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  • Inorganic Chemistry  (773)
  • 1990-1994  (773)
  • 1950-1954
  • 1991  (773)
  • 1
    ISSN: 0009-2940
    Schlagwort(e): Manganese-mediated cyclization ; Nine-membered carbocycles ; Manganese complexes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Photochemical Reactions of Transition Metal Organyl Complexes with Olefines, 31). - [4 + 5] Cycloaddition of Conjugated Dienes to Tricarbonyl(η5-2,4-dimethyl-2,4-pentadienyl)manganeseTricarbonyl(η5-2,4-dimethyl-2,4-pentadienyl)manganese [1] reacts photochemically with the acyclic conjugated dienes 1,3-butadiene [A], 2-methyl-1,3-butadiene [B], (E)-1,3-pentadiene (C), (E,E)-2,4-hexadiene (D), 2,4-dimethyl-1,3-pentadiene (E), 2,4-hexadien-1-ol (F), and methyl 2,4-hexadienoate (G) in a formal [4 + 5] cycloaddition to give tricarbonylmanganese complexes with η3:2-2,6-cyclononadien-1-yl ligands (2A-2G). In addition, the reaction of 1 with A yields thermolabile [η3:2:2-1-(3-butene-1,2-diyl)-1,3-dimethyl-2,6-cyclononadiene]dicarbonylmanganese (3A) and E,E and E,Z isomers of [η3-1-(2-butene-1,1-diyl)-1,3-dimethyl-2,6-cyclononadiene]tetracarbonylmanganese (4A, 4A] as byproducts. Similarly, 1 reacts with B to form tetracarbonyl[η3-1-(3-methyl-2-butene-1,1-diyl)-1,3,6-trimethyl1-2,6-cyclononadiene]manganese (4B) in a side reaction. The crystal and molecular structures of tricarbonyl(η3:2-1,3,5,5,7-pentamethyl-2,6-cyclononadien-1-yl]manganese (2E) and of 3A are determined by X-ray structure analyses. In each of the formally octahedral complexes unusual long manganese-carbon bonds are found for one coordinated CC double bond of the hydrocarbon ligands.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 17-23 
    ISSN: 0009-2940
    Schlagwort(e): (Borole)nickel complexes ; Nucleophilic substitution at boron ; 1H-Borole ; Dihydro-1H-borolediide ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Derivatives of Borole, XVI1), - Bis(borole)nickel Complexes2)The dilithium 1-(dialkylamino)dihydroborolediides Li2[C4H4-BNR2] 2a, b: R = Me, Et) react with NiCl2 · DME to give bis(borole)nickel complexes Ni(C4H4BNR2)2. Nucleophilic substitution reactions are used to produce a large variety of derivatives Ni(C4H4BR)2 1 (e.g. R = H, tBu, F, Cl, Br, I, OH, OMe). Treatment of Ni(C4H4BCl)2 (tg) with LiO(CH2)3OLi in THF produces a polymer and a dinuclear complex (μ-{η5:η5-[(CH2)3(OBC4H4)2]}2Ni2 (3) which crystallizes from CH2Cl2 as solvate 3 · CH2Cl2. The complexes 1g and 3 · CH2Cl2 are characterized by X-ray diffraction work. Barriers to internal ring-ring rotation are measured by variable-temperature NMR spectroscopy. The B - H bond of Ni(C4H4BH)2 (1a) is remarkably inert and does not react with H2O or with carboxylic acids in THF at room temperature. With PhCHO slow formation of the benzyloxy compound Ni(C4H4BOCH2Ph)2 (1 m) is observed at 100°C. For typical complexes such as the phenyl derivative 1e cyclic voltammetry in CH2Cl2 reveals an irreversible oxidation at 1.32 and a quasi-reversible reduction at -1.37 V vs. SCE.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 25-29 
    ISSN: 0009-2940
    Schlagwort(e): Borole complexes ; {η5-[1-(Diisopropylamino)borole]}metal complexes, internal rotation of, protonation of ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Derivatives of Borole, XVII1). - {η5-[1-(Diisopropylamino)borole]}metal Complexes: Syntheses, Protonation, Internal RotationNew complexes M(CO)4L (M = Cr, W), cis-M(CO)2L2 [M = Mo, W (not isolated)], and (COD)NiL have been prepared from the Diels-Alder dimer L2, where L is 1-(diisopropylamino)borole, C4H4BNiPr2. Complexes of L can be protonated at the nitrogen atom to give stable salts such as [Cr(CO)4(LH)]BF4, [Fe(CO)3(LH)]BF4, [(C6Me6)Ru(LH)]BF4, and [CpCo(LH)]BF4; B  -  N bond dissociation is not observed. Barriers to internal rotation have been determined by variable temperature NMR spectroscopy for Cr(CO)4L, (COD)NiL, and NiL2. Three processes have been identified: rotation of the NiPr2 group around the B  -  N bond, gear-mesh rotation of the isopropyl groups around the C  -  N bonds, and rotation of L with respect to the counter ligands.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 51-61 
