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  • Articles: DFG German National Licenses  (92)
  • General Chemistry  (90)
  • Calculations, ab initio, EH  (2)
  • Imidazoles  (2)
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  • Articles: DFG German National Licenses  (92)
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  • 1
    ISSN: 1434-1948
    Keywords: Boranes ; Ruthenium ; Sandwich Complexes ; Diboroles ; Triple-decker ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The addition products of lithium alkyls and the pentaalkyl-2,3-dihydro-1,3-diborole derivatives 5a-f react with [{(C5Me5)RuCl}4] and [{(C5Me4Et)RuCl}4] to form the violet sandwich compounds 2*c-f and 2∧c, f. These formally 16 VE complexes are in fact electron-poor 18 VE species, because a high-lying combination of σ(B-C) orbitals interacts with the dxz orbital of the Ru atom. Addition of tert-butyl isocyanide to 2*a, or 2*d leads to the isonitrile complexes 6*a, and 6*d, as indicated by the spectroscopic data and X-ray structure analyses. At low temperature the interaction of 2*a, c, or e with H2 yields the classic dihydride complexes 7*a, c, and e, respectively, which have been studied by NMR. Oxidative addition of H3B·THF to the ruthenium atom of 2*a or c, followed by a reductive elimination of H2 and migration of the boranediyl group gives the yellow closo-RuC3B3 ruthenacarboranes 8*a and 8*c, respectively. The reaction of [(C2H4)2RhCl]2 and 2*c generates the tetranuclear complex 9*c.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0009-2940
    Keywords: 1,3-Diborapentafulvene ; Iron tricarbonyl complexes ; Slipped triple-decker ; Calculations, ab initio, EH ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complexation of 1,3-Dihydro-1,3-diborapentafulvene Derivatives with Fe(CO)3 Fragments: Syntheses, Crystal and Electronic Structure of μ-(η4: η5-1,3-Dihydro-1,3-diborapentafulvene)-bis(tricarbonyliron) ComplexesReactions of the 1,3-diborapentafulvene derivatives 1a-c with (CO)3Fe(C8H14)2 lead to the violet dinuclear complexes 3a-c, which possess a slipped triple-decker structure. The X-ray structure analyses of 3b,c reveal that one Fe(CO)3 group is pentahapto-coordinated to the 1,3-diborole frame of C2B2C=C, whereas the other interacts with the Y-shaped B2C=C unit. The latter resembles the interaction of Fe(CO)3 with trimethylenemethane. An MO calculation indicates that the formation of 3 occurs by distortion of 1 · Fe(CO)3; the slippage of Fe(CO)3 from η5 to η4 bonding is followed by η5 coordination of the second Fe(CO)3 group.
    Additional Material: 4 Ill.
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  • 3
    ISSN: 0009-2940
    Keywords: Cobalt, (η5-cyclopentadienyl)(1, 3-dibora-4, 5-benzopentafulvene)- ; Iron tricarbonyl complexes ; Triple decker, mixed-metal, slipped ; Calculations, ab initio, EH ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complexation of 1, 3-Dihydro-1, 3, 10, 10-tetramethyl-1, 3-dibora-4, 5-benzopentafulvene with Fe(CO)3 and CpCo Fragments: Synthesis, Crystal and Electronic Structure of Tricarbonyl[(η5-cyclopentadienyl)cobalt][μ,η5:η4-(1, 3-dihydro-1, 3, 10, 10-tetramethyl-1, 3-dibora-4, 5-benzopentafulvene)]ironReaction of the 1, 3-dibora-4, 5-benzopentafulvene 1 with the isolobal organometallic fragments Co(C5H5) and Fe(CO)3 leads to the slipped triple-decker complex 5. It is also formed when 2 is stacked with the Co(C5H5) fragment. The X-ray structure analysis of 5 reveals that the Co(C5H5) fragment is coordinated to the 1, 3-diborole ring, and the Fe(CO)3 group interacts with the Y-shaped B2C=C unit. An MO calculation indicates that the formation of 5 occurs by distortion of 2 (η5- → η4-bonding) and complexation of the Co(C5H5) group. 5 is 16 kcal/mol more stable than its structural isomer 6.
    Additional Material: 1 Tab.
