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  • 1985-1989  (4,249)
  • 1988  (4,249)
  • Polymer and Materials Science  (3,199)
  • General Chemistry  (1,050)
  • 201
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: (E)-2-Methyl-1,3-pentadiene was polymerized with the AlEt2Cl-Nd(OCOC7H15)3-Al(iBu)3 system to a polymer consisting of 98-99% 1,4-cis-structure. The crude polymer was fractionated by successive extractions with boiling diethyl ether, heptane and toluene. Examination of the soluble fractions and of the residue to toluene extraction by NMR, X-ray and DSC techniques indicated that the crude polymer consists of macromolecules differing in stereoregularity. Evidence is reported that the crystalline residue after the toluene extraction has a 1,4-cis-isotactic structure. The existence of two different crystalline phases is shown and the respective cell parameters have been determined. α-Phase: a = 10,74, b = 13,04, c = 7,87 Å (-120°C), space group Pbca, Z = 8, Dc = 1,00 g · cm-3. β-phase: a = 9,30, b = 7,73, c = 7,90 Å (25°C), space group P212121Z = 4, Dc = 0,96 g · cm-3.
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  • 202
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Crystalline polymers of (E)-2-methyl-1,3-pentadiene, consisting almost exclusively of 1,4-cis units, obtained with the ternarycatalytic system AlEt2Cl-Nd(OCOC7H15)3-Al(iBu)3, exhibit two different crystalline forms. In this study, we determine the crystal structure of the form showing the highest melting point (175°C) through X-ray diffraction data from stretched and unstretched samples. Diffraction data from an unstretched (powder) sample were used to carry out a refinement procedure based on the Rietveld method. The space group is orthorhombic Pbca, the cell constants are a = 10,74, b = 13,04, c = 7,87 Å, and the polymer is isotactic.
    Additional Material: 4 Ill.
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  • 203
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Two non-ideal kinds of behaviour for solutions of liquid-crystalline side-chain polymer (LC polymer) solutes in nematic solvents of low molecular weight (LMW) are investigated, viz. immiscibility and induced smectic A phases. The former property already observed in the nematic state of some polysiloxanes is extended to polymethacrylates (or polyacrylates) leading to the conclusion that immiscibility is strongly influenced by the chemical structure of the whole macromolecule. The latter property responds in the same way as the former to molecular modifications, suggesting that they can be connected somehow.
    Additional Material: 9 Ill.
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  • 204
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of poly[oxy(2,6-dimethyl-1,4-phenylene)]s (PPE) (trivial names: polyphenylenether, polyoxyxylene, polyphenyleneoxide) with narrow molecular weight distribution were prepared by polymerization of 4-bromo-2,6-dimethylphenol and subsequent fractionation. The molecular weight dependence of the glass transition temperature obeys the Fox-Flory equation. Polystyrene (PS)/PPE blends (PS: number-average molecular weight M̄n = 144 000, ratio of weight- to number-average molecular weight M̄w/M̄n = 1,05) were prepared using PPE samples with molecular weights below the entanglement spacing of PPE, in order to obtain information about the influence of specific interactions on the linear viscoelastic properties in the plateau and terminal region. The iso-free-volume state turned out to be the most appropriate reference state to compare samples of various compositions. Low-molecular-weight PPE essentially acts as a solvent for polystyrene. The concentration dependence of the zero-shear viscosity η0 is proportional to φ3,6PS, φPS being the volume fraction of PS, and the temperature dependence of the logarithmic shift factor log aT indicates that interactions, which are responsible for the thermodynamic miscibility in this system, do not alter the linear viscoelastic properties of PS. The concentration dependence of the plateau modulus (G(0)N ∝ φ1,2 for PS/PPE-1500) blends is explained by an additional small elastic contribution of the short PPE chains to the plateau modulus at higher frequencies.
    Additional Material: 14 Ill.
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  • 205
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    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 189 (1988), S. 2219-2227 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of copolyesters 2 containing both linear mesogenic and non-linear non-mesogenic aromatic ester units was prepared and characterized for the ability of the latter to either modify or destabilize the liquid-crystalline (LC) properties of the former. The mesogenic units were formed from the reaction of 1,4-phenylene diacetate (3) with 4,4′-decamethylenedioxydibenzoic acid (5), whereas the non-mesogenic units were formed from reaction of the latter monomer with the diacetate of the non-linear biphenol, sulfonylbis(1,4′-phenylene) diacetate (4). The presence of the flexible spacer in each unit allows the copolyesters to form a nematic phase even at a content of non-mesogenic units as high as approximately 80 mole-%. Copolyester compositions with mesogenic unit contents approaching this limit for LC behavior appear to form melts which contain both nematic and isotropic phases below the isotropization transitions.
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  • 206
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    Die Makromolekulare Chemie 189 (1988), S. 2239-2243 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Equilibrium adsorption measurements of three anionic dyes on chitosan, under acid conditions, show that there is a 1 : 1 stoichiometry for the interaction of sulfonic acid groups on the dyes with protonated amine groups of the chitosan for mono-, di- and trisulfonated dyes. Comparison of the extents of N-acetylation calculated from equilibrium dye adsorption values with those determined by IR spectroscopy, for a series of chitosan samples covering a wide range of N-acetylation values, demonstrates that equilibrium adsorption measurements may be used for the analysis of chitin and chitosan.
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  • 207
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    Die Makromolekulare Chemie 189 (1988), S. 2269-2274 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The modification reaction of amylose with nicotinoyl chloride using pyridine as catalyst was studied. The structure of the resulting polymers was determined by means of IR, 1H and 13C NMR spectroscopy. A linear dependence of the reaction rate on polymer, nicotinoyl chloride and pyridine was found. The activation energy was found to be 32,2 kJ/mol. The hydrolysis in the heterogeneous phase showed that the release of the active compound is dependent upon the hydrophilic character of the modified amylose polymers, the temperature as well as the pH value of the medium.
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  • 208
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The synthesis and phase behaviour of liquid-crystalline acrylates and chloroacrylates with side-on fixed mesogenic groups are described. Polymers which have similar mesogenic groups but whose polymer backbones differ in chemical constitution exhibit identical liquid-crystalline to isotropic phase transformation temperatures (Tc). The glass transition temperature (Tg) decreases with increasing flexibility of the main chain and with increasing length of the terminal groups of the mesogenic side groups. All polymers with side-on fixed mesogenic groups exhibit a nematic phase. The domain texture indicates biaxial nematic phase behaviour. In copolymers consisting of mesogenic and non-mesogenic monomers, nematic phase behaviour is still observed, Tc is strongly depressed, and Tg is similar to that of the non-mesogenic homopolymer.
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  • 209
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    Die Makromolekulare Chemie 189 (1988), S. 2293-2302 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cold plasma can be applied to polymer chemistry especially when grafting is to be achieved. Multifunctional acrylate monomers could be grafted onto polypropylene after its surface was activated. Grafting, the final stage of this plasma-induced polymerization, is the consequence of a reaction of a macroradical, which has diffused to the surface of the substrate, with a reactive species created on the polypropylene surface. The rate of grafting was found to be smaller than the rate of monomer disappearance. The rate increases with the power, but no relation could be established between both.
    Additional Material: 8 Ill.
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  • 210
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Three techniques, i. e., the Lenka extrapolation method, the Stockmayer-Fixman method, and the extrapolation of the Mark-Houwink constants to a = 0,5 were applied to determine the unperturbed dimensions of ultrahigh-molecular-weight poly(isobutyl methacrylate). A correction term, depending on the exponent a of the Mark-Houwink relation, is suggested to be introduced into the Stockmayer-Fixman-Burchard equation.
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  • 211
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    Die Makromolekulare Chemie 189 (1988), S. 2357-2365 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Monte Carlo simulations are presented for binary (AB) symmetric polymer mixtures (chain lengths NA=NB=N) for the case that an attractive interaction ∊ exists between monomers of the same kind, and the limiting case that one species (B) is very diluted. It is shown that with increasing interaction strength ∊/(kB · T), T being the absolute temperature, the minority chains collapse to a very dense configuration, while the majority chains stay nearly Gaussian. Both chain radii, structure factors and numbers of nearest neighbour contacts are discussed.
