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  • Analytical Chemistry and Spectroscopy  (25,033)
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  • 1
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 17 (1986), S. 477-480 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Raman spectrum of the ν3 mode of allene has been studied as a function of temperature throughout the temperature range of the liquid. Analysis of the spectral band shape shows that the vibrational dephasing is a fast-modulation process. Evidence is presented for a vibrational-rotational coupling involving the tumbling reorientation of the molecule. Dilution studies in GeH4 indicated significant resonant vibrational energy transfer.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 20 (1997), S. 482-486 
    ISSN: 0935-6304
    Keywords: Volatile benzene alkyl derivatives ; Simple distillation ; Purge and trap ; Capillary gas chromatograph-mass spectrometry ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Simple distillation was used to prepare aqueous environmental samples (especially those with high content of accompanying dissolved and suspended organic and inorganic matter) for determination of benzene, toluene, ethylbenzene, and xylenes (BTEX) by means of purge and trap (PT) coupled to gas chromatography-mass spectrometry (GC-MS). The PT step was carried out with a laboratory-built device in which alalytes desorbed from a Primary trap (macrotrap) are focused in a microtrap (also with sorbent) and moisture is removed from purge gases by a Nafion tube (walls selectively permeable to water vapor). Recoveries, if only the first 10 ml distillate was collected, were of the order of 40% at optimum distillation parameters. At a probability level of 95% recoveries were independent of concentration in a studied concentration range of 0.50-30 ppb. Enrichment factors for distillation were of the order off 20. Real samples, i.e., raw and treated waste water were analyzedc for BTEX content by the developed medthod.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 19 (1984), S. 573-576 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A detailed energy-resolved study of the fragmentation of CH2=CHCH(OH)CD2CD3 (1-d5) has been carried out using metastable ion studies and charge exchange techniques, combined with collision-induced dissociation studies to establish the structures of fragment ions. At low internal energies (metastable ions) the molecular ion of 1-d5 rearranges to the 3-pentanone structure and fragments by loss of C2H5 or C2D5 leading to the acyl structure, [CH3CH2C≡O]+ or [CD3CD2C≡O]+, for the fragment ion. However, with increasing internal energy of the molecular ion this rearrangement process decreases rapidly in importance and loss of C2D5 by direct cleavage, leading to [CH2=CHCH=OH]+, becomes the dominant fragmentation reaction. As a result the [C3H5O]+ ion seen in the electron impact mass spectrum of 1-penten-3-ol has predominantly the protonated acrolein structure.
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 8 (1981), S. 312-315 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is shown that under field desorption conditions some less volatile or non-volatile compounds such as oligosaccharides, sulphonic acids and fatty acids can be ionized below the threshold of field electron emission by clustering with anions. In all cases the sample, together with polyethylene oxide 4000, is dissolved in water. The source of the clustering anion is provided either by a small amount of a salt added to this solution (sugars) or by the compounds themselves (sulphonic and fatty acids). The solution is applied to unactivated and/or slightly activated 10 μm tungsten wire cathodes. Suitable clustering ions for the sugars appear to be [Cl]-, [NO3]- and to a lesser extent [Br]- and [I]-. Most of the sulphonic acids studied give rise to the formation of [Mn - H]- ions (n≤5), but their potassium salts yield only unclustered sulphonate anions. However, the addition of a small amount of LiCl to the mixture of benzene sulphonic acid and polyethylene oxide 4000 promotes the formation of clustered anions, [(M - H)2Li]- being by far the most abundant if activated cathodes are used. This addition of some LiCl is essential in the case of fatty acids: without LiCl no anions may be desorbed at all from activated wires, but with the presence of LiCl both [M - H]- and the most abundant [(M - H)2Li]- anions are easily generated.
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  • 5
    Electronic Resource
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    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 18 (1983), S. 525-529 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The positive ion field desorption (FD) spectrum of arginine taken at the best anode temperature only contains a peak due to [M+H]+ ions. At higher emitter temperatures a considerable amount of fragmentation is induced and the [M+H—NH3]+ ions become most abundant. Specific 15N labelling reveals that the eliminated ammonia molecule, exclusively, contains one of the terminal nitrogen atoms of the guanidyl group. This also applies to the ammonia loss from metastably decomposing [M+H]+ ions. The positive ion fast atom bombardment (FAB) spectrum shows more fragmentation than the FD spectrum. In contrast with the FD results, the [M+H]+ ions generated upon FAB with ion lifetimes 〈10-6 s eliminate both ammonia containing one of the terminal nitrogen atoms of the guanidyl group and ammonia containing the α-amino group in the ratio of 1.35, as found by 15N labelling. The metastably decomposing [M+H]+ ions, however, eliminate only the former ammonia molecule. In the negative ion FD and FAB spectra no other peak than that corresponding to the [M—H]- ion is observed. Some attention has been paid to the thermal degradation of arginine on the basis of a few Curie-point pyrolysis experiments.
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  • 6
    Electronic Resource
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    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 23 (2000), S. 474-478 
    ISSN: 0935-6304
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---Solid-phase extraction, on-line derivatization, and measurement by ion trap mass spectrometry (ITD-MS) were used to investigate the biological degradation of pharmaceutical residues (clofibric acid, ibuprofen, diclofenac). The results of the single steps of sample pretreatment and analytical determination are reported. MS/MS measurements were performed on an ITD-MS by selecting collision induced dissociation of the molecular ions (M+) as parent ions to defined daughter ions. A pilot sewage plant and biofilm reactors operating under oxic and anoxic conditions were run as model systems with synthetic sewage water containing 10 to 50 mg/L dissolved organic carbon (DOC) and pharmaceuticals in concentrations of 10 μg/L. Clofibric acid displayed its persistent character in all cases. The pilot sewage plant and the oxic biofilm reactor showed comparable results for diclofenac and ibuprofen, which both were partly degraded. These results can explain the occurrence of these substances in sewage effluents and in the aquatic environment. A high degree of degradation was found especially for ibuprofen in the oxic biofilm reactor, which was attributed to adaptation of the biofilm to the residue. Two metabolites of ibuprofen could be identified on the basis of their mass spectra and comparison with literature data, viz. hydroxyibuprofen and carboxyibuprofen.
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 25 (1994), S. 849-854 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Low-wavenumber depolarized Raman spectra (-400 to 400 cm-1) for dioxane, water and glycerol are presented. Stokes and anti-Stokes spectra (-400 to 400 cm-1), are used to define a reduced spectrum, in which the effects of temperature and also flat backgrounds and symmetric central components are removed, without knowledge of these parameters. Comparison with the usual reductions shows that (i) all inelastically scattered photons must be considered as ‘true’ Raman signals, due to processes involving Boson-like excitations, (ii) if central scattering exists, then its intensity also depends on the population factor, (iii) the low-wavenumber Stokes signal is more intense than expected for a factor of n + 1 only, owing to non-linear effects, and (iv) the systematic use of reduced spectra is not essential, and can be hazardous in some cases.
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  • 8
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    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 3 (1980), S. 169-171 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Glass capillary columns ; Trimethylsilyl derivatives ; Pregnant mares' urine estrogens ; Estrone-equilin separation ; OV-225, Silar 10C stationary phases ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Glass capillary columns coated with OV-225 and Silar 10C were used to analyze estrogens (as their trimethylsilyl derivatives) present in pregnant mares' urine. Such columns provide better resolution in a shorter time than the corresponding packed columns, as exemplified by the separation of estrone from equilin.
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  • 9
    Electronic Resource
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    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 33 (1995), S. S114 
    ISSN: 0749-1581
    Keywords: electron paramagnetic resonance ; adriamycin ; metal chelation ; coordination structure ; iron ; free radical ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: EPR and Mössbauer studies demonstrate that iron chelation by adriamycin is complex, with several different chelation structures. At physiological pH in aqueous solution, three different EPR spectra are observed: a spectrum at g = 4.2 of Fe3+ in a rhombic crystal field (type 1); a spectrum at g = 2.01 with symmetric Gaussian lineshape linewidth 225 G (1 G = 10-4 T), suggestive of Fe3+ bound in an octahedral crystal field (type 2); and a broad spectrum centered at g = 2.0 suggestive of ferromagnetically coupled Fe3+ (type 3). The type 1 and 2 spectra are observed at adriamycin/Fe3+ ratios 〉4, the type 3 spectrum is observed at ratios 〈4 and at ratios 〈2 an increasing amount of Fe3+ gives rise to EPR silent iron(III) hydroxide polymers. At 4 K the type 1 and 2 complexes exhibit a broad doublet Mössbauer signal with an isomer shift δ = 0.56 (1) mm s-1 and quadrupole splitting δEQ = 0.74 (1) mm s-1. The type 3 complex gives rise to a sextet signal with isomer shift ΔEq = 0.47 (1) mm s-1 and hyperfine splitting HF = 476 (1) kG with exhibits superparamagnetic relaxation behavior with a blocking temperature of 23 K, consistent with a microcrystal size of 25 Å. Cu2+ binds to adriamycin at adriamycin/Cu2+ ratios 〉4:1 giving rise to an EPR spectrum with axial symmetry g∥ = 2.26, g⊥ = 2.066, A∥ = 188 G, while 2:1 complexes exhibit a single Gaussian line at g = 2.09 indicative of exchange-coupled Cu2+. The exchange-coupled Cu2+ and ferromagnetically coupled Fe3+ complexes can be explained by the formation of stacked 2:1 adriamycin-metal polymers. On titration of adriamycin with Fe3+-nitrilotriacetate a different spectrum is observed at g = 4.3 and its intensity plateaus at an adriamycin/iron ratio of 2. The iron adriamycin complexes cycle to reduce molecular oxygen and this cycle has been hypothesized to be a mechanism mediating the therapeutic and toxic effects of the drug. Both EPR and Mössbauer experiments demonstrate that the type 1 and 2 chelates reduce their Fe3+ to Fe2+ while the type 3 chelate does not. Therefore, the stoichiometry and method of complex preparation can profoundly effect the properties of these complexes.
