiene complexes 1 to complexed seven-membered ring ketones 2 and the further carbonylation to bicyclo[3.2.1]oct-3-ene-2,8-diones 3 the exo and endo isomers of (R)-(-)-α-phellandrene complex 7 were synthesized in pure form and in various isomeric ratios and converted. The optically active ring-enlargement products 11 and 12 obtained therefrom, as well as the enantiomerically pure bicyclooctenes 20-22, implicate a stereospecific reaction course under retention of the configuration predetermined by the starting material 6 and its complexes 7. This was confirmed by an X-ray determination of the absolute configuration of exo-12. Thus, the method is suitable for the diastereoselective synthesis of bicyclo[3.2.1]oct-3-ene-2,8-diones 3 from 1,3-cyclohexadiene complexes 1.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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