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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 50 (1985), S. 4171-4172 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 57 (2001), S. 868-869 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The title compound, 2,9-bis(3-nitrophenyl)-1-azatricyclo[3.3.1.13,7]decan-4-one, C21H19N3O5, has a tricyclic structure. The torsion angles may be used to describe the relationship of the carbonyl group to the adjacent faces, whereby it is seen that the angles on the face of the arylpiperidinone side [122.0 (3) and −122.0 (3)°] are greater than those on the cyclohexanone side [−119.8 (4) and 119.9 (4)°]. Although these differences may explain a facial selectivity during nucleophilic addition to the carbonyl group, the presence of the aryl rings is probably also important.
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  • 3
    ISSN: 1573-1111
    Keywords: [Ni(rac-Me6[14]aneN4)] ; 2,5-pyridinedicarboxylate ; preparation ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A bridged high-spin complex,bis-[Ni(II)(rac-5,5,7,l2,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane)]-2,5-pyridinedicarboxylate diperchlorate monohydrate has been obtained by reaction of [Ni(II)(rac-5,5,7, 12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane)](ClO4)2 and 2,5-pyridinedicarboxylic acid in aqueousalkaline (NH4OH) medium. C39H77Cl2N9Ni2O13, chemical formula weight 1068.42, orthorhombic, P212121, a = 11 .423(3) Å,b = 14.770(6) Å, c = 31.608(7) Å,α = β = γ =90.00°, V = 5333(3) Å3, Z = 4, Dcalc = 1.331 g cm-3, μcalc = 0.869 mm-1, F(000) = 2272, T = 293(2), R = 0.0870 for 2686 observed reflections [I 〉 2σ(I)]. The complexincludes two folded [Ni(rac- Me6[14]aneN4)]2+ units havingopposite diastereomeric configuration. They are bridged through a dianion of2,5-pyridinedicarboxylic acid, with one Ni-atom coordinated to the O-atom ofthe 2-carboxylic group and the pyridine N-atom (forming a 5-membered chelatering), and with the second Ni-atom coordinated to both O-atoms of the 5-carboxylic group (forming a 4-membered chelate ring). Hydrogen bonding involving macrocyclic NH groups, both 2- and 5-carboxylic groups, perchlorate anions and water molecules gives rise to the formation of an infinite supramolecular network in the title compound's crystals.
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  • 4
    ISSN: 1434-4475
    Keywords: Electron accepting ability of—CCl3 ; Schiff base
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Es wird über die Darstellung, Charakterisierung und Kristallstruktur derSchiff-Base berichtet, die aus 1,1,1-Trichloracetylaceton und Ethylendiamin erhalten wurde. Die Röntgenstrukturanalyse zeigte, daß es sich um 4,4′(1,1-Ethandiyldiimino)bis(1,1,1-trichlor-3-penten-2-on) handelt. Dies impliziert, daß die Elektronacceptorfähgkeit der CCl3-Gruppe eine größere Partialladung δ + im entfernteren Carbonyl induziert. Die Verbindung besitzt im Kristall zwei verschiedene Konformationen. Es wurde eine N-H----O-Wasserstoff-brückenbinding festgestellt.
    Notes: Abstract The preparation, characterization and crystal structure of theSchiff base obtained from 1,1,1-trichloroacetylacetone and ethylenediamine is reported. The structural determination shows that the compound is 4,4′(1,1-ethanediyldiimino)bis(1,1,1-trichloro-3-penten-2-one), it suggests that the electron accepting ability of the CCl3 group induces a larger δ + charge on the remote carbonyl. In the solid state it occurs in two different conformations and N-H ----O hydrogen bond is present.
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  • 5
    ISSN: 1434-4475
    Keywords: Arsenic, antimony complexes ; Dithiocarbamate complexes ; Dithiocarbamate X-Ray structure ; Monodentate group 15 dithio complex
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Es wurden eine Reihe von diheterocyclischen Dithiocarbamat-Komplexen des TypsRNCS2 MS2C2H4 mitR=Pyrrolidyl, 3-Pyrrolyl, 4-Morpholyl, 3-Methylpiperidyl undM=As oder Sb hergestellt und mittels IR,1H- und13C-NMR, MS und Elementaranalysen charakterisiert. Die Röntgenstrukturanalyse des 4-Morpholinocarbodithioats von 1,3-Dithia-2-arsa-cyclopentan zeigt ein monodentates Verhalten derRNCS2-Einheit.
    Notes: Summary A series of diheterocyclic dithiocarbamate complexes of the typeRNCS2 MS2C2H4, whereR=pyrrolidyl, 3-pyrrolyl, 4-morpholyl, 3-methlpiperidyl andM=As or Sb were obtained and characterized by IR,1H, and13C-NMR, mass spectroscopy and elemental analyses. The X-ray crystal structure determination of the 4-morpholinecarbodithioate of 1,3-dithia-2-arsa-cyclopentane shows a monodentate behaviour of theRNCS2 entity.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 25 (1995), S. 309-313 
    ISSN: 1572-8854
    Keywords: ent-kaurenoic acid ; trimer
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The crystal and molecular structure of the title compound has been determined by X-ray crystallographic analysis. The 12α-hydroxy-ent-kaur-16-en-19-oic acid previously isolated from other sources is found for the first time in a species of theMachaeranthera genus. The unit cell contains three closely similar independent molecules organized into trimers.