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  • 10
    Electronic Resource
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    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 15 (1992), S. 510-513 
    ISSN: 0935-6304
    Keywords: GC-MS ; Cl ; El ; Flavors ; Cola beverages ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: As part of a study directed at introducing GMP recommendations to the production of non-alcoholic beverages, combined Cl and El mass spectra have been used for the identification of compounds present in extracts of “Cockta” beverage following GC-MS analysis. The amount of useful information present both in the separate Cl and El spectra, and in two of the possible combinations of the spectra, is described.
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  • 11
    Electronic Resource
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    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 23 (2000), S. 681-687 
    ISSN: 0935-6304
    Keywords: Focused microwave assisted extraction ; close microwave-assisted extraction ; DDT ; soil samples ; experimental design ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---Optimization of focused microwave (FMW)-assisted extraction of 4,4′-DDE, 4,4′-DDD, and 4,4′-DDT from soil samples was carried out using central composite designs. All the extracts were analyzed with GC/MS and some of them also with GC/AED using columns of different polarities for each of the techniques. The extraction of the analytes was carried out in two ways: with acetic acid as microwave radiation absorbent solvent and n-decane to concentrate the analytes and with reagent water and iso-octane as solvents. In the first case, the influence of the extraction temperature, the extraction time, and the addition of sodium chloride were studied and the optimum conditions for the extraction of 1 g of soil with 5 mL of acetic acid and 2 mL of n-decane were 1.30 mol L-1 sodium chloride at 98°C for 9.3 min. In the second case, the temperature was kept constant (94°C) and the influence of the concentration of sodium chloride and the extraction time were studied. The optimum conditions were 5 mL of a 2.0 mol L-1 sodium chloride together with 2 mL of iso-octane for 15 min. The recoveries obtained by water-FMW extraction were significantly lower than those obtained by the acetic acid-FMW procedure. These last recoveries were in good agreement with those obtained by closed microwave assisted-extraction with acetone-n-hexane as solvent.
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  • 12
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    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 14 (1991), S. 361-362 
    ISSN: 0935-6304
    Keywords: Enantioseparation of α-Pinene ; Chiral mobile phase additive ; Cyclodextrins ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 13
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    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 16 (1993), S. 505-507 
    ISSN: 0935-6304
    Keywords: Enantioseparation of monoterpenes ; Cyclodextrins ; Chiral mobile phase additive ; UV-indirect detection ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 14
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    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 8 (1994), S. 906-912 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: A method of deriving peptide sequence information using partial acid hydrolysis in combination with accurate mass measurements and immonium ion analysis provided by high-resolution plasma desorption mass spectrometry has been developed. The technique is very simple in terms of the chemistry and involves a short-time (3-30 min) incubation of the peptide in 1N-6N HCl at 100-110°C with subsequent mass spectrometric analysis. Partial acid hydrolysis is found to produce sequence-specific segments, often ladder-like, although not always a complete set. Two application examples of the method are given: the linear peptide bradykinin and desmopressin, a peptide with an internal S—S bond and a non-amino-acid constituent. The technique has proved to be particularly useful in cases where some a priori information on the peptide structure was already known or where the automated Edman degradation technique might yield erratic results or not work at all.
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  • 15
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    Rapid Communications in Mass Spectrometry 5 (1991), S. 32-34 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: A new ionization technique based on a modification of the conventional plasma-desorption mass spectrometric apparatus is described. An electron avalanche produced by the microchannel plates of a secondary electron multiplier is found to desorb a sufficient amount of (quasi-)molecular ions of non-volatile thermally labile molecules. Spectra of several substances with molecular masses up to 1250 u are presented. The mechanism of electron avalanche desorption is now under investigation.
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  • 16
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    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 5 (1991), S. 276-277 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: A straightforward relationship between the average and the monoisotopic masses of peptides (proteins) and oligonucleotides is proposed which allows one to calculate the monoisotopic mass from aknown average mass with a 0.1 u order of precision. The approach offered here can be applied to any type of biopolymer.
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  • 17
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    Rapid Communications in Mass Spectrometry 5 (1991), S. 278-282 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Direct comparision of two ionization techniques, 252Cf plasma-desorption and electron-avalanche-desorption, is given in various aspect. signification differences were observed in the low-mass region, and in the spectra of volatile compounds and CsI samples, as well as in the fragmentation pattern of alanilnorleucine. On the other hand, a rather high degree of similarity was obtained in spectra of nitrocellulose and some cyclic depsipeptides, both in typical values of peak width and of the high-mass background character. The conclusion is made, that electron-avalanche desorption is a rather complex process involving various factors.
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  • 18
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    Journal of High Resolution Chromatography 2 (1979), S. 429-435 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Surface roughening by diatomaceous support (5 micron particles deposition) ; Organic glue (polar polymethacrylate acetate) used as intermediate material ; Reproducibility and durability of capillaries discussed ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A technique for adhesion of fine particles (ca. 5 μ) of the 405 white diatomaceous support on the inner wall of glass tube with organic glue [poly (diethylaminoethyl methacrylate) acetate] is described. The coated tube was drawn to capillary column by using a machine designed according to Desty's. The capillary column was then coated with stationary phase (such as squaiane, QF-1, Dexsil 300, PEG 20 M, OV-1, SE 30 and etc.) by the conventional dynamic or static method. This preparation method has proved easy to duplicate and is simple. The coating efficiency (UTE %) is within 60-90. The theoretical plate number per meter of an SE 30 column is about 4000, and per meter of a PEG 20 M column is about 2500. The columns thus prepared have been successfully used to analyze petroleum hydrocarbons, essential oils, petrochemicals, pheromone, steroid metabolites and others.
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  • 19
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    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 10 (1987), S. 100-101 
    ISSN: 0935-6304
    Keywords: Supercritical fluid chromatography, SFC ; Mass spectrometry ; Interfacing SFC/EI MS ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 20
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    Organic Magnetic Resonance 7 (1975), S. 470-474 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The diastereomers of 16 1,3-oxa-, 1,3-aza- and 1,3- thiaphospholanes were assigned by means of the coupling constants 2J(P—C—H) and 3J(P—C—CH3) and the linewidths of the 31P signals and 1H chemical shifts of CH3 groups. It is shown that the change in the 31P chemical shifts allows the estimation of the relative configuration in these compounds.
    Notes: Die Diastereomeren von 16 1,3 Oxa-, 1,3-Aza-und 1,3-Thiophospholanen wurden mit Hilfe der Kopplungs-konstanten 2J(P—C—H) und 3J(P—C—CH3), der Signalbreite der 31P-Signale und der 1H-chemischen Verschiebungen der CH3-Gruppen zugeordnet. Es wird gezeigt, daß auch die 31P-chemischen Verschiebungen eine Bestimmung der relativen Konfiguration dieser Verbindungen gestatten.
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  • 21
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    Organic Magnetic Resonance 6 (1974), S. 568-573 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The geometric factor G [G = (3 cos2 θ -1) r-3] of selected protons relative to a centre of co-ordination [Eu(dpm)3] is determined using Dreiding models of different conformers of 1,3-aza- and 1,3-oxaphospholanes. The centre of co-ordination is supposed to be joined to the oxygen of the carbonyl group or to the nitrogen and oxygen in the hetero-ring, respectively. The graphs of the geometric factors against the paramagnetic shifts of the relevant protons are straight lines only for the preferred conformers on the basis of a correct centre of co-ordination.As a measure for the paramagnetic shift of a proton the slope of the graph of chemical shift against the concentration of Eu(dpm)3 (in mol %) is chosen. By variation of the relative configuration at C-5 in the models and calculation of the geometric factor, it is possible to determine the different diastereomers, which are distinguished by the relative position of the substituent at phosphorus and C-5.
    Notes: An Dreiding-Modellen der verschiedenen Konformere von 1,3-Aza- und 1,3-Oxaphospholanen werden die Geometriefaktoren G [G = (cos2θ - 1)r-3] einzelner Protonen bezüglich eines Koordinationszentrums [Eu(dpm)3] bestimmt. Das Koordinationszentrum wird entweder an dem Sauerstoff der Carbonylgruppe oder an dem Stickstoff oder Sauerstoff im Heteroring gebunden angenommen. Die graphische Darstellung der Geometriefaktoren gegen die paramagnetischen Verschiebungen der betreffenden Protonen ergibt nur für die bevorzugten Konformere bei Zugrundelegung der richtigen Koordinationszentren Geraden. Als Maßzahl für die paramagnetische Verschiebung eines Protons wird die Steigung der Geraden gewählt, die sich beim graphischen Auftragen der chemischen Verschiebung gegen den Gehalt an Eu(dpm)3 (in Mol-%) ergibt. Durch Variation der relativen Konfiguration am C-Atom 5 an den Modellen und Berechnung der Geometriefaktoren ist es möglich, die unterschiedlichen Diastereomere zuzuordnen, die sich bezüglich der Substituentenstellung am Phosphor und am C-Atom 5 unterscheiden.
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  • 22
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    Organic Magnetic Resonance 21 (1983), S. 315-318 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The analysis of the 1H NMR spectra of 2,8-dithia-1,5-diphosphabicyclo[3.3.0]octane, 2,8-dithia-1-phospha-5-azabicyclo[3.3.0]octane and 2,8-dithia-1-arsa-5-phosphabicyclo[3.3.0]octane is supported by means of 2D- J-resolved NMR measurements. The spectra suggest a preferred conformer with strong puckering of the fused five membered rings.
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  • 23
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    X-Ray Spectrometry 19 (1990), S. 275-283 
    ISSN: 0049-8246
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Sub-micron spheres of pure materials prepared by electrohydrodynamic atomization were used to determine experimentally the x-ray distribution function, φ(ρz), for spheres using a dedicated HB501 scanning transmission electron microscope at 100 keV. The materials chosen were W, Pd, Ni, V and Al thin spheres. φ(ρz) was measured experimentally using a tracer technique. The thin film tracers used were Ir, Ag, Cr, Cu and SiO2, respectively. φ(ρz) for the above materials was also calculated using a Monte Carlo trajectory simulation modeled for the tracer technique. The experimental tracer φ(ρz) results show a pronounced scatter, especially for large-diameter spheres. Local variations in the tracer film thicknesses appear to be the reason for such scatter. The trends in the experimental and Monte Carlo results, however, are simple and show a strong dependence on the atomic number of the target material. A general expression for φ(ρz) for thin spheres is presented which fits the experimental tracer results. The Monte Carlo results agree well with the fitted data for elements of low atomic number and/or small-size spheres. For elements of higher atomic number (Pd and W), however, the Monte Carlo φ(ρz) curves peak too early with mass thickness. This problem may be due to inadequacies of the scattering cross-section models used in the analysis.
