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  • Inorganic Chemistry  (31)
  • Organic Chemistry  (3)
  • Absolute Configuration  (1)
  • CHEMISTRY AND MATERIALS (GENERAL)
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  • 1
    ISSN: 0040-4020
    Keywords: Absolute Configuration ; Crystal Structure Analysis ; Epoxidation ; Photochemistry
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 328 (1986), S. 156-162 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On the Interpretation of Relative Binding Constants of Complexes with Lanthanide N.M.R. Shift ReagentsThe determination of relative complex binding constants of lanthanide n.m.r. shift reagents (LSR) with organic molecules are based on the assumption that in all cases 1:1 complexes exist. A new interpretation of relative binding constants is given which is applicable also to 1:2 complexes. The new defined constant K* describes the relative tendency of the substrate under consideration to form LSR complexes.Using this method it is shown that Eu(fod)3 and Pr(fod)3 form other complexes than that of the 1 : 1 type.The K* of benzaldehyde-LSR complexes correlate linearly with the Hammett substituent parameters.The occurrence of other than 1:1 associates in the complex formation of para-substituted benzaldehydes with Eu(fod)3 and Pr(fod)3, respectively, could be shown; so we used the new model for these systems. The lg K* of the benzaldehydes in its reaction with the mentioned LSR, as well as with Eu(dpm)3, correlate linearly to the Hammett parameter of the para-substituents.
    Additional Material: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 175 (1928), S. 383-401 
    ISSN: 0863-1786
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 337 (1995), S. 299-306 
    ISSN: 0941-1216
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Peralkylthio-substituted Dibenzotetrathiafulvalenes (DBTTF) from BenzenehexathiolateElectrophilic and nucleophilic methylation of peralkylbenzo-1,3-dithiol-2-thiones are reported. The stable tetrakis(methylthio)-benzo-1,3-dithiolium triiodide 8a is characterized by X-ray structure analysis.The syntheses of novel 2,2′-bi-1,3,5,7-tetrathia-s-indacenylidenes 13, 16 and mixed substituted peralkylthio-dibenzotetrathiafulvalenes 15 are described.From selected representatives of 13, 15, 16 the ct-complex formation, the oxidation potentials and the uv-vis absorption range of the radical cations are reported and discussed with respect to the structures of the molecules. The electrical conductivities of the TCNQF4 complexes of 15 lie in the range of semiconductors (7·10-2-8·10-4 Scm-1).
    Additional Material: 2 Tab.
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  • 5
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The VIS-laser irradiation of enol lactones 1a, b and benzoquinone in an argon atmosphere led to the fenestrane-type oxetane 2a and the propellane-type oxetane 2b, with regioselective preference for the acetal structure. Under an oxygen atmosphere both regioisomeric fenestrane-type 1,2,4-trioxanes 4a and 5a were obtained from enol lactone 1a, while no oxygen trapping to the propellane-type trioxanes was observed with 1b. Significant quantities of photooxygenation products were obtained from both enol lactones 1a, b due to singlet oxygen derived from oxygen quenching of benzoquinone triplets. The present study demonstrates that Qinghaosu analoga are accessible via trapping of Paterno-Büchi triplet 1,4-diradicals by molecular oxygen.
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  • 6
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Structure and Properties of Homo- and Mixed-Ligand Bis-Complexes of Dimethyltetrathio-oxalate: [Ni(S2C2(SMe)2)2] and [Pd(S2C2(SMe)2) (PPh3)2][Ni(S2C2(SMe)2)2] was prepared photochemically under inert conditions from Ni(CO)4 and dimethyltetrathio-oxalate (ttoMe2) whereas [Pd(S2C2(SMe)2)(PPh3)2] was obtained thermally from Pd(PPh3)4 and ttoMe2 (beneath little [Pd(S2C2(SMe)2)2] as byproduct). In both neutral chelates the ligands are coordinated square planar round the metal atoms (space group for Ni complex C2/m, for Pd complex P1). From its electronic spectra, the IR, and cyclovoltammetric data the homo-ligand Ni complex can be interpreted as a dithiolene chelate. The mixed-ligand Pd complex shows interligand charge-transfer transitions. The Ni complex is an oxidant.
