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  • Digitale Medien  (20)
  • 1985-1989  (20)
  • 1989  (20)
  • Chemistry  (19)
  • Engineering General
  • Life and Medical Sciences
  • Physics
Materialart
  • Digitale Medien  (20)
Erscheinungszeitraum
  • 1985-1989  (20)
Jahr
  • 1
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 190 (1989), S. 1309-1317 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Acetylene was polymerized by (η-Cp)2Ti(PMe3)2 at room temperature to give predominantly trans-polyacetylene. All properties are within the ranges reported for polyacetylene produced with Ti(OBu)4/AlEt3 as catalyst.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 915-928 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Aromatic diamines containing —SO2— and —S— moieties have been used to prepare soluble polyimides with ditrifluoromethyl methane bis(phthalic anhydride) (F-series polyimides) and polyamic acid with pyromellitic dianhydride (P-series). Gamma radiolysis gave G(S) values for scission between 1 to 2 with no crosslinking. Significant weight loss occurred with radiolysis is attributable to efficient —SO2— bond scission for the F-series polyimides, as well as imidization in the cases of P-series polyamic acids.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 897-913 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Superactive Ziegler-Natta catalysts have been prepared from a soluble MgCl2·2-ethyl hexanol adduct in the presence of organic esters through reactions with TiCl4 and activated with AlEt3/phenyltriethoxy-silane. Electron paramagnetic spectra (EPR) were used to elucidate the nature and amount of those Ti+3 ions not bridged to another Ti+3 ion; the chlorine bridged Ti+3 ions are EPR silent. The EPR spectra were attributed to two rhombic Ti+3 sites with principal values for the g-tensors (1.967, 1.949, 1.915; and 1.979, 1.935, 1.887). The total amount of the EPR species, obtained by double integration of the EPR spectra, is in close agreement with the concentration of isospecific catalytic sites determined by radiotagging. This suggests that the nonspecific sites are EPR silent. When o-phthalic ester was present during the catalyst synthesis, there appears an EPR signal at the free electron g-value. This signal was attributed to a Ti+3 phthalate species with resonance stabilization and spin delocalization; it is absent in the catalysts made in the presence of monoesters such as ethyl benzoate. The effects of monomer, O2, H2O, and I2 on the EPR spectra were investigated. The changes in the EPR spectral intensity and the total Ti+3 ions, the latter determined by redox titrations during a polymerization or catalyst aging, are described. The results were extensively compared with those observed for supported Ziegler-Natta catalyst prepared with crystalline MgCl2.
    Zusätzliches Material: 14 Ill.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 1149-1160 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Copolymers of 2,2,2-trifluoroethyl methacrylate (TFEMA) and N-p-methoxyphenyl citraconimide (MCM) have been synthesized. The Tg varies with composition reaching 150°C with 34% MCM. The copolymer has good radiation sensitivity according to both G values for chain scission and E-beam measurements. Though they have lower contrast than PMMA, they have much higher resistance to plasma etching. The resistance increases markedly with MCM content to values comparable to that for polyimides. Therefore, TFEMA-MCM copolymers of high MCM content can be useful as high temperature plasma etchable positive E-beam resists.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 1499-1514 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A precise method for the determinations of Ti+2, Ti+3 and Ti+4 was developed. The CW-procatalyst before activation contains mostly Ti+4 ions with 6% Ti+3 and 4% Ti+2 ions. Activation with AlEt3 alone at room temperature reduced all the titaniums to lower valence states consisting of 71% Ti+3 and 29% Ti+2. Reduction is incomplete when methyl-p-toluate was present as external Lewis base during activation: at 25°C the distribution of Ti+4 : Ti+3 : Ti+2 is 36% : 25% : 38%; the distribution at 50°C is 37% : 22% : 40%. Aging of the activated catalyst caused little or no changes in the distribution of [Ti+n]; whereas the catalytic activity decays rapidly with aging. The aged catalysts have polymerization activity comparable to the decreased activity of the catalyst during a polymerization. The [Ti+n] was determined for the CW-catalyst during the course of a decene polymerization; they were found to be Ti+4 : Ti+3 : Ti+2 = 30% : 27% : 43%, which did not change with polymerization time. These results suggest that the reducibility of Ti+4 species by AlEt3 or 3AlEt3/MPT to different valence states is predicated by their structures. These species do not undergo further changes in their oxidation states during either aging or polymerization. Their decays probably involve nonreductive metathesis reactions like those known for zirconium alkyls. Possible structures for the stereospecific and nonspecific sites are proposed.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 1539-1557 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The initial active site concentrations, [C*]0, have been determined with CH3OT radiolabeling for the Cp2ZrCl2/MAO and CpZrCl3/MAO catalysts (Cp = η5 : cyclopentadienyl, MAO = methyl aluminoxane). Almost all the Zr are found to be catalytically active in 70°C ethylene polymerizations; [C*]0 = [Zr] and [C*]0 = 0.8[Zr] at Al/Zr ratios of 104 and 103, respectively. Lowering the temperature to 50°C and Al/Zr to 5.5 × 102 reduces [C*]0 to 0.2[Zr]. The rate constant of propagation at 70°C was calculated to be 1.6 × 103(M s)-1 for both catalysts at Al/Zr = 1.1 × 104; the values are decreased fivefold and tenfold, respectively, for the CpZrCl3 and Cp2ZrCl2 systems. The usage of 14CO to determine the propagating Zr-P species was investigated. With regard to the time of reaction of 14CO with the polymerization mixture, the initial phase is attributed to reversible CO complexation and reversible migratory insertion. The second slower phase may be due to the formation of enediolate. During the course of a batch polymerization the 14C radioactivity incorporated is small compared to the number of active sites found by CH3OT determination; it is only ca. 10% of [C*]0 at maximum rate of polymerization. Therefore, 14CO radiolabeling cannot be used to count C*.