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  • 24
    ISSN: 0049-8246
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Models of absorption and fluorescence corrections for characteristic x-rays emitted from electron-transparent spheres are presented for a stationary point probe and for a rastered or flooding beam. In both models, the primary inonzation event and subsequent x-ray emission are assumed to occur anywhere along the electron-beam axis within the sphere. Multiple scattering effects are not taken into account but absorption of the fluorescence radiation is taken into account. The integrals involved in both correction models are solved numerically and the results are compared with previous models of thin-foil, plane-parallel specimens. An analytical solution for the fluorescence correction is obtained when the primary x-ray generation is assumed to originate at the center of the sphere. Both corrections are found to be less severe for submicron spheres than the corresponding corrections for plane-parallel specimens.
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  • 25
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    Journal of High Resolution Chromatography 16 (1993), S. 188-191 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Thermostable WCOT columns ; PLOT columns ; Stainless steel ; Silicon layer for deactivation ; Simulated distillation ; PNA analysis ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A layer of elemental silicon has been deposited on the surface of stainless steel tubing by means of chemical vapor deposition (CVD). Two kinds of capillary column were prepared from the deactivated tubing: cross-linked, silanol-terminated polydime-thylsiloxane wall coated open tubular (WCOT) columns and molecular sieve 13X porous layer open tubular (PLOT) columns. Unlike fused silica capillary columns, stainless steel WCOT and PLOT columns can be operated at temperatures in excess of 400°C. High temperature simulated distillation has been performed successfully with a macro bore WCOT column and rapid PNA (paraffin, naphthene, and aromatic) analysis with a multidimensional gas solid chromatographic (GSC) system using PLOT columns.
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  • 26
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    Journal of High Resolution Chromatography 4 (1981), S. 6-10 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Retention index calculation by correlation techniques ; Use of n-dialkyl sulphides as standards ; Use of selective detectors ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Retention indices were determined for a homologous series of n-dialkyl sulphides on three stationary phases (SE-30, OV-17 and XE-60) under isothermal and linear temperature programming conditions. Under these two different GC conditions, equations were derived for each of the three stationary phases which showed the dependence of retention index on the number of carbon atoms and the boiling points for a homologous series of n-dialkyl sulphides. The equation for the correlation isothermal retention index was shown to be applicable to the identification of n-dialkyl sulphides using linear temperature programming. It was found that the GC behaviour of n-dialkyl sulphides makes these compounds suitable for use as a standard series instead of n-alkanes for the calculation of retention indices in GC analysis in which detectors insensitive to n-alkanes are employed. The use of the homologous series of n-dialkyl sulphides for the calculation of sulphide retention indices can be great practical importance in the microanalysis of natural compounds. We have used this method successfully in the analysis of pesticides containing S-atoms.
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  • 27
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    Journal of High Resolution Chromatography 6 (1983), S. 306-309 
    ISSN: 0935-6304
    Keywords: Liquid chromatography, HPLC ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A method is described for separation of low amounts of DHETX m. s. from human plasma, based on extraction and determination by high performance liquid chromatography with fluorimetric detection.
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  • 28
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of polyenic compounds of the type RC6H4(CH=CH)nCOPh, n=1, R=H,p-NMe2,p-OH,p-OMe,p-Cl,p-Br,p-NO2,m-NO2; n=2, R=H, p-NMe2, p-OMe,p-Cl,p-Br, p-NO2; n = 3, R = H, p-OMe,p-Cl, p-Br,p-No2 have been measured. The ratio of the intensities of the common ion PhCO (m/e 105) to the intensities of the molecular ions for these series is correlated with the Hammett-Brown equation with reaction constants p = 0.73 (when n = 1), 0.25 (when n =2), 0.11 (when n = 3). The transmission coefficients were calculated as π'=0.72,0.25 and 0.11 respectively [assuming p=1.01 for benzophenone series-see M. M. Bursey and F. W. McLafferty, J. Am. Chem. Soc. 89, 1 (1967)]. The contributions of the inductive mesomeric direct polar conjugation and non-additive interaction were calculated in accordance with the equation log Z/Z0= ρIσI + ρc+σc+ + ρI, cσIσc+. It was found that the inductive influence as well as the mesomeric influence of substituents decreases rapidly with the increase in the number of double bonds in the chain. The direct polar effect has a very small value in all series for all substituents with the exeption of NMe2. Non-additive interaction effects are large. They probably express the general influence of RC6H4(CH=CH)n on COPh.
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  • 29
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    Biological Mass Spectrometry 29 (1994), S. 253-259 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1- and 2-monoacylglycerols and 1,2- and 1,3-diacylglycerols of saturated and unbranched fatty acids with 8, 10, 12, 14, 16 and 18 carbon atoms were synthesized and subsequently derivatized with nicotinic acid chloride hydrochloride. The resulting nicotinoyl derivatives were examined by mass spectrometry in the case of pure substances and as mixtures by gas chromatography/mass spectrometry (GC/MS). From the electron impact mass spectra, differentiation between mono- and diacylglycerols and between the two positional isomers of mono-acylglycerols and diacylglycerols is possible. The molecular masses of the partial acylglycerols and the identities of the bonded fatty acid were also determined. Similarly to the nicotinoyl derivatives of saturated fatty alcohols, the nicotinoyl derivatives of partial acylglycerols produce a fragmentation pattern that reflects every methylene group of the alkyl chains. These results offer rules for the structure elucidation of partially acylated acylglycerols and probably for mixed diacylglycerols by means of GC/MS, which includes the detection of double bonds and methyl branch positions at the fatty acid alkyl chains. The molecular formulae of all the important fragments in the mass spectra of the nicotinoyl derivatives were confirmed by high-resolution mass spectrometry. Their structures and fragmentation pathways are proposed.
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  • 30
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    Biological Mass Spectrometry 30 (1995), S. 432-437 
    ISSN: 1076-5174
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The positional isomers of mono[(Z)-9-octadecenoyl] glycerol, di[(Z)-12-octadecadienoyl] glycerol were derivatized with nicotinic acid chloride hydrochloride. The resulting nicotinoyl derivatives were examined by gas chromatography/mass spectrometry. In their electron impact mass spectra, each methylene group and double bond of the alkyl chain is reflected by a fragmentation pattern in the high mass region. This is caused by radical-induced cleavage of the alkyl chains following random hydrogen abstraction by the pyridine nucleus. An accurate determination of double bond positions in mono- and diacylglycerols is possible by characteristic spacings between abundant diagnostic ions in this fragmentation pattern.
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  • 31
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    Biological Mass Spectrometry 20 (1985), S. 649-661 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Within the scope of a comparative study of the reactivities of odd- versus even-electron ions, the possible significance of the well-known McLafferty reaction for structural analysis in even-electron ions is investigated. In order not to compare reactions of different types with one another, a selective set of experimentally verifiable features is specified which must be met by a degradation reaction to justify its classification as a true McLafferty process. The literature is critically reviewed in the light of this restrictive specification and some ambiguous examples have been reinvestigated, applying modern techniques of selective metastable ion scrutiny together with specific 2H labelling. Only in a few specific cases are even-electron ions found to decay in a McLafferty fashion according to the postulated criteria, indicating a rather limited effectiveness of the reaction as a source of structural information in this field. Fundamental problems in unequivocally pinning down a very specific mechanistic course of a reaction are encountered in spite of using sensitive new techniques of measurement.
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  • 32
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    Journal of High Resolution Chromatography 13 (1990), S. 148-148 
    ISSN: 0935-6304
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 33
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    Journal of High Resolution Chromatography 2 (1979), S. 423-428 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, nickel ; „Transevaporator“ into packed pre-column as sampling technique prior capillary described ; Application to volatile metabolite body fluid analysis for early detection of disease ; Serum and human breast milk as examples ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Nickel capillary columns coated with moderately polarstationary phases such as Witconol can be used for the separation of the organic volatile fraction from biological fluids. A “transevaporator” sampling technique for the collection of the organic volatiles on glass beads from as little as 5 to 500 μl of biological fluids (e.g. urine, serum, amniotic fluid, breast milk, saliva, etc.) is described. The organic volatiles are thermally desorbed from the glass beads into a short precolumn cooled in liquid nitrogen, which overcomes the problems associated with sample introduction onto narrow-bore capillary columns. The application of the full analytical technique to problems associated with the early detection of disease is illustrated.
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  • 34
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    Journal of High Resolution Chromatography 7 (1984), S. 370-374 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Trace analysis ; On-column injection ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Large sample volume on-column injection (up to 250 μL) of n-pentane solutions of halogenated hydrocarbons has been employed for the direct measurement of both low-boiling and high-boiling compounds in what is essentially a single run. Two-bonded phase, fused-silica capillary columns are joined in series, through which the low-boiling compounds are first chromatographed and detected with an electron capture detector. High-boiling compounds are then trapped in a section joining the two columns, and subsequently chromatographed in the second column, using the same detector. This procedure permits analysis at the ppt level.
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  • 35
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    Biological Mass Spectrometry 17 (1982), S. 74-78 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The fragmentation pathways of RDX in chemical ionization mass spectrometry have been rationalized, using data from different reagent gases, including CD4 and iso-C4D10. The dependence of spectra taken with different gases on the acid strength of the reactant ions in the gases is accounted for.
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  • 36
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    Biological Mass Spectrometry 11 (1976), S. 388-393 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The methane and isobutane chemical ionization mass spectra of ten 2,4,6-trinitroaromatic compounds have been recorded. The mass spectra contain intense [M + 1]+ ions and usually little fragmentation. However, in some cases major fragmentation processes have been observed. Some unusual adduct ions have been found with isobutane as the reagent and their temperature dependence has been studied.
