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  • 1
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 57 (2001), S. o335-o337 
    ISSN: 1600-5368
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: 2-Phenyl-1-phenylthio-1-(tetrahydropyran-2-ylthio)propan-2-ol, C20H24O2S2, was synthesized as a mixture of four diastereoisomers. An isomer which crystallizes in the centrosymmetric monoclinic space group P21/c with the relative configuration (1S*,2R*,2′R*) is presented. Intermolecular hydrogen bonds between the hydroxyl group and the O atom of the tetrahydropyran ring of a neighbouring molecule [O...O 2.751 (2) Å] form zigzag chains in the c-axis direction. The tetrahydropyran ring has a chair conformation with an axial S-side chain.
    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. 69-71 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Two isostructural 9-thiophenanthrene derivatives, 9-dodecylthiophenanthrene, C26H34S, (I), and 9-tetradecylthiophenanthrene, C28H38S, (II), are reported. They crystallize in the monoclinic space group P21/c with four molecules in a unit cell. The S—Cphenanthrene bonds are 1.767 (2) and 1.772 (4) Å and S—Calkyl bonds are 1.809 (2) and 1.804 (4) Å for (I) and (II), respectively. The bond angles at S are 104.04 (11) and 104.0 (2)° for (I) and (II), respectively.
    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. 72-73 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The title compound, C28H18S2, crystallizes in the monoclinic space group P21/n and the structure shows pseudosymmetry close to the space group C2/c. At 193 K the compound has a long S—S bond of 2.1089 (12) Å and the S atom to anthracene bond distances are 1.776 (3) and 1.770 (2) Å. The C—S—S—C torsion angle is 76.06 (13)°.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 56 (2000), S. 1383-1385 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: In the synthesis of 1-phenyl-2-phenylthio-2-(tetrahydropyran-2-ylthio)ethanol, C19H22O2S2, four diastereoisomers are formed. Two non-centrosymmetric enantiomeric forms which crystallize in space groups P212121 and Pna21 are presented. The former has an intramolecular hydrogen bond between the hydroxyl group and the O atom of the tetrahydropyran ring. In the latter isomer, the hydroxyl group forms an intermolecular hydrogen bond to the O atom of the tetrahydropyranyl group of a neighbouring molecule, joining the molecules into chains in the c-axis direction; the O...O distances are 2.962 (4) and 2.764 (3) Å, respectively. The tetrahydropyran rings are in chair conformations in both isomers and the S side chain has an equatorial orientation in the former, but an axial orientation in the latter molecule.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 71 (1988), S. 1795-1800 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complexation of Cu2+ by N-isopropyl-2-methyl-1,2-propanediamine (L) has been studied by potentiometric and spectrophotometric titration. The dominant complexes formed in this system are [CuL]2+, [CuL2]2+, [Cu2L2(OH)2]2+, and [CuL(OH)2]. The data were thoroughly tested for different models with [CuL(OH)]+, [CuL(OH)]+, [Cu(OH)]+, and [Cu2(OH)2]2+ as additional species. The importance of steric factors is indicated by the d-d* spectra: for [CuL2]2+, (λmax = 499 nm) the absorption maximum is shifted by 50 nm to high energies relative to [Cu(en)2]2+, (λmax = 549 nm), whereas the opposite is true for the 1:1 complexes ([CuL]2+ : λmax = 712 nm,s [Cu(en)]2+ : λmax = 660 nm).
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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