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  • Crystal Structure  (5)
  • Aromatizität  (2)
  • 1
    ISSN: 0044-8249
    Keywords: Ab-initio-Rechnungen ; Aromatizität ; Bor ; Carbene ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 622 (1996), S. 863-866 
    ISSN: 0044-2313
    Keywords: Phosphorane Iminato Complex of Sulfur ; Synthesis ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: [(Me3PN)3SNS(NPMe3)2]Cl2, a Mixed Valenced Phosphorane Iminato Complex of SulfurThe title compound has been prepared from trithiazyl chloride and the silylated phosphaneimine Me3SiNPMe3 in acetonitrile solution, forming red crystals, which were characterized by IR spectroscopy and by a crystal structure determination.Space group P21/c, Z = 4, structure solution with 4250 independent reflections, R = 0.054. Lattice dimensions at 20°C: a = 1077.8, b = 2036.6, c = 1480.5 pm, β = 102.39°. The compound consists of dications [(Me3PN)3SNS(NPMe3)2]2+ and chloride ions. In the cations the sulfur atoms of oxidation number +VI and +IV are connected by an asymmetric, bent nitrido bridge with SN bond lengths of 156.9 and 167.0 pm.
    Notes: Die Titelverbindung entsteht als rote Kristalle bei der Reaktion von Trithiazylchlorid mit dem silylierten Phosphanimin Me3SiNPMe3 in Acetonitrillösung. Die Verbindung wird durch das IR-Spektrum und durch eine Kristallstruktur-analyse charakterisiert.Raumgruppe P21/c, Z = 4, Strukturlösung mit 4250 unabhängigen Reflexen, R = 0,054. Gitterabmessungen bei 20°C: a = 1077,8; b = 2036,6; c = 1480,5 pm, β = 102,39°. Die Verbindung besteht aus den Dikationen [(Me3PN)3SNS(NPMe3)2]2+ und Chloridionen. In den Kationen sind die Schwefelatome der Oxidationszahl +VI und +IV über eine asymmetrische, gewinkelte Nitridobrücke mit SN-Abständen von 156,9 und 167,0 pm verknüpft.
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  • 3
    ISSN: 0044-2313
    Keywords: Molybdenum ; Tungsten ; Halogenonitrosyl Complexes ; Syntheses ; IR Spectra ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Halogeno-Nitrosyl Complexes of Molybdenum and Tungsten. Crystal Structures of [Na2(15-Crown-5)2(CH3CN)][MoCl4(NO)2] and [Na(15-Crown-5)]2[MoF4Cl(NO)]MoCl2(NO)2 and WCl2(NO)2, respectively, react with excess sodium fluoride in acetonitrile at room temperature and in the presence of 15-crown-5 to give crystalline mixtures, which consist of the title compounds, respectively of [Na(15-crown-5)]2[WCl4(NO)2] and [Na(15-crown-5)]2[WF4Cl(NO)], and which can be separated by selection. The complexes are characterized by their i.r. spectra, the molybdenum compounds additionally by crystal structure determinations.[Na2(15-crown-5)2(CH3CN)][MoCl4(NO)2]: Space group P21, Z = 2, 5415 independent unique reflexions, R = 0.039. Lattice dimensions at -10°C: a = 984.3, b = 1231.1, c = 1483.0 pm, β = 105.67°. The compound consists of cations [Ne(l5-crown-5)(CH3CN)]+, in which the sodium ion is surrounded by the five O-atoms of the crown ether and by the N-atom of the acetonitrile molecule, as well as of anions, which form an ion pair {Na(15-crown-5)[MoCl4(NO)2]}-. In the in pairs the sodium ion is coordinated by the five oxygen atoms of the crown ether and by two chlorine atoms of the [MoCI4(NO)2]2- unit. The nitrosyl ligands take the cis-position a t the molybdenum atom which is in a distorted octahedrally fashion.[Na(15-crown-5)]2[MoF4Cl(NO)]. Space group C2/c, Z = 4, 1933 independent unique reflexions, R = 0.078. Lattice dimensions at -7O°C: D : 1.585.8, b = 1171.5, c = 1771.5 pm, β = 114.91°. The compound forms an ion triple, in which the sodium ions are linked to five oxygen atoms each of the crown ether molecules, and to two F-atoms of the [MoF4Cl(NO)]2- unit. The F-atom which is arranged in trans-position to the nitrosyl ligand coordinates with both sodium ions; thus an unusual T-shaped arrangement results for this F-atom. The sole terminal F-Atom and the Cl-atom are disordered in two positions.