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    Biological Mass Spectrometry 11 (1976), S. 1114-1119 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Fatty acids with a hydroxyl moiety at the C-3 position are found widely in bacterial lipids, but only rarely in mammalian lipids. The mass spectra of the methyl ether derivative of these hydroxy acids exhibit an intense ion at m/e 75, rather than the rearrangement ion at m/e 74 more typical of fatty acid methyl esters. The mass spectrometric behavior of several 3-methoxy fatty acid methyl esters were studied, and the origin of the unique ion at m/e 75 was established using 18O and 2H labeled analogs and metastable ion transitions. this ion was shown to arise from the loss of ketene from the 3,4 cleavage ion at m/e 117.
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  • 38
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    Biological Mass Spectrometry 25 (1990), S. 517-521 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass fragmentation behaviour of 3,4-dihydro-1H-2,3-benzothiazine 2,2-dioxides was studied. The rationalizations suggested are supported by accurate mass measurements, metastable evidence and deuterium labelling.
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  • 39
    ISSN: 0935-6304
    Keywords: Capillary gas chromatography ; Time-of-flight mass spectrometry ; Hyphenated analytical techniques ; REMPI laser ionization ; Selective ionization ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Analysis of environmental samples usually requires time consuming sample preparation and clean-up procedures prior to instrumental detection. Faster analysis requires an enhanced instrumental selectivity in order to reduce the necessary clean-up effort. In this context we present a novel concept for coupling gas chromartography/mass spectrometry (GC-MS) with high resolution UV spectoscopy to increase selectivity. We use UV-laser induced, resonance-enhanced multi-photon ionization (REMPI)as a compound specifie ion source for time-of-flight mass spectrometry (TOFMS). The REMPI ionization involves the UV absorption spectroscopy into the ionization process as an aditional analytical dimension. The heart of the GC-REMPI-TOFMS coupling is a specially designed valve, which repetitively (20 Hz) expands the chromatographic eluent as short supersonic jet gas pulses (≈ 150 μs duration) into the vacuum of the mass specrtrometer. The sample molecules are cooled down to temperatures of 10-40 K within the jet expansion. Under these conditions, UV absorption spectriscopy (i.e. REMPi spectroscopy) becomes highly compound selective, even able to distinguish isomeric compounds. The ions formed by REMPI ionization are mass analyzed in the TOFMS. Thus the GC-REMPI-TOFMS coupling presented here is actually a three-dimensional analytical instrument, providing gas chromatographic (retention time) as well as mass spectrometric (molecular mass) and UV -spectroscopic (excitation laser wavelength) selectivity. In combination with gas phase sampling and concentration techniques for semi-volatile organic air pollutants based, e.g., on silicone rubber traps the GC-LAMS technique can be a powerful tool for fast environmental target analysis, e.g. for industrial emission control purposes.
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    Journal of Raman Spectroscopy 26 (1995), S. 435-441 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The groove binding dye Hoechst 33258 was investigated both in aqueous solution and in the adsorbed form on silver colloids and island films. Fourier transform Raman, resonance Raman and surface enhanced resonance Raman spectra were used together with the results of a normal coordinate analysis for a comprehensive assignment of the rich vibrational spectrum. Relative band intensities in the SERRS spectra indicate that the molecule is adsorbed with its long axis oriented along the silver surface and with the planes of the benzimidazole rings approximately parallel to the surface. The molecule is bound to the surface as a cation protonated at a piperazine nitrogen atom and is desorbed on complete deprotonation.
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  • 41
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    Organic Magnetic Resonance 6 (1974), S. 346-354 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A large series of cyclohexane and cyclopentane spiro compounds has been studied by carbon-13 NMR. Increments have been derived in terms of α, β, γ spiro substituent effects, one ring being considered as the substituent of the other. As usual α and β effects are paramagnetic and γ effects are diamagnetic. They are compared with the corresponding effects associated with the introduction of a gem dimethyl group into a cyclohexane or cyclopentane ring. The size of the two rings involved in the spirane structure has a marked influence especially on the chemical shift of the spirane carbon atom. Comparison between monospiro and dispiro derivatives gives information about the so-called 1,5 or δ effect which is paramagnetic. From an analytical point of view, carbon-13 NMR appears to be a powerful method of detecting the spirane structure, apparently including the relative size of the rings.
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    Organic Magnetic Resonance 6 (1974), S. 492-493 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The 13C NMR spectral study of epoxy bicyclo [2.2.1]-heptanes reveals a strong influence on the chemical shift of the bridging 13C, due to the endo or exo orientation of the heterocyclic ring. The difference between the 13C and 1H Δδ shows that the observed results cannot be explained by the ring current alone.
    Notes: L'étude RMN 13C de composés époxybicyclo[2.2.1]-heptaniques fait ressortir une forte influence de l'orientation endo ou exo de l'hétérocycle sur le glissement chimique du 13C pontal. La différence entre les variations de glissements chimiques en 13C et 1H montre que l'effet de courant de cycle ne peut seul rendre compte des résultats observés.
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  • 43
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    Journal of High Resolution Chromatography 9 (1986), S. 111-115 
    ISSN: 0935-6304
    Keywords: Liquid chromatography, LC ; Exclusion chromatography ; Glass microcolumns ; Protein association ; Surfactants ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The application of microcolumn exclusion chromatography to the determination of equilibrium and kinetic association constants for proteins is described. Taking phospholipase A2 as an example, the relationship between association and enzymatic activity was investigated. A procedure for determination of the critical concentration of micelle formation (CCM) in surfactants was developed.
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  • 44
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    Biological Mass Spectrometry 4 (1977), S. 155-158 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of antipyrine metabolites show characteristic fragmentation patterns which depend on the presence and position of functional groups. A substituent at position 4 is indicated by an intense key fragment at m/e 56 and a substituent at the methyl group in position 3 causes a significant increase in the intensity of the peak at m/e 82. The fragment at m/e 96, which is characteristic for antipyrine itself, is suppressed if there is a substituent in either position 3 or 4. Mass spectra of the glucuronides of 4-hydroxyantipyrine and 3-hydroxymethylantipyrine are also discussed.
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  • 45
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    Biological Mass Spectrometry 13 (1978), S. 65-73 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of nine diastereoisomeric pairs of 4-methyl-2-X-2-Y-1,3,2-dioxaphosphorinanes have been examined. The differences between the intensities of particular ions in the mass spectra of geometrical isomers are reported and rationalized in terms of the conformations adopted by compounds.
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  • 46
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    Journal of High Resolution Chromatography 11 (1988), S. 639-646 
    ISSN: 0935-6304
    Keywords: Liquid chromatography ; HPLC ; Electrochemical detection ; Fluorescence detection ; UV detection ; Cysteine derivatives ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electrochemical (ECD), fluorescence (FLD), and UV spectrophotometric (UVD) detection were used to monitor various S-alk(en)yl-L-cysteines and their corresponding sulfoxide isomers following pre-column derivatization with o-phthaldialdehyde-tert-butylthiol and separation by reversed-phase HPLC. Recording of hydrodynamic voltammograms, FLD stop-flow scanning, and on-line captured UV spectra were methods used for establishing optimal detector settings which were defined as a compromise between favorable selectivity and high sensitivity. Optimal detector settings were found at: (A) 750 mV vs. Ag/AgCl for ECD; (B) excitation at 230 nm and emission at 420 nm for FLD; and (C) 337 nm for UVD. Various aspects of detector practicability such as selectivity, baseline disturbances due to excessive reagent, scanning possibilities, as well as detection limits were evaluated and compared. Minimal detectable amounts of the compounds were in the range of 130-160 fmol for ECD, and 2.5-3.5 pmol and 13-16 pmol for FLD and UVD. In addition, the possibilities and benefits of detector coupling were examined.
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    Journal of Raman Spectroscopy 26 (1995), S. 493-494 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 48
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    Journal of Raman Spectroscopy 21 (1990), S. 769-779 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Recent experimental and theoretical developments in spontaneous hyper-Raman spectroscopy (HRS) are reported. The scope of the general review of HRS presented summarizes the results of this non-linear scattering technique during the past 10 years. In particular, those aspects of HRS studies which allow novel observations as compared with other spectroscopic techniques are emphasized. HRS investigations of crystals, liquids and surface and electronic resonance enhancement are highlighted.
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  • 49
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Raman scattering of two vibrational overtones of benzene is found to undergo strong preresonance enhancement as the excitation frequency approaches the 1B2u state, the lowest lying, forbidden electronic transition at 265 nm. These preresonance active modes are the first overtone of the 606 cm-1 e2g fundamental, which is responsible for the vibronically induced 1B2u intensity, and the first overtone of the 848 cm-1 e1g fundamental, an out-of-plane C—H bending mode. In order to treat this overtone preresonance Raman behavior theoretically, the molecular polarizability is consistently expanded to second order in nuclear displacements, and thus we consider all preresonance contributions of this order. The leading contributions of strictly dipole-forbidden electronic transitions to the scattering cross-section of overtones are exposed. Within this theoretical context it is seen how scattering cross-section for each of these resonance active overtones is derived from different sources. The preresonance scattering of the 606 cm-1 overtone results from the vibronic activity of this fundamental in the 1B2u transition. On the other hand, the 848 cm-1 overtone derives its 1B2u resonance activity from the change in its fundamental frequency (to 585 cm-1) in this excited electronic state. Furthermore, the 848 cm-1 overtone activity is built upon signifficant background preresonance contributions from other higher lying electronic transitions.
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    Organic Magnetic Resonance 30 (1992), S. 387-392 
    ISSN: 0749-1581
    Keywords: Vasopressins ; Peptide dynamics in solution ; NMR relaxation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dynamic behaviour of [Lys8]-vasopressin derivatives, especially of N-Gly-Gly-Gly-[Lys8]-vasopressin in solution, was investigated by NMR relaxation studies. One can derive a set of dynamics data which describe the molecular tumbling in solution from 13C spin-lattice relaxation times, T1, spin-spin relaxation times, T2, and heteronuclear nuclear Overhauser enhancements (NOE). Two different approaches, the scheme proposed by Jardetzky and co-workers and the ‘model-free’ approximation of Lipari and Szabo, are used to analyse the dynamics and a comparison of the corresponding data is given. In addition to a mobility of 108-109 s-1, we observe a faster mobility of the order of 109-1010 s-1 in addition to slow dynamic contributions. The latter can be associated by means of T1, measurements with a motion involving the S—S linkage in the vasopressin. Some additional motion is described as the overall mobility of an associate. The results from 13C relaxation were corroborated by 15N T1 measurements, performed at the 15N natural abundance level by an INEPT-reverse INEPT method, and by 15N NOE investigations.