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  • 212
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    Die Makromolekulare Chemie 189 (1988), S. 2367-2379 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 2H NMR is used to study the mobility of the alkylene chain in solid poly[(dimethyliminio)-alkylene]s (α,ω-ionenes) complexed with poly(styrenesulfonate). In 10, 10-ionene the alkylene chain motion was probed on samples selectively deuterated at the 1-, 2-, and 4-position as well as in the methyl part of the quaternary ammonium groups. 2H NMR spectra show that all positions in the polymethylene chains are involved in conformational jumps between trans and gauche states. The mobility of the methylene units adjacent to charged centres was found to be significantly reduced compared with that of units in the inner part of the chain. The charged quaternary ammonium groups themselves, however, do not take part in trans-gauche isomerization. An increase in mobility resulting from increasing the length of the alkylene chains between the charge centres was observed in 3,3-, 6,6- and 10,10-ionene complexes labelled in the 2-position. The differences in chain dynamics were also detected via EPR line shapes of small spin probe molecules incorporated into the complexes.
    Additional Material: 6 Ill.
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  • 213
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An original method based on IR spectroscopy has been developed in order to follow real-time photopolymerizations that take place in less than one second. Conversion versus time curves were directly recorded for various multiacrylic monomers irradiated in condensed phase, thus allowing an immediate evaluation of both the rate of polymerization and the amount of residual unsaturation in the UV-cured polymer. This method proved well suited to study the effect on the polymerization rate of the photoinitiator efficiency, the monomer reactivity, the light intensity, the film thickness, and the O2 inhibition. The dark polymerization that develops just after the UV exposure was investigated as a function of the degree of conversion and was shown to represent up to 60% of the total process. A comparison with other methods of kinetic analysis shows the unique advantages of real-time infra-red (RTIR) spectroscopy which permits to follow quantitatively and in situ ultra-fast polymerizations.
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  • 214
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Aromatic polyethers were prepared by bulk condensation of 2,6-difluoropyridine (1) with various silyalated diphenols and benzelnediols at temperatures between 140 and 240°C. Colorless products were obtained with inherent viscosities in the range of 0,4-1,4 dl/g. DSC measurements revealed that the polyethers derived from bisphenol-A, phenolphthalein, 4,4′-oxydiphenol and phenylhydroquinone are amorphous with glass-transition temperatures in the range of 90-190°C. Polyethers derived from hydroquinone or 4,4′-biphenyldiol are crystalline with melting points in the range of 200-270°C. Thermogravimetry in air indicates thermostabilities up to 450°C (at 5% loss of weight). Poly(pyridinediylether-co-ketoether)s (4) and poly(pyridinediylether-co-arylsulfoether)s (5) were obtained by cocondensation of 1 with 4,4′-difluorobenzophenone or 4,4′-difluorodiphenyl sulfone and various silylated aromatic diols. For these copolyethers inherent viscosities in the range of 0,6-1,0 dl/g were found, and tough films could be cast from solution. Incorporation of the pyridinediyl units was found to significantly lower the glass-transition temperatures. The copolyethers obtained from 1, 4,4′-difluorobenzophenone and hydroquinone or 4,4′-biphenyldiol are crystalline. Thermodynamical analyses indicate high heat-distortion temperatures (〉200°C) for annealed samples of these crystalline polyethers. Thermogravimetry conducted at a heating rate of 10°C/min in air only indicates a moderate thermostability.
    Additional Material: 6 Ill.
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  • 215
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    Die Makromolekulare Chemie 189 (1988), S. 2323-2330 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: α-(3-Dimethylaminopropyl)-ω-dimethylaminomethylpoly(oxyethylene)s (2a-e) were prepared from α-(3-aminopropyl)-ω-aminomethylpoly(oxyethylene)s (1a-e) (M̄n = 430-2300 g·mol-1), by the Wallach-Leuckart reaction, with a degree of transformation of —NH2 into —N(CH3)2 groups of 70-98%. The samples were characterized by means of IR spectrometry and Siggia's acylation method, adjusted for microdetermination. The polymers terminated with 3-dimethylaminopropoxy groups were transformed into the corresponding derivatives bearing quaternary ammonium end groups, and characterized both as dihydroxides and dichlorides. The content of the quaternary ammonium groups was found to differ considerably for the individual samples in the range of 19-97%. The reason for this variability was found not to be a low efficiency of the quaternization reaction, but the Hofmann-degradation giving rise to terminal vinyl groups of the polyether chain.
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  • 216
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The anionic ring-opening polymerization of mixtures of 2,2-dimethyltrimethylene carbonate and ∊-caprolactone in toluene as solvent, with sec-butyllithium or potassium dihydronaphthylide as initiator, results in the formation of polymers of the (A-X-B)n type, where A represents a poly(2,2-dimethyltrimethylene carbonate) block, B represents a poly(∊-caprolactone) block and X stands for a block of the two monomers with a composition gradient; n represents the number of portions by which the monomer mixture is added to the initiator or the living system. From the time-conversion curves it follows that the reactivity of the carbonate monomer is higher than that of the lactone. This difference in reactivity of the monomers is the reason for the special polymer architecture represented by (A-X-B)n. The properties of these polymers depend upon the ratio of the monomers and the number n of additions. The polymers are characterized by spectroscopic, thermoanalytical, and thermomechanical measurements.
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  • 217
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    Die Makromolekulare Chemie 189 (1988), S. 2341-2355 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dependence of viscous and elastic rheological functions on molar mass and molar mass distribution was investigated under shear flow conditions using concentrated solutions of polyacrylamides and polyacrylamide mixtures. The zero-shear viscosity η0 correlates with the weight-average molar mass M̄w; with increasing shear rate the corresponding controlling molar mass average tends to change to the number-average molar mass M̄n. It is shown that the analysis of the shape of the whole flow curve is a simple way to obtain qualitative information about molar mass distribution. Elastic forces are influenced mainly by the high-molar-mass tail of a molar mass distribution. The zero normal stress coefficient ψ0 depends on a molar mass average between M̄w and z-average molar mass M̄z·ψ0 increases with the 7,4th power of the molar mass for the polyacrylamides (not for the mixtures). The steady-state compliance Je(0) is, for the investigated system, independent of the absolute molar mass, but increases with the 5,5th power of the ratio M̄z/M̄w. The elasticity modulus G0(A) can be correlated with M̄n of the polyacrylamide samples and their mixtures. These investigations show that the analysis of various rheological functions can lead to a wealth of information about the molar mass distribution of a polymer.
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  • 218
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    Die Makromolekulare Chemie 189 (1988), S. 2719-2730 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The copolymerization of sulfur dioxide with methyl, ethyl, butyl or 2-ethylhexyl acrylate was studied. The influence of the composition of monomer feed and reaction temperature on the composition of the copolymers was investigated. The maximum content of sulfonyl units in the copolymers, obtained at -78°C, was found to be ca. 30 mol-% and to decrease with increasing temperature. The sequence distribution in the copolymers was determined by 13C NMR spectroscopy. It was proved that acrylates do not undergo alternating propagation with SO2, and the minimum number of acrylate monomeric units in a homosequence is 2. The results obtained were compared with those obtained from studies on the copolymerization of SO2, with other monomers, and are discussed in terms of the alternating copolymerization theory and the penultimate model.
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  • 219
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Chemical reactions leading to crosslinking were followed by rheometrical studies during curing at different temperatures and compositions of compatible species. The condensation reactions between two copolymers of styrene and maleic anhydride, and several α,ω-dihydroxyoligostyrenes, lead to an experimental variation of the elastic modulus (G′)t. A kinetic scheme is proposed, selecting the most reliable reactions, which describes the experimental behaviour adequately. According to this scheme, the rate constants of interpolymeric condensation reactions were evaluated. It appears that the values obtained for grafting and crosslinking are quite the same. They depend mainly, in absence of a catalyst, on the molecular weight of the oligomer and on the local viscosity, which is a function of composition. In presence of a catalyst, there is a large increase of the constant, indicating that the chemical step is dominating the diffusion process.
