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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 389-396 
    ISSN: 0887-624X
    Keywords: polyethylene ; polypropylene ; oxidation ; biodegradation ; C—H bond activation ; functionalization ; XPS ; ATR-IR ; surface ; Gif ; oxidase ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Modification of polyethylene and polypropylene film and powder surfaces with oxygen and hydrogen peroxide is promoted by nonporphyrinic, nonfree radical based iron reagents such as Fe3O(OCOCH3)6(C6H5N)3.5 and FeCl3 • 6H2O/picolinic acid. These oxidation systems introduced small amounts of carbonyl groups onto the surface of these hydrocarbon polymers. The most visible manifestation of this reaction was increased polyolefin wettability toward water. IR spectroscopy, XPS spectroscopy, and chemical derivatization all were used to verify that the reaction had occurred and that a chemically derivatizable surface had been prepared. The overall process produced a fraction of the density of functional groups introduced by conventional etching chemistry.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2049-2053 
    ISSN: 0887-624X
    Keywords: polyethylene ; grafting ; polymerization ; surface ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 27 (1992), S. 1266-1270 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A rapid method was developed for the analysis or polar conjugated bile acids by combined packed column super-critical fluid chromatography/mass spectrometry. Direct coupling of the column to the mass spectrometer was effected with a modified thermospray interface operated in the filament-on mode. Maximum sensitivity for the bile acid conjugates was achieved by recording the negative ions generated in the ionization process. The effects of vaporizer and source temperatures, repeller voltage and discharge conditions on the bile acid response were investigated. The mass spectra obtained for the common glycine and taurine conjugates yielded only the [M - H]- pseudo-molecular ions. In contrast with the taurine derivatives, the glycine forms produced a weak ion current and exhibited broad hands. The applicability of the technique is illustrated with a sample of human bile.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The preparation and characterization of DNA dumbbells that contain the 16 base-pair duplex sequences 5′G-C-A-T-A-G-A-T-G-A-G-A-A-T-G-C3′ (set 1) and 5′G-C-A-T-C-A-T-C-G-A-T-G-A-T-G-C3 ′(set 2) are reported. The dumbbells of set 1 have the duplex stem nucleated on both ends by Tn (n = 2, 3, 4, 6, 8, 10, and 14) loops. The dumbbells of set 2 have Tn (n = 2, 4, 8, 10) end loops. For the molecules of set 1, effects of end loop size on the electrophoretic mobility, CD and UV absorbance spectra, and cleavage by restriction enzymes, were investigated. Effects of loop size on the CD spectra and restriction enzyme cleavage of the molecules of set 2 were also examined. Optical melting curves of the molecules of set 1 were collected as a function of sodium ion concentration from 30 to 120 mM. These investigations revealed that as loop size decreases, the electrophoretic mobilities, rates of enzyme cleavage, and optical melting temperatures increase. For end loops with at least three T's the observed increases are inversely proportional to loop size. The behavior of the dumbbell with T2 end loops departs from this linear dependence and is anomalous in every experimental context. For molecules with end loops comprised of at least four T's CD spectra were virtually indistinguishable. However, these spectra differed considerably from the CD spectrum of the T2-looped molecule. The CD spectrum of the dumbbell with T3 end loops displayed features common to the dumbbells with larger loops and T2 end loops. Thermodynamic evidence that the terminal G · C base pairs (bps) nucleating the T2 end loops were intact was obtained from a comparison of the melting temperature of this molecule with that of a DNA dumbbell containing the 14 central bps of the set 1 duplex sequence linked instead by end loops comprised of the four base sequence, C-T-T-C. The tm of this latter molecule was determined to be 9°C less than that of the former dumbbell assumed to contain a 16-bp stem and T2 end loops. One- and two-dimensional proton nmr measurements performed on the dumbbell of set 2 with T2 end loops and the same sequence with unpaired T's on the ends also verified formation of the T2 end loops, indicated the duplex residues of the dumbbell were in the B form, and showed that the first 3 bps adjoining the loops are distorted. Results are compared with several recently published relevant studies.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 32 (1992), S. 1695-1702 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Helix propagation of the S-peptide sequence (residues 1-19 of ribonuclease A) in 2,2,2-trifluoroethanol (TFE) solutions has been investigated with CD and nmr Overhauser effect spectroscopies. In this study, the S-peptide helix is covalently initiated at the N-terminus through disulfide bonds to a helix scaffold derived from the N-terminal sequence of the bee venom peptide apamin. The entire S-peptide sequence of this hybrid sequence peptide becomes helical at high proportions of TFE. Residues 14-19 of the S-peptide are not helical in the free peptide in TFE, nor are they helical in ribonuclease A. The “helix stop” signal encoded by the S-peptide sequence near residue 13 does not persist at high TFE with this hybrid sequence peptide. The helix-stabilizing effects of TFE are due at least in part to facilitated propagation of an extant helix. This stabilizing effect appears to be a general solvation effect and not due to specific interaction of the helical peptide with TFE. Specifically these data support the idea that TFE destabilizes the coil state by less effective hydrogen bonding of the peptide amide to the solvent. © 1992 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0749-1581
    Keywords: 1H and 13C NMR chemical shift assignments ; Tricyclic ketoalcohol ; COSY ; RELAYH Long-range HETCOR ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Diels-Alder cycloaddition of a mixture of 1- and 2-methylcyclopentadienes (1a and 1b, respectively) to 2-methoxy-p-benzoquinone (2) gave a mixture of isomeric endo [4 + 2] cycloadducts (3a-3d). Fractional recrystallization of this product mixture from EtOAc-hexane gave 6-methoxy-1-methyl-1α,4α,4aα,8aα-tetrahydro-1,4-methanonaphthalene-5,8-dione (3a). Reaction of 3a with NaBH4 in the presence of cerium(III) chloride resulted in the selective reduction of the less hindered C=O group in 3a, thereby affording 8-hydroxy-7-methoxy-4-methyl-1α,4α,4aα,8β,8aα-tetrahydro-1,4-methanonaphthalen-5(1H)-one (4). The 1H and 13C NMR spectra of 4, a novel tricyclic ketoalcohol, have been completely assigned by using a combination of one- and two-dimensional NMR techniques.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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