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    Organic Magnetic Resonance 30 (1992), S. S3 
    ISSN: 0749-1581
    Keywords: Transient NOE experiments ; Synchronous nutation experiments ; NAD stack interactions ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cross-relaxation interactions between the nicotinamide moiety and the adenine moiety of NAD in D2O solution were unambiguously revealed by steady-state NOE experiments, transient NOE experiments and synchronous nutation experiments. The experimental results, which allow a concise description in terms of auto-relaxation and cross-relaxation, are interpreted as the result of a stacking interaction. Studies of 13C relaxation and investigations on ternary mixtures with 6-methylpurine give evidence for an inter- rather than intra-molecular stack interaction, at least in the NMR concentration range.
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  • 52
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    Organic Magnetic Resonance 29 (1991), S. 580-586 
    ISSN: 0749-1581
    Keywords: [Lys8]-vasopressin homologues ; NMR assignments in peptides ; Conformational analysis ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The assignment of proton NMR signals and the conformational analysis of N-(Gly)-[Lys8]-vasopressin and N-(Gly—Gly—Gly)—[Lys8]-vasopressin in dimethyl sulfoxide solution by means of one- and two-dimensional NMR techniques are presented. Dihedral angles obtained from 3J (HN—C—α-H) vicinal couplings, intramolecular distances estimated from nuclear Overhauser enhancements (NOEs) and two-dimensional experiments in the rotating frame (ROESY), as well as temperature dependences of the amide protons, suggest a more or less rigid ring conformation with an inverse γ-turn for both cyclic peptides.
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  • 53
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    Biological Mass Spectrometry 19 (1990), S. 13-26 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The determination of the amino acid composition and sequence of a peptide, using both conventional and tandem fast atom bombardment mass spectrometry, is presented. First a list of potential empirical formulae is generated using the accurate mass and isotopic peak intensity ratios from the molecular ion cluster. The formulae are mathematically analyzed to ensure that they correspond to linear peptides composed of 19 common amino acids. Then using the ions below m/z 160 Da, which are characteristic of the amino acid content of the peptide, the formulae are decomposed into possible amino acid compositions. From each composition sequences are generated and their predicted fragment ions are compared to ions present in the mass spectrum. A score based on the intensities and the occurrence of consecutive sequence fragments is calculated. Finally sequences with the ten highest scores are retained. Analyses performed on typical peptides with molecular weights below 1500 Da indicate that identification can generally be achieved using this approach.
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  • 54
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: SERS and SERRS spectra in aqueous silver sol for Ru(II) polypyridine complexes with 2,2′-bipyridine (bpy) and 1,1′-biisoquinoline (Q) [Ru(bpy)2+3, RuQ2+3, Ru(bpy)2Q2+ and Ru(bpy)Q2+2] were observed with 457.9, 488.0, 514.5 and 632.8 nm excitation. The vibrational modes of the conjugated ring system in the 1600-1400 cm-1 region are enhanced by the resonance effect. Some bands in the SERS spectra of the four complexes show remarkably high intensities with longer wavelength excitation. This may be explained by surface selection rules.
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  • 55
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The ion-molecule reactions of allyl bromide with the molecular ion of allyl bromide and with its major fragment, the allyl ion, yield the C6H7+ and C6H9+ ions. The structure of these product ions was explored by means of photofragmentation with laser light in the 10 μm region and by proton transfer reaction to selected reagents. These product ions were also formed by other reactions and their reactivities compared. In both cases the presence of at least two populations is demonstrated. For C6H9+ these two populations are initially present, whereas for C6H7+ an isomer is formed by the infrared light before the loss of H2. When this ion is produced by photofragmentation of C6H7+, at least one third, stable isomer is formed. Two isomers of C6H5+ are formed in the photofragmentation of C6H7+, but only one form photofragments further by loss of C2H2. The use of non-linear least-squares fitting does not allow definite conclusions to be drawn concerning the kinetics of the consecutive photofragmentations.
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  • 56
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    Rapid Communications in Mass Spectrometry 9 (1995), S. 1315-1320 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Matrix-assisted laser desorption/ionization (MALDI) was used for several small proteins (such as insulin) and for peptides. It was found that the detection efficiencies of MALDI for the insulin B chain and the insulin A chain are drastically different. Similar phenomena were also observed for various types of peptides. The positive-ion signal of MALDI in detecting proteins or peptides was found to be greatly enhanced by the presence of a basic amino acid in their chains. The experimental results indicate that this enhancement may arise from proton transfer in solution by an acid-base reaction between the protein/peptide and matrix molecule. This pre-protonated mechanism provides a low energy barrier for the ionization of peptides in a MALDI process, and greatly reduces the energy threshold of MALDI. Matrix effects on the ionization mechanism are discussed.
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  • 57
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    Journal of High Resolution Chromatography 22 (1999), S. 449-453 
    ISSN: 0935-6304
    Keywords: Capillary electrophoresis ; experimental design ; cyclodextrin ; chiral separation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---Orthogonal design and uniform design were used for the optimization of separation of enantiomers using 2,6-di-O-methyl-β-cyclodextrin (DM-β-CD) as a chiral selector by capillary zone electrophoresis. The concentration of DM-β-CD, buffer pH, running voltage, and capillary temperature were selected as variable parameters, their different effects on peak resolution were studied by the design methods. It was concluded that orthogonal design offers a rapid and efficient means for testing the importance of individual parameters and for determining the optimum operating conditions. However, for a large number of both factors and levels, uniform design is more efficient. The effect of addition of methanol and citric acid buffer on the separation of enantiomers was also examined.
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  • 58
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    Journal of High Resolution Chromatography 17 (1994), S. 563-564 
    ISSN: 0935-6304
    Keywords: Capillary electrophoresis ; Electrolysis ; Electrolytic effect ; pH Variation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 59
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    Biological Mass Spectrometry 25 (1990), S. 260-264 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A field desorption mass spectrometric method is proposed for the analysis of mixtures of surfactant and inorganic salts. Different compounds in the mixture are determined with different heating currents and distinguished on the basis of the exterior character of the mass spectrum. The effectiveness of the method is demonstrated with known mixtures of surfactants and inorganic salts. Two unknown additives for electric tin plating were tested with the method.
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  • 60
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: N-Trifluoroacetyl-n-butyl ester derivatives of deuterium-labelled valine, leucine, isoleucine and phenylulanine were analysed by the isotope dilution technique and gas chromatography/mass spectrometry (GC/MS). Selected ion retrieval and peak-area integration were applied. The conditions adopted gave good separations with a short experimental time and high intensity. Ratios of the total isotopic abundance and metabolic kinetic curves were obtained. The regression coefficient of the standard dilution curve was 0.99 and the relative standard deviation was 0.3%. The stabilities of the amino acid derivatives were also tested.
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  • 61
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    Biospectroscopy 2 (1996), S. 301-309 
    ISSN: 1075-4261
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: Femtosecond pump-probe experiments are used to study the photophysics and photochemistry of heme proteins on ultrafast time scales. Using electronic relaxation measurements combined with reaction-driven coherence signals, we determine that, after the photoexcitation of myoglobin (Mb)NO, the bond-breaking time is on the order of the electronic dephasing time (∼ 20 fs) and the electronic ground state of deoxy Mb appears on a time scale of 80 ± 30 fs. This latter time scale is linked to the Fe-His bond compression (TFe-His/2 ∼ 75 fs), which is initiated by the photolytic depletion of electron density from the antibonding dz2 orbital. The subsequent depression of the dx2-y2 orbital energy, and its population as the iron moves out of plane, leads to the formation of the S = 2 electronic ground state and drives the doming of the heme (Tdome/4 ∼ 100 fs). Thus, the initial stage of heme doming is completed in TFe-His/2 + Tdome/4 ∼ 180 fs. Samples of hemoglobin (Hb)NO display a strong coherent Fe-His stretching vibration at 230 cm-1, which appears immediately (∼ 200 fs) after photodissociation. The data also show a lower-frequency component at 95 cm-1, which we assign to heme doming. The reaction driven coherence of HbNO is observed to be much stronger than the impulsively stimulated Raman coherence of Hb, as might be expected, based on the large relative displacement between reactant and product equilibrium position. The Raman coherence of deoxy Mb is also studied as a function of temperature. As the temperature decreases from 290 to 10 K, the amplitude of the 370 cm-1 mode increases while the amplitude of the 220 cm-1 Fe-His stretching mode decreases. Finally, we report preliminary observations of the first Raman coherences in samples of another heme protein, cytochrome P450. © 1996 John Wiley & Sons, Inc.
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    Journal of Raman Spectroscopy 26 (1995), S. 527-534 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ultra-fast pulsed laser measurements in the time domain have several advantages over traditional frequency-domain spectroscopy. For example, very low frequency modes are more easily probed, fluorescent samples can be studied and vibrational modes that are directly coupled to chemical reactions are revealed. This study demonstrated some of these advantages using heme protein samples. Low-frequency modes are observed in deoxymyoglobin (deoxyMb), fluorescence rejection is demonstrated with metMb and product-state vibrational coherence is revealed with MbNO.
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  • 63
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    Journal of Chemometrics 9 (1995), S. 363-372 
    ISSN: 0886-9383
    Keywords: PLS regression ; orthogonal expansion ; optimization ; Lagrange multipliers ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A simple iteration algorithm that is faster and less memory-intensive than the NIPALS iteration algorithm for PLS regression is presented. The iteration algorithm is obtained by treating the orthogonal expansion or decomposition of a matrix X as an extremum problem subject to normalization and orthogonality constraint conditions and then solving the problem by use of the method of Lagrange multipliers. The main idea in this method is to find the transformation vector r. The latent variable t is expressed exactly as the linear combination of X-variables with the vector r so that the final regression coefficients can be conveniently provided. In the algorithm the recursion of the orthogonal projection is needed, which is derived by use of a matrix inverse formula. Algorithms are established from the equation for calculating the vector r that are suitable for dealing with three cases of large data sets. The first case is when the number of objects is very large, the number of variables is relatively small and the number of Y-variables is equal to or greater than the number of X-variables. The second case is when the number of objects is very large, the number of variables is relatively small and the number of X-variables is greater than the number of Y-variables. The last case is when the number of variables, either X- or Y-variables, or both, is very large and the number of objects is small.