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  • 220
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    Die Makromolekulare Chemie 189 (1988), S. 409-417 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Emulsion copolymerization of unsaturated polyesters (UP) with styrene was initiated by potassium peroxodisulfate and by azodiisobutyronitrile (AIBN). The decay rates of both initiators were compared and influences of temperature, electrolyte and concentration of the reaction components studied. Initiation radicals from the persulfate partly add to unsaturated UP units and decarboxylate terminal acid groups of the UP. Initiation by AIBN predominantly occurs in the aqueous phase, and side reactions with this initiator are neglectable.
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  • 221
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    Die Makromolekulare Chemie 189 (1988), S. 437-445 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Results of group transfer polymerization of methyl methacrylate (MMA) in acetonitrile with tetraethylammonium cyanide (Et4NCN) and tris(dimethylamino)sulfonium difluorotrimethylsilicate (TASF2SiMe3) as catalysts and trimethylsilyl cyanide as initiator are presented. It is shown, that both catalysts behave similarly with respect to catalysis of the initiation and the propagation step and of the termination step of the growing chains with the solvent, TASF2SiMe3 being more active than Et4NCN.
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  • 222
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    Die Makromolekulare Chemie 189 (1988), S. 845-849 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Copolymers of ethylene and ethylene-d4 were prepared, and their composition and comonomer sequence distribution determined from high-field 13C NMR spectra. For a conventional Ziegler-Natta catalyst, deuterium was shown to decrease the reactivity of ethylene.
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  • 223
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    Die Makromolekulare Chemie 189 (1988), S. 851-861 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order to modify the properties of low density polyethylene (LDPE), the radically initiated polymerization of ethylene can be performed at pressures below 1200 bar and moderately high temperatures. Under such conditions the reaction mixture separates into a less dense phase, rich in monomer, and a dense phase, rich in polymer. The polymerization proceeds mainly in the monomer-rich phase. When the polymer concentration exceeds the solubility limit, polymer precipitates from the monomer-rich phase and moves into the polymer-rich phase. By polymerization under two-phase conditions, polyethylene resins with a narrow molecular weight distribution can be obtained.
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  • 224
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Irreducible sequences in n-ary copolymers are defined. An exhaustive and non-redundant lexicographically ordered list of irreducible sequences of comonomers in binary (n = 2), ternary (n = 3), quaternary (n = 4) and quinquenary (n = 5) copolymers is presented. The numbers of irreducible sequences may be found either by an explicit formula in terms of the number n of comonomers and of the length m of the sequences, or by applying the Polya-de Bruijn theorem, as shown in detail in the first two parts of this series. For stereoregular vinyl homopolymers, or for the geometrical (E/Z) isomerism in polyalkenes, irreducible sequences are the same as in binary copolymers. A nomenclature is proposed for m-ads in stereoregular homopolymers with m 〉 2, i. e. beyond isotactic for m = 1, and syndiotactic for m = 2.
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  • 225
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    Die Makromolekulare Chemie 189 (1988), S. 871-880 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Differential scanning calorimetry and scanning electron microscopy were carried out in order to study the relation between the structure and properties of poly(vinyl alcohol) hydrogels prepared by repeated cycles of freezing-thawing. The effect of the number N of repeated cycles of freezing-thawing, of the degree of saponification (DS), and of the degree of polymerization (DP) on structure and properties was examined. The elastic modulus and the endothermic enthalpy, estimated from the area surrounded by the endothermic peak, increase with increasing N, DS, and DP. The melting temperature Tm shifts to higher temperatures with increasing DS and DP, but it is almost independent of N for gels with high DS or DP. In PVA gels with lower DP or DS, Tm shifts to higher temperatures with increasing N. The temperature dependence of the elastic modulus is discussed on the basis of a theory on thermoreversible gels.
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  • 226
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    Die Makromolekulare Chemie 189 (1988), S. 881-898 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Four different samples of α-dimethylvinylsilyl-ω-vinylpoly(oxydimethylsilanediyl) (α,ω-divinylPDMS) chains of different molar masses have been endlinked in the absence of solvent to form “model” polymer networks. These networks have been subjected to swelling experiments at 30°C in toluene and toluene/methanol mixtures. The volume fraction of polymer in the gel at equilibrium swelling v3 is determined gravimetrically. The preferential sorption coefficient λ is found using interferometry. Large preferential sorption effects prevent the solvent mixtures from being treated as pseudo-one-component solvents. The variation of swelling and preferential sorption with network and solvent composition is discussed. The thermodynamic properties of α,ω-divinylPDMS chains in dilute solution with toluene, toluene/methanol mixtures, and tetrahydrofuran are determined at 30°C using intrinsic viscosity measurements. Polymer-solvent interaction parameters and Mark-Houwink constants as well as unperturbed dimensions are determined in both the pure solvents and solvent mixtures.
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  • 227
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    Die Makromolekulare Chemie 189 (1988), S. 899-909 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It is shown that the mechanism of polyacetylene (PA) reduction (or n “doping”) by alkaline carbanionic salts and butyllithium is a simple electron transfer without addition. In this reduction reaction the dicarbanionic dimer of 1,1-diphenylethylene (DD2- Na2+) is quantitatively converted to 1,1-diphenylethylene. The reduction by 3-methyl-1,1-diphenylpentyllithium produces free radicals which deactivate in solution by coupling and disproportionation. But the strong dependence of the ratio of disproportionation to coupling of these radicals on solvent polarity is unusual: no coupling is observed in diethyl ether or pentane, while it is the most important reaction in THF. sec-Butyllithium in pentane also reduces PA by a simple electron transfer process. The “doping” levels can be deduced accurately from the quantitive analysis of the by-products by gas chromatography.
    Additional Material: 13 Tab.
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  • 228
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    Die Makromolekulare Chemie 189 (1988), S. 961-967 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystal structure of polythiophene is analyzed by the Rietveld whole-fitting method on the X-ray diffraction powder profile. Experimental data allow only a bidimensional characterization of the structure in the plane orthogonal to the chain axis with a pgg symmetry (a = 7,79; b = 5,53 Å). Best fitting is obtained by assuming rigorous coplanarity of thiophene rings along the chain. The presence of few and weak layer-peaks is interpreted in terms of only partial ordering of chains along their axes. The final disagreement factor, in terms of ∑|I0 - Ic|/∑ Inet, is 0,125.
    Additional Material: 3 Ill.
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  • 229
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Using NMR and infrared (IR) spectroscopy, the effect of crosslinking on the aggregation of syndiotactic (s) poly(methyl methacrylate) (PMMA) in toluene or o-dichlorobenzene gels was investigated. A conclusion was drawn from the integrated band intensities in the 1 H NMR high resolution spectra that the values of fractions of aggregated units decrease with increasing crosslinking, and that the corresponding aggregates of crosslinked s-PMMA decompose (melt), compared with uncrosslinked s-PMMA, at somewhat lower temperatures. Already loose crosslinking markedly slows down the aggregation process. The IR spectra showed that fractions of long s-sequences, which form helices having a high number of units per turn (conformation close to the all-trans one), are greatly reduced due to crosslinking, and the structure of aggregated sequences is less defined. Unlike the uncrosslinked s-PMMA, the structures arising by aggregation in gels of crosslinked s-PMMA do not persist in the solid state.
    Additional Material: 8 Ill.
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  • 230
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(dimethylsiloxane) (poly(DMS))/poly(N-tert-butylaziridine) (poly(TBA)) block copolymer was synthesized by two different techniques; (1) the coupling reaction of poly(DMS) having a dimethylaminopropyl end-group (1) with living poly(TBA) (2) which was prepared with methyl trifluoromethanesulfonate as an initiator, and (2) the polymerization of N-tert-butylaziridine (5) using poly(DMS) having a p-toluenesulfonyl ester end-group (4) as macromolecular initiator, respectively.
    Additional Material: 5 Ill.
