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  • 1
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Acetylene Complexes of Molybdenocene: Synthesis via Ligand Substitution Reactions of Bis(η5-cyclopentadienyl)[(Z)-stilbene]molybdenum, a Molybdenocene Derivative with Substitution-labile OlefinThe reinvestigation of the reaction of molybdenocene dihydride, Mo(C5H5)2H2 (1), with diphenylacetylene led to the isolation and characterization of the (Z)-stilbene complex of molybdenocene, Mo(C5H5)2[(Z)-C6H5CH=CHC6H5] (3). The olefin ligand in this complex is found to be rather labile and substitution reactions with various substituted acetylenes RC≡CR′ readily gave the acetylene complexes of molybdenocene, Mo(C5H5)2(RC≡CR′) (2f-cm). The effect of the acetylene substituents R and R′ in these compounds is discussed in terms of their electronic properties.
    Notes: Bei der Wiederholung der Reaktion von Molybdänocendihydrid, Mo(C5H5)2H2 (1), mit Diphenylacetylen konnte das (Z)-Stilben-Addukt des Molybdänocens, Mo(C5H5)2[(Z)-C6H5CH=CHC6H5] (3), isoliert und charakterisiert werden. Der olefinische Ligand in 3 erweist sich als substitutionslabil: Verschiedene substituierte Acetylene RC≡CR′ reagieren mit 3 glatt zu den Acetylen-Komplexen 2f-m des Molybdänocens, Mo(C5H5)2(RC≡CR′). Der Einfluß der Acetylensubstituenten R und R′ in dieser Verbindungsklasse wird im Hinblick auf ihre elektronischen Eigenschaften untersucht.
    Additional Material: 1 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 1575-1577 
    ISSN: 0009-2940
    Keywords: Oxidative coupling of cyclopentadienide anion ; Dihydrofulvalene, molecular structure ; Migration of trimethylsilyl group ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reaction of 1,2,4-tris(trimethylsilyl)cyclopentadienyllithium with ferric chloride in THF at -95°C leads to the formation of a thermally sensitive iron(III) complex which decomposes to the new dihydrofulvalene derivative 3,7-dihydro-1,3,3,5,7,7-hexakis(trimethylsilyl)fulvalene (1).
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 122 (1989), S. 1259-1260 
    ISSN: 0009-2940
    Keywords: Sterically demanding cyclopentadienyl ligand ; Iron(trimethyl phosphite) complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A direct synthesis of iron(trimethyl phosphite) half-sandwich complexes [η5-C5H2(SiMe3)3]Fe[P(OMe)3]2X starting from FeX2(X = Cl, Br, I) and Li[η5-C5H2(SiMe3)3] is described. Their reactivity toward tBuMgCl and CO has been studied.
    Additional Material: 1 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 123 (1990), S. 87-88 
    ISSN: 0009-2940
    Keywords: Cyclopentadienyl ligand, sterically demanding / Titanium alkyl complex / Cyclopentadienyl, 1,2,4-tris(trimethylsilyl)- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new polyalkyl complex of titanium, trimethyl[l,2,4-tris(trimethylsilyl)cyclopentadienyl]titanium, [η5-1,2,4-(SiMe3)3C5H2]-TiMe3, has been synthesized and found to be thermally stable up to 110°C.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 122 (1989), S. 1075-1077 
    ISSN: 0009-2940
    Keywords: Cobaltocenes, highly substituted ; Cyclopentadienyl ligand, sterically demanding ; Ferrocenes, highly substituted ; Hindered rotation of ring ligands ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complexes with Sterically Demanding Ligands, V. - Synthesis of 4-tert-Butyl-1,2-bis(trimethylsilyl) cyclopentadienyl Complexes of Iron and Cobalt2-tert-Butyl-5,5-bis(trimethylsilyl)-2,4-cyclopentadiene (1) is prepared in a one-pot synthesis starting from 1,1-dimethylfulvene. Deprotonation of 1 with n-butyllithium yields the lithium derivative Li[C5H2(CMe3)(SiMe3)2] (2) which is treated with FeBr2· DME and CO to cleanly give [C5H2(CMe3)(SiMe3)2]Fe(CO)2Br (3). Ferrocene and cobaltocenium cation derivatives [C5H2-(CMe3)(SiMe3)2]2M (M = Fe: 4; M = Co⊕ PF6⊖: 5) have also been synthesized using 2. Variable-temperature 1H-NMR spectroscopy shows that rotation of the five-membered ring about the metal-ring axis is hindered in these metallocenes.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 123 (1990), S. 1641-1648 
    ISSN: 0009-2940
    Keywords: Cyclopentadienyl ligand, functionalized ; Half-sandwich complexes ; Cobalt complexes ; Intramolecular C=C bond coordination ; Reductive complexation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermolysis of [1-(3-butenyl)-2,3,4,5-tetramethylcyclopentadienyl]carbonyldiiodocobalt, (η5-C5Me4CH2CH2CH=CH2)-Co(CO)I2 (2), in boiling octane affords the dimeric diiodide [(η5-C5Me4CH2CH2CH=CH2)-COI2]2 (3) without any interference of the 3-butenyl chain with the cobalt center. 2 reacts with various two-electron ligands L (L=P(OMe)3, P(OPh)3, PPh3, PMe3, PMe2Ph, tBuNC] to give a series of cobalt(III) complexes of the general formulae (η5-C5Me4CH2CH2CH=CH2)-Co(L)I2 (4-9). Sodium amalgam reduction of these “open-chain” complexes 4-9 yields novel cobalt(1) complexes containing an intramolecularly coordinated C=C bond (η5:η2-C5Me4CH2CH2CH=CH2)-Co(L). For L=CO (12), P(OMe)3 (13), and P(OPh)3 (14) low-melting crystals are isolated and fully characterized by analytical and spectroscopic methods.