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  • 64
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    Biological Mass Spectrometry 19 (1990), S. 782-786 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Proteolytic digests of human antithrombin III (ATIII) have been analyzed by a combination of reversed-phase high-performance liquid chromatography and fast atom bombardment (FAB) mass spectrometry for disulfidecontaining peptides which are diagnostic for disulfide linkages in ATIII. These results indicate that disulfide bonds join Cys 8 and Cys 128, Cys 21 and Cys 95, and Cys 247 and Cys 430. In addition, these results demonstrate that systematic searches of the amino acid sequence of a large protein for segments with molecular weights matching FAB mass spectral information is a viable method for identifying peptides independent of the specificity of the enzyme used to fragment the protein.
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  • 65
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    Journal of High Resolution Chromatography 19 (1996), S. 643-646 
    ISSN: 0935-6304
    Keywords: Enantioselective gas chromatography ; Polysiloxane-anchored chiral crown ether stationary phase ; Chirasil-man-18C6-25 ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 66
    ISSN: 1075-4261
    Keywords: brown pigment stone ; PAGE ; mid-IR spectroscopy ; far IR spectroscopy ; FT-Raman ; bezoar ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: Spectroscopic studies of various types of gallstones carried out in China are reviewed. Three basic classes of gallstones are surveyed: cholesterol stones, brown pigment stones, and black pigment stones. The emphasis of this review is on brown gallstones. The primary spectroscopic methods used in the studies surveyed are Fourier transform infrared absorption and Fourier transform Raman scattering. Chemical components studied in gallstones include cholesterol, bile pigments, glycoproteins, proteins, bilirubin metal complexes, and salts of calcium and other metals. Further studies are needed characterize the relationship of these components to more complex features of gallstones. © 1997 John Wiley & Sons, Inc. Biospectroscopy 3: 371-380, 1997
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  • 67
    ISSN: 0935-6304
    Keywords: Gas Chromatography ; Stationary phase ; Liquid crystalline crown ether ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new kind of side chain liquid crystalline polysiloxane containing a crown ether with a longer spacer (PSC-11) has been prepared and coated on a fused silica capillary column. The main chroma-tographic characteristics including efficiency, polarity, and selectivity have been examined. The phase exhibits the retention properties of both liquid crystal and crown ether stationary phases and possesses higher efficiency and better selectivity than PSC-3, which has a shorter spacer between the main polysiloxane chain and liquid crystalline side chain.
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    Rapid Communications in Mass Spectrometry 9 (1995), S. 1516-1521 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Electrospray ionization of four structurally diverse natural products, actinomycin D, digitoxin, reserpine and quercetin was investigated. Specific attention was paid to the molecular ions formed under typical reversed-phase high-performance liquid chromatography (RP-HPLC) conditions. The response characteristics of [M + H]+, [M + NH4]+ and [M + Na]+ Ions, observed upon addition of formic acid, ammonium formate and sodium acetate were studied. It was found that the highest response for these molecular ions was obtained with proton, ammonium and sodium ion concentrations of approximately 10-3 ∼ 10-4 M. This critical concentration appears to be correlated with the equilibrium between the thermodynamically controlled molecular ions in solution and electrospray produced gas-phase ions. Gas-phase ion reactions in the ion transfer region were investigated for digitoxin, and the mechanism of gas-phase ion formation is briefly discussed.
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    Journal of High Resolution Chromatography 3 (1980), S. 440-446 
    ISSN: 0935-6304
    Keywords: High performance thin-layer chromatography ; β-adrenoceptor blocking drugs ; Continuous development ; Multiple development ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: High performance thin-layer chromatography was used for the separation of nine therapeutically important and structurally similar β-adrenoceptor blocking drugs on silica gel plates. In situ scanning of the plate in the reflectance mode gave detection limits in the low nanogram range depending on the individual drug and the wavelength selected for its determination. Scanning the HPTLC plate at several wavelengths can be used to aid the identification of partially resolved components. Continuous development and continuous multiple development techniques are compared for the simultaneous separation of the drug mixture.
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    Rapid Communications in Mass Spectrometry 6 (1992), S. 671-678 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Measurements of kinetic energy distributions of molecular ions ejected into an extraction field by matrix-assisted laser desorpton re reported. The measurements were made in a time-of-flight mass spectrmeter with an electrostatic mirror by measuring the reflected signal as a function of the difference between the accelerating voltage and the voltage applied t the mirror. The molecular ions ere found to have less kinetic energy than the extraction field alone would normally provide, i.e. we observed an nergy deficit. Under conditons typical for a matrix-assisted laser desrptio experiment, the deficit is about 24 eV for oleclar ions of insulin. The size of the deficit increases with the intensity of the molecular ion signal, and the molecular weight of the protein; t is also larger for negative molecular ions than for positive molecular ions.
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    Organic Magnetic Resonance 31 (1993), S. 194-199 
    ISSN: 0749-1581
    Keywords: 2D NMR (COSY, ROESY, HETCOR, FLOCK) ; Conformation ; Computer modeling ; Molecular dynamics simulation ; Yuanhuacin ; Thymelaeaceae ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Stereochemical assignments of yuanhuacin were performed through two-dimensional COSY, ROESY, 1H and 13C shift correlation spectroscopy (HETCOR and FLOCK), and ambiguous assignments were resolved through molecular modeling comparisons. This combination of techniques is applicable for the assignment of 1H and 13C chemical shifts of polycyclic compounds containing high percentages of quaternary carbons.
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    Journal of Chemometrics 4 (1990), S. 323-330 
    ISSN: 0886-9383
    Keywords: Target factor analysis ; Spectrophotometry ; Amino acids ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The UV spectra of mixture solutions consisting of tyrosine, tryptophane, phenylalanine, cystine, histidine and 3,4-dihydroxyl phenylalanine have been measured. The numbers, identities and concentrations of the amino acids in the mixtures have been determined successfully using target factor analysis. The effects of the wavelength range and the selected sampling interval on the results are discussed. Twenty-five synthetic mixture samples have been analysed successfully. The average recoveries are 98.9 for Tyr, 96.5 for Trp, 105.6 for Phe, 98.1 for Cys, 98.9 for His and 106.4 for Di-phe. The results obtained are in good agreement with those obtained by the Kalman filter method.
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    Rapid Communications in Mass Spectrometry 8 (1994), S. 735-736 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Phthalates (dimethyl, diethyl, dibutyl, diallyl and dinonyl) and p-toluenesulfonates (methyl and ethyl) have been investigated as matrices for the fast-atom bombardment mass spectrometric analysis of fullerenes for the first time. Compared with spectra obtained using 3-nitrobenzyl alcohol and 2-nitrophenyl octylether as matrices, the fast-atom bombardment mass spectra of fullerenes with the two classes of compounds listed above as matrices are simple and show no fragment ions or adduct ions of fullerenes, and the matrices produce no background interference in the mass range of fullerenes.
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    Rapid Communications in Mass Spectrometry 8 (1994), S. 481-483 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: A method for obtaining fast-atom bombardment mass spectra of samples on paper is described in which a scrap trimmed from the paper of interest is adhered to the FAB probe tip with a strip of double-faced adhesive tape. After addition of suitable matrix (e.g. glycerol or thioglycerol) to the scrap, the probe is introduced into the mass spectrometer to obtain mass spectra in the usual manner. The method is demonstrated by analysing some paper containing hexadecyltrimethylammonium bromide, sodium dodecylbenzene sulfonate and vanillic acid. The method is also used to characterize paper chromatographic spots, by which the fractions of a mixture of three amino acids (L-glutamic acid, L-proline and L-valine) separated by paper chromatography are easily determined. The detection limit of the method is well below 10 ng with respect to hexadecyltrimethylammonium bromide.
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    Rapid Communications in Mass Spectrometry 9 (1995), S. 570-572 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The formation of singly charged oligomers and multiply charged monomers has been studied under different conditions with matrix-assisted laser desorption/ionization and it has been found that the concentration of analyte in matrix solution, as well as the matrix and substrate used, are factors that influence this process. The concentration of analyte in the matrix solution has a strong influence on the formation of singly charged oligomers. When α-cyano-4-hydroxycinnamic acid is used as matrix, more doubly charged monomeric molecular ions are observed than when sinapinic acid is used. By using a nitrocellulose membrane instead of a silver plate as substrate, we find more multiply charged monomers and dimers in the spectra, especially in the case of high mass proteins, such as albumin. It seems that the formation of multiply charged monomers and oligomers is influenced by the overall amount of charge that the sample carries.
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    Journal of Raman Spectroscopy 21 (1990), S. 203-205 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Fourier deconvolution technique was applied to the analysis of Raman OH stretching spectra in H2O2—H2O mixtures. An intensity decrease and a low-frequency shift of the resolved high-frequency component at 3635 cm-1 was established and can be used in the elucidation of physical models explaining the existence of weakly hydrogen-bonded OH oscillators in liquid water.
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  • 77
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The OD stretching spectra of D2O for temperatures from 5 to 90°C and for concentrations (D2O in H2O) from 100 to 10 mol-% were studied. These spectra were treated by means of the Fourier deconvolution technique for the first time.Using the positions of the resolved components the coupling constants for intra- and inter-molecular and Fermi resonance interactions and all parameters according to the presented model, for all investigated temperatures, were evaluated. A gradual decrease in all interactions was observed in the concentration study, in accordance with expectations and in agreement with the results for dilute solutions of H2O in D2O.The temperature behaviour of the coupling constants and other parameters were in accordance with the corresponding data for H2O. The only exception is the temperature behaviour of the intramolecular coupling constant. The greater mass of the D atom is one of the probable reasons that lead to the smaller sensitivity of OD frequency to the hydrogen bond fluctuations.All the results verify the assignments and assumptions made according to the model presented and support the continuous model for the water structure.
