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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 112 (1979), S. 2413-2418 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Molecular Structure of a Metal Cluster with Cubane Structure, [η5-C5H5Mo(CO)3HgMo]4(4)The compound [η5-C5H5Mo(CO)3HgMo]4 has been isolated as an additional product of the reaction between [η5-C5H5Mo(CO)3]2, 2-butenyl chloride, and sodium amalgam. The X-ray structure (R = 0·050) analysis of this novel species revealed that the compound has a slightly distorted cubane structure, for the first time the cubane unit being built up by two different metal atoms (Mo and Hg).
    Notes: Die Verbindung [η5-C5H5Mo(CO)3HgMo]4 (4) wurde als weiteres Produkt der Reaktion zwischen [η5-C5H5Mo(CO)3]2, 2-Butenylchlorid und Natriumamalgam isoliert. Die Röntgenstrukturanalyse dieser neuartigen Spezies zeigt eine leicht verzerrte Cubanstruktur, bei der das Cubangerüst erstmals aus zwei verschiedenen Metallatomen (Mo und Hg) aufgebaut ist. Der R-Wert beträgt 0·050.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 422 (1976), S. 182-192 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Übergangsmetall-Chlorid-Chelate mit 1.10-Phenanthrolin-N-Oxyd1.10-Phenanthrolin-N-Oxyd(L) reagiert mit 3d Metall-Chloriden unter Bildung folgender Chelate: [CrL2Cl2]Cl · H2O; [FeL2CI2]Cl; [FeLCl2]x (x = 1 oder 2); [MnL2Cl2]; [ClLMnCl2MnLCl] · 2 H2O; [CoL2Cl2] · H2O; [CoLCl2] · H2O; [NiL2Cl2] · 2 H2O; [CuL2Cl]Cl · 2H2O oder [CuL2Cl2] · 2 H2O; und [ZnL3][ZnCl4] · 2 H2O. Diese Chelate wurden mittels Infrarot- und Elektronen-Spektren und magnetischer, röntgenographischer und konduktometrischer Messungen charakterisiert.
    Notes: 1,10-Phenanthroline N-oxide(L) interacts with 3d metal chlorides to yield the following chelates: [CrL2Cl2]Cl · H2O; [FeL2Cl2]Cl; [FeLCl2]x (x = 1 or 2); [MnL2Cl2]; [ClLMnCl2MnLCl] · 2 H2O; [CoL2Cl2] · H2O; [CoLCl2] · H2O; [NiL2Cl2] · 2 H2O; [CuL2Cl]Cl · 2 H2O or [CuL2Cl2] · 2 H2O; and [ZnL3][ZnCl4] · 2 H2O. These complexes were characterized by means of their infrared and electronic spectra, magnetic susceptibilties, X-ray powder diffraction patterns and molar conductivities.
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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: Investigations on the Catalysis of Ammonia Synthesis and Nitrogen Isotope Exchange by Lamellar Compounds of Graphite with Iron, Ruthenium, and OsmiumThe catalytic activity of transition metal potassium-graphite lamellar compounds for the synthesis of ammonia from the elements and the catalysis of the equilibration by isotope exchange of the isotopic nitrogen molecules are shown to correlate. Connections between the state of metal in the catalyst exist with iron as metal which is shown by Mössbauer spectroscopy and the catalytic activity in relation to the potassium content.
    Notes: Die katalytische Aktivität von Übergangsmetall-Kalium-Graphitverbindungen bei der Synthese von Ammoniak aus den Elementen und bei der Einstellung des Isotopenaustauschgleichgewichts der isotopen Stickstoffmolekeln korrelieren miteinander. Im Falle von Eisen als Metall sind Beziehungen zwischen dem durch Mößbauer-Spektroskopie ermittelten Zustand des Metalls im Katalysator und der katalytischen Aktivität in Abhängigkeit vom Kaliumgehalt erkennbar.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 443 (1978), S. 269-278 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Komplexe von TrialkylphosphinoxidenEs wird über neue Komplexe von Trimethyl-, Tris(hydroxymethyl)-, Triethyl-, Tripropyl-, Tri-isopropyl-, Tributyl-phosphinoxid berichtet. Aussagen über die Strukturen der Komplexe werden mit Hilfe der Schwingungs- und Ligandenfeld-Spektroskopie erzielt. Die verschiedenen Faktoren, welche die Strukturen beeinflussen, werden diskutiert.