    Notes: Die Synthese von [Ni(S2C2(SMe)2)2] gelang photochemisch unter Inertbedingungen aus Ni(CO)4 und Dimethyltetrathiooxalat (ttoMe2) und von [Pd(S2C2(SMe)2)(PPh3)2] thermisch aus Pd(PPh3)4 und ttoMe2 (daneben fällt wenig [Pd(S2C2(SMe)2)2] an). In beiden Neutralchelaten sind die Liganden quadratisch-planar um Ni (Raumgruppe C2/m) bzw. Pd (Raumgruppe P1) koordiniert. Elektronenspektrum, IR-Daten und Cyclovoltammogramm lassen den reinligandigen Ni-Komplex als Dithiolenchelat interpretieren. Im gemischtligandigen Pd-Komplex treten Interligand-charge-transfer-Übergänge auf. Der Ni-Komplex wirkt oxydierend.
    Additional Material: 5 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 562 (1988), S. 17-22 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Structure of 1,3-Dimethyl-1,1,3,3-tetraphenyldisiloxane1,3-Dimethyl-1,1,3,3-tetraphenyldisiloxane 1 crystallizes monoclinically (P21/n; a = 2237.5; b = 801.4; c = 1396.6 pm, β = 106.29°; Z = 4). The X-ray structural analysis shows a bent configuration of the molecule with Si—O—Si angle = 140°, d(Si—O) = 163.8 pm. The staggered conformation of the six Si—C bonds is distorted. The methyl groups are in gauche position.The results are discussed with respect to an intramolecular H…O interaction in the structure of 1,1,3,3-tetraphenyldisiloxane.
    Notes: 1,3-Dimethyl-1,1,3,3-tetraphenyldisiloxan 1 kristallisiert monoklin (P21/n; a = 2237,5; b = 801,4; c = 1396,6 pm; β = 106,29°; Z = 4). Die Kristallstrukturanalyse ergab eine gewinkelte Konfiguration des Moleküls mit Si—O—Si = 140° und d(Si—O) = 163,8 pm. Die Substituenten an dem Silicium-Atom zeigen eine Abweichung von einer gestaffelten Anordnung der sechs Si—C-Bindungen. Die Methylgruppen sind in gauche-Position.Die Ergebnisse werden im Zusammenhang mit der Struktur des 1,1,3,3-Tetraphenyldisiloxans hinsichtlich einer intramolekularen H…O-Wechselwirkung diskutiert.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 621 (1995), S. 557-561 
    ISSN: 0044-2313
    Keywords: TlEu[PS4] ; Tetrathiophosphate(V) ; Crystal Structure ; Vibrational Spectrum ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Kristallstruktur und Schwingungsspektrum von Thallium(I)-Europium(II)-tetrathiophosphat(V), TlEu[PS4]TlEu[PS4] wurde aus den Elementen bei 1 150 K in einer evakuierten Quarzampulle dargestellt. Die Verbindung bildet transparente, orangefarbene, luft- und feuchtigkeitsbeständige Nadeln, die orthorhombisch, Pnma (Nr. 62) mit a = 12,157(2), b = 6,581(1), c = 8,802(2) Å, Z = 4 kristallisieren. Charakteristisch sind diskrete [PS4]3--Anionen, die durch Tl+ und Eu2+ verbunden sind. Sie sind verzerrt tetraedrisch mit P—S-Abständen zwischen 2,028 und 2,043 Å und so angeordnet, daß Liganden benachbarter Gruppen trigonale S6-Prismen bilden, entlang [0 0 1] zu Säulen verknüpft, die parallel (1 0 0) über gemeinsame Kanten zu gewellten Schichten kondensiert sind. Dazwischen sind leere, verzerrte Halbwürfel und zur Hälfte mit P-Atomen besetzte Tetraederlücken Durch die alternierende Besetzung mit Tl+ und Eu2+ sind diese Prismen leicht verzerrt. Man kann daher diese Struktur als eine geordnete, teilweise aufgefüllte Überstruktur des InNi2-Typs auffassen (InInNi4□2tet ≙ TlEuS4P□1tet), aber auch als zentrosymmetrische Variante der TlSn[PS4]-Struktur (Raumgruppe Pna21). Das Schwingungsspektrum entspricht der Strukturbestimmung, die beobachteten Raman- und Infrarotbanden lassen sich zwanglos auf der Basis von [PS4]3- -Einheiten mit C2v-Symmetrie zuordnen.
