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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 128 (1995), S. 1199-1205 
    ISSN: 0009-2940
    Keywords: Copper(I) complexes ; Copper(II) complexes ; N,S-Donor ligands ; Macrocyclic ligands ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis and characterization of seven copper coordination compounds with the 14-membered macrocyclic cis-N2S2 dibenzo ligand 6,7,13,14,15,16,17,18-octahydrodibenzo[e,m]-[1,4,8,11]dithiadiazacyclotetradecine (L1) and its N,N'-bisacetato and -bis(methylpyridyl) functionalized derivatives H2L2 and L3 are described. The structures of five compounds were determined by single-crystal X-ray diffraction. The tetrahedrally distorted square-planar coordination geometry of [CuL1](ClO4)2 (1) changes upon reduction of copper to a severely distorted tetrahedral geometry in [CuL1]Br · MeCN (2). The Cu-N bond lengths increase from 1.988(3) to 2.029(5) Å; the Cu-S bond lengths decrease from 2.293(1) to 2.255(2) Å. Copper(II) is hexacoordinated in [CuHL2]HSO4 · 2.5 H2O (5) and [CuHL2]ClO4 · H2O (6). Both compounds exhibit very similar overall structures in the cationic part. The macrocyclic ring of the ligand is folded along an N⃜S axis, the octahedral geometry is strongly Jahn-Teller distorted, with O and S donor atoms in the apical positions. Compound 5 contains one very short [2.271(3) Å] and one long [2.701(3) Å] Cu-S (thioether) bond. In [CuL3](ClO4)2 · 2 H2O (7) one thioether group of the ligand L3 remains uncoordinated. The coordination polyhedron is rather irregular: Cu-S 2.506(3) and Cu-N 1.960(7)-2.107(8) Å. The compounds were further characterized by electronic and EPR spectroscopy and by cyclic voltammetry. Some relationships to the structural and spectroscopic properties of “blue” copper proteins were found.
    Additional Material: 5 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 611 (1992), S. 158-164 
    ISSN: 0044-2313
    Keywords: Oxo-sulfato-vanadates(V) ; syntheses ; crystal structures ; Raman spectra ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation, Raman Spectra, and Crystal Structures of V2O3(SO4)2, K[VO(SO4)2], and NH4[VO(SO4)2]The oxo-sulfato-vanadates(V) V2O3(SO4)2, K[VO(SO4)2], and NH4[VO(SO4)2] have been prepared as crystals suitable for X-ray structure determination. In all structures sulfate acts as an unidentate ligand only toward a single vanadium atom. The structure of V2O3(SO4)2 consists of a threedimensional network of pairs of cornershared VO6 octahedra with one terminal oxygen atom each, and SO4 tetrahedra. All oxygen atoms of the sulfate ions are coordinated. NH4[VO(SO4)2] and K[VO(SO4)2] are isostructural. VO6 octahedra with one terminal oxygen atom and pairs of sulfate tetrahedra form infinite chains by corner sharing. The chains are weakly interlinked to layers. The sulfate ions are distorted towards planar SO3 molecules and single oxygen atoms attached to vanadium. This structural detail gives an explanation for the mechanism of the reversible reaction K[VO(SO4)2] ⇄ K[VO2(SO4)] + SO3 at 400°C. Raman spectra of the compounds have been recorded and interpreted with respect to their structures.Crystal data: V2O3(SO4)2, monoclinic, space group P21/a, a = 947.2(4), b = 891.3(3), c= 989.1(4) pm, β = 104.56(3)°, Z = 4, 878 unique data, R(Rw) = 0.039(0,033); K[VO(SO4)2], orthorhombic, space group P212121, a = 495.3(2), b = 869.6(9), c = 1 627(1)pm, Z = 4, 642 unique data, R(Rw) = 0,11(0,10); NH4[VO(SO4)2], orthorhombic, space group P212121, a = 495.3(1), b = 870.0(2), c = 1 676.7(4)pm, Z = 4, 768 unique data, R(Rw) = 0.088(0.083).
