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  • Electronic Resource  (8)
  • 1985-1989  (5)
  • 1970-1974  (3)
  • Analytical Chemistry and Spectroscopy  (8)
  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 14 (1987), S. 131-140 
    ISSN: 0887-6134
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mixtures of both synthetic and naturally occurring (human plasma) cholesteryl esters have been examined by capillary gas chromatography/mass spectrometry (GC/MS). A magnetic sector mass spectrometer was used and a variety of ionization modes were assessed with a view to obtaining structural information on intact cholesteryl esters. By employing ammonia as reagent gas, with negative ion scanning, spectra were produced from which the nature of steryl and fatty acyl moieties could be readily deduced. Analyses were performed at an ion source temperature of 300°C in order to maintain the integrity of the gas chromatographic profile. The technique described is of general use for the GC/MS analysis of steryl esters, particularly in conjunction with magnetic sector instruments.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 1 (1974), S. 269-273 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An azurin, a small respiratory copper protein from the bacterium Pseudomonas fluorescens biotype G, has been studied by mass spectrometry to determine sequence information. The study of homologously related proteins by mass spectiometry is particularly attractive, since the correct nature of major parts of the deduced sequences can be confirmed by comparison with the sequences of the protein from related organisms. An oxidized tryptohan residue has been identified amongst the products from a cyanogen bromide digest of this wild type azurin. In the same digest, a product is also found to arise from cleavage of the peptide chain at the C-terminal side of the same tryptophan residue. These results are rationalized.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Metastable ions arising from pseudomolecular [M — H]- ions produced by fast-atom bombardment negative-ion mass spectrometry of a range of free ecdysteroids, ecdysteroid conjugates and polar metabolites were investigated by means of linked scanning at constant B/E. Free ecdysteroids displayed daughter-ion spectra which allow 20-hydroxyecdysteroids and ecdysteroids lacking C-20 hydroxylation to be readily distinguished. The ejection of acetic acid from acetylated ecdysteroids was also readily detectable. Characteristic metastable-ion decomposition of ecdysteroid acids was not observed, presumably as a result of charge localization. High-mass daughter ions were also lacking in the case of phosphate conjugates.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Acetylacetone (Hacac) admitted as a gas to an ion source containing CoCl2 adsorbed on a field ionization/field desorption emitter produces the ion [Co(acac)Cl]+. Similar ions arising from interaction of adsorbed salt and a ligand admitted as a gas were found for CoCl2 and trifluoroacetyl acetone, and for FeCl2 and acetylacetone. The chelation process represents a new kind of reaction of chemisorbed species in field ionization mass spectrometry.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 20 (1985), S. 445-453 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The hydrogen chemical ionization (H2 CI) mass spectra of a range of metal(II) (Ni, Cu, Co, Pt), metal (III) (Al, Mn, Ga, Fe (bearing a single axial ligand)) and metal(IV) (Si, Ge, Sn (bearing two axial ligands) and V (as V=O2+)) porphyrins have been determined, The spectra are highly dependent on the coordinated metal, rather than the axial ligand(s) (where present). Ni(II), Cu(II), Mn(II or III), Ga(III), Ge(IV), Fe(III) and Sn(IV) porphyrins fragment via hydrogenation and demetallation, followed by cleavage of the resulting porphyrinogens at the meso(bridge) positions to give mono- and di-pyrrolic fragments. Tripyrrolic fragments are also observed in the case of Ni(II), Cu(II) and Sn(IV). Fragmentations of this type are similar to those observed for free-base porphyrins. In the case of Pt(II), Co(II), Al(III), Si(IV) and V(IV) (as vanadyl), the dipyrrolic fragment ions are either very weak or completely absent; hence their H2CI spectra contain limited structural information. This variable CI behaviour may be related to the relative stabilities of the metalloporphyrins together with the multiple stable valency states exhibited by several metals.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 3 (1970), S. 387-393 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A probability distribution of internal energies is derived for aromatic molecular ions which can decompose to give only a single product whose relative intensity and appearance potential are each a function of Hammett sigma constants, with certain simplifying assumptions.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 17 (1986), S. 471-475 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Apparatus is described for the acquisition of Raman spectra with excitation at wavelengths as short as 184 nm. The H2 Raman-shifted output of an Nd:YAG laser is directed on to a free-flowing sample, and the Raman photons are collected and dispersed by a scanning 1.26 m single monochromator equipped with a 2400 groove holographic grating and a solar blind phototube with integrating electronics, or by a 0.5 m spectrograph with an 1800 groove holographic grating and a reticon multi-channel detector. Data for air-sensitive samples are obtained by enclosing the sample jet in an inert gas purged shroud equipped with a UV-transparent optical window. Raman spectra are reported for phenylalanine at a series of excitation wavelengths down to 184 nm. They show a sharp transition between 200 and 192 nm from vibronic to Franck-Condon scattering. At 200 nm, the intensities of the vibronically induced ν8a and ν8b modes, at 1606 and 1586 cm-1, are nearly the same as that of the 1000 cm-1 ν1 ring breathing mode, whereas at 192 nm the relative intensities of the former bands are dramatically dimished. In contrast, the ν8a and ν8b modes of tyrosine continue to show enhancement comparable to the ring breathing modes at 192 nm, the maximum of the strong 1Bα, b tyrosine absorption. The spectrum of insulin at 192 nm shows comparable contributions from tyrosine, phenylalanine and amide vibrations, whereas at 200 and 218 nm excitation the aromatic contributions are dominant.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 16 (1985), S. 171-173 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Comparison of Raman spectra of octahedral Ru(pyridine)6(BF4)2 with those of Ru(bipyridine)(pyridine)4(ClO4)2 provides an opportunity to analyse the orientation of Ru(pyridine)6 at silver over a wide potential range. At the more positive potentials, the Ru(pyridine)6 appears to be bonded through two pyridine ligands, while at more negative potentials, the orientation is probably C4ν, indicating bonding through one pyridine. Previously reported potential dependences of Raman scattering intensities show mobility of the complex on the electrode surface and probable conversion between these two orientations. Possibilities for further orientation changes at more positive and more negative potentials are obscured by electrode oxidation and complex desorption, respectively.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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