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    Journal of Raman Spectroscopy 19 (1988), S. 405-412 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The structure of the Raman OH stretching band of water has been investigated from 4 to 90 °C using a Fourier deconvolution technique. The overlapped components in the isotropic and anisotropic spectra have been resolved. The information on the positions of the components in the deconvoluted spectra was used for calculation of the constants for intra- and inter-molecular coupling and Fermi resonance and for an estimation of the component frequencies according to the model presented. For the first time, the value of the asymmetric Fermi resonance constant and the temperature dependences of all coupling constants have been obtained. Their temperature behaviour is in good agreement with the data in the literature concerning the different phases of water. It was established that the intramolecular coupling constant increases and the intermolecular coupling constant decreases as the temperature increases. The Fermi resonance constant for symmetric components tends to decrease with increasing temperature. The decrease in the symmetric Fermi resonance interaction with increasing temperature is due to the increase in the distance between the unperturbed fundamental and overtone band positions. The asymmetric Fermi resonance constant tends to increase with increasing temperature and this determines the strengthening of the asymmetric Fermi resonance interaction, which exhibits a limiting value at high temperatures.
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    Journal of Microcolumn Separations 4 (1992), S. 411-417 
    ISSN: 1040-7685
    Keywords: capillary electrophoresis ; superox-coated capillaries ; proteins ; protein digests ; peptides ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Fused silica open tubular columns treated with Superox 0.6 and 4 for capillary electrophoresis were evaluated. Excellent separations of proteins were obtained. Column effeiciencies of over 700,000 theoretical plates were achieved for basic proteins. The relative standard deviations (RSDs) in migration times for these proteins were below 1%. Comparisons were made of the electropherograms of α-, β-, γ-, and δ-chymotrypsins. Three different protein digestion reagents were used to produce complex peptide mixtures for analysis: trypsin, chymotrypsin, and pepsin. Each reagent produced a unique mixture of peptides. Capillary electrophoresis was used to elute the peptides, yielding highly efficient and reproducible separations.
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  • 80
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Positive ion fast atom bombardment mass spectrometry of N-diisopropyloxyphosphoryl dipeptides and tripeptides showed a novel cleavage pattern in that only the N-phosphoryl fragment ions gave intense peaks while the C-terminal series of ions was suppressed. The base peak was the N-phosphoryl imino ion responding to the N-terminal residue. These advantages are superior to those of other types of N-protecting groups.
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  • 81
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    Journal of Microcolumn Separations 5 (1993), S. 331-339 
    ISSN: 1040-7685
    Keywords: capillary electrophoresis ; chemiluminescence detection ; sheath flow cuvette ; post-column reaction ; amino acids ; isoluminol thiocarbamyl derivatives ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A post-column reactor was designed for chemiluminescence detection in the capillary electrophoresis separation of isoluminol thiocarbamyl derivatives of amino acids. This system was characterized with respect to hydrogen peroxide concentration and flow rate, surfactant concentration, microperoxidase concentration, and mixing distance. A linear calibration curve (R 〉0.999) was constructed for isoluminol ranging from at least 30 femtomoles to the detection limit of 40 attomoles injected; the dynamic range of the instrument is at least three orders of magnitude. Detection limit for the isoluminol thiocarbamyl derivative of valine was 500 attomoles. The theoretical plate counts for the raw data are typically 1 × 105 for labeled amino acids, and a factor of two better for isoluminol.
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  • 82
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    Biological Mass Spectrometry 27 (1992), S. 428-434 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photofragmentation of an equimolar mixture of cycloheptatriene and [1, Me-13C2]toluene was studied with photons of wavelength 488 nm in order to obtain a direct comparison between the two isomers. The idea was to check the extent to which these photons could be used as a probe to study the fragmentation processes. Whenever feasible, the data were treated by a kinetic scheme and rate constants were obtained by a non-linear regression. It could be shown that the decay of both isomers follows a time behaviour described by two exponential decays. Evidence is presented that the faster decay leads to the benzyl ion. The photofragmentation of the [C7H7]+ ions follows a complex behaviour that can be superimposed by selective ion-molecule reactions.
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  • 83
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    Journal of High Resolution Chromatography 16 (1993), S. 689-692 
    ISSN: 0935-6304
    Keywords: Solid phase microextraction (SPME) ; Headspace analysis ; Headspace solid phase microextraction ; Environmental analysis ; Water analysis ; Solid samples ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The analysis of samples contaminated by organic compounds is an important aspect of environmental monitoring. Because of the complex nature of these samples, isolating target organic compounds from their matrices is a major challenge. A new isolation technique, solid phase microextraction, or SPME, has recently been developed in our laboratory. This technique combines the extraction and concentration processes into one step; a fused silica fiber coated with a polymer is used to extract analytes and transfer them into a GC injector for thermal desorption and analysis. It is simple, rapid, inexpensive, completely solvent-free, and easily automated. To minimize matrix interferences in environmental samples, SPME can be used to extract analytes from the headspace above the sample. The combination of headspace sampling with SPME separates volatile and semi-volatile analytes from non-volatile compounds, thus greatly reducing the interferences from non-target compounds.This paper reports the use of headspace SPME to isolate volatile organic compounds from various matrices such as water, sand, clay, and sludge. By use of the technique, benzene, toluene, ethyl-benzene, and xylene isomers (commonly known as BTEX), and volatile chlorinated compounds can be efficiently isolated from various matrices with good precision and low limits of detection. This study has found that the sensitivity of the method can be greatly improved by the addition of salt to water samples, water to soil samples, or by heating. Headspace SPME can also be used to sample semi-volatile compounds, such as PAHs, from complex matrices.
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  • 84
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    Journal of High Resolution Chromatography 19 (1996), S. 155-160 
    ISSN: 0935-6304
    Keywords: Solid phase microextraction (SPME) ; Headspace analysis ; Gastight syringe ; Water analysis ; Volatile organic compounds (VOCs) ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Headspace solid phase microextraction (headspace SPME) has been demonstrated to be an excellent solvent-free sampling method. One of the major factors contributing to the success of headspace SPME is the concentrating effect of the fiber coating toward organic compounds. The affinity of the fiber coating toward very volatile analytes, such as chloromethane, may, however, not be large enough for detection at the parts per trillion concentration level. Static headspace analysis, on the other hand, is very effective for these very volatile compounds. As analyte volatility decreases, the sensitivity of static headspace analysis drops. The complementary nature of these two sampling methods can be exploited by combining the SPME device with a gastight syringe. The sensitivity of the new sampling device is better than that of SPME for very volatile compounds or that of static headspace analysis for less volatile compounds. This new method can sample a wide range of compounds from chloromethane (b.p. -24°C) to bromoform (b.p. 149°C) with estimated limits of detection at the low parts per trillion level.
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  • 85
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    Journal of High Resolution Chromatography 21 (1998), S. 291-297 
    ISSN: 0935-6304
    Keywords: Gradient ; liquid chromatography ; micro-HPLC ; mixer ; electrospray mass spectrometry ; cytochrome c ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---This paper describes a new method for gradient elution at low flow rate. By adjusting the solvent composition flowing into a dynamic mixer, we can program the concentration of solvent, B, inside a dynamic mixer to form a time-resolved solvent gradient delivered to the column. The input gradient is related to the output gradient by the equation, Bin = Bout + τ × dBout/dt, in which τ is the gradient response time constant at specified flow rate, and Bin and Bout are input and output concentration of solvent B, respectively.
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  • 86
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    Organic Magnetic Resonance 27 (1989), S. 846-851 
    ISSN: 0749-1581
    Keywords: ESR ; Spin trapping ; Stereospecificity ; Cyclic nitrone ; Free radical ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The ability of ten cyclic nitrones, 5-alkyl-5-methyl-1-pyrroline N-oxides, to trap a variety of short-lived free radicals has been investigated using ESR spectroscopy. Stereospecific spin trapping by these nitrones has been demonstrated by comparison of the ESR spectra of their adducts with the ESR spectra of the corresponding 5-alkyl-5-methyl-1-tetrahydropyrrolyl-1-oxyls. Phenyl radical trans addition to these nitrones has also been proved.
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  • 87
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    Organic Magnetic Resonance 33 (1995), S. S154 
    ISSN: 0749-1581
    Keywords: EPR spin trapping ; 6,6,-dimethyl-3,4,5,6-tetrahydropyridine N-oxide ; 6-alkoxyl-2,2-dimethylpiperidine-1-oxyl ; aminoxyl (nitroxide) ; conformation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The addition reactions of CH3(CH2)3O·, (CH3)2CHCH2O·, (CH3)2CHCH2CH2O·, (CH3)3CO· and (CH3)2C(CN)O· radicals to a novel six-membered cyclic nitrone, 6,6-dimethyl-3,4,5,6-tetrahydropyridine N-oxide (M2PyO), generate the corresponding 6-alkoxyl-2,2-dimethylpiperidine-1-oxyl aminoxyl (nitroxide) spin adducts. In benzene solution at room temperature, the preferential conformation of these spin adducts appears to be the anomeric conformer with the alkoxyl group in the axial position according to EPR spectroscopic conformational analysis of these aminoxyls. The anomeric effect in these aminoxyls might be the combination of electrostatic and molecular orbital interactions.
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  • 88
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    Organic Magnetic Resonance 32 (1994), S. 36-39 
    ISSN: 0749-1581
    Keywords: NQR ; Natural hybrid orbitals ; Halogenated hydrocarbons ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The natural hybrid orbitals of halogen atoms in various halogen-substituted alkanes and benzenes have been calculated by the Fenske-Hall MO SCF method and natural hybrid orbital theory. Four consistent parameters i, s, d and π are derived to describe the nuclear quadrupole coupling constant (QCC) of the halogen isotopes 35Cl, 81Br and 127I, with modification by the asymmetry parameter η. A semi-empirical expression is proposed from a different point of view.
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  • 89
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    Journal of High Resolution Chromatography 18 (1995), S. 579-581 
    ISSN: 0935-6304
    Keywords: Deactivation ; Packed column SFC ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Residual adsorptive activity of reversed phase (RP) column packings used in supercritical fluid chromatography (SFC) can be significantly reduced by a dynamic in-situ silanization with diphenyltetramethyldisilazane (DPTMDS). RP-materials thus deactivated were characterized both chromatographically and by solid-phase 29Si NMR.