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  • 231
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence of the number of oxyethylene repeating units in the oligomeric derivatives of ethylene bis(4-chlorocarbonylbenzoate) (1, n = 3, 6,4, 13, 22,3, 45 and 68) on the reactivity of the chlorocarbonyl end groups in the acceptor-catalytic esterification was determined by means of thermodynamic and kinetic investigations in diluted solutions. The violation of the principle of equal reactivity was found to be caused by the far-order effect, when with increasing chain length the effective local concentration of oxyethylene repeating units increases in the environment of the end group whose reactivity is determined by the ratio between the “solvating ability” of the repeating units and the solvent. The far-order effect influences not only the kinetics, but also the reaction mechanism.
    Additional Material: 6 Ill.
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  • 232
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    Die Makromolekulare Chemie 189 (1988), S. 993-1000 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The thermal expansivity of semicrystalline polymers is interpreted within the framework of the composite model which has already been found useful in describing mechanical and optical properties as well as the thermal conductivity of a large number of polymers. The model assumes the polymers to be an aggregate of units composed of crystalline and amorphous phases. The thermal expansivities of the unit are calculated in terms of those of the constituents. In the undrawn state the units are distributed randomly, and the isotropic thermal expansivity of the bulk results. The development of strong anisotropy in thermal expansivity on drawing is explained in terms of preferred orientation of the units. The orientational changes on drawing have been directly calculated from the birefringence versus draw ratio data. The results of these investigations indicate that the present model is quite successful in interpreting thermal expansivity data for poly(oxymethylene) and poly(propylene) over the entire draw ratio and temperature range.
    Additional Material: 2 Ill.
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  • 233
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Water-soluble polymers 6-17 containing covalently bound moieties of porphyrin derivatives were prepared by reaction of poly(methacrylic acid) (4) and poly(N-vinylpyrrolidone-co-methacrylic acid) (5) with the low-molecular-weight substituted tetraphenylporphyrin 1 b, phthalocyanines 2 b and 2 d and naphthocyanine 3 c. Besides binding of one porphyrin derivative, also combined binding of two or three different porphyrin derivatives to the polymers could be achieved. The resulting polymers are negatively charged (polymers 6-11) or uncharged (polymers 12-17).
    Additional Material: 2 Ill.
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  • 234
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    Topics: Chemistry and Pharmacology , Physics
    Notes: Positively charged polymers 6-13 containing covalently bound moieties of tetraphenylporphyrin (1), phthalocyanine 2 and naphthocyanine 3 were obtained by reaction of poly(chloromethylstyrene) with low-molecular weight substituted porphyrins (1 b, 2 b, 2 d, 3 c) in the presence of triethylamine. The water-soluble polymers contain moieties of one or of two or three different porphyrin derivatives.
    Additional Material: 1 Ill.
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  • 235
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: By ring-opening copolymerization of 1,6-anhydro-2,3,4-tri-O-octadecyl-β-D-glucopyranose (1) with 1,6-anhydro-2,3,4-tri-O-benzyl-β-D-glucopyranose (2) using phosphorus pentafluoride as initiator in dichloromethane at 0°C, stereoregular copolymers 3, with M̄n = 6 · 103 to 24 · 103 were obtained. For debenzylation of copolymers 3, either the reduction with sodium in liquid ammonia or radical bromination-hydrolysis was applied, depending on solubility and copolymer composition. Poly[2,3,4-tri-O-octadecyl-α-D-glucopyranosyl-(1→6)-stat-α-D-glucopyranosyl-(1→6)] (4,) exhibits characteristic solution properties arising from its amphiphilic structure. Polysaccharide 4, with mole fractions of trioctadecylated unit (x) below 0,03, are water-soluble and interact with magnesium 1-anilino-8-naphthalenesulfonate (ANS) in water. The polysaccharide 4 (x = 0,29), which is soluble in chloroform, was found to solubilize an aqueous methyl orange solution in chloroform. Formation of micelles in water and reversed micelles in chloroform is suggested.
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  • 236
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    Die Makromolekulare Chemie 189 (1988), S. 1027-1033 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Crosslinked polymers containing pendant tris(bipyridyl)ruthenium(II) complexes [Ru(bipy)32+] were synthesized and examined as sensitizers for the light-induced formation of hydrogen in the heterogeneous system H2O/immobilized Ru(bipy)32+/ethylenediamine-tetraacetic acid/platinum. Hydrogen generation rates of 0,037 ml/h were obtained with Ru(bipy)32+ -complexes immobilized with spacer groups onto hydrophilic carriers based on sucrose-methacrylates as well as hydrophobic carriers based on crosslinked poly(4-aminostyrene), whereas carrier bound complexes without spacer gave lower efficiencies in hydrogen production. The hydrogen generation rates were linear for more than 8 days.
    Additional Material: 2 Ill.
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  • 237
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    Die Makromolekulare Chemie 189 (1988), S. 1035-1042 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The reactive species (radicals, ions, etc.) or the UV-visible radiation emitted by the excitated species initiate the cold plasma induced polymerization of a monomer in the liquid or solid state. The residual CC double bond concentration of an acrylic monomer depends on the plasma characteristics (gas nature, pressure, discharge power, etc.), but also on the polymerization conditions. The UV-visible radiation emitted in a cold plasma has more influence on the thickness of the film than the reactive species bombardment. Two simple mathematic laws describe these phenomena.
    Additional Material: 5 Ill.
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  • 238
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    Die Makromolekulare Chemie 189 (1988), S. 447-458 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystallographic interactions between the toluenesulfonate-substituted diacetylene 2,4-hexadiynylene di-p-toluenesulfonate (TS), its corresponding polymer (PTS) and polyethylene (PE) have been established in detail with the help of the polymer decoration technique. Although monomer and polymer are known to be isomorphous, the decoration patterns observed on their (100) crystal surface differ significantly, revealing some subtle structural changes on solid-state polymerization. The single and twofold orientations obtained on TS and PTS, respectively, are discussed and shown to be of epitaxial character. The PE contact planes for the two decoration orientations are however, significantly different, since the chain packing distances at play are 5,26 Å (or 4,94 Å) and 7,47 Å, respectively. From the very close similarity in crystal structures, it is anticipated that favourable interactions may also exist in many other polydiacetylene/polymer binary systems.
    Additional Material: 8 Ill.
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  • 239
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The temperature changes caused by adiabatic pressure changes were studied in a polymersolvent system at high pressures. It is shown that the temperature determination by means of light scattering measurements is in good agreement with thermodynamic calculations of the temperature change for adiabatic pressure changes. The directly measured temperature changes by use of a thermocouple are found to be far too small.
    Additional Material: 5 Ill.
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  • 240
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Bile pigments covalently anchored to beads of a polystyrene-based resin show in gel-phase 13C NMR spectroscopy hydrogen-bond interactions between the anchored groups. Such interactions are similar to those observed in homogeneous solution: attached 5(1 H)-pyrromethenones in aprotic solvents show dimer formation analogously to what happens in homogeneous solution.
    Additional Material: 1 Ill.
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  • 241
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    Die Makromolekulare Chemie 189 (1988), S. 1569-1577 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In the past morphological changes, caused by uni-axial drawing of flexible polymers have been studied mostly under conditions, quite different from the drawing conditions. This could give rise to certain artefacts, leading to mis-interpretations. Up to now very little was known about this possibility. Therefore, X-ray patterns obtained by conventional drawing studies and by real-time X-ray drawing studies are compared in this paper. It will be shown, that although some results on melt-crystallized polyethylene discussed here show indeed small differences, conventional X-ray studies can be used without any problem for qualitative studies. However, studies of deformation phenomena in elastic deformable regions as well as quantitative X-ray studies require real-time measurements.
    Additional Material: 5 Ill.
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  • 242
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cross polarization/magic angle spinning 13C NMR has been applied to the investigation of some solid organometallic compounds of the general formulae TiCl4 · n RCOOR′, MgCl2 · n RCOOR′ (RCOOR′ = p-CH3—C6H4COOCH3 and C6H5COOC2H5, n = 1; 2; and 0,15). Compounds with n = 1 and 2 show narrow resonance lines indicative of crystalline regular structures while for MgCl2 · 0,15 RCOOR′ a disordered structure is found with the organic ligands strongly bonded to the surface of MgCl2 crystallites. For n = 2 splitting into a doublet is found for some resonances due to the spatial non-equivalence of the two ligands induced by crystalline packing. A shift has been found for some resonances in going from Mg to Ti complexes which reflects the different Lewis acidity of the two metal atoms.
