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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 685-693 
    ISSN: 0887-624X
    Keywords: photoreactive polyimides ; chalcone-containing polymers ; photocrosslinking ; photosensitive ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two chalcone-derivative isomers, 4,4′-diaminochalcone (4DAC) and 3,3′-diaminochalcone (3DAC), were synthesized and used as monomers together with tetracarboxylic dianhydrides to prepare novel photosensitive polyimides that contain a chalcone moiety in the main chain. The polyimides were characterized and their photochemical behavior was investigated as thin films and in solutions with the aid of ultraviolet and infrared spectroscopy. Compared with 4DAC-based polyimides, the 3DAC-based polyimides exhibited lower glass transition temperatures and higher photocrosslinking rates of the carbon-carbon double bond as well as higher photosensitivities obtained from the exposure characteristic curves, suggesting that an increase in the photoreactivity of the 3DAC-based polyimides might arise from the improved flexibility of their backbones. The polyimide from 3DAC and 6FDA (2,2-bis[3,4-dicarboxypheny]hexa-fluoropropane dianhydride) showed a photosensitivity of 33 mJ/cm2 with a contrast of 1.5 upon light irradiation using a Xenon lamp. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 685-693, 1998
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 23-42 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Statistical radii of gyration, second virial coefficients, and intrinsic viscosities of sharp fractions (M̄w/M̄n ≈ 1.1) of polyisobutylene (PIB) covering a wide range of molecular weight (1.6 × 105 to 4.7 × 106) were determined in isoamyl isovalerate (IAIV) at a number of temperatures ranging from 20 to 60°C, in n-heptane at 25°C, and in cyclohexane at 25°C by light-scattering and viscosity measurements. It was found that IAIV at 22.1°C is a theta solvent for PIB. Analysis of the data by the methods described in preceding papers of this series indicated that, except for minor differences, the conclusions derived from similar studies with polychloroprene, polystyrene, and poly-p-methylstyrene hold equally for solutions of the typical linear polymer investigated here. In particular, no decisive evidence for the drainage effect was found.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 5 (1994), S. 56-62 
    ISSN: 1042-7147
    Keywords: Photoinitiator ; Photopolymerization ; Laser imaging ; Laser spectroscopy ; Photochemistry ; 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
    Notes: The design of an efficient photosenzitizer/photoinitiator combination is partly governed by a better understanding of the excited state processes involved. In the present paper, the photochemistry of a thiopyrylium salt (TP) as photosensitizer and of a tetraperester of benzophenone, tetra t-butyl peroxycarbonylbenzophenone (BTTB) as initiator, used in laser imaging applications has been investigated. The reactivity of the triplet states of both compounds BTTB and TP was studied by time-resolved laser absorption spectroscopy. The laser excitation of TP leads to a long-lived triplet state (lifetime 20-25 μsec) and a second species arising from the triplet state which cannot yet be characterized. Under laser excitation, BTTB gives a longlived transient arising from the cleavage of the peroxy bond. The short-lived triplet state cannot be observed on the nanosecond timescale. The triplet state lifetime has been evaluated from quenching experiments and found to be about 1 ns in acetonitrile. The deactivation of the TP triplet state by BTTP was considered, the deactivation constant was found to be equal to 6.6 × 107 m-1/sec in acetonitrile. The initiation mechanism is discussed.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aus Carpophoren von Amanita muscaria (L.′ ex Fr.) HOOKER wurden neu β-n-Butyl-D-glucopyranosid, (-)-R-4-Hydroxy-pyrrolidon-(2), Uracil, Hypoxanthin und (-)-1,2,3,4-Tetrahydro-1-methyl-β-carbolin-3-carbonsäure isoliert.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 52 (1969), S. 808-812 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Caryopteris clandonsis BUNGE (Verbenaceae) enthält in der Wurzelrinde mehrere Farbstoffe, von denen einer, α-Caryopteron, C15H12O4, kristallisiert und rein erhalten werden konnte. Er wurde als 9-Hydroxy-α-dehydrolapachon (Ia) erkannt, wobei die Lage der Hydroxylgruppe unter Beiziehung der para-ortho-Chinonmlagerung nach PATERNÒ;-HOOKER, am Dihydroderivat festgelegt wurde.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 19 (1981), S. 143-147 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 23 (1985), S. 521-524 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 20 (1982), S. 45-51 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: No Abstract
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 18 (1980), S. 481-486 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Publication Date: 2015-07-14
    Description: Inference of gene sequences in ancestral species has been widely used to test hypotheses concerning the process of molecular sequence evolution. However, the approach may produce spurious results, mainly because using the single best reconstruction while ignoring the suboptimal ones creates systematic biases. Here we implement methods to correct for such biases and use computer simulation to evaluate their performance when the substitution process is nonstationary. The methods we evaluated include parsimony and likelihood using the single best reconstruction (SBR), averaging over reconstructions weighted by the posterior probabilities (AWP), and a new method called expected Markov counting (EMC) that produces maximum-likelihood estimates of substitution counts for any branch under a nonstationary Markov model. We simulated base composition evolution on a phylogeny for six species, with different selective pressures on G+C content among lineages, and compared the counts of nucleotide substitutions recorded during simulation with the inference by different methods. We found that large systematic biases resulted from (i) the use of parsimony or likelihood with SBR, (ii) the use of a stationary model when the substitution process is nonstationary, and (iii) the use of the Hasegawa-Kishino-Yano (HKY) model, which is too simple to adequately describe the substitution process. The nonstationary general time reversible (GTR) model, used with AWP or EMC, accurately recovered the substitution counts, even in cases of complex parameter fluctuations. We discuss model complexity and the compromise between bias and variance and suggest that the new methods may be useful for studying complex patterns of nucleotide substitution in large genomic data sets.
    Print ISSN: 0016-6731
    Topics: Biology
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