    Notes: A number of new complexes containing trimethylphosphine oxide, tris(hydroxymethyl)phosphine oxide, triethylphosphine oxide, tripropylphosphine oxide, triisopropylphosphine oxide and tributylphosphine oxide is reported. The structures of the complexes have been deduced with the aid of physical measurement such as vibrational and ligand-field spectroscopy. The various factors that influence the structure of phosphoryl solvates and adducts are discussed.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 109 (1976), S. 125-131 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Crystal and Molecular Structure of C7H7RuC7H9 - (1-5-ν- Cycloheptadienyl)(1-5-ν-cyclohepatrienyl)ruthenium(II)The structure of the title compound 5 has been determined by X-ray diffraction. The compound crystallizes in the space group P21/n, a = 644.2 ± 0.1 pm, b = 01775.8 ± 0.2 pm., c = 989.9 ± 0.1 pm, β = 97.72 ± 0.02°, Z = 4 (R = 0.035). The ruthenium atom is coordinated by a cyclohephtadienyl and cycloheptatrienyl ligand, both functioning as five electron ligands. One double bond of the cycloheptarienyl ligand does not interact with the central atom.
    Notes: Mittels Röntgenanalyse wurde die Struktur der Titelverbindung 5 bestimmt. Der Komplex kristallisiert in der Raumgruppe p21/n, a = 644 ±0.1pm, b = 1775.8 ± 0.2pm, c = 989 ± 0.1pm, β = 97.72 ± 0.02°, Z = 4 (R + 0.035). Das Ruthenium ist im Komplex jeweils von einem Cycloheptadienyl- und Cycloheptarienylliganden koordiniert. Beide fungieren als 5-Elektronenliganden, wobei im Cycloheptarienylligand eine Doppelbindung nicht in Wechselwirkung mit dem Zentralatom ist.
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  • 6
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: I. R. Laser-specific Reactions of Boron Compounds, VMercaptoboranes from the Reaction of Diborane with Hydrogen SulfideThe new and unstable compounds HB(SH)2 (1) and HB(SD)2 are formed by CO2-laser irradiation of a gaseous mixture of B2H6 and H2S or D2S, respectively. In addition, μ-mercapto-diborane, HSB2H5 (2), has been obtained. None of these compounds is produced in the thermal reaction of B2H6 and H2S.
    Notes: Die neuen, instabilen Verbindungen HB(SH)2 (1) und HB(SD)2 bilden sich bei der CO2-Laserbestrahlung eines Gasgemisches von B2H6 und H2S bzw. D2S. Außerdem wurde μ-Mercaptodiboran, HSB2H5 (2), erhalten. Keine dieser Verbindungen entsteht bei der thermisch angeregten Reaktion von B2H6 mit H2S.
    Additional Material: 5 Ill.
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  • 7
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Di-p-hydrido-bis[1,3-propanbis(dicyclohexylphosphin)]dinickel(Ni—Ni) - Der Bindungszustand in einem Dreizentren-Wasserstoff-überbrückten Ni—Ni-SystemDie Kristallstruktur der Titelverbindung [(C6H11)2PCH2CH2CH2P(C6H11)2NiH]2 (1) wurde aus 4051 Reflexen abgeleitet und zu einem R-Wert von 0.044 verfeinert. Lageparameter aller Wasserstoffatome konnten einer Differenz-Fourier-Synthese entnommen werden. Die Struktur der diamagnetischen Verbindung setzt sich aus zwei P2Ni-Untereinheiten zusammen, welche zweifach mit Wasserstoffatomen (Ni—H 1.6 Å) überbrückt sind. Hierdurch ergibt sich ein bindender Ni—Ni-Abstand von 2.441(1) Å. Im Kristallgitter bilden die Ebenen durch die P2Ni-Untereinheiten einen Interplanarwinkel von 63.3°. Theoretische Betrachtungen sagen für das freie Molekül eine quadratisch planare Anordnung voraus, doch ergibt sich für die Drehbewegung zur beobachteten Geometrie nur eine flache Potentialenergiefläche. Die gefundene Verdrillung resultiert aus starken intramolekularen Abstoßungskräften zwischen den Cyclohexylgruppen der zwei P2Ni-Einheiten.