    Notes: TlEu[PS4] was synthesized from the elements in a sealed quartz ampoule at 1 150 K. The compound forms transparent orange needles, stable in air and moisture. It crystallizes in the orthorhombic system, space group Pnma (No. 62), with cell dimensions a = 12.157(2), b = 6.581(1), c = 8.802(2) Å, Z = 4. The crystal structure consists of discrete [PS4]3- anions interconnected by Tl+ and Eu2+. The tetrahedral [PS4]3- groups are slightly distorted with P—S bond lengths in the range 2.028 to 2.043 Å. These tetrahedral anions are arranged in such a way that the sulfur atoms form columns of distorted trigonal S6 prisms along [0 0 1]. The columns are condensed via common edges to puckered layers parallel to (1 0 0). The interlayer region consists of empty distorted half-cubes and tetrahedral holes, half of them filled by P atoms. The trigonal prisms in the columns are centered alternately by Tl+ and Eu2+. In this way, the structure can be regarded as an ordered superstructure of the InNi2 type, where half of the tetrahedral holes are filled by phosphorus atoms: InInNi4□2tet ≙ TlEuS4P□1tet. TlEu[PS4] is a centrosymmetric variant of the TlSn[PS4] structure type (space group Pna21). The vibrational spectrum is in accordance with the X-ray crystal structure, the Raman and infrared vibrations are assigned on the basis of [PS4]3- units with C2v symmetry.
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  • 9
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Formation and Structure of tert-Butyl(tert-butylamino) [tris(tert-butyloxy)silylthio]-boraneThe smooth addition of the SH bond of (tBuO)3SiSH to the BN bond of tBuB≡NtBu gives the title compound, which crystallizes in the triclinic system, space group P1, with an unexpectedly short BN bond, d(BN) = 137 pm, in a Z configuration.
    Notes: Die SH-Bindung von (tBuO)3SiSH addiert sich glatt an die BN-Bindung von tBuB≡NtBu unter Bildung der Titelverbindung. Diese kristallisiert triklin, Raumgruppe P1, mit einer unerwartet kurzen, Z-konfigurierten BN-Bindung, d(BN) = 137 pm.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 377-384 
    ISSN: 0044-2313
    Keywords: One-pot reactions of tri-t-butoxychlorosilane, K-t-butanolate and substituted anilines. Crystal structure analyses of N-(tri-t-butoxysilyl)-aniline, C18H33NO3Si ; N-(tri-t-butoxysilyl)-p-nitroaniline, C18H32N2O5Si ; N-Methyl-(N-tri-t-butoxysilyl)-p-nitroaniline C19H34N2O5Si ; N-(tri-t-butoxysilyl)-p-cyanoaniline, C19H32N2O3Si ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Formation and Structures of N-(tri-t-butoxysilyl)aniline CompoundsPara-substituted N-(tri-t-butoxysilyl)anilines (t-BuO)3SiNRC4H4X-p, R = H, CH3, with substituents of high electron affinity (X = CN, NO2) were prepared by a one-pot reaction of tri-t-butoxychlorsilane, potassium t-butanolate and substituted anilines. Corresponding compounds with substituents of low electron affinity (X = OMe, H) preferably were prepared by metalation of anilines with sodium amide. Four crystal structures were determined. N-(tri-t-butoxysilyl)-p-nitro-aniline, N-methyl-(N-tri-t-butoxysilyl)-p-nitroaniline and N-(tri-t-butoxysilyl)-p-cyanoaniline crystallize at 298 K monoclinically, N-(tri-t-butoxysilyl)aniline crystallizes orthorhombically.
    Notes: Derivate des para-substituierten N-(Tri-t-butoxysilyl)anilins (t-BuO)3SiNRC6H4X-p, R = H, CH3 mit Substituenten hoher Elektronenaffinität (X = CN, NO2) wurden nach einem neuen Eintopfverfahren aus Tri-t-butoxychlorsilan, Kalium-t-butanolat und dem entsprechend substituierten Anilin dargestellt. Für Substituenten niederer Elektronenaffinität (X = OMe, H) wird die Methode der Metallierung von Anilinen mit Natriumamid bevorzugt. Vier Kristallstrukturen wurden bestimmt. N-(Tri-t-butoxysilyl)-p-nitroanilin, N-Methyl-(N-tri-t-butoxysilyl)-p-nitroanilin und N-(Tri-t-butoxysilyl)-p-cyanoanilin kristallisieren bei 298 K monoklin, N-(Tri-t-butoxysilyl)anilin kristallisiert orthorhombisch.
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