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  • 4
    ISSN: 1434-1948
    Keywords: Boranes ; Homogeneous catalysis ; Ab initio calculations ; Donor-acceptor systems ; X-ray analysis ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The catechol-substituted diboranes(4) 1 react with the catechol-substituted diborylacetylenes 2, in the presence of [Pt(PPh3)2(C2H4)] or [Pt(PPh3)4], to give tetra- and hexaborylethane derivatives. When [Pt(cod)2] is used as catalyst, the tetraborylethene 5a is formed exclusively. Catalytic hydrogenation of 5a affords the 1,1,1′,1′-tetraborylethane 4a, which has been studied by an X-ray structure analysis. Natural Bond Orbital (NBO) analyses for the RHF/3-21G optimized geometries of 4a and 5a reveal intramolecular stabilization of the boron pz orbital. This covers B-O, B-B, and agostic interactions. The photoelectron spectrum of 5a is reported
    Additional Material: 7 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 393-398 
    ISSN: 1434-1948
    Keywords: Boranes ; Bipyridine ; Crystal structures ; Donor-acceptor interaction ; Heterocycles ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 6,6′-Bis(diethylboryl)-2,2′-bipyridine (1a) was obtained in low yield by in situ deprotonation of 2,2′-bipyridine in the presence of diethyl(methoxy)borane. 6,6′-Dilithio-2,2′-bipyridine reacts with various alkoxyboranes leading to bipyridinediborates 2 in good yields. The derivatives 2b and 2c allow the formation of the free diborylbipyridines 1b and 1c. The coordination properties of the diboryl-bipyridines as tetrafunctional donor-acceptor compounds have been used for the formation of the copper complex 4 and of the adduct 5 which is built from diborylbipyridine and a dihydroxydiboroxan derivative. The composition of the products follows from spectroscopic data and from X-ray structure analyses for 2f, 4, and 5.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 459-463 
    ISSN: 1434-1948
    Keywords: 1,2-Diboraheterocycles ; Carbon monoxide insertion ; Isonitrile insertion ; Dimerisation ; Spiro insertion products ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The insertion of CO into the B-B bond of 1,2-bis(diisopropylamino)-2,5-dihydro-1H-1,2-diborole (1b) and 1,2-bis(diisopropylamino)-3-methylidene-1,2-diborolane (1c) leads to the dimeric spiro products 1,7,9,14-tetrakis(diisopropylamino)-6,13-dioxa-1,7,9,14-tetraboradispiro[4.2.4.2]tetradeca-2,10-diene (4b) and 1,7,9,14-tetrakis(diisopropylamino)bismethylidene-6,13-dioxa-1,7,9,14-tetraboradispiro[4.2.4.2]tetradecane (4c). Insertions of CO into the B-B bonds of the cyclic organo-1,2-diborane compounds 5, 6, and 7 are not observed. The reaction of 1b with tert-butyl isocyanide and 2,6-dimethylphenyl isocyanide in THF leads to the formation of the monomeric insertion products 1,3-bis(diisopropylamino)-2-tert-butylimino-1,3-diboracyclohex-4-ene (10b) and 1,3-bis-(diisopropylamino)-2-(2′,6′-dimethylphenylimino)-1,3-diboracyclohex-4-ene (11b). The treatment of 1cwith the isonitriles yields 2-tert-butylimino-1,3-bis(diisopropylamino)-4-methylidene-1,3-diboracyclohexane (10c) and 1,3-bis(diisopropylamino)-2-(2′,6′-dimethylphenylimino)-4-methylidene-1,3-diboracyclohexane (11c). The steric requirements of the isonitrile insertion products 10b, c and 11b, c prevent their dimerisation and rearrangement. 11b rearranges to 1-(diisopropylamino)-2-(diisopropylaminohydroxyboryl)-2-(2′,6′-dimethylphenylamino)-1-boracyclopent-3-ene (12b) upon reaction with water from sodium sulfate decahydrate. The compositions of the compounds are derived from the 1H-, 11B-, 13C-NMR data as well as from mass-spectral and C, H, N analyses. In the cases of of 4b and 12b they have been proven by X-ray structure analyses.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1434-1948