    Notes: The crystal structure of the title compound, [(C6H11)2PCH2CH2CH2P(C6H11)2NiH]2 (1), has been determined from 4051 reflections and refined to a final R-value of 0.044. The positions of the hydrogen atoms (bridging and non-bridging) have been determined from a difference Fourier synthesis. The molecular structure of the diamagnetic compound consists of subunits doubly-bridged by hydrogen atoms. The Ni—Ni and average Ni—H distances are 2.441 and 1.6 Å, respectively. In the solid state the two planes of the P2Ni units form a dihedral angle of 63.3°. Theoretical considerations predict a square-planar structure for the idealized molecule with a soft potential energy surface for a twisting motion towards the observed geometry. The observed twist is the result of severe intramolecular repulsions between the cyclohexyl groups of the two P2Ni units.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 2212-2218 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Vinyl Cations, 20. Synthesis and Solvolysis of Bicyclo[5.3.0]dec-l-ene-2-yl TriflateBicyclo[5.3.0]dec-1-ene-2-yl triflate (6) and Δ1(8a)-octalinyl triflate (7) were synthesized and the solvolyses of both compounds were investigated in different solvents. 6 reacts in 50% aqueous ethanol and in 70% trifluoroethanol mostly with rearrangement to 1-decalone (3). Similarly, a rearrangement to the octalinyl system occurs in absol. TFE, in which the enol ether 11 is formed. In contrast, 7 solvolyses in the same solvents mostly with retention of structure. A rearrangement to the bicyclo[5.3.0]decane system was observed only in small amounts. - The triflate 6 solvolyses in 50% aqueous ethanol 343 times faster than 7. The product analyses as well as the kinetics show that the solvolyses occur via vinyl cation intermediates. The octalinyl cation 2 would appear to have a higher stability than the bicyclic vinyl cation 4.
    Notes: Bicyclo[5.3.0]dec-1-en-2-yl-triflat (6) und Δ1(8a)-Octalin-1-yl-triflat (7) wurden synthetisiert und ihre Solvolysereaktionen in verschiedenen Lösungsmitteln untersucht. 6 reagiert in 50proz. wäßr. Äthanol und in 70proz. Trifluoräthanol weitgehend unter Umlagerung zum 1-Decalon (3). In absol. Trifluoräthanol tritt ebenfalls Umlagerung in das Octalinylsystem ein, wobei der Enoläther 11 erhalten wird. 7 solvolysiert in den gleichen Lösungsmitteln weitgehend unter Strukturerhaltung, eine Umlagerung in das Bicyclo[5.3.0]decan-System wird nur in untergeordnetem Maße beobachtet. - Das Triflat 6 solvolysiert in 50proz. wäßr. Äthanol 343 mal schneller als 7. - Die Produktanalysen sowie die Kinetik zeigen, daß die Solvolysen über Vinyl-Kationen ablaufen, wobei das Octalinyl-Kation 2 sich durch eine höhere Stabilität gegenüber dem bicyclischen Vinyl-Kation 4 auszeichnet.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 2312-2319 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 1-Amino-2,6-hexacosamethylen-4-pyridon, a Potential Starting Compound for the Synthesis of a CatenaneFour synthetic pathways to the 2,6-disubstituted 1-amino-4-pyridone 16 from 9,12-heneicosa-diyne-11-one (10) are described. The synthesis of the title compound 22 is performed by cyclisation of 2,6-di(12-tridecynyl)-4-pyridone (19c), followed by catalytic hydrogenation of the triple bonds and N-amination with chloroamine/sodium hydride in DMF. O-Amino-4-pyridones (17, 23) are formed as by-products during this procedure.
    Notes: Vier Synthesewege für das 2,6-disubstituierte 1-Amino-4-pyridon 16 aus 9,12-Heneicosadiin-11-on (10) werden beschrieben. Die Titelverbindung 22 wird dargestellt durch Cyclisierung von 2,6-Di-(12-tridecinyl)-4-pyridon (19c), katalytische Hydrierung der Dreifachbindungen und N-Aminie-rung mit Chloramin/Natriumhydrid in Dimethylformamid. Als Nebenprodukte bilden sich bei diesem Verfahren O-Amino-4-pyridone (17, 23).
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 109 (1976), S. 132-138 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Crystal and Molecular structure of C6H6RuC8H12 - (Benzene) 1, 5-cyclooctadiene)ruthenium(0)The crystal structure of the title compound 1 has been determined by X-ray diffraction. The Complex crystallizes in the space group p21/n, a = 648 ± 0.1 pm, b = 1188.3 ± 0.2 pm, c = 1486.1 ± 0.2 pm, β = 91.43 ± 0.02°, Z = 4 (R = 0.034). In the molecule the diolefin 1.5-cyclooctadiene functions as a four electron ligand, that is the ligand is π-bonded to the central ruthenium atom with its two double bonds. The coordination of the ruthenium 1/s completed by the six electron ligand benzene.
    Notes: Mittels Röntgenanalyse wurde die Struktur der Titelverbindung 1 bestimmt. Der Komplex kristallisiert in der Raumgruppe p21/n, a = 648 ± 0.1 pm, b = 1188.3 ± 0.2 pm, c = 1486.1 ± 0.2 pm, β = 91.43 ± 0.02°, Z = 4 (R = 0.034). Im Komplexmolekül fungiert das Diolefin 1,5-Cyclooctadien als Vierelektronenligand, d. h. der Ligand ist über seine beiden Doppelbindungen an das zentrale Rutheniumatom π-gebunden. Der Sechselektronenligand Benzol vervollständigt die Koordination des Rutheniums.
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