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  • 1
    ISSN: 1434-1948
    Keywords: Copper chelates ; EPR spectroscopy ; Electronic structure ; Schiff base ligands ; Structure elucidation ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of tetrahedrally distorted copper(II) complexes with thiolate and imine coordination were synthesized. Schiff bases derived from 4-benzoyl-3-methyl-1-phenyl-2-pyrazoline-5-thione and various diamines were used as tetradentate ligands to obtain tetrahedrally distorted metal chelates with [CuN2S2] complex units. Crystal structures of the complexes 1, 2, 5 and 6 and of ligand H25 have been determined by means of single-crystal X-ray structure analysis. The structure data show a strong influence of the diamine building blocks on the tetrahedral distortion of the copper(II) complexes. Results of Extended Hückel LCAO calculations correlate strongly with structural, electrochemical, UV/Vis- and EPR-spectroscopic features obtained experimentally. The calculations confirm for the whole complex series a strong delocalization of the frontier orbitals. The highest fully occupied molecular orbital shows a weak contribution, resulting from thiolate donor atoms, whereas the antibonding singly occupied molecular orbitals (SOMOs) are distributed between the copper(II) centre (ca. 35-40%) and the N2S2 donor set. The SOMO energy significantly lowers with increasing tetrahedral distortion of the coordination sphere. The influence of the tetrahedral distortion of copper(II) complexes on redox potentials, UV/Vis and EPR spectra is discussed.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1434-1948
    Keywords: Cobalt(III) ; Dithionate ; Trithionate ; Sulfato ligand ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Crystal structures of amminehalocobalt(III) compounds with di- or trithionate anions have been determined in order to know whether they interact to adopt specific molecular packing patterns and whether di- and trithionate anions undergo the S-S bond cleavage reactions as has been found for the S4O62- ion. In the structures of p-[Co(tren)(NH3)Cl]S2O6·H2O (1) and t-[Co(tren)(NH3)Cl]S2O6 (2), the configurational differences in the cations dictate the hydrogen-bonding pattern with the dithionate anion to lead to racemic structures. cis-[Co(en)2(NH3)Br]S3O6 (3) also crystallizes in a racemic space group P21/c in which the ions form a macrocyclic hydrogen-bonded network. Aqueous solutions of S3O62- and p-[Co(tren)(NH3)Cl]2+ produce p-[Co(tren)(NH3)(OSO3)]ClO4 (4) which is believed to be derived from the hydrolytic cleavage of S-S bond in the trithionate anion. These results reinforce our previous observation of the S-S cleavage reactions for the tetrathionate anion.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 651-656 
    ISSN: 1434-1948
    Keywords: Secondary carbaboranyldiphosphane ; Transition-metal complexes ; Crystal structure ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: When a mixture of stereoisomers of rac- and meso-1,2-bis(phenylphosphanyl)-1,2-dicarba-closo-dodecaborane(12) (1a, b; 1a/1b = 3:1) is treated with [Cp2ZrMe2] in boiling toluene for 2 h, the formation of three phosphorus-containing products, namely meso-[Cp2Zr(PPh)3] (3), (PPh)4 (4) and (PPh)5 (5), ratio 2.8:1.1:1.0, was observed by 31P-NMR spectroscopy. In the 11B-NMR spectrum of the reaction mixture, only signals for 1,2-dicarba-closo-dodecaborane(12) were observed. When zirconocene, prepared in situ from [Cp2ZrCl2] and BuLi, was treated with 1a, b at low temperature and then heated to reflux in toluene for 2 h, only formation of 3 and 1,2-dicarba-closo-dodecaborane(12) was observed. The mixture of stereoisomers of 1a, b reacts with CuCl in THF to give rac- and meso-[CuCl(THF){1,2-(PHPh)2C2B10H10}] (7a, b), which is only stable in THF solution and loses THF in vacuo over several hours to yield the insoluble colorless complex [CuCl{1,2-(PHPh)2C2B10H10}]n (8). In THF solution, 7 reacts with PPh3 to give the stable isolable complex [CuCl(PPh3){1,2-(PHPh)2C2B10H10}] (9). No reaction of 1a, b is observed with [Cp′Mo(CO)3]2 (Cp′ = C5H4Me) in boiling THF, while only decomposition occurs in boiling toluene. However, [(NBD)Mo(CO)4] (NBD = norbornadiene) reacts smoothly with 1a in toluene at room temperature to give cis-rac-[Mo(CO)4{1,2-(PHPh)2C2B10H10}] (10). Compounds 7, 9, and 10 were characterized spectroscopically (1H, 31P, 11B, 13C NMR, IR), and an X-ray structure determination was carried out on 10.
    Type of Medium: Electronic Resource
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