    Additional Material: 6 Ill.
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  • 243
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    Die Makromolekulare Chemie 189 (1988), S. 541-547 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The reaction of 1,3-benzenedithiol (1) with 1,4-diethinyl-benzene (2) at room temperature yields polymers with thio-1,3-phenylenethiovinylene-1,4-phenylenevinylene repeating units. The polymerization proceeds without addition of an initiator and without UV-irridiation. Because of the resulting structure a radical mechanism is suggested. However, the molar mass/conversion relation shows similarities with a step-growth polymerization. Because of this behaviour this reaction was successfully used for the preparation of telechelics in which molar mass and end groups are controlled simply by the unstoichiometric ratio of the educts.
    Additional Material: 1 Ill.
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  • 244
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    Die Makromolekulare Chemie 189 (1988), S. 559-566 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Vinyl alcohol (VA)/4-vinylpyridine (4VP) graft copolymers were prepared by the macromonomer method. After domain fixing of the PVA matrix of this graft copolymer, the water/1-propanol mixed solution of poly(sodium p-styrenesulfonate) (PSSS)/P4VP polymer blends was cast on the microheterophase surface of VA/4VP graft copolymer which served as a support membrane. The surface characterization of this composite membrane was carried out by means of transmission electron microscopy (TEM) and Electron Spectroscopy for Chemical Analysis (ESCA). The TEM observation indicated that charge mosaic microdomains formed by means of epitaxial growth are oriented perpendicularly to the film surface. The ESCA results clearly indicated that the two-phase composition of the surface (in sampling depths of ≈ 1 and ≈ 5 nm) is proportional to the overall bulk composition of the polymer blends.
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  • 245
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    Die Makromolekulare Chemie 189 (1988), S. 1603-1612 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Macrocyclization equilibrium data from metathesis reactions of cycloolefins (cyclobutene, cyclooctene, and cyclododecene) are compared with predictions of a novel, simple rotational isomeric state (RIS) scheme for polyalkenes with at least three single bonds between adjacent double bonds. The predictions agree with experiment within the combined experimental errors, supporting the conformational models and confirming that macrocyclization equilibrium has indeed been established in the metathesis reactions.
    Additional Material: 3 Ill.
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  • 246
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    Die Makromolekulare Chemie 189 (1988), S. 1613-1625 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An apparatus for turbidimetric measurements of demixing temperatures under shear flow is presented, and the results of experiments with trans-decahydronaphthalene/polystyrene (TD/PS) solutions, investigating molecular weights ranging from 100 kg/mol to 1770 kg/mol, are compared with viscometric data. It is found that the sign and magnitude of shear effects depend on molecular weight (Mw), polymer concentration (c2), and shear rate (\documentclass{article}\pagestyle{empty}\begin{document}$ \dot \gamma $\end{document}). For the first time, it was possible to study a solution which exhibits shear dissolution at low shear rates but shear demixing at high shear rates.
    Additional Material: 11 Ill.
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  • 247
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    Die Makromolekulare Chemie 189 (1988), S. 1657-1669 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Deviations in the determination of the unperturbed dimensions of polymers arising in ternary polymer systems (solvent (1)/solvent (2)/polymer) can be explained by the inaccurate use of an interaction parameter independent of polymer molecular weight. On this basis, a new formalism for the calculation of the second virial coefficient from intrinsic viscosity is proposed. This formalism was tested (and compared with well established formalisms) for all ternary polymer systems with simultaneous intrinsic viscosity and second virial coefficient data in the literature.
    Additional Material: 6 Ill.
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  • 248
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The glass transition temperatures Tg of homogeneous binary blends of the homo- and the statistical copolymers of the system poly(styrene-co-methyl methacrylate) were studied. Some of the blends, which are in the equilibrium phase separated, were forced into homogeneity. Tg (φ) of the homopolymer blends (PS/PMMA)φ follows the Fox equation, while Tg (x) of the pure copolymers P(SxMMA1 - x) exhibits a minimum. This minimum can be effectively removed by blending the copolymers with small fractions (φ ≈ 0,2) of one of the two homopolymers or a differently composed copolymer P(SyMMA1 - y).
    Additional Material: 7 Ill.
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  • 249
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    Die Makromolekulare Chemie 189 (1988), S. 1685-1692 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A relation is proposed which yields the occupied volume by macromolecular chains in solution. The experimental verification of the model is carried out by a viscometric study of the ternary system polymer A/polymer B/solvent. More precisely the viscometric study permits the determination of the critical concentration c** corresponding to the incipient overlap of spherical coils.
    Additional Material: 6 Ill.
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  • 250
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    Die Makromolekulare Chemie 189 (1988), S. 715-715 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 251
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of polymerization of β-lactones  -  β-propiolactone, α-ethyl-α-phenyl- and α-benzyl-α-ethyl-β-propiolactone  -  was investigated using nickel carboxylate/phosphine complexes as initiators. The apparent rate constants of initiation and propagation, ki and kp, were calculated assuming first order kinetics. The variations of ki values with monomer concentration suggest that the mechanism is more complex, with a reaction order which is not as admitted for calculation. The infrared study has shown that the polymerization initiated by the complex is of zwitterionic type, and the kinetic curves indicate that the nickel carboxylate participates in the reaction.
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  • 252
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    Die Makromolekulare Chemie 189 (1988), S. 743-754 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(β-aminoester)s 7 - 12, containing in the repeating unit ethylenebis(carbonyloxy-1,4-phenylene)carbonyloxy groups interconnected by polymethylene segments of different length and coupled by diamino spacers, were synthesized from mesomorphic diacrylates and secondary diamines. The thermal behavior and the solution properties of the polymers were investigated. Depending on the structure of the repeating unit, the polymers were found to give rise to either isotropic or anisotropic melts. The incidence and extension of the mesophase are favored in poly(β-aminoester)s based on even numbered methylene segments and 2-methylpiperazinediyl spacers. The polymer samples were found to degrade at room temperature, when dissolved in solutions containing water, an organic base or an acid. Based on a macromolecular model compound (14) a degradation process is suggested involving a selective cleavage of the benzoate ester groups assisted by the amino groups in β-position.
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  • 253
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    Die Makromolekulare Chemie 189 (1988), S. 1997-2005 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Difunctional poly(dimethylsiloxane) (PDMS) macromonomers were synthesized. Emphasis was put on the synthesis of short PDMS chains exhibiting a narrow molecular weight distribution. This was achieved by the selection of an efficient initiator and under polymerization conditions such as to minimize reshuffling reactions. The macromonomers were subsequently obtained by deactivation of the living sites with an electrophilic unsaturation. Accurate characterization of the macromonomers (GPC, end-group analysis) was performed.
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  • 254
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    Die Makromolekulare Chemie 189 (1988), S. 1987-1996 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Several series of thermotropic copolyesters with different spacers, containing the moieties of 1,4-butanediol (4a or 4b), 1,6-hexanediol (6a or 6b), bisphenol-A (10a), bisphenol-S (10b) or a telechelic polysulfone (12a or 12b) were synthesized. The mesomorphic properties of the resulting copolyesters were examined by visual observation of stir-opalescence and birefringence under a polarizing microscope. Copolyesters 4a, 4b, 6a or 6b with mole fractions of mesogenic units over a broad extent (≥0,2) being thermotropic within wide mesomorphic temperature ranges, regardless of the spacers based on 1,4-butanediol or 1,6-hexanediol, have microstructures of block sequence distribution and do not retain liquid-crystallinity if the mean lenghts of mesogenic segments are shorter than that of the triad with three phenyl rings. For the thermotropic copolyesters 10a, 10b, 12a or 12b the minimum mole fraction of mesogenic units needed is not higher than 0,10, despite of the different varieties and lengths of rigid spacers.
