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  • Atomic, Molecular and Optical Physics  (11)
  • Inorganic Chemistry  (9)
  • Analytical Chemistry and Spectroscopy  (8)
  • 42.75
  • General Chemistry
  • Surface physics, nanoscale physics, low-dimensional systems
  • 1980-1984  (28)
Collection
Keywords
Publisher
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 17 (1980), S. 651-671 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ab initio MO calculations, using both minimal (STO-3G) and extended (Roos-Siegbahn) basis sets are reported for the systems methanethiol-imidazole, methanethiol-imidazole-formaldehyde, and methanethiol-imidazole-formamide, which, together with a point-change representation of a long α-helix, form models for the active site of papain. It is shown that the large electric field exerted by the helix in the active-site region is responsible for the presence of the essential residues Cys 25 and His 159 in the form of an ion pair RS- ··· ImH+, which is crucial for a recently proposed mechanism for the catalytic action of the enzyme. Also, an explanation is given for the anomalies in measured pK values for these residues. Detailed studies on the (sub)systems show that minimal basis sets lack the flexibility necessary for describing the type of proton transfer involved. We conclude that α-helices are essential parts of enzymes and that they play a significant role in the catalytic process.
    Additional Material: 8 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 3 (1980), S. 298-298 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Closing technique for static coating ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 5 (1982), S. 19-26 
    ISSN: 0935-6304
    Keywords: Gas chromatography, glass capillary ; Selective detection ; Nitrated polycyclic aromatic hydrocarbons ; Carbon black ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Glass capillary gas chromatography has been investigated as a method for the analysis of nitrated polycyclic aromatic hydrocarbons (nitro-PAH) using both splitless and on-column injection techniques. The nitro-PAH showed good chromatographic performance and thermal stability under the GC conditions used. Retention times and response factors of several nitro-PAH were compared to those of conventional PAH.Simultaneous flame ionization and thermionic nitrogen selective detection was used to facilitate identification of nitro-PAH in complex samples. The feasibility of the method is demonstrated on two samples of commercial carbon black. Besides 1-nitropyrene several isomeric dinitropyrenes have been identified.
    Additional Material: 7 Ill.
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  • 4
    ISSN: 0935-6304
    Keywords: Thin-layer chromatography, TLC ; Reversed phase TLC ; Chemically bonded stationary phases ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An overview is given of the literature publisned in the field of thin-layer chromatography on chemically bonded phases. Aspects which merit further attention are: quantitative analysis, organic solvent selection, stationary phase characteristics, surface modification of precoated silica plates, ion-pair chromatography and correlation of thin-layer and column chromatographic data.
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  • 5
    ISSN: 0935-6304
    Keywords: Thin-layer chromatography, (HP)TLC ; Pre-chromatographic derivatization ; Quantitation of estriol, cortisol, selenium ; Biological matrix ; Water analysis ; Ready-for-use column extraction ; Fluorescence enhancement ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 9 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 7 (1980), S. 109-114 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electron impact mass spectra of various methoxyhalobiphenyls have been reinvestigated. Previous findings, concerning the effect of the methoxy group upon the main fragmentation routes, have been confirmed and extended. In addition, studies of unimolecular and collision induced fragmentations of ions, using linked scan techniques, have been made. Such an approach permits the identification of substances with a minimal chromatographic separation prior to mass spectrometry. It has also led to some clarification of the fragmentation pathways leading to the observed cracking patterns.
    Additional Material: 2 Ill.
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  • 7
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Phosphorus. 115. Synthesis and Properties of the Tetraphospha-silaspiro[2.2] pentane (PBut)2Si(PBut)2The first spirocyclic phosphorus-silicon three-membered ring compound, 1,2,4,5-tetra-tert-butyl-1,2,4,5-tetraphospha-3-silaspiro[2.2]pentane, (PBut)2Si(PBut)2 (1), has been synthesized by cyclocondensation of K(But)P—P(But)K with silicon tetrachloride in the molar ratio of 2:0.9. It was characterized by elemental analysis, cryoscopic molecular weight determination and its mass, magnetic resonance and vibrational spectra. 1 is formed as a mixture of two diastereomers 1a and 1b. These differ in the relative arrangement of the trans-oriented organyl substituents at the two three-membered rings; both isomers could be obtained in a pure state. The sterically less favoured isomer 1b rearranges into the comparatively more stable isomer 1a.
    Notes: Die erste spirocyclische Phosphor-Silicium-Dreiringverbindung, das 1,2,4,5-Tetra-tert-butyl-1,2,4,5-tetraphospha-3-silaspiro[2.2]pentan, (PBut)2Si(PBut)2 (1), wurde durch Cyclokondensation von K(But)P—P(But)K mit Siliciumtetrachlorid im Molverhältnis 2:0,9 synthetisiert. Die Charakterisierung erfolgte durch Elementaranalyse, kryoskopische Molmasse-Bestimmung, Massen-, Kernresonanz- und Molekülschwingungsspektren. 1 entsteht als Gemisch von zwei Diastereomeren 1a und 1b, die sich in der Anordnung der jeweils trans-ständigen Organylgruppen beider Dreiringe zueinander unterscheiden; beide Isomere konnten rein erhalten werden. Das sterisch ungünstigere Isomer 1 b lagert sich in das vergleichsweise beständigere Isomer 1 a um.
