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  • Analytical Chemistry and Spectroscopy  (14)
  • 2015-2019
  • 1990-1994  (14)
  • 1930-1934
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Chemometrics 4 (1990), S. 61-77 
    ISSN: 0886-9383
    Keywords: Infrared ; Spectroscopy ; Spectrometry ; Retrieval ; Confirmation ; Chemometrics ; Adequate peaks ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the series of analytical techniques for identification of chemical substances, infrared spectrometry presents by far the highest information content. However, the information is most complicated too. It concerns a multitude of band positions, band intensities and band shapes, which, moreover, can be disturbed by matrix and other effects. The high redundancy, however, allows conclusions to be made by a qualitative, subjective procedure.IR is often used to prove the equality between a sample and a reference material, e.g. in quality control of a production process. In forensic control, the question to be answered is mostly not to prove equality, but whether or not the presence of a compound in a sample, e.g. a drug, can be proved. Moreover, testing has to be performed according to objective rules.To fulfil these requirements, a new retrieval algorithm, the ‘Adequate Peaks Search’, is presented. It concerns representing the reference spectra by sets of adequate peak positions and the sample spectrum by a set of all peak positions, whereafter the cross-sections of the sample set and the reference sets are determined. The concept ‘adequate peak’ is defined and criteria have been formulated to evaluate the results into a positive (presence of the analyte is proved) or negative (presence is not proved) conclusion.The detection limit when the Adequate Peaks Search (APS) method was applied was four to seven times lower than that attained by a number of experts.
    Additional Material: 8 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 28 (1993), S. 635-642 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The potent endectocide 23-(O-methyloximino)-F28249α and related compounds were identified and characterized by mass spectrometry. The fragmentation pathway of 23-(O-methyloximino)-F28249α was identified by its high-resolution mass spectrum and the electron impact unit mass spectra of its homologs. This fragmentation pathway is presented and discussed.
    Additional Material: 6 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 29 (1991), S. S118 
    ISSN: 0749-1581
    Keywords: 103Rh NMR ; 31P NMR ; Inverse 2D NMR ; Square planar ; Cation ; Diphosphine ; Paramagnetic shift ; Chemical shift correlation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of new and known Rh(I) complexes [Rh(R2P(CH2)nPR2)2]Y and [Rh(diene)(R2P(CH2)nPR2)]Y (R = Me, Et, Ph, C6F5, C6H4CF3; Y = Cl, ClO4, PF4, BF4, OSO2CF3; diene = norbornadiene, cyclooctadiene) were prepared and their 103Rh NMR spectra were recorded on a 100-MHz spectrometer by using inverse two-dimensional 31P, 103Rh{1H} NMR. This technique provides quick access to 103Rh NMR data (2-8 h for ca. 0.1 M samples) when dealing with Rh-phosphine complexes. The 103Rh NMR data are discussed. All δ(103Rh) of the cationic Rh(I) complexes appear at the lower frequency end of the Rh(I) range, i.e. between -1350 and + 200 ppm, which is in agreement with the fact that the Rh shift is determined by σp and with a large ΔE in square-planar d8 complexes. The relative change in ΔE between complexes is not large and the changes in paramagnetic shift for these complexes are essentially determined by their relative σ-donor capacities. δ(103Rh) shows an inverse correlation with δ(31P), which was rationalized by invoking the chelate ring size containing the Rh centre and the bidentate phosphine ligands.
    Additional Material: 1 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 6 (1992), S. 46-53 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Substituted cinnamic acids were dimerized, under fluorescent or UV light, as a glassy coating on a vial then subsequently analysed by GC/MS. Mass Spectrometric analysis of the dimers formed by each acid allowed the assignment of the dimer as a truxillic or truxinic structure since these structures had distinctive fragmentation patterns; the breakdown of the truxillic acids involves a McLafferty rearrangment before fragmentation occurs, whereas the truxinic acids, which have both carboxy groups on one side and both aromatic groups on the other, fragment asymmetrically to give characteristic stilbene and dicarboxylate fragments. It is apparent from the results of the dimerization of the lcinnamic acids that, under the conditions used here, if the monomeric acid had the capacity for hydrogen bonding using the ring substituent as well as the carboxy group, the dimerization products would be overshelmingly truxillic in structure. However, if only the carboxy group could hydrogen bond, the products would be almost exclusively traxinic in structure.
    Additional Material: 9 Ill.
