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  • Wiley-Blackwell  (40)
  • 1980-1984  (40)
  • 1980  (40)
  • 1
    Electronic Resource
    Electronic Resource
    Evaluation of MINDO/3 calculated structures. II. Branching errors in alkanes and cycloalkanesFor Part I see ref. 1. (1980)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Computational Chemistry 1 (1980), S. 233-239 
    Details
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: MINDO/3 calculations have been carried out for a series of branched chain alkanes in order to assess effects of branching on calculated geometries and heats of formation (ΔHf). With vicinal branching, MINDO/3 calculates the central C—C bond to be too long. Bond angles are also found to be distorted. Errors in calculated heats of formation are large when geminal branching is present and significant with vicinal branching. Branching error corrections for ΔHf have been derived and applied to a separate series of branched acyclic and cyclic compounds. For the test sample, application of the branching error corrections gave calculated structures of acyclic branched hydrocarbons with heats of formation having an average absolute error of 1.3 kcal/mole rather than 17.3 kcal/mole before correction. Cyclic branched hydrocarbons are shown to be less well corrected. Calculations of heats of reaction have also been carried out for some isomerization and cyclization reactions using the MINDO/3 and MNDO methods. It is clear from the comparisons that MNDO calculations give less severe errors for highly branched compounds but the errors are still substantial. For prediction of heats of reaction, the error-corrected calculations are shown to be superior to the “raw” calculations obtained by MINDO/3 or MNDO.
    Additional Material: 7 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jcc.540010304
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  • 2
    Electronic Resource
    Electronic Resource
    Crystal and molecular structure of isoleucinomycin, cyclo[-(D-Ile-Lac-Ile-D-Hyi)3-](C60H102N6O18) (1980)
    New York : Wiley-Blackwell
    Biopolymers 19 (1980), S. 1517-1534 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The crystal structure of a synthetic analog of valinomycin, cyclo[-(D-Ile-Lac-Ile-D-Hyi)3-] (C60H102N6O18), has been determined by x-ray diffraction procedures. The crystals are orthorhombic, space group P212121, with cell parameters a = 11.516, b = 15.705, c = 39.310 Å, and Z = 4. The atomic coordinates for the C, N, O atoms were refined in the anisotropic thermal motion approximation and for the H atoms in the isotropic approximation. Values of standard (R) and weighted (Rw) reliability factors after refinement are 0.073 and 0.056, respectively. The structure is completely asymmetric. The cyclic molecular backbone is stabilized by six intramolecular hydrogen bonds N—H…O=C, five bonds being of the 4→1 type and one being of the 5→1 type. The side chains are located on the molecular periphery. The conformational state of isoleucinomycin in the crystal is intermediate between the corresponding crystalline states of valinomycin and meso-valinomycin. The observed conformation suggests that complexation could proceed via entry of the ion at the face possessing the L-Lac residues, the less crowded face.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.1980.360190808
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  • 3
    Electronic Resource
    Electronic Resource
    Micellar Solubilization of Biopolymers in Hydrocarbon Solvents III. Empirical Definition of an Acidity Scale in Reverse Micelles (1980)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 63 (1980), S. 2302-2311 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This paper deals with the problem of defining, and measuring, the pH inside the water pool (which we define as pHwp) of reverse micelles, i.e. micelles formed by surfactants dissolved in apolar solvents in the presence of minimal amounts of water. The conceptual and experimental difficulties are discussed, and it is argued that no absolute determination of pHwp is possible, mostly because water in the water pools of reverse micelles is a new solvent, for which no standardization of acidity is available. The problem can be approached only on the basis of an empirical acidity scale.An empirical acidity scale for water pools in reverse micelles of bis (2-ethyl-hexyl) sodium sulfosuccinate (AOT) in isooctane has been defined by measuring the 31P-chemical shifts of phosphate buffers. The chemical shifts in bulk water were compared to those found in reverse micelles under the assumption that the pK of phosphate ion is the same in the two systems. It was found that in most cases there was little difference (less than 0.4 pH units) between pHwp and the pH of the starting buffer in bulk water (which we define as