    ISSN: 0009-2940
    Schlagwort(e): Selenocarbonyl compounds, perfluorinated ; 1,3-Diselenetanes, perhalogenated ; 2-Selenabicyclo[2.2.1]hept-5-enes ; 1,3-Diselenetan-2-ylium hexafluoroarsenates ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Preparation of (Perfluoroalkyl)halogeno-1,3-diselenetanes from the Corresponding Selenocarbonyl Fluorides and Reactions with Boron Trichloride or Arsenic Pentafluoride1)Reactions of Hg(SeRt)2 (Rt = C2F5, C3F7, CF3) with (C2H5)2 All or All3 in octamethylcyclotetrasiloxane produce the unstable perfluoroalkaneselenocarbonyl fluorides 1 [R1 = CF3 (1 a), C2F5 (1 b), CF3Se (1 c)]. These compounds are very reactive and polymerize to rubberlike products. On heating the polymers decompose almost quantitatively to the monomers or dimers. In CFCl3 solution 1 dimerizes at 20°C in sunlight to the corresponding cis/trans-1,3-diselenetanes 2. The structure of 2 b is determined by single crystal X-ray diffraction. Different selenocarbonyl derivatives add to unsymmetrically substituted 1,3-diselenetanes 3. 1 a and 1 b react with cyclopentadiene to form the [4 + 2] cycloaddition products 4a and 4c. Halogen exchange reactions take place between 2a  -  d and BCl3. The cis-isomers react much faster than the trans-isomers to give a mixture of cis-, trans-forms of 5. When 2c,d is treated with BCl3 it is possible to isolate and characterize the pure trans-isomer 2d, which is separated by preparative gas chromatography from 5c,d. Fluorine abstraction with formation of 1,3-diselenetan-2-ylium ions (6a  -  f) are accomplished by reactions of 2 or 3 with AsF5 in SO2.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 87-88 
    ISSN: 0009-2940
    Schlagwort(e): Alkylidenesulfur difluoride oxide ; Carbon-sulfur double bond ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Hg[C(COF) = SF2 = O]2 is prepared by the reaction of FCO — CH = SF2 = O with HgF2. This compound represents the third known example of an alkylidenesulfur difluoride oxide. Its molecular structure is the same as that of the most abundant of the three isomers of FCO-CH = SF2 = O. This is assumed to be the result of weak intramolecular Hg… O contacts. With the exception of the fluorine atoms bound to sulfur, all atoms lie approximately in one plane.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 103-109 
    ISSN: 0009-2940
    Schlagwort(e): Asteranes ; Cage compounds ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Asteranes, XXII1).  -  Synthesis of a Double Tetraasterane: Nonacyclo[10.8.0.02,11.04,9.04,19.06,17.07,16.09,14.014,19]eicosane1,4,5,8-Tetrahydronaphthalene-2,3-dicarboxylic anhydride (9) is dimerized by UV light in dioxane yielding four isomeric [2 + 2] adducts whose methyl ester derivatives are elucidated spectroscopically. The structures of the major products 14 and 16 have been confirmed by X-ray structure analysis. Degradation of the carboxylic groups of 14 afforded the title compound 5.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 157-162 
    ISSN: 0009-2940
    Schlagwort(e): Fluoro compounds, aromatic ; Nitrite exchange by fluoride ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Synthesis of Aromatic Fluoro Compounds by Nucleophilic Exchange of Nitro Groups by FluorideThe synthesis of aromatic fluoro compounds from the respective nitro compounds by nucleophilic substitution of nitrite by fluoride is described. Reasonable yields in case of nonactivated nitro compounds are only obtained if the nitrite formed in the reaction is eliminated by acylation. 1-Fluoro-3-nitrobenzene (2) was obtained from 1,3-dinitrobenzene (1), and 1-fluoro-3,5-dinitrobenzene (9) as well as 1,3-difluoro-5-nitrobenzene (10) from 1,3,5-trinitrobenzene (8) in yields up to 92% by reaction of nitro compounds with potassium fluoride in sulfolane at 180 - 200°C in the presence of phthaloyl dichloride (6); 1,2-difluoro-4-nitrobenzene (12) was formed in 58% yield from 2,4-dinitro-1-fluorobenzene (11) in the presence of pyromellitoyl tetrachloride (13).