    Additional Material: 1 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 498 (1983), S. 153-160 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions on the Thermal Behaviour of Sulfates. VI. On the Chemical Transport of CuSO4, Cu2OSO4, and CuOA powder of anhydrous CuSO4 can be prepared by heating CuSO4 · 5 H2O in air or in an argon atmosphere. In the same way it is possible to get a powder of Cu2OSO4. But up to now, it was difficult to get crystals of CuSO4 and there was no method known to synthesize crystals of Cu2OSO4. Investigations concerning chemical transport reactions of anhydrous heavy metal sulfates showed, that it is possible to get well formed crystals of CuSO4 and Cu2OSO4 by deposition from a vapour phase. As transport agents for CuSO4, Cl2 and HgCl2 are especially suitable. Less appropriate are HCl, NH4Cl, and I2.The chemical vapor deposition of Cu2OSO4 proceeds well with HgCl2. In course of these investigations we recognized, that for CuO in addition to the well approved transport agents also Cl2, HgCl2 or I2 (NH4Cl less suitable) can successfully be used.
    Notes: Wasserfreies CuSO4 ist in Pulverform durch thermischen Abbau der Hydrate leicht zugänglich, pulverförmiges Cu2OSO4 läßt sich dementsprechend aus CuSO4 darstellen. Kristalle waren dagegen bisher von CuSO4 nur sehr schwierig und von Cu2OSO4 noch nicht synthetisch zu gewinnen. Wie sich im Rahmen einer Untersuchung zum chemischen Transport wasserfreier Schwermetallsulfate zeigte, sind gut ausgebildete Kristalle von CuSO4 und Cu2OSO4 durch Abscheidung aus der Gasphase zugänglich. Als Transportmittel für CuSO4 sind besonders Cl2 und HgCl2 geeignet, weniger brauchbar sind HCl, NH4Cl oder I2. Das Oxidsulfat ist mit HgCl2 und NH4Cl, weniger gut mit I2 zu transportieren. Dabei fanden wir, daß für CuO außer den dafür bereits erprobten Transportmitteln auch Cl2, HgCl2 und I2 (NH4Cl weniger gut) verwendbar sind.
    Additional Material: 2 Ill.
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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: Structural Chemistry of Phosphorus Containing Chains and Rings. 11. Crystal and Molecular Structures of the Two Stereoisomers of Tetraphospha-silaspiro[2.2]pentane (PBut)2Si(PBut)2The spirocyclic compound 1,2,4,5-tetra-tert-butyl-1,2,4,5-tetraphospha-3-silaspiro[2.2]pentane exists in tow diastereomers of point symmetry 4 and 2. The isomer with symmetry 4 even in the solid crystallizes tetragonally in I41/a with a = 1247.0, c = 1505.5 pm and Z = 4. The isomer of fairly exact symmetry 2 crystallizes triclinically in P1 with a = 612.8, b = 996.3, c = 1017.2 pm, α = 75.63, β = 72.38, γ = 88.71° and Z = 1. In this disordered structure the surroundings of Si is slightly distorted due to the influence of the substituents. The (average) bond lengths are (4, 2): d(Si—P) = 220.09(9), 221.5(5); d(P—P) = 225.5(2), 224.2(5); d(P—C) = 189.4(3), 190(2); d(C—C) = 151.4(4), 152(3) pm. The geometry of the substituents in both isomers is quite normal.
    Notes: Die Spiroverbindung 1,2,4,5-Tetra-tert-butyl-1,2,4,5-tetraphospha-3-silaspiro[2.2]pentan liegt in zwei Diastereomeren der Punktsymmetrie 4 und 2 vor. Das Isomer der auch im Festkörper exakten Symmetrie 4 kristallisiert tetragonal in der Raumgruppe I41/a mit a = 1247,0, c = 1505,5 pm und Z = 4. Das sterisch weniger günstige Isomer der im Festkörper nicht streng erfüllten Symmetrie 2 kristallisiert triklin in der Raumgruppe P1 mit a = 612,8, b = 996,3, c = 1017,2 pm, α = 75.63, β = 72,38, γ = 88,71° und Z = 1. In dieser nur fehlgeordnet beschreibbaren Struktur wird die Umgebung des Si durch Substituenteneinflüsse etwas verzerrt. Die (mittleren) Bindungslängen betragen (4, 2): d(Si—P) = 220,09(9), 221,5(5); d(P—P) = 225,5(2), 224,2(5); d(P—C) = 189,4(3), 190(2); d(C—C) = 151,4(4), 152(3) pm. Die Geometrie der Substituenten ist in beiden Isomeren normal.
    Additional Material: 3 Ill.
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  • 10
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ni(PF3)4 (1) tauscht mit Lithiumorganylen und Grignard-Reagentien Fluor gegen Organyl-Gruppen aus, wobei die Komplexe (10-32) Ni(PF3)4-n(PF2R)n (n = 1, 2 und 3), Ni(PF3)3(PFR2), Ni(PF3)2(PF2R)(PFR2) und Ni(PF3)3(PR3) (R = organ. Rest) gebildet werden. Für den Reaktionsablauf wird ein Vierzentren-Synchron-Mechanismus vorgeschlagen.Fluorine Exchange in Trifluorophosphane Metal Complexes. X. Reactions of Tetrakis(trifluorophosphane)nickel(0) with Metal OrganylsThe fluorine atoms in Ni(PF3)4 (1) can be partially substituted by organyl groups yielding the complexes (10-32) Ni(PF3)4-n(PF2R)n (n = 1, 2 and 3), Ni(PF3)3(PFR2), Ni(PF3)2(PF2R)(PFR2) and Ni(PF3)3(PR3) (R = organyl group). The mechanism of these peripheric reactions is discussed by assuming a four centered type intermediate.
    Additional Material: 5 Tab.
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