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  • 7
    ISSN: 0009-2940
    Keywords: Titanium complexes ; Bidentate phenoxy ligands ; Bulky phenols ; Lewis acidity ; Pentacoordination ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of new titanium complexes of the general type Ti(mbmp)X2 (X = Br, I; OMe, OiPr, OtBu), containing a bidentate bis(phenoxy) ligand derived from 2,2′-methylenebis(6-tert-butyl-4-methylphenol) (mbmpH2), was prepared. The 1H-chemical shifts for the protons of the methylene link were found to vary considerably as a function of the ligand X. Reaction of Ti(OiPr)4 with two equivalents of mbmpH2 gave the C2-symmetric spiro-titanate complex Ti(mbmp)2. The crystalline labile solvent adducts of the dichloro complex Ti(mbmp)Cl2 with THF and DME were isolated and characterized. A single-crystal X-ray structural analysis revealed the THF adduct to be a mono(THF) adduct with a trigonal-bipyramidal configuration, the bidentate mbmp ligand spanning an apical and equatorial site and the THF ligand occupying the remaining apical position.
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 121 (1988), S. 1899-1905 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Complexes with Sterically Demanding Ligands, II. - Synthesis and Structure of 1,1′,2,2′,4,4′-Hexakis(trimethylsilyl)ferroceneReaction of iron(II) halides FeX2 (X = Cl, Br, I) with tris(trimethylsilyl)cyclopentadienyllithium Li[C5H2(SiMe3)3] at -40°C yields 1,1′,2,2′,4,4′-hexakis(trimethylsilyl)ferrocene, Fe[η5-C5H2(SiMe3)3]2 (2). Preparation of two mixed ferrocene derivatives Fe(η5-C5R5)[η5-C5H2(SiMe3)3] (R = H, 3; R = Me, 4) bearing one tris(trimethylsilyl)cyclopentadienyl ligand is also reported. An X-ray structure determination of 2 confirms the sandwich structure with significantly long Fe—C(ring) distances of average 2.082(1) Å and virtually eclipsed five-membered rings. According to variable-temperature 1H- and 13C-NMR spectroscopic analysis, 2 shows in solution a hindered rotation of the two cyclopentadienyl rings around the metal-ligand vector (ΔG≠ = 11.0 kcal/mol).
    Notes: Die Umsetzung von Eisen(II)-halogeniden FeX2 (X = Cl, Br, I) mit Tris(trimethylsilyl)cyclopentadienyllithium Li[C5H2(SiMe3)3] bei -40°C ergibt 1,1′,2,2′,4,4′-Hexakis(trimethylsilyl)ferrocen, Fe[η5-C5H2(SiMe3)3]2 (2). Die gezielte Darstellung der Ferrocene Fe(η5-C5R5)[η5-C5H2(SiMe3)3] (R = H, 3; R = Me, 4) mit einem Tris(trimethylsilyl)cyclopentadienyl-Liganden gelingt ebenfalls. Die Röntgenstrukturanalyse von 2 bestätigt die Sandwichstruktur mit vergleichsweise langen mittleren Fe—C(Ring)-Abständen von 2.082(1) Å, praktisch auf Deckung stehenden Fünfring-Liganden und einer angenähert C2-symmetrischen Konformation. In Lösung beobachtet man laut temperaturabhängiger 1H- und 13C-NMR-spektroskopischer Analyse eine gehinderte Rotation der beiden Cyclopentadienyl-Ringe relativ zueinander (ΔG≠ = 11.0 kcal/mol).
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 123 (1990), S. 1649-1651 
    ISSN: 0009-2940
    Keywords: Cyclopentadienyl ligand, functionalized ; Amido ligands ; Titanium complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: [(tert-Butylamino)dimethylsilyl]cyclopentadienes C5H5-n-(CMe3)n(SiMe2NHCMe3) (n=1, 2) and C5H4(SiMe3)(SiMe2-NHCMe3) have been prepared and the complexation of their lithium derivatives with FeCl2(THF)1.5 and TiCl4(THF)2 investigated.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 122 (1989), S. 1645-1647 
    ISSN: 0009-2940
    Keywords: Cobalt carbonyl complexes ; Cyclopentadienyl ligand, functionalized ; Intramolecular C=C bond coordination ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of 1-(3-butenyl)-2,3,4,5-tetramethylcyclopentadienyl cobalt complexes without and with intramolecular C-C double-bond coordination is reported.
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