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  • 5
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A peptide comprising 37 amino acids of the antigen binding site of a monoclonal antibody directed against glycoprotein D of herpes simplex virus was synthesized. The synthetic peptide and the impurities formed in the synthesis were characterized by capillary electrophoresis/ionspray mass spectrometry and by 252Cf plasma desorption-time of flight mass spectrometry. The measured average molecular mass of the synthetic peptide was 4627.16 Da, which was only 0.08 Da higher than the calculated value (4627.08 Da). The plasma desorption mass spectrum of the synthetic peptide showed a protonated molecule at m/z 4624.1, which was 4 Da lower than the calculated one (4628.09 Da). The amino acid sequence of the peptide was confirmed in part by electrospray (ionspray) mass spectrometry using a high nozzle skimmer voltage difference. Five impurities were separated and identified by capillary electrophoresis/mass spectrometry and two of them also appeared in the plasma desorption mass spectrum.
    Additional Material: 6 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 23 (1994), S. 71-74 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Using gas chromatography/mass spectrometry we have observed six peaks in the single ion chromatograph at m/z 674 of the alkaline extract of barley straw cell walls. The breakdown pattern of these ions suggests that they could all be isomers of 5,5′-bis-dehydroferulic acid. Since only the 5,5′ linkage is reported to be present in plants this tentatively suggests that these compounds exhibit stable orientational isomerism about this bond. Plausible breakdown mechanisms are presented which allow for the complete assignment of structure to all the isomers. These mechanisms suggest that the two pairs of breakdown ions at m/z 556 and 467, and 265 and 193 are representative of trans and cis double bonds, respectively.
    Additional Material: 5 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 25 (1990), S. 317-322 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dicyandiamide (DCDA) is used as a chemical additive in the fast atom bombardment (FAB) matrix 3-mercaptopropane-l,2-diol (thioglycerol) and propane-l,2,3-triol (glycerol). It is demonstrated that DCDA can be used to generate adduct ions [M + H + DCDA]+ for a variety of common organic functional groups to confirm the molecular ion [M + H]+. It is particularly useful for aromatic and alkyl amines and these compounds were therefore investigated in greater detail. Primary and secondary amines on heating react with DCDA to produce biguanides. DCDA can be used as a derivatizing reagent, but the reaction times are typically longer than 12 h and, therefore, it has limited utility. Biguanides can be detected at the nanogram level in full-range FAB mass spectral analysis.
    Additional Material: 3 Ill.
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  • 8
    ISSN: 0749-1581
    Keywords: Tigogenin ; DQCOSY ; TOCSY ; HMQC ; HMBC ; Selective reverse INEPT ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A glycoside extracted from the rhizomes of Agave americana was identified as 3-O-[{{β-D-xylosyl(1 → 3)}{β-D-xylosyl(1 → 3) - β - D - glucopyranosyl(1 → 2)} - β - D - glucopyranosyl(1 → 4)} - β - D - galactopyranosyl] - (25R) - 5α - spirostan-3β-ol by concerted use of proton and carbon-13 2D NMR methods. Complete assignments for the sugar resonances were obtained with standard methods, but the presence of chemical shift degeneracies prevented an unequivocal determination of two of the glycosidic linkage points by the HMBC experiment. Further two-dimensional experiments failed to resolve the ambiguity, but a clear identification of the linkages was obtained using a selective reverse INEPT experiment with homonuclear double resonance.
    Additional Material: 6 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 32 (1994), S. 552-553 
    ISSN: 0749-1581
    Keywords: NMR ; 15N NMR ; Cyanamide ; Phenylcyanamides ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 15N NMR chemical shifts are reported for cyanamide, phenylcyanamide and nine substituted phenylcyanamide derivatives. Results are discussed in terms of the degree of the π interaction between the cyanamide moiety and the aromatic ring and the stereoelectronic influence of the substituents.
    Additional Material: 1 Tab.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 22 (1991), S. 1-9 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Raman spectra were obtained from PtO, Pt5O6, Pt3O4, α-PtO2, β-PtO2, MxNayPt3O4 (M = Co, Ni), PtCoO2 and MPt3O6 (M = Mn, Co, Cd). An enumeration of the allowed Raman modes is made for all of these oxides except Pt5O6, for which the structure is unknown. Polarization measurements allow symmetry species assignments to be made for the lines from α-PtO2 and PtCoO2, and a likely assignment of the lines from β-PtO2 is made by analogy with rutile-structured materials with the rutile structure.
    Additional Material: 15 Ill.
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