ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Chemistry  (39)
  • Inorganic Chemistry  (28)
  • Arenkomplexe  (1)
  • 1995-1999  (39)
  • 11
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 12
    ISSN: 0044-8249
    Keywords: Carbanionen ; Kupfer ; Phosphazene ; Zink ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 13
    ISSN: 0044-8249
    Keywords: Cobaltverbindungen ; Heterocubane ; Manganverbindungen ; Phosphaniminatokomplexe ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 14
    ISSN: 0044-8249
    Keywords: Ab-initio-Rechnungen ; Imine ; Phosphorverbindungen ; Schwefelverbindungen ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 15
    ISSN: 0044-2313
    Keywords: Phosphorane Iminato Complexes of Aluminium, Gallium and Antimony, Syntheses, Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Syntheses and Crystal Structures of the Phosphorane Iminato Complexes [MCl2(NPPh3)]2 with M = Al and Ga, [SbCl2(NPMe3)(DMF)]2, and of the Phosphorane Imine Complex [Ph3PNH · BF3] · THFThe phosphorane iminato complexes [MCl2(NPPh3)]2 with M = Al and Ga and [SbCl2(NPMe3)(DMF)]2 are formed as colourless crystals by reactions of the anhydrous trichlorides MCl3 (M = Al, Ga, Sb) with the corresponding silylated phosphorane imines Me3SiNPR3 in acetonitrile and in dimethyl formamide, respectively. The phosphorane imine derivative [Ph3PNH · BF3] · THF is formed from Me3SiNPPh3 and boron trifluoride etherate in boiling tetrahydrofuran. The compounds are characterized by their i. r. spectra and by crystal structure analyses.[AlCl2(NPPh3)]2: Space group P1, Z = 1, structure solution with 1 585 observed unique reflections, R = 0.061. Lattice dimensions at -70°C: a = 917.6, b = 1 053.5, c = 1 145.2 pm, α = 111.72°, β = 100.80°, γ = 109.95°.[GaCl2(NPPh3)]2: Space group P1, Z = 1, structure solution with 2 586 observed unique reflections, R = 0.066. Lattice dimensions at -70°C: a = 917.5, b = 1 058.3, c = 1 153.7 pm, α = 105.52°, β = 107.75°, γ = 109.88°.In both compounds the metal atoms are linked to planar M2N2 four-membered rings via the N-atoms of the phosphorane iminato groups.[SbCl2(NPMe3)(DMF)]2: Space group P21/n, Z = 4, structure solution with 3 805 observed unique reflections, R = 0.038. Lattice dimensions at -70°C: a = 1 913.0, b = 726.8, c = 2 040.7 pm, β = 113.62°. The unit cell contains two symmetry independent dimeric molecules, in which the antimony atoms are centrosymmetricly μ2 linked via the N-atoms of the phosphorane iminato groups. Along with the oxygen atom of the dimethyl formamide molecule the Sb atoms achieve a ψ-octahedral environment.[Ph3PNH · BF3] · THF: Space group C2/c, Z = 8, structure solution with 2 048 observed unique reflections, R = 0.058. Lattice dimensions at -70°C: a = 2 460.4, b = 869.2, c = 1 978.0 pm, β = 116.35°.