    Notes: MoCl2(NO)2 bzw. WCl2(NO)2 reagieren mit überschüssigem Natriumfluorid in Acetonitril bei R.T. und Anwesenheit von 15-Krone-5 zu Kristallgemischen, die aus den Titelverbindungen bzw. aus [Na(15-Krone-5)]2[WCl4(NO)2] und [Na(15-Krone-5)]2[WF4Cl(NO)] bestehen, und die sich durch Auslesen trennen lassen. Die Komplexe werden durch ihre IR-Spektren, die Molybdänverbindungen zusätzlich durch Kristallstrukturanalysen charakterisiert.[Na2(15-Krone-5)2(CH3CN)][MoCl4(NO)2]: Raumgruppe P21, Z = 2, 5415 unabhängige beobachtete Reflexe, R = 3,9%. Gitterabmessungen bei -10°C: a = 984,3; b = 1 251,1; c = 1 483,0 pm, β = 105,67°. Die Verbindung besteht aus Kationen [Na(15-Krone-5)(CH3CN)]+, in denen das Natriumion von den fünf O-Atomen des Kronenethers und von dem N-Atom des Acetonitrilmoleküls umgeben ist, sowie aus Anionen, die ein Ionenpaar {Na(15-Krone-5)[MoCl4(NO)2]}- bilden. In ihnen ist das Natriumion durch die fünf O-Atome des Kronenethers und durch zwei Chloratome der [MoCl4(NO)2]2--Einheit koordiniert. Die Nitrosylliganden nehmen die cis-Positionen am verzerrt oktaedrisch koordinierten Molybdänatom ein.[Na(15-Krone-5)]2[MoF4Cl(NO)]: Raumgruppe C2/c, Z = 4, 1933 unabhängige beobachtete Reflexe, R = 7,8%. Gitterabmessungen bei -70°C: a = 1 585,8; b = 1 171,2; c = 1 771,5 pm; β = 114,91°. Die Verbindung bildet ein Ionentripel, in dem die Natriumionen mit je fünf O-Atomen der Kronenethermoleküle und mit zwei F-Atomen der [MoF4Cl(NO)]2--Einheit verbunden sind. Das in trans-Position zum Nitrosylliganden angeordnete F-Atom koordiniert mit beiden Natriumionen, so daß für dieses F-Atom eine ungewöhnliche T-förmige Anordnung resultiert. Das einzige terminal gebundene F-Atom und das Cl-Atom sind in zwei Positionen fehlgeordnet.
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  • 4
    ISSN: 0044-2313
    Keywords: Silanolato Complexes of Titanium and Zirconium ; Synthesis ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Silanolato Complexes of Titanium and Zirconium. The Crystal Structures of Cp2TiCl(OSiPh3) and Cp2ZrCl(OSiPh3)The title compounds have been prepared by the reaction of Cp2MCl2 (M = Ti, Zr) with triphenylsilanole in diethylether in the presence of piperidine. They form only sparingly moisture sensitive orange (Ti) or colourless (Zr) crystal needles, which were characterized by X-ray crystallography.Cp2TiCl(OSiPh3): Space group P21/n, Z = 4, structure solution with 3961 observed unique reflections, R = 0.057. Lattice dimensions at 20°C: a = 1029.6, b = 1719.3, c = 1388.9 pm, β = 100.69°. The compound forms monomeric molecules with bond lengths TiO of 184.2 pm, SiO of 161.5 pm, and a TiOSi bonding angle of 164.5°.Cp2ZrCl(OSiPh3): Space group P3, Z = 18, structure solution with 2799 observed unique reflections, R = 0.047. Lattice dimensions at -20°C: a = b = 3518, c = 1058.3 pm. The structure consists of three symmetry-independent monomeric molecules, which differ only slightly. The bond lengths are (in average): ZrO 196.4 pm, SiO 162.1 pm, the ZrOSi bond angle is 173.7°.