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  • 255
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    Die Makromolekulare Chemie 189 (1988), S. 2029-2037 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The syntheses and properties of a series of para-linked aromatic homopolyesters with 2,2′-dimethylbiphenylylene units are described. In the 2,2′-dimethyl-substituted biphenylylene unit the phenyl rings are forced into a non-coplanar conformation, which decreases the interchain interactions. The combination of such a biphenylylene unit with a monosubstituted unit further reduces the regularity of the substituents along the polyester backbone. As a result, soluble and completely amorphous liquid-crystalline (LC) aromatic polyesters with low phase transition temperatures are obtainable. Ternary solutions, consisting of a soluble aromatic LC polyester, a conventional randomly coiled thermoplastic and chloroform as solvent, can be used for the preparation of films and fibers.
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  • 256
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    Die Makromolekulare Chemie 189 (1988), S. 1819-1834 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The steady state of reversible polymer-analogous reactions was simulated by Monte Carlo calculations. The length of the simulated copolymer chains was chosen large enough to yield data with an acceptable degree of statistical fluctuation. Two types of sets of relative rate constants K were investigated, first K1 = K2 = K3, and second K1 ≠ K2, K1 ≠ K3, K2 ≠ K3, with K1 · K3 = K22. The relative rate constants K are defined as K1 = k(AAA)/k(ABA), K2 = k(AAB+)/k(ABB+), and K3 = k(BAB)/k(BBB), where k is the ordinary rate constant pertaining to the reaction of the central monomeric unit in the triad given in parentheses, with two different types of monomeric units A and B in the binary copolymer. For both types of sets of relative rate constants the simulation showed a detailed balance to prevail for the kinetics in the steady state. It was also shown that the same kinetics and statistics were obtained in the steady state when starting the simulation first from a homopolymer consisting of A-monomeric units, and then from a homopolymer of B-monomeric units. Based on the finding of a detailed balance and on the definition of K, it could be shown by analysis that the first type of the sets of K leads to a Bernoullian statistics of the copolymers in the steady state, while the second type leads to a first-order Markov statistics. Correspondingly, equations are given which allow to calculate the relative rate constants from statistics and vice versa. The equations have also been confirmed by Monte Carlo simulation. In addition, the equations for the interrelations between the standard Gibbs free energies of the individual reactions for the central units in the triads are given.
    Additional Material: 6 Tab.
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  • 257
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    Die Makromolekulare Chemie 189 (1988), S. 1845-1854 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The 125 MHz 13C NMR spectra of some poly(dialkyl fumarates) (PDAF) and poly(dicycloalkyl fumarates) (PDCF) prepared by radical polymerization are measured in CDCl3 solution at 60°C. The multiplet resonances of the main-chain carbon atoms and the ester carbonyl carbon atoms are assigned to stereochemical triad and pentad sequences, respectively, using model compounds as well as computer simulation. From these results it is found that PDAF and PDCF exhibit essentially atactic structures with meso addition favoured over racemic addition, and that the ratio of meso to racemic content varies with different kinds of alkyl and cycloalkyl groups. The tactic sequence proportions of the polymers cannot be explained by one-parameter Bernoullian statistics, but can be successfully explained by modified Bernoullian trial.
    Additional Material: 7 Ill.
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  • 258
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Light scattering, neutron scattering and viscosity measurements on a nematic and a smectic polymethacrylate demonstrate the presence of molecularly disperse coils in solution. For the nematic polymer, toluene is a theta solvent, the behaviour familiar from conventional polymers (unperturbed coil conformation) being exhibited at the theta point. The isotropic melts likewise contain unperturbed coils; in the case of the nematic polymers, however, the coils in the melt have a radius of gyration which is about 30% smaller than that in solution at the theta point. In the liquid-crystalline phase, the mean radii of gyration in both cases are identical to the corresponding parameters in the isotropic melt. In the nematic material, however, the coils can be shown to have a substantial anisotropy, the radius of gyration parallel to the director being about 20% smaller than that at right angles to this direction. On the basis of a theoretical chain simulation, a model for the main-chain conformation has been developed which takes into account both short-range interactions along the main chains and three-dimensional interactions by the oriented side groups. This model indicates the degree of orientation from which a change in the mean radius of gyration can be expected. Wide-angle neutron scattering experiments on smectic polymer provide information about the main-chain distribution in the smectic phase. The main chains are present in a substantially higher concentration between the smectic layers, but there are hints that they do not have a true two-dimensional arrangement.
    Additional Material: 9 Ill.
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  • 259
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A comprehensive study of the propagation step of 1-heptyne polymerization initiated by a dinuclear μ-alkylidene complex of tungsten, was carried out. Kinetic orders, apparent rate constants and thermodynamic parameters were determined. The structure of the active species and that of the organic side-products appearing during this step, were analyzed by NMR and mass spectroscopy. According to the experimental data, a mechanism of the propagation reaction is proposed: the propagating species could derive from inactive metalated oligomers by loss of a carbonyl ligand; the monomer then coordinates at the free site of the transition metal of the μ-alkylidene active species and inserts into the C—W bond. In competition with the normal insertion of the monomer molecule, termination and transfer reactions occur (including or not the monomer and/or the polymeric chain).
    Additional Material: 9 Ill.
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  • 260
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    Die Makromolekulare Chemie 189 (1988), S. 2395-2408 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: We measured the tensio-active properties of octamethylene dimethacrylate (1), octamethylene diisobutyrate (2) and octamethylene isobutyrate methacrylate (3) at the oil-water interface. The results indicate that these molecules are strongly adsorbed at the boundary between oil and water. The amphiphatic compounds in the monolayer can be polymerized and cross-linked by UV irradiation. The kinetics of surface gelation was studied by measuring the two-dimensional shear modulus as a function of the time of irradiation. A two-dimensional sol-gel transition was observed which is in fairly good agreement with percolation theories. The kinetics of the two-dimensional polymerization can be completely interpreted in terms of a simple reaction scheme. The elasticity of the two-dimensional films depends strongly on the surface concentration of the cross-linking agent. The rheological properties of the polymerized films exhibit typical features of rubber-elastic systems and there exists an interesting analogy to corresponding structures of three-dimensional networks.
    Additional Material: 9 Ill.
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  • 261
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    Die Makromolekulare Chemie 189 (1988), S. 2419-2423 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thin films (thickness 0,3 μm) of a mixture of phthalocyaninatozinc(II) (1) and poly(1-vinylcarbazole) (2) are prepared by coating from a solution on ITO glass. The blue coloured films are investigated in an electrochemical cell under irradiation with visible light. In the presence of dioxygen from air the films exhibit an intensive cathodic photocurrent. The action spectrum of the photocurrent corresponds to the absorption spectrum of the phthalocyanine. The results show a device which can be switched by air and visible light.
    Additional Material: 5 Ill.
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  • 262
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The apparent viscosity η of semi-dilute solutions of cellulose nitrate in ethyl acetate was measured as a function of shear rate at 20°C by rotational viscometry. The mass concentration c of the solutions was chosen such that the product between c and the intrinsic viscosity was 8 〈 c · [η] 〈 22, lying in the range of viscosity-average degrees of polymerization covered by the employed samples 550 〈 DPη 〈 7600. The experimental flow curves were interpreted in terms of Graessley's theory for non-Newtonian flow of polydisperse polymers. The polydispersities derived for five individual samples according to the theory of Graessley were used for calculating the resulting theoretical curves belonging to four binary mixtures each between two of them. The reasonable good agreement between calculated and experimental reduced flow curves of blends indicates consistency of the theory when applied to the present system of a semi-rigid polymer. This and other results point to a flow behaviour of semi-rigid cellulose nitrate being similar to that of linear flexible polymers.
    Additional Material: 3 Ill.
