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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1343-1350 
    ISSN: 1434-1948
    Keywords: Indium ; O ligands ; N ligands ; C ligands ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New heteroleptic indium compounds have been synthesized starting from indium(III) halides and hexamethyldisilazyllithium to form MeXInN(SiMe3)2 [X = Cl (1), Br (2)], and then subsequent alcoholysis to afford the molecules [ClMeIn(OtBu)]2 (3), [BrMeIn(OtBu)]2 (4), {ClMeIn[O(C6H4)OMe]}2 (5), {[(SiMe3)2N]MeIn(OtBu)}2 (6) and [MeIn(OtBu)2]2 (7). The molecular structures of molecules 3-7 have been obtained by single crystal X-ray diffraction studies. The structures of the compounds 3-7 are almost identical: 3-5 crystallize in the monoclinic crystal system with two dimeric molecules per unit cell in the space group P21/c, 6 crystallizes in the monoclinic space group C2/c with four molecules per unit cell, and compound 7 crystallizes in the triclinic crystal system with one dimeric molecule per unit cell in the space group P-1. The central centrosymmetric In2O2 ring, common to all the compounds, is achieved by two bridging oxygen atoms. Due to the additional coordination by an oxygen atom of the methoxy group, the coordination number of the metal center rises from 4 to “4+1” if the OtBu ligand (compounds 3, 4, 6, and 7) is exchanged for a methoxyphenol ligand (compound 5). In addition to the In2O2 ring the compound 5 possesses two annealed five-membered InO2C2 rings. The common indium methyl group of all compounds, which is transfered by an original route from the silicon to the indium atom, is used to compare structural and spectroscopic properties of the molecules, as there is a correlation between the In-C bond length and the chemical shift of the methyl group which depends on the ligand system used.
    Additional Material: 2 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 1327-1332 
    ISSN: 1434-1948
    Keywords: Barium ; Zirconium ; O ligand ; Heterometal alkoxides ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Manipulable metal ratios are accessible in a series of heterometal Ba-Zr alkoxides by changing the size and the charge of the ligands. The synthesis and characterisation of four mixed-metal Ba-Zr species [BaZr2(OtBu)10] (1), [Ba2Zr(OtBu)8(tBuOH)(THF)2] (2), [BaZr(OtBu)6(THF)2] (3) and [BaZr(OH)(OiPr)5(iPrOH)3]2 (4), based on different Ba/Zr stoichiometries, are reported. The molecular structures of 1, 2, and 4 have been determined by single-crystal X-ray diffraction studies. 1 exhibits a bow-tie structural motif in which a trigonally distorted six-coordinate barium atom is chelated by two bipyramidal {Zr(OtBu)5}- units. 2 reveals a triangular “Ba2Zr(μ3-OtBu)2(μ2-OtBu)3” core structure formed by the fusion of three octahedra built about two Ba atoms and a Zr atom. The structure is unique in terms of the distribution of terminal ligands at each of the metal centers. One of the barium atoms possesses one -OtBu and one tBuOH as terminal ligands, while the terminal ligands on the second barium atom are two THF molecules; the zirconium center bears -OtBu groups as the terminal ligands. Hydrolysis of compound 3 with one equivalent of water, followed by alcoholysis (iPrOH) of the resulting product, gave 4. The structure of 4 shows a planar tetrametallic Ba2Zr2 frame capped by two μ3-hydroxo ligands. The coordination figure of the zirconium atoms resembles a distorted octahedron, whereas the geometry of the barium centers is best described as capped trigonal prisms. Both 3 and 4 are excellent precursors to morphologically pure BaZrO3 ceramic by the sol-gel process.
