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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 117 (1995), S. 2361-2362 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Organometallics 14 (1995), S. 2133-2135 
    ISSN: 1520-6041
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Organometallics 13 (1994), S. 5173-5176 
    ISSN: 1520-6041
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 57 (2001), S. m103-m105 
    ISSN: 1600-5368
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The X-ray crystal structure of the title compound, lithium 1,2,3,6-tetrahydro-2,6-dioxo-4-pyrimidinecarboxylate monohydrate, Li+·C5H3N2O4−·H2O, was redetermined at a temperature of 110 (2) K. It was now possible to locate all H atoms in the difference Fourier map. The hydrogen-bonding pattern can now be completely described, as well as the coordination mode of the water molecule to the lithium center.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 57 (2001), S. o1136-o1138 
    ISSN: 1600-5368
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The X-ray crystal structure of the title compound (2,5-furandione), C4H2O3, was redetermined at 130 (2) K. The C=C double bond, previously reported to be unusually short, was accurately measured as 1.3322 (9) Å and thus proved to be fairly standard. The relatively high melting point of the compound is attributed to the intermolecular dipole–dipole interactions between carbonyl groups.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    [s.l.] : Macmillian Magazines Ltd.
    Nature 406 (2000), S. 970-974 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Considerable effort is being devoted to the fabrication of nanoscale devices. Molecular machines, motors and switches have been made, generally operating in solution, but for most device applications (such as electronics and opto-electronics), a maximal degree of order and regularity is ...
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 56 (2000), S. 720-722 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The title compound, C4H11NO6P2, reveals a two-dimensional network of P—O—H...O=P and N—H...O=P hydrogen-bond interactions, forming molecular slabs parallel with the (010) plane. One O—H...O interaction is distinct within these sets: whilst forming the shortest intermolecular hydrogen bond, it possesses a short P—O(H) bond of 1.5291 (10) Å. Weak C—H...O contacts link individual stacks to produce a three-dimensional array. The compound is zwitterionic: one H atom from a P—O—H group has transferred to the pyrrolidine ring N atom.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 56 (2000), S. 577-579 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The title compounds contain very short intramolecular hydrogen bonds of the type C—O—H...O—N. The O...O distances are 2.425 (2) Å in picolinic acid N-oxide (2-carboxypyridine N-oxide), C6H5NO3, (I), and 2.435 (2) Å in quinaldic acid N-oxide (2-carboxyquinoline N-oxide), C10H7NO3, (II). In (II), this is associated with slight molecular distortion from planarity, while in (I), such an effect cannot be observed because the molecule crystallizes on a mirror plane.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1434-1948
    Keywords: Polymeric copper complexes ; Group-subgroup relationships ; 2D-sheets ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis and characterisation of two new polymeric CuII complexes is described, i.e. {[Cu(btp)2(CH3CN)(H2O)](CF3SO3)2}n (1) and {[Cu(btp)2(CH3CN)2](ClO4)2}n (2), in which btp = [1,3-bis(1,2,4-triazol-1-yl)propane]. Compound 1 crystallizes in space group P21/c with a = 11.9337(15) Å, b = 20.108(6) Å, c = 12.748(6) Å, β = 92.247(14)°, and Z = 4. Compound 2 crystallizes in space group Pna21 with a = 18.770(8) Å, b = 12.648(8) Å, and c = 12.019(8) Å. The structures refined to R1 values of 0.0683 for 1 and 0.0846 for 2. In both structures the CuII ions are linked by the bridging ligands, resulting in two-dimensional networks. Two such curved layers are arranged on top of each other with center-to-center of layer distances of 2.12 Å in 1 and 1.98 Å in 2. Such double layers are separated from each other by 10.05 Å in 1 and 9.385 Å in 2. The space between the double layers is occupied with interstitial anions. No significant interaction between CuII ions is observed by EPR and magnetic susceptibility measurements. The compounds form a new class of a lattice engineered system held together by the CuII ions. - The coordination geometry of the copper ions is distorted octahedral, with the equatorial plane formed by the N4 nitrogens of the four triazole groups and the axial sites occupied by solvent molecules; acetonitrile and water in structure 1 and two acetonitrile molecules in structure 2. The two structures are related by a group-subgroup relationship, which appears to be the first such case in supramolecular chemistry. - The Cu-N vibrations in the FIR region are found at 274 cm-1 for 1, and at 276 cm-1 for 2. The ligand-field maxima are observed at about 16·103 cm-1, with a shoulder at about 12·103 cm-1. The νCN stretching vibrations of the acetonitrile molecules are found at 2303 and 2261 cm-1 for 1, and at 2313, 2294, 2278, and 2260 cm-1 for 2.Supporting information for this article is available on the WWW under -//_/_http://www.wiley-vch.de/contents/jc_2005/2000/99211_s.pdf or from the author.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0941-1216
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1-aza-2-azoniaallene salt 8 prepared from 3-acetyl coumarin via the hydrazone 6 and the (chloroalkyl)azo derivative 7 reacts with nitriles to afford the 3-(3-chromenyl)-1,2,4-triazolium salts 11a-d. With diisopropylcarbodiimide the triazolium salt 13 and with norborene a tricyclic pyrazolium salt 14 are obtained. Concurrent to these cycloadditions the by-product 12 is formed by intramolecular cyclization of the cumulene 8. Similarly, the intramolecular cyclization product 18 is isolated as the sole product when the 1-aza-2-azoniaallene salt 17a (prepared from the ethyl carbazone of camphor by chlorination and treatment of the product 16a with SbCl5) was treated with nitriles, carbodiimides or alkenes. In contrast, 1,2,4-triazolium salts 20a-c, 23c, respectively pyrazolium salts 20d-f, and 1,3,4-thiadiazolium salts 23a,b are obtained by reaction of the 1-aza-2-azoniaallene salt 17b with nitriles, respectively alkenes, alkynes, diisopropylcarbodiimide, and isothiocyanates. The constitutions of two of these products (20e, 23a) were secured by X-ray structural analysis.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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