    Zusätzliches Material: 16 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 1525-1538 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The reactions occurring between the components of metallocene and methylaluminoxane (MAO) catalyst leading to the reduction of the former were studied by electron paramagnetic resonance (EPR). At low Al/Zr ratios, CpZrCl3 (Cp = η5-cyclopentadienyl) was reduced to simple trivalent Zr species (g = 1.998, a(91Zr) = 12.3 G) without other superhyperfine splittings. At higher Al/Zr ratios the reactions proceed further to form two CpZr(III) hydrides (g = 1.991, a(H) = 5.5 G; and g = 2.00, a(H) = 3 G). Two CpTi(III) hydrides were also produced by the reaction of MAO with CpTiCl3 (g = 1.989, a(H) = 7.4 G, a(Ti) = 8 G; and, g = 1.995, a(H) = 4.5 G, a(Ti) = 8 G). In the case of Cp*TiCl3 (Cp* = η5-pentamethyl cyclopentadienyl) initially a multitude of paramagnetic species were formed. After long reaction time the final products show EPR features consistent with two η3: η4-(1,2,3-trimethyl-4,5-dimethylene cyclopentadienyl)hydrido Ti(III) species: the abundant one with g = 1.999, (H, sextet) = 9.5 G, a(Ti) = 9.5 G, and a weaker one of g = 1.975, a(H) = 4.8 G. All the five protons of these species and as well as those in the Cp hydrido complexes of Ti and Zr undergo facile H—D exchanges with D2. MAO is important in the formation of these hydrides because they are not formed by trimethyl aluminum reduction. The presence of tetrahydrofuran suppresses the hydride formation. The possible structures for the hydrido species and reactions producing them are discussed.
    Zusätzliches Material: 14 Ill.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 1571-1588 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Acetaldehyde and chloral were copolymerized using triethyl aluminum catalyst. The copolymer (ACC) obtained with equimolar monomer feed is not alternating in structure as it was once thought to be; it is comprised of two fractions differing in MW and composition. ACC has good thermal stability which is further improved by endcapping. Radiolysis in vacuo caused depolymerization with a G(M) value (number of monomers produced per 100 eV) of about 4000 to 80% completion. The G(S) value for chain scission is 1.9. These processes are effectively inhibited by benzoquinone. Oxygen markedly increases G(M) to ca. 18,000 and 〉 97% completion. Addition of tetrabutyl ammonium salt or tetramethyl urea has no effect on the depolymerization, whereas the addition of di-t-butyl-p-cresol causes an induction period after which normal unzipping ensues. Even UV photolysis of ACC in the presence of oxygen produces monomer with a quantum yield of 1.7, but very little photolysis occurs in the absence of oxygen. Gamma radiolysis sensitized by (C6H5)2IPF6 has G(M) value of 32,700. These results are very similar to the radiolysis and photolysis of the homopolymer of monochloroacetaldehyde and reinforce the mechanisms proposed for them. The E-beam sensitivity of ACC is about 3 × 10-6 C cm-2.
    Zusätzliches Material: 13 Ill.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 3343-3352 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Polyamic acids synthesized from di-trifluoromethyl methane bis(phthalic anhydride) and 4,4′-diaminophenyl sulfone and 4,4′-diaminophenyl ether were found to have excellent negative E-beam resist properties. The best materials contain about 90% imidized structural units having sensitivities of 1.5-2.5 μC cm-2 and contrast of 1.0-1.3. Polyamic acid of pyromellitic dianhydride and 4,4′-diaminophenyl sulfone imidized to 97% exhibits useful positive E-beam resist properties. Radiation induces imidization or chain scission to alter the solubility of the resist polymers resulting in the formation of latent images.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Proteins: Structure, Function, and Genetics 6 (1989), S. 231-239 
    ISSN: 0887-3585
    Schlagwort(e): phosphotyrosine linkage ; protein-DNA transesterification ; enzyme mechanism ; DNA-protein covalent complex ; Chemistry ; Biochemistry and Biotechnology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Medizin
    Notizen: Tyrosine 319 of E. coli topoisomerase I is shown to be the activesite tyrosine that becomes covalently attached to a DNA 5′ phosphoryl group during the transient breakage of a DNA internucleotide bond by the enzyme. The tyrosine was mapped by trapping the covalent complex between the DNA and DNA topoisomerase I, digesting the complex exhaustively with trypsin, and sequencing the DNA-linked tryptic peptide. Site-directed mutagenesis converting Tyr-319 to a serine or phenylalanine completely inactivates the enzyme. The structure of the enzyme andits catalysis of DNA strand breakage, passage, and rejoining are discussed in terms of the available information.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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