pHst). However, this difference between pHwp and pHst may become much larger in certain cases.The difference (pHwp-pHst) is measured under a variety of conditions, and this permits the determination of an operational acidity in the micelle water pools as a function of the pHst with which the aqueous micelles are prepared. The significance of such data for interpreting the behaviour of enzymes confined in the micelles water pool is discussed. Based on the pHwp scale, the apparent pKa of phenol-red and 4-nitrophenol were determined in reverse micelles containing different buffers and different water content. The pKa values obtained were rather sensitive to changes of both these factors, which was taken to signify that organic dies have only a very limited applicability to measure the acidity of the water pools of reverse micelles.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19800630820
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  • 4
    Electronic Resource
    Electronic Resource
    Binding energies of ionized donor-exciton complexes in polar crystals (1980)
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 18 (1980), S. 583-586 
    Details
    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: Binding energies of ionized donor-exciton complexes in crystals of CdSe, CdTe, and ZnSe are calculated using the most realistic effective potentials available for the electron-hole interaction.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/qua.560180230
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  • 5
    Electronic Resource
    Electronic Resource
    The evaluation of the error term in some numerical quadrature formulae: An addendum (1980)
    Chichester [u.a.] : Wiley-Blackwell
    International Journal for Numerical Methods in Engineering 15 (1980), S. 157-160 
    Details
    ISSN: 0029-5981
    Keywords: Engineering ; Engineering General
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mathematics , Technology
    Notes: In a previous paper the author deduced a method of evaluating the error term arising in some quadrature formulae. This method depended on the analytic evaluation of a Hilbert transform. The result is now extended to all quadrature formulae used for the calculation of integrals over finite intervals by approximating the Hilbert transform.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/nme.1620150113
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  • 6
    Electronic Resource
    Electronic Resource
    Modeling of rotating biological contactor systems (1980)
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 22 (1980), S. 2055-2064 
    Details
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: An investigation of the rotating biological contractor (RBC) process variables to determine the efficiency of biological oxygen demand (BOD) removal is presented. Operating parameters including influent BOD content (〈355 mg/liter), flow rate, disk surface area, hydraulic loading, disk rotational speed, liquid retention time, stage number, and wastewater temperature were evaluated. The BOD predictive model was developed using literature data with multiple regression analysis. This study shows that influent BOD concentration, hydraulic loading, stage number, and wastewater temperature are the most significant variables in predicting the RBC system performance. The model presently developed was verified by field data concerned with the treatment of both domestic and low-strength industrial wastewaters. Also, the results calculated by this model were compared to those obtained from Weng's model.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bit.260221006
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  • 7
    Electronic Resource
    Electronic Resource
    Comparison of dynamically coated SE-54, SP-2250 and carbowax 20M wall-coated open tubular (WCOT) glass capillary columns, prepared after surface pretreatment with Superox™-4 or with BaCO3 (1980)
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 3 (1980), S. 115-123 
    Details
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Preparation of deactivated capillaries for routine analysis ; Easy deactivation and pretreatment steps described in detail ; Comparison of different modes given ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new surface pretreatment for the preparation of wall-coated open tubular (WCOT) glass capillary columns has been evaluated. This technique involves the application of a non-extractable layer of Superox™-4, a 4,000,000 MW polyethylene glycol, to the glass surface as a pretreatment and deactivation agent. Unlike other polyethylene glycols, Superox-4 is stable at high temperatures (〉 300°C) in the absence of oxygen, coats smoothly onto a bare glass surface and resists droplet formation. WCOT columns (SE-54, Carbowax 20M, and SP-2250) prepared using this technique are compared to columns prepared using a modified Grob [2,3] BaCO3 procedure. The Superox-4 pretreated columns were equal or superior in quality to the BaCO3 pretreated columns, based on the appearance of an activity standard and the effective theoretical plates (Neff) per meter. Chromatograms showing practical application of the WCOT columns prepared using both methods is given.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jhrc.1240030303
