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  • Chemistry  (7)
  • Polymer and Materials Science  (6)
  • 1970-1974  (4)
  • 1960-1964  (3)
  • 1930-1934
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  • 1
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Infrared and Raman spectra of aqueous poly(rA-rU)·poly(rA-rU), the double-helical complex containing strands of alternating riboadenylate and ribouridylate residues, display significant differences from one another and from corresponding spectra of poly(rA)·poly(rU), the double-helical complex of riboadenylate and ribouridylate homopolymers. Parallel studies on the copolymer and homopolymer complexes by cesium sulfate density gradient centrifugation, ultraviolet absorption spectroscopy, hydrogenion titration, 1-N oxidation of adenine residues by monoperphthalic acid and X-ray diffraction reveal, however, that the geometry of base pairing between adenine and uracil is closely similar in each complex and apparently of the Watson-Crick type. Therefore the differences observed between vibrational spectra of poly (rA-rU)·poly (rA-rU) and poly(rA)·poly(rU) are not due to different base-pairing schemes but may be attributed to differences in vibrational coupling between vertically stacked bases. Vibrational coupling may also account for the differences between infrared and Raman spectra of the same complex. Thus, the present results indicate that infrared and Raman frequencies of RNA in the region 1750-1550 cm-1 should be dependent on the base sequence.
    Additional Material: 10 Ill.
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  • 2
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Four fragments (named K, L, M, and N) of Escherichia coli formylmethionine transfer RNA have been prepared by a partial digestion with ribonuclease T1 followed by a chromatographic separation with a DEAE-Sphadex (A-25) column and then a DEAE-cellulose column. The fragment K is the anticodon fragment with 19 nucleotides (previously reported). L is a fragment with 57 nucleotides involving the 3′-terminal (CCA). M is a fragment with 51 nucleotides which is equal to L except that M lacks 6 nucleotides at the 3′-terminal. N is a fragment with 20 nucleotides which involved the 5′-terminal and corresponds to the complementary half to L. The infrared absorption spectrum has been observed of each of these fragments and two equimolar mixtures L + N and M + N in D2O solutions at several temperatures. The results indicate that at 37°C, K has about 4 hydrogen-bonded base-pairs, L about 11, and M about 13. On the other hand, fragment N is found to have only three weak G-C pairs. For both L + N and M + N, 15-17 strong base pairs are found. The observations give direct support to the clover-leaf structure and at the same time provide information on the stability of each of the four arms in the structure.
    Additional Material: 13 Ill.
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  • 3
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Infrared absorption and x-ray diffraction measurements have been made of D,L-copoly-γ-benzylglutamate fibers (cast from dioxane solutions) with various D/L ratios and with various degrees of polymerization. It was found that each chain of these copolymers consists of a random coil portion and an α-helix portion and that the conformation of the latter is similar to the α-helix of pure poly-γ-benzyl-L-glutamate. It was also found that the fraction of the α-helix portion increases with the degree of polymerization of the copolymer. A simplified polymerization mechanism has been proposed for mixtures of D- and L-amino acid N-carboxyanhydrides. A model of the molecular conformation of the D,L-copolypeptide chains derived from this proposed polymerization mechanism is in good agreement with infrared, x-ray, and other measurements. Based on the results of these observations, we discuss the number of L- or D-residues linked in succession that is required for initiating the formation of an α-helix during the course of polymerization.
    Additional Material: 12 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 14 (1970), S. 2357-2376 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Gelation of poly(ethylene terephthalate) by heating at 263°-300°C was investigated. Under nitrogen flow, crosslinks were scarcely formed. However in air, degradation and crosslinking were common, and these were accelerated by purging gaseous and sublimable degradation products out of the system with a stream of air. The main component of the sublimate was terephthalic acid. Infusible and insoluble gel was treated with methanol at 260°C, and then the methanolysis products were separated into two parts. The methanol-insoluble part exhibited a polyene structure with ester groups, and the methanol-soluble part contained dimethyl terephthalate, ethylene glycol, and some 1,2,4-butanetriol. To clarify the relation between the crosslinking and the formation of vinyl ester groups, the degradation of vinyl methyl terephthalate was studied. Thermoxidative degradation of linear polyesters other than poly(ethylene terephthalate) was also studied. Poly(ethylene isophthalate) and poly(ethylene sebacate) were easily gelated. However, poly(trimethylene terephthalate) and poly(neopentyl terephthalate) were scarcely gelated. The primary reaction leading to crosslinking is assumed as follows. At first, the random scission of polyester chain may take place forming carboxylic acids, vinyl esters, aldehydes, etc. After accumulation of vinyl esters to some extent, vinyl polymerization of the esters takes place and network structures are formed.
    Additional Material: 14 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 1 (1963), S. 47-49 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 2 (1974), S. 609-621 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Raman specrum of β-adenosine-5′-phosphoric acid has been observed in its aqueous solution with 6471, 5145, 4880, 4579, 4579, and 3511 Å excitation. An examination of the manner of increase of the intensities of the Raman lines at 1580 and 1484 cm-1 of the adenine residue indicated that the electronic excited state corresponding to a weak absorption band at 276 nm is responsible for these Raman scatterings. This idea has been supported by a similar examination of the Raman spectrum of β-adenosine-3′,5′-cyclic phosphoric acid and an examination of the effect of temperature on the Raman spectra of poly rA and poly(rA-rU). A discussion is included of the geometrical structure of the adenine residue in its lowest-singlet electronic excited state, based on the vibrational structure of the fluorescence spectrum, the result of a normal coordinate treatment, and the result of a semiempirical Pariser-Parr-Pople calculation, as well as the Raman data.
    Additional Material: 7 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 1 (1963), S. 531-534 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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