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  • Articles: DFG German National Licenses  (11)
  • 2000-2004  (8)
  • 1995-1999  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 56 (2000), S. e278-e279 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The crystal and molecular structure of the title compound, (C4H12N)2[Mo6O19]·H2O, has been determined from X-ray diffraction data. The polyoxoanion [Mo6O19]2− is built up from six distorted MoO6 octahedra sharing common edges and one common vertex at the central O atom, and has crystallographic m3m (Oh) symmetry. The cation has crystallographic \overline 43m symmetry.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 56 (2000), S. 1164-1167 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The crystal structures of the first stable α-diol from the α-halogenopyruvamide series, 3-chloro-2,2-dihydroxy-3-phenylpropanamide, C9H10ClNO3, and three products [3-(4-chlorophenyl)-2-cyano-2,3-epoxypropanamide, C10H7ClN2O2, 3-bromo-2-cyano-2-hydroxy-3-p-tolylpropanamide, C11H11BrN2O2, 3-bromo-2-oxo-3-p-tolylpropanamide, C10H10BrNO2] obtained during the systematic synthesis of α-halogenopyruvamides are reported. The crystal structures are dominated by hydrogen bonds involving an amide group. The stability of the geminal diol could be ascribed to hydrogen bonds which involve both hydroxyl groups.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 56 (2000), S. 890-891 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: In the title compound, C22H24N4O11, the N-glycosidic torsion angles O′—C′—N—C and O′—C′—N—N are −34.1 (6) and 148.8 (3)°, respectively. The molecule displays an α-D configuration with the ribofuranose moiety in an O′-exo–C′-endo pucker. There are only weak C—H...O and C—H...N intra- and intermolecular interactions.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 57 (2001), S. 246-247 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The title centrosymmetric cluster octakis(4-isopropylpyridine-N)-di-μ4-oxo-hexa-μ3-oxo-octa-μ2-oxo-decaoxooctamolybdenum(V)dimolybdenum(VI), [Mo10O26(C8H11N)8], consists of ten Mo atoms connected together by bridging oxo groups. Pentavalent Mo atoms are linked into four Mo2V pairs by metal–metal single bonds with lengths of 2.5637 (6) and 2.6132 (6) Å.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 56 (2000), S. e443-e444 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The crystal and molecular structure of bis(tetramethylammonium) dichlorotetra-μ2-methoxo-di-μ2-oxo-octooxotetramolybdate(VI), (C4H12N)2[Mo4O10(OCH3)4Cl2], has been determined from X-ray diffraction data. The crystallographically centrosymmetric anion is built up of four edge-sharing octahedra, two MoO6 and two MoO5Cl.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 57 (2001), S. 409-411 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The reaction of 3,4,5,6-tetrahydropyrimidine-2-thione (H4pymtH) with mercury(II) iodide in methanol in a 1:1 molar ratio resulted in the formation of single crystals of the title compound, [Hg(C4H8N2S)I2]. The Hg atom is coordinated by one S atom from H4pymtH at 2.456 (2) Å and by two I atoms at distances of 2.6872 (7) and 2.7044 (6) Å, and has a characteristic deformed trigonal coordination geometry. The molecule has crystallographic m symmetry but the Hg atom is disordered above and below the mirror plane.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 57 (2001), S. 546-548 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The title compounds, tetrakis(μ-benzoato-O:O′)bis(2,6-diaminopyridine)-1κN,2κN-dicopper(II)–acetonitrile (1/2), [Cu2(C7H5O2)4(C5H7N3)2]·2C2H3N, (I), and bis(acetonitrile)-1κN,2κN-tetrakis(μ-benzoato-O:O′)dicopper(II)–acetonitrile (1/1.5), [Cu2(C7H5O2)4(C2H3N)2]·1.5C2H3N, (II), crystallize as acetonitrile solvates exhibiting different stability. They have similar molecular structures with discrete dimeric units located at crystallographic inversion centres. The copper ions are bridged by four benzoate groups and neutral N-donor ligands, viz. 2,6-diaminopyridine in (I) and acetonitrile in (II), are coordinated at apical positions. The diverse stability is probably due to hydrogen-bond interactions of the solvated acetonitrile molecules with neighbouring dimers in compound (I).