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  • 8
    Electronic Resource
    Electronic Resource
    Fabrication of gas-chromatographic glass capillary columns of high efficiency with liquid crystal stationary phases (1980)
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 3 (1980), S. 355-356 
    Details
    ISSN: 0935-6304
    Keywords: Gas-liquid chromatography (GLC) ; Open tubular glass capillary columns ; Blended stationary phases ; Liquid crystals ; Polycyclic aromatic hydrocarbons (PAH) ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jhrc.1240030710
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  • 9
    Electronic Resource
    Electronic Resource
    Gas-chromatographic separation of underivatized steroids using a BPhBT liquid crystal stationary phase (1980)
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 3 (1980), S. 333-336 
    Details
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Liquid crystal ; N,Ń, Bis (p-phenylbenzylidene)-α, α′-bi-p-toluidine (BPhBT) ; Steroids ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A gas-chromatographic separation of underivatized steroids is described, in which the liquid crystal N,Ń-bis(p-phenylbenzylidene)α,α′-bi-p-toluidine (BPhBT) was used isothermally at 265°C for the stationary phase. The nematic range of this crystal is 247 to 403°C. Use of the BPhBT crystal allowed operations in a temperature range where steroids are volatile and unlikely to display broad elution peaks and long retention times.With columns precoated with 2.5 weight percent of BPhBT, steroids containing minor structural differences in the ring system were readily differentiated. For example, 5-androsten-17α-ethinyl-3β, 17β-diol was found to elute more rapidly than its 3-keto analog, ethisterone. Ethisterone was distinguished readily also from its 19-nor analog, norethisterone. Additionally, differences in side-chain functionality and resultant molecular dimensions facilitated the separation of steroids of identical ring structure, as in the comparison of cholesterol with methyl 3β-hydroxy-5-cholenate and 25-hydroxycholesterol.An enhancement of separation according to the molecular length-to-breadth ratio was observed; in general, the larger this length-to-breadth ratio, the greater the retention period on the column.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jhrc.1240030705
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  • 10
    Electronic Resource
    Electronic Resource
    A quaternary solvent system for the reverse-phase liquid-chromatographic separation of polycyclic aromatics (1980)
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 3 (1980), S. 634-640 
    Details
    ISSN: 0935-6304
    Keywords: HPLC ; Reverse-phase ; UV detection ; Fluorescence detection ; Polycyclic aromatic hydrocarbons ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Modern liquid chromatographic (LC) conditions which effect a separation of polycyclic aromatic hydrocarbons (PAH) containing up to ten rings are described. The LC conditions include reverse-phase chromatographic columns in combination with a quaternary solvent system. Methanol and water are combined to form solvent system A, while tetrahydrofuran and acetonitrile form solvent system B. Solvent systems A and B are then combined in a linear gradient relationship to effect the separation. The separation of benzo(a)pyrene and perylene along with benzo(ghi)perylene and indeno (1,2,3-cd)pyrene is achieved. In the same chromatogram the PAHs, coronene, dibenzo(a,e), (a,i), (a,h)pyrene and tribenzo(a,e,i)pyrene are also separated. An increase in column temperature from 45°C to 55°C is shown to shorten the elution time and increase chromatographic resolution of many of the PAHs examined. At least 25 PAHs ranging in molecular weight from 178 to 536 are examined for their chromatographic behavior. As examples, the application of this method to samples from a coal liquefication process are included. The samples are examined with both a UV detector and fluouescence detector to demonstrate the utility of dual detectors when analyzing for PAHs in complex matrices. With minor modification of the gradient this method is applicable to PAHs containing ring systems other than those reported here.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jhrc.1240031206
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