    Notes: Die Oxo-sulfato-vanadate(V)V2O3(SO4)4, K[VO(SO4)2] und NH4[VO(SO4)2] wurden dargestellt und ihre Strukturen röntgenographisch ermittelt. Die Struktur von V2O3(SO4)2 besteht aus einem dreidimensionalen Netzwerk von SO4-Tetraedern und Paaren eckenverknüpfter VO6-Oktaeder. Die Sauerstoffatome der Sulfationen sind an vier verschiedene Vanadinatome koordiniert. K[VO(SO4)2] und NH4[VO(SO4)2] sind isostrukturell. VO6-Oktaeder, mit einem endständigen Sauerstoffatom, und Paare von SO4-Tetraedern sind über Ecken zu Ketten verknüpft. Diese bilden über weitere gemeinsame Ecken Schichten. Die Sulfationen sind in Richtung planarer SO3- Moleküle und eines Sauerstoffatoms, das an Vanadium gebunden ist, verzerrt. Dies gibt eine Erklärung für den Mechanismus der bei 400°C reversiblen Reaktion K[VO(SO4)2] ⇄ K[VO2(SO4)] + SO3. Die Ramanspektren der genannten Verbindungen wurden gemessen und zugeordnet.Kristalldaten: V2O3(SO4)2, monoklin, Raumgruppe P21/a, a = 947,2(4), b = 891,3(3), c = 989,1(4)pm, β = 104,56(3)°, Z = 4, 878 unabhängige Reflexe, R(Rw) = 0,039(0,033); K[VO(SO4)2], orthorhombisch, Raumgruppe P212121, a = 495,3(2), b = 869,6(9), c = 1627(1) pm, Z = 4, 642 unabhängige Reflexe, R(RW) = 0,11(0,10); NH4[VO(SO4)2], orthorhombisch, Raumgruppe P212121, a = 495,3(1), b = 870,0(2), c = 1676,7(4) pm, Z = 4, 768 unabhängige Reflexe, R(Rw) = 0, 088(0,083).
    Additional Material: 5 Ill.
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  • 3
    ISSN: 0044-2313
    Keywords: Fluoro antimonates(III) ; protonated azacrownethers ; host-guest complexes ; crystal structures ; Mößbauer spectra ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Anionic Antimony(III) Fluoro Complexes with protonated Azacrownethers as Counterions. Crystal Structures and Mößbauer Spectra of [H2cyclam]2[Sb4F16] · 2H2O, [H4cyclam][Sb2F10] · 2 HF, and [H4(tetramethyl)cyclam]2[Sb4F15][HF2][F]4 (cyclam = 1,4,7,11-Tetraazacyclotetradecane)The title compounds are formed by reaction of SbF3 with the respective azacrownether. [H2cyclam]2[Sb4F16] · 2 H2O contains tetrameric anions which weakly associate to chains. The [H2cyclam]2+ ions possess an unusual conformation due to intramolecular hydrogen bonds. [H4cyclam][Sb2F10] · 2HF contains the dimeric hitherto unknown [Sb2F10]4- ion; two HF molecules are attached to it by hydrogen bonds. The structure of [H4(tetramethyl)cyclam]2[Sb4F15][HF2][F]4 is made up of the two dimensional polymeric [HSb4F17]4- anion. The tetra-protonated tetramethylcyclam ions form host-guest complexes with fluoride ions.
    Notes: Die Titelverbindungen entstehen durch Reaktion von SbF3 mit dem betreffenden Azakronenether. [H2cyclam]2[Sb4F16] · 2H2O enthält tetramere, schwach assoziierte [Sb4F16]4--Anionen. Die Kationen [H2cyclam]2+ liegen infolge intramolekularer H-Brückenbindungen in einer ungewöhnlichen Konformation vor. [H4cyclam][Sb2F10] · 2 HF enthält das dimere [Sb2F10]4--Ion, an das zwei HF-Moleküle gebunden sind. In [H4(tetramethyl)cyclam]2[Sb4F15][HF2][F]4 liegt ein zweidimensional polymeres Anion der Formel [HSb4F17]4- vor. Fluoridionen und protonierte Azakronenether bilden Wirts-Gast-Komplexe.
    Additional Material: 7 Ill.
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