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  • Wiley-Blackwell  (4)
  • International Union of Crystallography (IUCr)  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 56 (2000), S. 407-411 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The sodium salt of a complex anion formed between gadolinium(III) and three variously deprotonated chelidamic acid (4-hydroxypyridine-2,6-dicarboxylic acid) ligand moieties, assigned as Na5[Gd(C7H2NO5)2(C7H3NO5)]·16H2O, i.e. pentasodium (4-hydroxypyridine-2,6-dicarboxylate)bis(4-oxidopyridine-2,6-dicarboxylate)gadolinium(III) hexadecahydrate, forms as colourless monoclinic crystals upon vapour diffusion of ethanol into its aqueous solution. The ligand moieties, assigned as two trianionic and one dianionic chelidamate species, are all tridentate in the complex anion of tricapped trigonal prismatic donor-atom geometry. The geometry of the ligands and that of the primary coordination sphere is very similar to that of the analogous anionic tris(ligand)–rare earth complexes of the pyridine-2,6-dicarboxylate (dipicolinate) dianion.
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  • 2
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A room-temperature single-crystal X-ray structure determination of the title compound, C21H20O8, confirms the stereochemical assignment made previously on the basis of spectroscopic studies [Shaari & Waterman (1994). J. Nat. Prod. 57, 720–724].
    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. 448-450 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Chelidamic acid, 4-hydroxypyridine-2,6-dicarboxylic acid, is found to be zwitterionic in its solid monohydrate form, C7H5NO5·H2O, with the aryloxide and one carboxylate group remaining protonated, but the other carboxylate group losing its proton to the pyridine N atom. In this, it is unlike its parent, dipicolinic acid (pyridine-2,6-dicarboxylic acid), which also crystallizes as a monohydrate, but one in which the acidic H atoms remain bound to the carboxylate groups. In both structures, the water molecule is a component of an extended hydrogen-bonded network.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 543-545 
    ISSN: 1434-1948
    Keywords: Lanthanoid(II) complexes ; Ytterbium ; Thallium ; η2-Pyrazolate complexes ; Diphenylmercury ; Redox transmetallation ; X-ray crystal structure ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ytterbium metal reacts with thallium(I) 3,5-diphenylpyrazolate, or with diphenylmercury and 3,5-diphenylpyrazole (Ph2pzH) in tetrahydrofuran or 1,2-dimethoxyethane (DME) giving, after appropriate isolation, the first lanthanoid(II) pyrazolate complex, [Yb(Ph2pz)2(DME)2]. The molecular structure reveals eight coordinate ytterbium(II) with two cisoid η2-3,5-diphenylpyrazolate and two chelating 1,2-dimethoxyethane ligands.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 751-761 
    ISSN: 1434-1948
    Keywords: Lanthanide(II) complexes ; Ytterbium ; Europium ; Samarium ; Redox transmetallation ; Thallium ; Diphenylmercury ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complexes [Yb(bind)2(DME)2], [Yb(MePhpz)2(DME)2], [Yb(azin)2(DME)2], and [Eu(Ph2pz)2(DME)2] (bindH = 4,5-dihydro-2H-benz[g]indazole; MePhpzH = 3-methyl-5-phenylpyrazole; azinH = 7-azaindole; Ph2pzH = 3,5-diphenylpyrazole; DME = 1,2-dimethoxyethane) have been prepared by redox transmetallation between ytterbium or europium metal and the corresponding thallium(I) pyrazolate in tetrahydrofuran (THF) in the presence of mercury metal, followed by work up with DME. The thallium reagents were obtained by treatment of the appropriate pyrazole with thallium(I) ethoxide. Both [Yb(Ph2pz)2(DME)2] and [Sm(Ph2pz)2(DME)2] have been prepared by metathesis from LnI2(THF)2 and K(Ph2pz) in THF, whilst the former has also been obtained by redox transmetallation from [Hg(Ph2pz)2] and ytterbium metal and by reaction of 3,5-diphenylpyrazole with Yb(C6F5)2, and the latter from protolysis of [Sm{N(SiMe3)2}2(THF)2] with Ph2pzH, followed in each case by crystallisation of the crude product from DME. Europium(II) 3,5-di-tert-butylpyrazolate was synthesised by a redox transmetallation/ligand exchange reaction between europium metal chunks, diphenylmercury(II), and 3,5-di-tert-butylpyrazole (tBu2pzH) in the presence of mercury metal in THF, and [Eu(tBu2pz)2(DME)2] was isolated on crystallisation of the crude product from DME. The X-ray crystal structures of [Ln(L)2(DME)2] (Ln =Yb, L = bind or azin; Ln = Eu or Sm, L = Ph2pz; Ln = Eu, L = tBu2pz), each of a different crystallographic form, reveal eight-coordinate lanthanoid complexes with two η2-pyrazolate and two chelating DME ligands, but the structures differ in the relationship (cisoid or transoid) between the pyrazolate ligands. Thus cen-Ln-cen (cen = centre of the N-N bond) angles of 106.7° [Yb(bind)2(DME)2] (3a), 141.4° [Yb(azin)2(DME)2] (3c), 142.2° [Eu(Ph2pz)2(DME)2] (4a), 107.4° [Eu(tBu2pz)2(DME)2] (4b), and 102.1° [Sm(Ph2pz)2(DME)2] (5) are observed.
    Additional Material: 6 Ill.
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  • 6
    ISSN: 1434-1948
    Keywords: Thiacalixarene ; Trimetallic sandwich ; Cobalt ; Zinc ; Divergent receptors ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reaction between deprotonated p-tert-butyltetrathiacalix[4]arene and CoII or ZnII under strictly defined conditions leads to the formation of sandwich species in which a trimetallic unit is held between two opposed, divergently oriented, staggered O- and S-bound calixarene ligands in the cone conformation. Despite the isomorphous nature of the crystalline compounds, there is a subtle difference in the coordination of CoII and ZnII, presumably related to the differences in metal radius and electron configuration combined with structural restrictions imposed by the calixarene framework, in that whereas all three Co atoms may be considered six-coordinate (and approximately octahedral), only two of the Zn atoms appear so, the third being five-coordinate and more nearly trigonal bipyramidal in its coordination geometry.
    Additional Material: 2 Ill.
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  • 7
    ISSN: 0268-2605
    Keywords: X ray structure ; triphenyltin ; p-ethoxybenzoic acid ; acetylsalicylic acid ; phthalic acid ; salicylaldehydato ; polymer ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Triphenyltin(IV) compounds of p-ethoxybenzoic acid and acetylsalicylic acid contain molecular units with Sn-O bonds and distorted tetrahedral tin centers. The phthalic acid derivative contains two four-coordinate tin atoms between which the phthalic acid unit effectively forms a bridge. The salicylaldehydato compound is polymeric with trigonal bipyramidal tin centers in which the phenyl groups take equatorial positions. The polymerization occurs via the aldehyde oxygen atom bonding to a neighboring tin atom. © 1998 John Wiley & Sons, Ltd.
    Additional Material: 3 Ill.
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