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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 10 (1977), S. 676-681 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 9 (1976), S. 701-704 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 9 (1976), S. 705-710 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The addition reaction of the radicals formed from 2,2∢zobisisobutyronitrile(AIBN), diisopropyloxydicarbonate(DISOP), or benzoyl peroxide(BPO) to methyl methacrylate-β-d2(MMA-β-d2) or methyl tiglate(MTA) has been investigated at 30°C by the spin trapping technique. The tail and head addition of the radicals were detected for MMA-β-d2, and only the tail addition was observed for MTA.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 8 (1982), S. 141-146 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The interaction of γ-cyclodextrin(γ-CD) with sodium 1-pyrenesulfonate(PS) was studied spectrophotometrically. γ-CD was found to cause much larger decrease in the absorption maxima of PS than β-CD. The fluorescence spectra of PS in the presence of γ-CD showed excimer emission, while those of PS with β-CD showed only monomer emission, indicating that γ-CD forms 1∶2 (γ-CD∶PS) complexes in which two PS molecules are included in the γ-CD cavity in a face-to-face fashion. The binding isotherm showed a sigmoidal curve. The association constants were estimated by computer simulation of the binding curve. The 1∶2 (CD∶PS) complex was found to be much more stable (K=106 M−1) than the 1∶1 complex (K=1 M−1). At high concentration of γ-CD another γ-CD cooperates in binding two PS molecules, resulting in the formation of a 2∶2 complex.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 5 (1981), S. 19-24 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Various polymers of aromatic vinyl compounds having haloalkyl groups at the both chain-ends were prepared by terminating the living anionic polymers with 1,2-dichloroethane or 1,4-dibromobutane. Using these polymers as initiators, 2-methyl-2-oxazoline was polymerized to result in the block copolymers.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The rate of radical copolymerization of optically active acryloyl-d-phenylglycine methyl ester (APM) with methyl methacrylate (MMA) or with methyl acrylate(MA) was dilatometrically measured in optically active solvents, D-or L-ethyl mandelate. The copolymerization rate of D-monomer in D-solvent was higher than that in L-solvent. The origin of the difference in the copolymerization rate was discussed using data of UV and 13C-NMR chemical shift and spin lattice relaxation time, T1, and the asymmetric solvent effect was concluded to be due to the difference in the interaction between propagating radical and solvent.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 11 (1984), S. 175-178 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The interaction of polyelectrolytes with ionic surfactants is studied by turbidimetry and electron micrography. The turbidity of the mixed solution of PVS (poly(vinyl sulfate)) and CTAB (cetyltrimethylammonium bromide) showed a sharp maximum at the mole ratio of 1∶1, indicating quantitative binding between PVS and CTAB. A multilayer structure was observed on the electron micrograph only at the mole ratio of PVS:CTAB=2∶1 with a spacing of about 25A. At the mole ratio of PVS:CTAB=1∶1, a single strand structure was observed. The system of ionene polymer (3,4) $$\left( {\begin{array}{*{20}c} + \\ {\text{N}} \\ \end{array} {\text{CH}}_{\text{2}} )_3 - \begin{array}{*{20}c} + \\ {\text{N}} \\ \end{array} {\text{CH}}_{\text{2}} )4} \right)$$ -SDS (sodium lauryl sulfate) forms a multilayer structure at the equivalent ratio of 1∶1 with a spacing of 20A.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In an expectation as potential media for photosensitized electron transfer reactions, polymers carrying both strong electrolytic and hydrophobic segments were prepared by the copolymerization of 2-acrylamido-2-methylpropanesulfonic acid (AMPS) and styrene. The AMPS segments were found to have a remarkable power to solubilize the hydrophobic segments into water, i.e., even a copolymer with a styrene mole fraction of 0,72 is still soluble in water. Salt effect on the reduced viscosity, broadening of NMR spectra in D2O, and enhanced excimer fluorescence of styryl groups in aqueous solution indicated a pronounced hydrophobic interaction of a number of styryl groups along the chain in the copolymer with high styrene content. 8-Anilinonaphthalene-1-sulfonic acid, 1,6-diphenyl-1,3,5-hexatriene, and a cyanine dye were used as fluorescent probes for the hydrophobic microdomains. The results suggested that the microdomains are highly hydrophobic in nature but less capable to solubilize the fluorescent probes than the surfactant micelles. An electron microscopic image of the copolymer was also discussed as a supporting evidence for the presence of microdomains.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 12 (1985), S. 255-263 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The magnetic properties of polymers containing nitroxyl, tetraphenylporphin (TPP)-Cu(II), -Ag(II), or -Co(II) in the side chains were studied by ESR and magnetic susceptibility(χM) measurements. The values of χM for the polymers containing nitroxyl, TPP-Cu(II), and -Co(II) were found to obey the Curie-Weiss law, and their magnetic moments showed the occurrence of a weak antiferromagnetic interaction between paramagnetic species. The value of χM for the polymer containing TPP-Ag(II) showed the presence of strongly interacting sites. This strong interaction possibly arises from a hyperexchange interaction through the C—O group situated among the Ag(II) ions. Polymers containing TPP-Co(II) adsorb oxygen below 180 K and the ratio of O2:Co(II) was found to be 1:1 at 77 K.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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