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1572-8854
    Keywords: Chromium(III) ; molybdenum(III) ; 4-ethylpyridine complexes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The structures of trichlorotris(4-ethylpyridine)chromium(III), [CrCl3(C7H9N)3] (I), and trichlorotris(4-ethylpyridine)molybdenum(III), [MoCl3(C7H9N)3] (II), consist of neutral molecules where three 4-ethylpyridine and three chloro ligands coordinate to the metal with a meridional configuration. Compound I crystallizes in a trigonal space group P31 with a = 11.515(2) Å and c = 15.378(3) Å. Compound II crystallizes in a monoclinic space group C2/c with a = 24.200(3) Å, b = 18.089(3) Å, c = 22.6004(7) Å and β = 106.7137(6)°.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1434-4475
    Keywords: Keywords. Ca2(SeO3)(Se2O5); Ba(SeO3); Ba(Se2O5) ; Crystal structure; Crystal chemistry.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung.  Die Verbindungen Ca2(SeO3)(Se2O5), Ba(SeO3) und Ba(Se2O5) wurden unter niedrig-hydrothermalen Bedingungen aus wäßrigen Lösungen von SeO2 durch Reaktion mit den jeweiligen Erdalkalikarbonaten erhalten. Die Kristallstrukturen wurden aus Einkristallröntgendaten mittels direkter Methoden bestimmt. Ca2(SeO3)(Se2O5): Raumgruppe P*, Z=2, a=5.517(1), b=8.210(2), c=8.716(2) Å, α=92.47(2), β=95.92(2), γ=97.15(2)°, V=389.0(2) Å3, R 1=0.017; Ba(SeO3): Raumgruppe P21/m, Z=2, a=4.677(2), b=5.645(2), c=6.851(3) Å, β=107.16(2)°, V=172.8(1) Å3, R 1=0.022; Ba(Se2O5): Raumgruppe P21/c, Z= 4, a= 4.553(1), b=11.724(3), c=9.758(2) Å, β=92.66(2)°, V=520.3(2) Å3, R 1=0.027. Alle drei Verbindungen besitzen Gerüststrukturen; im Fall des Ca2(SeO3)(Se2O5) können Einheiten von kantenverknüpften CaOn Polyedern hervorgehoben werden, die Schichten parallel zu (010) bilden. Ba(SeO3) gehört dem KClO3-Strukturtyp an. In Ba(Se2O5) treten Ketten von flächenverknüpften BaO9 Polyedern entlang [100] auf. Die Calciumatome sind 7- und 8-koordiniert mit mittleren Ca–O Bindungslängen von 2.42 und 2.48 Å: die beiden Bariumatome weisen neun Sauerstoffliganden mit mittleren Ba–O Bindungslängen von 2.87 Å auf.
    Notes: Summary.  The compounds Ca2(SeO3)(Se2O5), Ba(SeO3), and Ba(Se2O5) were obtained at low-hydrothermal conditions from aqueous solutions of SeO2 by reaction with the respective earth alkaline carbonate. The crystal structures were determined by direct methods from single crystal X-ray diffraction data. Ca2(SeO3)(Se2O5): space group P*, Z=2, a=5.517(1), b=8.210(2), c=8.716(2) Å, α=92.47(2), β=95.92(2), γ=97.15(2)°, V=389.0(2) Å3, R 1=0.017; Ba(SeO3): space group P21/m, Z=2, a=4.677(2), b=5.645(2), c=6.851(3) Å, β=107.16(2)°, V=172.8(1) Å3, R 1=0.022, Ba(Se2O5): space group P21/c, Z=4, a=4.553(1), b=11.724(3), c=9.758(2) Å, β=92.66(2)°, V=520.3(2)Å3, R1=0.027. All three compounds have framework structures; in the case of Ca2(SeO3)(Se2O5), subunits of edge-sharing CaO n polyhedra forming sheets parallel to (010) can be emphasized. Ba(SeO3) belongs to the structure type of KClO3. In Ba(Se2O5), chains of face-sharing BaO9 polyhedra along [100] are present. The calcium atoms are 7- and 8-coordinated with mean Ca–O bond lengths of 2.42 and 2.48 Å, the barium atoms have nine oxygen ligands with mean Ba–O bond lengths of 2.87 Å.
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  • 10
    ISSN: 1434-1948
    Keywords: Ruthenium ; Coordination chemistry ; Paramagnetic complexes ; Magnetic properties ; Ion exchange ; Antitumor agents ; Colon tumors ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Indazolium trans-tetrachlorobis(indazole)ruthenate(III) exhibits excellent results against different tumor models in vitro and in vivo. To improve the water solubility necessary for the introduction of this tumor-inhibiting compound into clinical trials, we synthesized the corresponding sodium salt in a two-step ion exchange via the tetramethylammonium salt. The sodium salt shows a 35-fold higher solubility in water relative to the indazolium salt. We also synthesized the n-butylammonium, n-octylammonium, and tetraphenylphosphonium salts, all of which showed improved solubility in organic solvents. The X-ray crystal structure of the latter could be solved, proving the trans configuration of the complex anion. In spite of the paramagnetic RuIII center an assignement of the coordinated indazole protons could be made with the help of a COSY experiment.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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