    Notes: Die Phosphaniminatokomplexe [MCl2(NPPh3)]2 mit M = Al und Ga und [SbCl2(NPMe3)(DMF)]2 entstehen bei Reaktionen der wasserfreien Trichloride MCl3 (M = Al, Ga, Sb) mit den entsprechenden silylierten Phosphaniminen Me3SiNPR3 in Acetonitril bzw. in Dimethylformamid als farblose Einkristalle. Das Phosphanimin-Derivat [Ph3PNH · BF3] entsteht aus Me3SiNPPh3 und Bortrifluorid-Etherat in siedendem Tetrahydrofuran. Die Verbindungen werden durch ihre IR-Spektren und durch Kristallstrukturanalysen charakterisiert.[AlCl2(NPPh3)]2: Raumgruppe P1, Z = 1, Strukturlösung mit 1 585 beobachteten unabhängigen Reflexen, R = 0,061. Gitterkonstanten bei -70°C: a = 917,6; b = 1 053,5; c = 1 145,2 pm; α = 111,72°; β = 100,80° γ = 109,95°.[GaCl2(NPPh3)]2: Raumgruppe P1, Z = 1, Strukturlösung mit 2 586 beobachteten unabhängigen Reflexen, R = 0,066. Gitterkonstanten bei -70°C: a = 917,5; b = 1 058,3; c = 1 153,7 pm; α = 105,52°; β = 107,75°; γ = 109,88°. In beiden Verbindungen sind die Metallatome über die N-Atome der Phosphaniminatogruppen zu planaren M2N2-Vierringen verknüpft.[SbCl2(NPMe3)(DMF)]2: Raumgruppe P21/n, Z = 4, Strukturlösung mit 3 805 beobachteten unabhängigen Reflexen, R = 0,038. Gitterkonstanten bei -70°C: a = 1 913,0; b = 726,8; c = 2 040,7 pm; β = 113,62°. Die Elementarzelle enthält zwei symmetrieunabhängige dimere Moleküle, in denen die Antimonatome zentrosymmetrisch ψ2 über die N-Atome der Phosphaniminatogruppen verknüpft sind. Zusammen mit dem O-Atom des Dimethylformamid-Moleküls erreichen die Sb-Atome ψ-oktaedrische Umgebung.[Ph3PNH · BF3] · THF: Raumgruppe C2/c, Z = 8, Strukturlösung mit 2 048 beobachteten unabhängigen Reflexen, R = 0,058. Gitterkonstanten bei -70°C: a = 2 460,4; b = 869,2; c = 1 978,0 pm; β = 116,35°.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 16
    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.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 17
    ISSN: 0044-2313
    Keywords: Magnesium Compounds ; Phosphoraneiminato Complexes ; Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Phosphaneimine and Phosphoraneiminato Complexes of Magnesium. The Crystal Structures of [MgBr1,25I0,75(Me3SiNPMe3)(OEt2)], [MgI2(Me3SiNPMe3)2], [Mg2I2(Me3SiNPMe2CH2)(Me3SiNPMe2CH2CH(Me)O)(OEt2)], and [MgBr(NPMe3)]4 · C7H8By reactions of the silylated phosphaneimine Me3SiNPMe3 with the Grignard reagents EtMgBr and MeMgI, respectively, the carbanionic phosphoraneiminato derivatives [XMg(CH2PMe2NSiMe3)]n (X = Br, I) can be isolated as main products. The by-products of these reactions, [MgBr1.25I0.75(Me3SiNPMe3)(OEt2)], [MgI2(Me3SiNPMe3)2] and [Mg2I2(CH2PMe2NSiMe3)(O(Me)CHCH2PMe2NSiMe3)(OEt2)] were identified by crystal structure determinations. The phosphoraneiminato complex [MgBr(NPMe3)]4 · C7H8 with hetero cubane structure is formed by a metathesis reaction of [ZnBr(NPMe3)]4 with RMgBr (R = Ph. Mes).
    Notes: Als Hauptprodukte der Umsetzungen des silylierten Phosphanimins Me3SiNPMe3 mit den Grignard-Reagentien EtMgBr und MeMgl wurden die carbanionischen Phosphaniminato-Derivate [XMg(CH2Pme2NSiMe3)]n (X = Br, I) isoliert. Als Nebenprodukte wurden [MgBr1,25I0,75(Me3SiNPMe3)(OEt2)], [Mgl2(Me3SiNPMe3)2] und [Mg2I2(CH2PMe2NSiMe3)(O(Me)CHCH2PMe2NSiMe3(OEt2)] durch röntgenographische Strukturanalysen identifiziert. Den Phosphaniminato-Komplex [MgBr(NPMe3)]4 · C7H8 mit Heterocuban-Struktur erhielten wir durch Metathese-Reaktion aus [ZnBr(NPMe3)]4 und RMgBr (R = Ph, Mes).