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  • 263
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    Die Makromolekulare Chemie 189 (1988), S. 2425-2432 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(γ-methyl-L-glutamate) membranes with α-helix structure and with ß-sheet structure were prepared by casting. The electrical membrane potentials of the membranes in LiCl, NaCl, and KCl solutions were measured in order to obtain information on the mobility of ions within the membranes. In the membranes with α-helix structure the relative ionic mobilities of Na+ and Li+ to K+ are larger than in aqueous solutions. In the membranes with ß-sheet structure the mobility of cations within the membrane is extremely restricted. The partition coefficient of KCl in this membrane at low concentrations is greater than 10. The permeability and diffusion coefficients of KCl depend on the concentration of KCl, and the values are higher, when compared with those for the membrane with α-helix structure. These results reflect the differences between the secondary structures of the polymers. The specific behaviour of the partition coefficient and of the permeability found in the membranes with ß-sheet structure is explained by an interaction between the carbonyl groups of the main chain and the cations.
    Additional Material: 6 Ill.
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  • 264
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order to follow the process of aggregation, viscosity measurements in dilute aqueous solution were performed with two carbohydrate amphiphiles: (i) N-octylgluconamide (C8-GA) and (ii) N-decanoyl-N-methylglucamide (C10-MGA). Both compounds ten to form a gel on cooling, the former at 65°C, the latter at 10°C. Electron micrographs have shown that the gels are composed of a loose network of thin, regularly twisted helical ropes. By viscosity measurements over a wide range of temperatures and concentrations, typical changes of the reduced viscosity were observed. Results are discussed with respect to the critical micelle concentration (CMC), the Krafft point, i. e. the critical temperature of crystallization (Tc), and the cloud point (Tcp). It is concluded that micellar aggregation to rod-shaped particles, quasi-crystalline aggregation to highly hydrated gels, and crystallization of monomers, the latter mediated by hydrogen bonding, are involved and compete with each other.
    Additional Material: 8 Ill.
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  • 265
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Diffusion processes taking place across the boundary between the two compatible polymers poly(methyl methacrylate) (PMMA) and poly(vinylidene difluoride) (PVDF) were studied by means of small angle X-ray scattering. The excess scattering resulting from thermal concentration fluctuations was used to monitor the diffusion process as a function of the molecular weight of the PMMA component and the diffusion geometry. The results obtained were analyzed on the basis of simplified versions of the interdiffusion theories proposed by Brochard (slow-mode model) and by Kramer (fast-mode model). This, however, required, the introduction of approximations with respect to the concentration dependences of monomer mobilities and interaction parameter and with respect to the role of molecular weight distribution. Using these approximations it is possible to account quantitatively for all experimental findings on the basis of the slow-mode approach. Discrepancies between experimental results and theoretical predictions were found for the model based on the fast-mode approach.
    Additional Material: 8 Ill.
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  • 266
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Doubly labeled poly(methacrylic acid) (PMA) samples with two different concentrations of carbazole and anthracene labels were prepared, and one sample was divided into two fractions of different molecular weight. Emission spectra were recorded in solutions without added salt, at ionic strengths 0,05 and 0,40 and in a 2 : 1 water-methanol mixture, as a function of pH. The nonradiative energy transfer (NET) from carbazole donor to anthracene acceptor decayed as the PMA coils expanded. On mixing solutions of the labeled PMA with buffer solutions of varying ionic strength in water or aqueous methanol in a stopped-flow apparatus, the expansion of the PMA was monitored by the decrease in anthracene emission intensity when the solution was irradiated in the carbazole absorption band. Only part of the process could be followed, since the initial expansion occurred in a sub-millisecond time. Some studies were also carried out on the kinetics of chain contraction when partially neutralized PMA solutions were acidified. The changing NET with the conformational transition of PMA was correlated with the change in the intrinsic viscosity of the polymer. The kinetic data obtained were generally in excellent agreement with those of an earlier study in which conformational changes of PMA were monitored by the changing emission of a dansyl label. In particular, the surprising slowness of the final approach to equilibrium was substantiated.
    Additional Material: 4 Ill.
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  • 267
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    Die Makromolekulare Chemie 189 (1988), S. 2485-2501 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The tacticity and the nature of irregularities and end-groups in poly(styrene oxide) samples prepared using potassium alcoholates and anionic coordinated systems as initiators were studied by 13C NMR at 62,89 MHz. It was found that the polymerization initiated with potassium alcoholates fits a first-order Markov propagation model. Head-to-head (H—H) and tail-to-tail (T-T) irregularities are detected in all the samples studied, but more than 95% of the opening of the oxirane ring occurs in the β-position with potassium alcoholates as initiators while about 10% of α-scission may be observed with coordinated systems. Secondary hydroxyl terminal groups and initiator moieties are identified in polymers prepared with potassium alcoholates. Poly(styrene oxide) was found to undergo chain-scission by aging at 25°C. Among the various structures produced by the oxidative degradation process, benzoate and secondary hydroxyl groups are identified.
    Additional Material: 6 Ill.
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  • 268
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    Die Makromolekulare Chemie 189 (1988), S. 2503-2512 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Quantum yields of photocyclization of a fulgide 1a and its corresponding fulgimide 1b upon irradiation with ultraviolet light, and of the back decoloration reaction of the cyclic product 3 on irradiation with visible light, were determined in different solvents and in polymer matrices. The isomerization of the (Z)-isomers to the (E)-isomers is very sensitive to the glass transition temperature Tg of the matrix, especially in the case of copolymers of N-styrylfulgimides 1c with styrene where the photochrome is linked to the polymer chain.
    Additional Material: 4 Ill.
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  • 269
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    Die Makromolekulare Chemie 189 (1988), S. 2513-2520 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polyureas and polythioureas were prepared under mild conditions by direct polycondensation of carbon dioxide and carbon disulfide, respectively, with diamines in the presence of diethyl N-acetyl-N-methylphosphoramidite or its analogs containing an active P—N bond. The influence of the substituents in the phosphoramidite, of the CO2 pressure, solvent, organic base and diamine structure on the yield and inherent viscosity of the polymer was investigated. A reaction mechanism involving the intermediate formation of a mixed anhydride of dialkylphosphorous and alkyl(aryl)carbamic acid is discussed.
    Additional Material: 1 Ill.
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  • 270
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    Die Makromolekulare Chemie 189 (1988), S. 2533-2543 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: (18-Crown-6)-bridged phthalocyanine network polymers 4-8 as well as a low-molecular-weight model compounds with only one phthalocyanine unit (3a, b) were prepared from tetracyanodibenzo-18-crown-6 (2a). The cyano end groups were partially converted into imido groups during the cyclotetramerization reaction, as detected from the IR spectra. In order to obtain structurally uniform compounds with the same end groups, the —C ≡ N groups were hydrolyzed into imido groups with conc. sulfuric acid. The metal-free phthalocyanine polymer 4a was obtained by the reaction of 2a either with hydroquinone or PbO in ethylene glycol. The chlorides of Cu(II), Ni(II), and Co(II) were empolyed in order to synthesize the corresponding metal-phthalocyanine polymer, and Fe(CO)5 was used for the preparation of the Fe-analog 7a. For the preparation of the Co-containing polymer 8a ammonium molybdate has to be added as catalyst. The selectivity of 7a for Rb+ was found to be highest in the heterogeneous phase extraction experiments. Polymers 4-8 are also capable of binding silver from aqueous and methanolic solutions.
    Additional Material: 5 Tab.
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  • 271
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 1-Phenylethylpotassium (5), an efficient anionic polymerization initiator in tetrahydrofuran (THF) solution serving as a substitute for 1-methyl-1-phenylethylpotassium in most of its applications, was obtained by cleavage of bis(1-phenylethyl) ether (1) with potassium. Ether cleavage reactions were carried out in THF at mole ratios potassium/1 = 2/1 and 1/1, and the resulting solutions were submitted to careful analysis. All by-products formed in the reaction media were unambiguously identified and their mole fractions in the resulting mixture determined. The presence of these by-products was found not to influence the initiator efficiency.
    Additional Material: 5 Ill.