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  • 90
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    Journal of Microcolumn Separations 6 (1994), S. 217-221 
    ISSN: 1040-7685
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We have developed a new method to quantitatively determine ionized calcium and total calcium by using high performance capillary electrophoresis (HPCE) with indirect photometric detection. Other cations such as Na+, K+, and Mg+ can also be quantitatively determined. A 70 cm × 50 μm i.d. fused silica capillary was used for the separation. The detection window was located 25 cm from the cathodic end, and the detection wavelength was set at 214 nm. A 100 mM imidazole solution at pH 7.4 (adjusted with 5% H2SO4) containing 0.1% hydroxypropylmethylcellulose (HMC, 4000 centipoise) was used as background electrolyte. Whole serum was injected for 5 s at 15 kV for the determination of ionized calcium. The total calcium levels in a number of human serum samples were determined by HPCE and compared with the NIST reference method (atomic absorption), and the results agree with each other within 95% confidence. Two NIST standards were analyzed by HPCE, and the results fit each other perfectly. The ionized calcium levels in sera by this HPCE method have been compared with those obtained with ion-selective electrode (ISE) method, and the results were lower than those of ISE, which was what we anticipated. The effects of sample temperature and buffer pH were studied.
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  • 91
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    Journal of High Resolution Chromatography 13 (1990), S. 683-688 
    ISSN: 0935-6304
    Keywords: Capillary gas chromatography ; Recycle gas chromatography ; Microvalve ; Connectors ; Band broadening and peak distortion ; Activity ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Sources leading to band broadening and peak distortion have been studied in a capillary column recycle system, based on a commercial microvalve. The ferrule system was a major contributor to band broadening. It was found that the quality of connections is very critical but the internal volume of the valve is not important. The pressure pulses resulting from each switching operation produced some band broadening with substances that had just been transferred through the valve but no adverse effects were noticed when they had travelled some distance into the column. Flow into valve cavities and through tees also produced a drop in efficiency. It is not clear whether this is solely due to problems in column connection or if changes in flow pattern also contribute.The activity of the valve toward polar substances was also assessed. No attempt was made to deactivate valve surfaces. The components of the Grob test mixture were almost unaffected but highly polar and acidic compounds such as nitrophenol showed severe losses. No evidence for catalysis was found.
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  • 92
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    Journal of Raman Spectroscopy 21 (1990), S. 127-131 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence on silver colloids of the addition of KCI was directly investigated by means of transmission electron microscopy (TEM). It was found that the particle size increased and the surfaces of the crystal particles of the silver became covered with an overlayer. Additionally, the pattern of aggregation was found to be chain-like. These changes were very different from those caused by adding pyridine. The mechanism affecting the colloid and the intensity of the surface-enhanced Raman scattering signals of adsorbed molecules on adding KCl to silver colloid is discussed.
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  • 93
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    Journal of Raman Spectroscopy 25 (1994), S. 515-520 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Raman spectra excited at two laser wavelengths are used to study the damage in self-implanted silicon. Depending on the implantation conditions, a three-layer structure can be constructed: a damaged surface crystalline layer (dsc-Si), an amorphous layer (a-Si) and a damaged interior crystalline layer (dic-Si). Raman spectra can provide the structural details of these layers, together with the Rutherford backscattering-chanelling technique. Examination of the scattering intensities shows that the contribution to the Raman signals from different layers can be distinguished and separated. Further analysis of the Raman data reveals a defect-activated low-frequency band in the dsc-Si layer which is sensitive to the damage and may be used for the characterization of dsc-Si. For totally amorphlzed samples the two Raman spectra excited at 457.9 and 647.1 nm show different scattering intensity ratios for the optical- and acoustic-like phonons. This novel result may indicate a depth-dependent variation of the disordering in the amorphous layer. Quantitative comparison between the calculated and measured Raman scattering intensities provides the scattering efficiency ratios of dsc-Si and a-Si in samples comprising both dsc- and a-Si layers.
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  • 94
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    Biological Mass Spectrometry 27 (1992), S. 991-994 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several approaches have been proposed for the use of mass spectra from collisionally activated dissociation (CAD) to determine the isomeric composition of mass analyzed ions. As originally proposed, measurement at collision gas pressures (≍ 30% transmittance) yielding maximum CAD cross-sections provides improved precision, whereas differential isomeric scattering should not be an appreciable problem, despite earlier warnings. For the C2H4O+· ions from butan-1,3-diol, this CAD method found [CH3CHO+·] = 50 ± 4%, in agreement with values of 44 ± 6 and 45 ± 6% from two methods of neutralization-reionization mass spectrometry, but in contrast with 66 ± 5% from a proposed CAD methodology using high transmittance measurements. The agreement of the three methods also shows that the principle of linear superposition of spectra is applicable to CAD as well as to electron ionization mass spectra.
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  • 95
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    Organic Magnetic Resonance 27 (1989), S. 451-454 
    ISSN: 0749-1581
    Keywords: Photolysis ; Ketones ; CIDNP ; Exciplex ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photolysis of 4-acetyl-4-ethoxyformylcyclohexanone and 4-acetyl-4-phenylcyclohexanone in deuteriochloroform showed an unusual polarization which suggests that a singlet exciplex of the ketone with deuteriochloroform may be involved in the Norrish type I reaction.
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  • 96
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    Journal of High Resolution Chromatography 22 (1999), S. 666-670 
    ISSN: 0935-6304
    Keywords: Capillary electrochromatography ; mixed packing technique ; electroosmotic flow ; retention mechanism ; fast analysis ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mixed packing capillary electrochromatography (MP CEC) with the stationary phase comprising a physical mixture of strong cation exchange (SCX) phase and octadecysilyl (ODS) phase was developed. With the existence of a sulfonic acid group on the surface of SCX, not only could the electroosmotic flow (EOF) remain high at low pH, but also the hydrophilicity of the stationary phase was increased greatly, leading to broad adaptable ranges of both pH and organic modifier concentration in the mobile phase. At the same time, with the coexistence of C18 on the surface of ODS, both the retention and the resolution of samples were improved. Accordingly, MP CEC combined the advantages of both SCX and ODS columns. Effects of operation parameters on EOF and the capacity factors of solutes as well as the retention mechanism of such a column were studied systematically. In addition, MP CEC columns were used in the analysis of strong polar solutes as well as for the high speed separation of acidic, basic, and neutral compounds in a single run.
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  • 97
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    Journal of High Resolution Chromatography 23 (2000), S. 445-448 
    ISSN: 0935-6304
    Keywords: O-Aryl,O-(1-methylthioethylideneamino)phosphates ; retention prediction ; quantitative structure-retention relationship (QSRR) ; reversed-phase HPLC ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---Using factor analysis and stepwise linear regression methods, two parameters - CMR and ECCR - were selected from eight solute-related structure parameters as the most retention-influencing parameters. The relationships between the retention data (k ´) and the two structure parameters were established for 13 O-aryl,O-(1-methylthioethylideneamino)phosphate compounds under a wide range of experimental conditions. The retention data (k ´) of another seven compounds with similar structures were predicted using these QSRR equations. Good agreement was obtained between the experimental k ´ values and predicted ones.
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  • 98
    ISSN: 1076-5174
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Novel cystathionine metabolities, cystathionine sulfoxide and NAc-cystathionine sulfoxide, were identified in the urine of a patient with cystathioninuria using liquid chromatography/mass spectrometry with an atmospheric pressure chemical ionization interface system. NAc-cystathionine sulfoxide was discovered as a new metabolite of cystathionine in the urine of a cystathioninuric patient. The concentrations of cystathionine sulfoxide and NAc-cystathionine sulfoxide in this urine were also determined for the first time using this method, and were 28.69 ± 0.44 and 10.51 ± 0.49 mg g-1 creatinine, respectively. Neither compound was detected in the urine of healthy subjects.
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  • 99
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Arachidonic acid is oxidized to regioisomeric 5(S)-, 12(S)- and 15(S)-hydroxyeicosatetraenoic acids by the corresponding 5-, 12- and 15-lipoxygenases. These hydroxylated fatty acids can then be incorporated into cellular phos-pholipids. Negative liquid secondary ion tandem mass spectrometry using a high-energy collision regime in a tandem four-sector mass spectrometer was used to characterize regioisomeric hydroxyeicosatetraenoic acids and the corresponding hydroxyeicosatetraenoic phosphatidylcholine species. Collision-induced dissociation (CID) of the [M - H]- negative ion at m/z 319 from the hydroxyeicosatetraenoic acids regioisomers produced some similar product ions, such as m/z 301 [M - H - H2O]- and m/z 257 [M - H - (H2O + CO2)]-. In addition, product ions characteristic of the particular hydroxyeicosatetraenoic acid were formed from α cleavages adjacent to the hydroxyl moieties. Negative liquid secondary ion mass spectrometry of purified hydroxyeicosatetraenoate phosphatidylcholine species gave an ion at m/z 810 [M - CH3] -. CID of the m/z 810 ion gave product ions at m/z 283 and m/z 319, corresponding to stearate at the sn-1 position and hydroxyeicosatetraenoate at the sn-2 position, respectively. From CID of the negative ion at m/z 319 and examination of the product ion spectra, the hydroxyeicosatetraenoate regioisomer present in the phosphatidylcholine could be identified.
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  • 100
    ISSN: 0887-6134
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Long-chain unsaturated fatty acids (UFA) can easily be converted on a microgram scale to the corresponding 2-alkenyl-4,4-dimethyloxazolines by condensation with 2-amino-2-methylpropanol (AMP). These modified molecules with a ‘hidden’ carboxyl group have been proved to be a class of useful derivatives for gas chromatography/mass spectrometry (GC/MS) of UFA mixtures. While possessing very good GC characteristics, the title compounds show regular, well-recognizable diagnostic ion peaks of the double bond position in the chain. Detailed description of the method as well as electron impact (E1) mass spectra of derivatives resulting from mono-, di and polyenoic (maximally containing six double bonds) acids are presented.
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