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  • 7
    ISSN: 1572-8854
    Keywords: 1,4,10,13-Tetraoxa-7,16-diazacyclooctadecane ; 2,5-pyridinedicarboxylic acid ; 2,2′-dithiosalicylic acid ; hydrogen bonding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract A 1:2:2 complex of 1,4,10,13-tetraoxa-7,16-diazacyclooctadecane with 2,5-pyridinedicarboxylic acid and water (1) and its 1:1:1.75 complex with 2,2′-dithiosalicylic acid and water (2) have been obtained and characterized by x-ray diffraction. C26H40N4O14 (1), triclinic, $$P\bar 1$$ , a = 9.574(1) Å, b = 9.632(1) Å, c = 9.723(1) Å, α = 112.70(1)°, β = 91.07(1)°, γ = 115.45(1)°, V = 728.35(13) Å3, Z = 1. C26H39.5N2O9.75S2 (2), M = 600.22, triclinic, $$P\bar 1$$ , a = 10.492(1) Å, b = 10.945(1) Å, c = 14.535(2) Å, α = 102.74(1)°, β = 109.08(1)°, γ = 90.68(1)°, V = 1532.2(3) Å3, Z = 2. In complex 1, both N-atoms of the macrocyclic ring are protonated. The following types of H-bonding have been found: (1) between protonated aza groups of the macrocycle and ionized carboxylic groups; (2) between the protonated aza groups and N-atoms of the pyridine nuclei (D–A distance slightly exceeds 3 Å); (3) between water molecules and C=O groups of the non-ionized carboxylic groups; and (4) between the nonionized and ionized groups of the carboxylic acid. The above interactions give rise to the formation of a developed supramolecular network in the crystals of 1. In complex 2, despite the presence of several types of hydrogen bonds involving the aza crown, 2,2′-dithiosalicylic acid and water, the aromatic anions are H-bound only to the two other components, and not to each other. The H-bonds found in complex 2 are between (1) one of the protonated aza groups and water, (2) protonated aza groups and O-atoms of the ionized carboxylic groups, (3) water molecule and carboxylic O-atom, (4) water molecule and sulfur atom, and (5) water molecule and O-atom of diaza-18-crown-6.
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  • 8
    ISSN: 1572-8854
    Keywords: 5,7-Dioxo-1,4,8,11-tetraazacyclotetradecane ; 2,6-dihydoxyanthraquinone ; hydrogen bonding ; supramolecular network
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract A complex of 5,7-dioxo-1,4,8,11-tetraazacyclotetradecane (dioxocyclam) and 2,6-dihydoxyanthraquinone (anthraflavic acid) has been obtained. The complex (crystals grown from water-ethanol solution) has a stoichiometry dioxocyclam-anthraflavic acid 1:1:5. C31H32N4O8, chemical formula weight 588.61, triclinic, P − 1, a = 10.542(3) Å, b = 11.936(2) Å, c = 12.206(2) Å, α = 104.00(1)°, β = 92.68(2)°, γ = 103.64(2)°, V = 1439.4 (5) Å3, Z = 2, Dx = 1.358 g cm−3. Only one of the two amine N-atoms of the macrocycle is protonated due to very weak acidic properties of 2,6-dihydoxyanthraquinone. Due to the rather poor quality of the crystals and structure refinement, reliable determination of H-bonds is complicated. Nevertheless, several types of H-bonding responsible for the formation of a developed supramolecular network can be suggested: between the protonated amino groups and macrocycle's C=O moieties; between non-protonated amino groups and macrocycle's C=O moieties; between protonated and non-protonated amino groups; between the amide NH and C=O groups of anthraflavic acid; and between protonated and deprotonated hydroxy groups of the acid. Two types of anthraflavic components can be distinguished in the lattice: those having a parallel orientation with respect to the macrocyclic fragments and forming hydrogen bonds with the latter, and those lying in an approximately perpendicular plane and not involved in H-bonding with the macrocycles.
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  • 9
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The title compound, Rb2H4M3, is C9H10O12Rb2, triclinic,P¯1,a=7.254(2),b=9.683(2),c=11.514(3) Å,α=107.05(2),/gb=103.81(2), γ=93.89 (2)°. The structure was solved by the heavy-atom method and refined by least-squares techniques to anR factor of 0.043 for 1649 observed reflections. Rb2H4M3 occurs as three independent molecules, two HM− and one H2M with different conformations. Rb2H4M3 has a type B2IR spectrum and has four short, intermolecular and unsymmetrical hydrogen bonds. Rb(1)+ and Rb(2)+ ions are coordinated to nine and ten carboxylate oxygen atoms, respectively. The coordination polyhedron for each Rb+ ion is a distorted tricapped trigonal prism.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 17 (1987), S. 207-219 
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The title compound, IBA-PIC, is 2C12H13NO2·2C6H3N3O7, triclinic,P¯1,a=7.137(1),b=15.355(4),c=18.282(5) Å,α=79.72(2),β=79.85(2), γ=76.87(2)°. The structure was solved by direct methods and refined by least-squares techniques to anR factor of 0.068 for 3395 observed reflections. The IBA-PIC complex occurs as two independent molecules with different conformations. The crystallographic evidence for a prominent overlapping between the phenyl and indole rings corroborates earlier conclusions from UV spectroscopy. Molecules of both IBA and picric acid lie approximately parallel to (100) in layers and π-bonding interactions across the 3.55 Å spacing. The angles between the indole ring and carboxyl-group planes are 82.9 and 86.9° for the A and B molecules, respectively.
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