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 18
    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.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 19
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 623 (1997), S. 1306-1310 
    ISSN: 0044-2313
    Keywords: Lithium Cluster ; Carbdianion ; NMR spectra ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: [Li7(CHPMe2NSiMe3)3(OSiMe2nBu)]2, a Mixed-Ligand-Li14 Cluster with the Carbdianion (CHPMe2NSiMe3)2-The title compound is formed as colourless moisture and oxygen sensitive crystals by the reaction of [LiCH2PMe2NSiMe3]4 with zinc or cobalt chloride in a toluene suspension in the presence of silicongrease (-OSiMe2-)n and n-butyllithium. It is characterized by multinucleus NMR spectroscopy and by crystal structure determinations of two different crystal individuals.1. Space group P1, Z = 1, lattice dimensions at -70 °C: a = 1272.0, b = 1392.6, c = 1417.6 pm, α = 115.33°, β = 96.75°, σ = 106.81°; R = 0.042.2. Space group P21/n, Z = 2, lattice dimensions at -50 °C: a = 1424.8, b = 1457.1, c = 1997.0 pm, β = 90.32, R = 0.069.
    Notes: Die Titelverbindung (farblose, feuchtigkeits- und sauerstoffempfindliche Kristalle) entsteht bei der Reaktion von [LiCH2PMe2NSiMe3]4 mit wasserfreiem Zink- oder Cobaltchlorid in einer Toluolsuspension in Gegenwart von Siliconfett (-OSiMe2-)n und n-Butyllithium. Sie wird durch Multikern-NMR-Spektroskopie und durch Kristallstrukturanalysen zweier kristallchemisch verschiedener Individuen charakterisiert.1. Raumgruppe P1, Z = 1, Gitterkonstanten bei -70 °C: a = 1272,0; b = 1392,6; c = 1417,6 pm; α = 115,33°; β = 96,75°; σ = 106,81°; R = 0,042.2. Raumgruppe P21/n, Z = 2, Gitterkonstanten bei -50 °C: a = 1424,8; b = 1457,1; c = 1997,0 pm; β = 90,32°; R = 0,069.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 20
    ISSN: 0044-2313
    Keywords: Zinc Complexes ; Syntheses ; IR Spectra ; Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Syntheses and Crystal Structures of the Zincates [Na(12-Crown-4)2][Zn{N(SiMe3)2}3] and [Na(12-Crown-4)2]2[Zn(C≡C-Ph)3(THF)][Zn(C≡C-Ph)3]The homoleptic amido complex [Na(12-crown-4)2][Zn{N(SiMe3)2}3] (1) is prepared from Zn[N(SiMe3)2]2 and NaN(SiMe3)2 in toluene solution in the presence of 12-crown-4. Single crystals of 1 · 0,5 C6H14 can be obtained from diethylether/hexane solutions. 1 reacts with phenylacetylene to give [Na(12-crown-4)2][Zn(C≡C-Ph)3] (2) which forms single crystals 2 · 0.5 THF from tetrahydrofurane solutions. The complexes were characterized by IR spectroscopy and by crystal structure determinations.
    Notes: Der homoleptische Amidokomplex [Na(12-Krone-4)2][Zn{N(SiMe3)2}3] (1) entsteht aus Zn[N(SiMe3)2]2 und NaN(SiMe3)2 in Toluol-Lösung in Gegenwart von 12-Krone-4. Einkristalle von 1 · 0,5 C6H14 erhält man aus Diethylether/Hexan-Lösungen. 1 reagiert mit Phenylacetylen unter Bildung von [Na(12-Krone-4)2][Zn(C≡C-Ph)3] (2), das nach Kristallisation aus Tetrahydrofuran Einkristalle 2 · 0,5 THF bildet. Die Komplexe werden IR-spektroskopisch und durch Kristallstrukturanalysen charakterisiert.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...