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 13-16 
    ISSN: 0009-2940
    Schlagwort(e): Diphosphines, tetrakis(diisopropylamino) ; Phosphinous anhydrides ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Synthesis and Structure of Bis[bis(diisopropylamino)phosphino]chalcogenidesPhosphorodiamidous chalcogeno-anhydrides [(R2N)2P]2X (R = Me2CH; X = S, Se, Te) (2a-c) have been obtained by insertion of elemental sulfur, selenium, or tellurium into the P-P bond of the corresponding diphosphane (1). The structure of 2a and 2c has been confirmed by an X-ray diffraction.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 31-38 
    ISSN: 0009-2940
    Schlagwort(e): Fluorosulfonium salts, reaction with nucleophiles ; (Perfluoroakyl)(dimethylamino)sulfonium salts, preparation and structures of ; Methoxysulfinyl hexafluoroarsenate, alkylation with ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: (Perfluoroalkyl)(dimethylamino)sulfonium HexafluoroarsenatesMeN = S(CF3)2 (5) is alkylated by Me3O⊕ AsF⊖6 to Me2N-S(CF3)⊕2 AsF⊖6 (4). From 5 and MeOSO⊕ AsF⊖6 (6) MeOS(O)-N(Me)S(CF3)⊕2 AsF⊖6 (7) is formed as a relatively stable primary product. Decomposition of 7 gives the expected 4 only in poor yield. Nucleophilic substitution of the sulfur-bonded fluorine in CF3SF⊕2 AsF⊖6 (8) by Me3SiNMe2 yields CF3S(NMe2)⊕2 AsF⊖6 (9). Similarly, (CF3)2CFSF⊕2 AsF⊖6 (10) reacts with dimethyl(trimethylsilyl)amine to give (CF3)2CFS(NMe2)⊕2 AsF⊖6 (11). The structures of 4 and 9 are elucidated by X-ray analyses, and the influence of the substituents on the bonding is discussed.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 63-67 
    ISSN: 0009-2940
    Schlagwort(e): Dinuclear gold complex ; Silyl complex ; Gold-gold interaction ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Transition-Metal Silyl Complexes, 361).  -  On the Question of Gold-Gold Interactions in Ph2P[CH2]t(2)PPh2-Bridged Dinuclear Gold Silyl ComplexesDinuclear silyl gold complexes of the type dppm(AuSiR3)2 (1) or dppe(AuSiR3)2 (2) are prepared by the reaction of dppm-(AuCl)2 or dppe(AuCl)2 with two equivalents of LiSi(aryl)3 or LiSi(SiMe3)3 The complex dppe[AuSi(SiMe3)3]2 (2 c) exhibits crystallographic inversion symmetry, and therefore the distance between both gold atoms is a maximum. In dppm-(AuSiPh3)2 (1b) a gold-gold interaction between both gold atoms is observed [Au  -  Au 316.80(3) pm].
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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