    Notes: Die Titelverbindungen werden aus Cp2MCl2 (M = Ti, Zr) und Triphenylsilanol in Diethylether in Gegenwart von Piperidin hergestellt. Sie bilden nur wenig feuchtigkeits-empfindliche orange (Ti) bzw. farblose Kristallnadeln (Zr), die wir kristallographisch charakterisiert haben.Cp2TiCl(OSiPh3): Raumgruppe P21/n, Z = 4, Strukturlösung mit 3961 unabhängigen, beobachteten Reflexen, R = 0,057. Gitterkonstanten bei -50°C: a = 1029,6; b = 1719,3; c = 1388,9 pm, β = 100,69°. Die Verbindung bildet monomere Moleküle mit Abständen TiO von 184,2 pm, SiO von 161,5 pm und einem TiOSi-Bindungswinkel von 164,5°.Cp2ZrCl(OSiPh3): Raumgruppe P3, Z = 18, Strukturlösung mit 2799 unabhängigen, beobachteten Reflexen, R = 0,047. Gitterkonstanten bei -20°C: a = b = 3518; c = 1058,3 pm. Die Struktur enthält drei symmetrieunabhängige monomere Moleküle, die sich nur wenig voneinander unterscheiden. Die Abstände ZrO betragen im Mittel 196,4 pm, SiO im Mittel 162,1 pm und die Bindungswinkel ZrOSi im Mittel 173,7°.
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  • 5
    ISSN: 0044-8249
    Keywords: Ab-initio-Rechnungen ; Aromatizität ; Bor ; Carborane ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 623 (1997), S. 1203-1204 
    ISSN: 0044-2313
    Keywords: Ytterbium Complex ; Amido Compound ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: [Yb3OBr4{N(SiMe3)2}3(THF)3], an Amido Complex of Ytterbium with a Clusterlike StructureThe title compound has been prepared from YbBr3 and NaN(SiMe3)2 in THF suspension, forming yellow single crystals from hexane solutions which were characterized by a crystal structure determination. Space group P1, Z = 2, lattice dimensions at -100°C: a = 1085.4(1), b = 1410.2(1), c = 1912.0(1) pm; α = 78.62(1)°, β = 80.61(1)°, γ = 73.45(1)°, R = 0.025.In the molecular structure of [Yb3OBr4{N(SiMe3)2}3(THF)3] the three ytterbium atoms together with the μ3-oxygen atom and a μ3-bromine atom form a distorted trigonal bipyramid. In addition, three μ2-Br atoms coordinate the Yb atoms in the equatorial plane, whereas the THF molecules and the N(SiMe3)2- ligands are terminally coordinated, thus forming a distorted octahedrally surrounding of the Yb atoms.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 623 (1997), S. 1035-1036 
    ISSN: 0044-2313
    Keywords: Titanium compound ; Phosphorane iminato derivatives ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tetrakis(triphenylphosphoraneiminato)titanium, [Ti(NPPh3)4]The title compound has been prepared by the reaction of [TiCl2(NPPh3)2] with methyllithium and cyclopentadienyllithium, respectively, in hexane solution. [Ti(NPPh3)4] · 3 C7H8 crystallizes from toluene solution to form colourless, only slightly moisture sensitive crystals which were characterized by a crystal structure determination. Space group I41/a, Z = 8, lattice dimensions at -80°C: a = b = 2160.7(2), c = 3334.2(3) pm, merohedral (110) twin, R = 0.077. The compound forms monomeric molecules with tetrahedrally coordinate titanium atoms and bonding parameters of TiN = 187.3 pm, PN = 155.1 pm, TiNP 150.4° in average.
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