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  • 3
    ISSN: 0947-6539
    Keywords: alkoxides ; clusters ; Group 15 complexes ; Lewis acids ; oxygen bridges ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: As(OtBu)3 does not form adducts with alkali metal tert-butoxides MOtBu (M = Li, Na, K, Rb and Cs), whereas the corresponding Sb(OtBu)3 (2) and Bi(OtBu)3 (3) react with MOtBu (M = K, Rb, Cs) to yield M(OtBu)4Sb (M = K (6), Rb (7), Cs (8)) and M(O-tBu)4Bi (M = 9), respectively. X-ray structure determinations for 6 and 9 show them to be one-dimensional coordination polymers composed of E(OtBu)4 (E = Sb, Bi) units linked through potassium atoms. These E(OtBu)4 units display a ψ-trigonal-bipyramidal coordination around the metal atom (Sb—O = 1.971(2) and 2.181(2) Å, Bi—O = 2.068(8) and 2.275(8) Å). Both the structures exhibit a planar four-coordinate environment of oxygen around the potassium atoms (K—O = 2.650(2)-2.967(2) Å in 6, 2.53(1)-3.15(1) Å in 9). Compound 2 reacts with two equivalents of KOtBu to afford K2Sb(OtBu)5 · dioxane (10), which contains Sb2K2O5 cage units and can be described as an O5 trigonal bipyramid with metal atoms inserted in the equatorial edges. Each metal atom is tetracoordinated by oxygen atoms of the cage (Sb—O = 1.979(3)-2.144(3) Å. K—O = 2.592(3)-2.778(2) Å). The dioxane molecules increase the coordination number at each potassium atom to five by forming bridges between the molecules through K—O bonds. Reaction of 2 and 3 with NaOtBu produce the cluster compounds Na4Sb2O(OtBu)8 (4) and Na4Bi2O-(OtBu)8 (5) in high yields. K4Sb2O-(OtBu)8 (11) is obtained in almost quantitative yield by heating KSb(OtBu)4 in benzene for 24 h. Compounds 4, 5 and 11 crystallise in rhombohedral lattices; the crystal structure analyses show a superposition of molecules. With an isotropic oxygen-centred M6 octahedron. The formation of these oxo-tert-butoxides is accompanied by evolution of isobutene. Addition of four equivalents of THF to 11 gives K4Sb2O(OtBu)8 · 4 THF (12). X-ray diffraction studies reveal a cis arrangement of the Sb atoms in the central OSb2K4 unit. K4Sb2O2(OiPr)12 (13) is obtained as the major product on heating KSb(OtBu)4 and subsequent reaction with isopropyl alcohol. In the crystal structure, two oxygen-centred Sb2K2 tetrahedra (K—O 2.693(4) Å, Sb—O = 1.982(5) Å) linked through iPrO—K bonds (2.726(7)-2.738(7) Å) are observed. In the reactions of KSb(OtBu)4 (6) with the metal halides CaCl2, TlCl and CuI, a halide ion is transferred to potassium; this results in formation of potassium halide, the corresponding alkoxide and Sb(OtBu)3.
    Additional Material: 8 Ill.
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  • 4
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Das durch Oxidation von Lithium-tris(trimethylsilyl)hydrazid erstmals dargestellte hellblaue, thermolyse- und hydrolyseunbeständige, an Luft selbstentzündliche, extrem reaktionsfähige Bis(trimethylsilyl)diimin (BSD) wirkt aufgrund von Elektronenwechsel-, Säure-Base- oder Radikal-Reaktionen insbesondere als (präparativ nutzbares) Redoxsystem und „Azo“-ierungsmittel. Redoxreaktionen führen dabei unter Oxidation bzw. Reduktion der Reaktionspartner von BSD um zwei Oxidationsstufen zu Hydrazinderivaten bzw. molekularem Stickstoff und im Falle elektrochemischer Reduktion zu BSD-Radikalanionen. Azogruppen-Übertragungen ergeben hingegen neue anorganische Azoverbindungen ohne Oxidationsstufenwechsel der Diimingruppe.
    Additional Material: 2 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 88 (1976), S. 384-385 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 87 (1975), S. 287-288 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 92 (1980), S. 408-409 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 100 (1988), S. 1418-1421 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 9
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
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  • 10
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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