    Keywords: 3,4-Bis(isopropylidene)-1,2,5-thiadiborolane ; nido-2,4,5-Thiadicarbahexaboranes(5) ; Isomeres ; Thiadicarbanonaborane(8) ; IGLO ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 3,4-bis(isopropylidene)-2,5-dichloro-1,2,5-thiadiborolane (5b), obtained from 3,4-bis(dichloroboryl)-2,5-dimethyl-2,4-hexadiene (4) and (Me3Si)2S, reacts with Li[RBH3] (R = H, C6H5, C6Me4H) to yield the corresponding derivatives of the nido-4,5-diisopropyl-2,4,5-thiadicarbahexaboranes 2. Replacements of the chlorine atoms in 5b with two hydrido, or with one hydrido and one aryl (phenyl or duryl) group, followed by the hydroboration of the isopropylidene substituents with RBH2 (R = H, C6H5, C6Me4H) lead to four nido-2,4,5-thiadicarbahexaboranes (2a-d) in low yields. Their composition follows from MS and NMR data; not refined X-ray structural data of 2d support the proposed skeletal structure. In addition to 2a, larger thiacarboranes were detected by GC/MS and 11B NMR. The structure of the nine-vertex cluster 6a could be identified by applying the ab initio/IGLO/NMR method. Geometry optimizations at the MP2(fc)/6-31G* level rule out the Csnido-SC2B6H8 isomer 7. The C2v structure of 6 consists of a nine-vertex cluster with two elongated B-B distances. As this 22e cluster 6 represents an exception to the Wade rules, the nature of the bonding of nine-vertex clusters with different electron counts is discussed.
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 7-9 
    ISSN: 1434-1948
    Keywords: Boranes ; Diazaboroles ; Heterocycles ; Ketiminoboranes ; Crystal Structures ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The cyclocondensation reaction of benzil-bis(trimethylsilylimin) (3) and Cl2B-NiPr2 via silicon-boron exchangeresults in the solvent-dependent formation of the 1,3,2-diazaborole 1a or the 1,3,6,8,2,7-tetraazadiborecin 2a. Using the more rigid 9,10-bis(trimethylsilylimino)phenanthrene instead of 3 only the five-membered heterocycle 4,5-biphenylene-2-diisopropylamino-1,3,2-diazaborole (1b) is formed. The cyclic ketiminoboranes are characterized by NMR and X-ray diffraction data. The 1,3,2-diazaborole ring is almost planar, while the conformation of the 1,3,6,8,2,7-tetraazadiborecin has the shape of a figure-eight loop.
    Additional Material: 2 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 399-404 
    ISSN: 1434-1948
    Keywords: Boranes ; 1-Alkylpyrroles ; Porphyrinogenes ; Lithiation ; Tin-boron exchange ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of 2,5-dilithiated 1-methylpyrrole (1a) with ClB(NR2)2 lead to the novel 2,5-diboryl-1-methylpyrroles 2a and 2b. Accordingly, 2,5-diboryl-1-benzylpyrrole 2d is obtained. 1a and Cl2BNiPr2 form the aminochloroboryl-substituted derivative 2c and the di(5-boryl-2-pyrrolyl)borane 4 in 29% and 15% yield, respectively. The 2,5-distannyl-1-methylpyrrole 1c is used for the synthesis of the aryloxy-boryl derivative 2e. Reacting monolithiated 1-methyl- and 1-benzylpyrroles with Cl2BNiPr2 yields the di(2-pyrrolyl)boranes 3e and 3f, respectively. NMR and MS data are in agreement with the compositions of the compounds, which are confirmed by X-ray structure analyses for 2a, 2b, 2d, und 3e.
    Additional Material: 3 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 789-793 
    ISSN: 1434-1948
    Keywords: Boranes ; Carbenes ; Heterocycles ; Imidazoles ; X-ray structures ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The nucleophilic carbene 3-borane-1,4,5-trimethylimidazol-2-ylidene anion (1-) reacts with the electrophiles CH3I, (CH3)3SiCl, (CH3)3SnCl, and the bromodiazaboroline 7 to form the 2-substituted imidazoles 4, 5, 6, and 8. With triethylborane, the anionic carbene borane adduct 9- is obtained. An unexpected result was achieved when chlorodimethoxyborane and HBCl2 · S(CH3)2 were used as electrophiles. In both cases only the imidazabole 14a could be isolated. Imidazole 5, the imidazole borane adduct 3a and the imidazabole 14a were characterized by X-ray structure analyses.
    Additional Material: 3 Ill.
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