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  • 272
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The redox catalyzed addition of compounds such as Cl3C—CF2—CCl3 and Cl3C—CF2—CCl2—CH2—CHCl—CH2—OCOCH3 to allyl acetate was studied with the purpose of obtaining telechelic products. RuCl2[P(C6H5)3]3 was used as catalyst, and its action was compared to that of cooper- or iron-based catalysts. The products were isolated and their structures studied by means of 13C, 19F and 1H NMR spectroscopy. The reaction mechanism was studied to improve the yield of the diaddition product for its utilisation as monomer in polycondensation reactions. It was found that the low reactivity for a second addition is not due to the presence of a chlorine atom in β-position of the acetate function. When allyl acetate was replaced by allyl bromide or chloride in the first addition, the second addition to allyl acetate occurred normally.
    Additional Material: 2 Tab.
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  • 273
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The photodecomposition of diphenyl-2,4,6-trimethylbenzoylphosphine oxide (1) was studied both in solution at 40°C and in thin films in the presence of 1,1-di-p-tolylethylene as a model substrate for vinyl monomers. Both primary radicals resulting from α-cleavage of 1 were found to add to the olefinic double bond of the model substrate (initiation). The diphenylphosphinoyl radical (3) proved to be twice as effective as the 2,4,6-trimethylbenzoyl radical (2) under all conditions. Oxygen (air) considerably reduced the initiating efficiencies fp, in particular fp(2) (of radical 2). The addition of triethylamine partially restored the overall initiating efficiency in all likelihood by oxygen scavenging. A direct contribution of triethylamine-derived radicals to the initiation was not observed.
    Additional Material: 1 Ill.
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  • 274
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 1-Alkanesulfonic and 4-alkylbenzenesulfonic esters of α-hydroxymethylbenzoin were shown to photoinitiate the polymerization and crosslinking of acrylates. The overall rate of polymerization in bulk and of crosslinking in solution, respectively, proved to be constant within each series of homologues. However, in thin films in an air atmosphere, the overall rate of crosslinking (curing rate) proved to increase with increasing alkyl chain-length within each series of homologues. Moreover, the curing rate obtained with the 1-hexanesulfonic ester and its higher homologues substantially surpassed the curing rates obtained with a number of established photoinitiators, provided a small amount of an alkali metal salt (preferably a lithium salt) is present. The curing mechanism of the sulfonic esters of α-hydroxymethylbenzoin and the role of the alkali metal salt are explained.
    Additional Material: 1 Ill.
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  • 275
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The possibility of making block copolymers at room temperature from the monomer pairs 2a,b/1, 4/1, 5/1 and 5/3 (1 = norbornene = bicyclo[2.2.1]hept-2-ene; 2a,b = anti- and syn-7-methylbicyclo[2.2.1]hept-2-ene; 4 = methyl endo-bicyclo[2.2.1]hept-5-ene-2-carboxylate; 5 = endo-bicyclo[2.2.1]hept-5-ene-2-carbonitrile; 3 = 1,5-cyclooctadiene) was explored using as initiator of metathesis polymerization in CD2Cl2. The reactions of successive small amounts of the monomers with the catalyst were first followed by 1H NMR to determine the rate of the reaction and the stability of the metal-carbene propagating species. AB and ABA type block copolymers were prepared on this basis and analysed by GPC. An increase in molecular weight after each addition was observed in most cases. Secondary metathesis reactions of double bonds in the polymer chains appear to be significant only for blocks formed from 3.
    Additional Material: 3 Ill.
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  • 276
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The free radical oligomerization of methyl methacrylate using different tetraphenylethane initiators [1,2-diphenoxy-1,1,2,2-tetraphenylethane (4), tetraphenylsuccinonitrile (5), and 1,1,2,2-tetraphenyl-1,2-bis(trimethylsiloxy)ethane (6)] gives telechelics 1 - 3 with end groups originating from the initiator. These telechelics were characterized by gel permeation, thin layer, and high performance chromatography. By adsorption chromatography, the separation does not only proceed in accordance with the molecular weight of the oligomers, but also with their tacticity as well. The free radical oligomerization is a process in which syndiotactic structures are favoured above isotactic ones.
    Additional Material: 6 Ill.
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  • 277
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    Die Makromolekulare Chemie 189 (1988), S. 2823-2837 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The commercially available poly(1-octenylene) Vestenamer® formed by the metathetic polymerization of cyclooctene with a tungsten catalyst, is highly crystalline at room temperature; it shows specific properties as a blend component, thus favourably influencing the processing characteristics and the final product quality. Differential scanning calorimetry, infrared and torsion pendulum experiments indicate that the melting temperature and the degree of crystallinity depend on the concentration of trans double bonds, on their distribution along the polymer chain as well as on the sample history. The formation of crosslinks induced by very intensive UV irradiation of 100 μm thin films leads to a reduction of the melting temperature and the crystallinity. A correlation between stiffness (shear modulus G′) and crystallinity was found for samples with varying amounts of trans double bonds.
    Additional Material: 12 Ill.
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  • 278
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    Die Makromolekulare Chemie 189 (1988), S. 2839-2846 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polymerizations of various olefins (ethylene, propene, 1-butene, 4-methyl-1-pentene,1-hexene, and 1-octene) were carried out using the Solvay-type TiCl3 catalyst combined with Cp2TiMe2. The polymers produced were characterized by DSC, solvent fractionation, GPC, and 13C NMR. It was found that the present catalyst gives linear polyethylene without ethyl branches and extremely highly isotactic poly(α-olefins) containing very few steric defects. The catalyst seems to be most isospecific among the Ziegler-Natta catalysts reported so far.
    Additional Material: 7 Ill.
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  • 279
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    Die Makromolekulare Chemie 189 (1988), S. 2847-2860 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cross-linked poly(vinyl alcohol) beads were functionalized by derivatization of their hydroxyl groups with succinic acid anhydride, 1,6-hexamethylene diisocyanate, 3-aminopropyltriethoxysilane, 2-chlorophenylbis(1,2,4-triazol-4-yl) phosphate and different sulfhydryl reagents. The resulting 8 gels carry isocyanato, carboxyl, amino, phosphate and mercapto residues in concentrations of 1 to 3 mmol per gram of polymer. The derivatives obtained from the starting poly(vinyl alcohol) beads are mechanically stable, resistent to hydrolysis in the pH range between 1 and 14 and stable up to 100°C. The functionalized, cross-linked polymer beads, applicable in aqueous systems as well as in organic solvents, should find a wide application in chromatography, as supports in the preparative solid phase synthesis and as basic carriers for polymeric reagents.
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  • 280
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    Die Makromolekulare Chemie 189 (1988), S. 2861-2874 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The development of polymer optical fibers (POF) leads to the fundamental question about the lowest loss attainable with organic polymers. In the present paper, we address this question with experimental and theoretical work on vibrational overtone absorption of different molecular bonds, which is the dominant loss contribution in POF's. The investigations, the first of their kind for several bonds, show good agreement between experiment and theory for the experimentally accessible CH-, CD-, and OH-vibrations. Applied to CF-, CCl-, and (C=O)- vibrations, the calculations lead to the conclusion that in the most important wavelength region 600 - 900 nm fully halogenated polymers show a negligible loss contribution due to overtone absorption. In these cases, the theoretical lower loss limit should be a few dB/km.
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  • 281
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    Die Makromolekulare Chemie 189 (1988), S. 2875-2883 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(vinyl acetate) (PVAc) and poly(tert-butyl methacrylate) (PBMA) macromonomers with vinyl end-groups were synthesized by radical or anionic polymerizations. 4-Vinylpyridine (4VP)/vinyl acetate (VAc) and 4VP/tert-butyl methacrylate (BMA) graft copolymers were prepared by radical copolymerization of these macromonomers with 4VP as a comonomer. The 4VP/vinyl alcohol (VA) graft copolymer was derived from alkaline hydrolysis of 4VP/VAc graft copolymer. After having fixed the microdomains of 4VP/VA graft copolymer film, the solution of graft copolymer (or polymer blends) was cast on a support film of 4VP/VA graft copolymer. It was shown that the domain structure of the upper layer is governed by epitaxial growth of the microdomain pattern of the support film surface.
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  • 282
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Three different methods to synthesize star-shaped poly(ethylene oxide) are discussed in the present article. In all three cases, the branches are grown from a plurifunctional initiator. It is established that even though the early stages of the polymerization occur in heterogeneous phase, the consequences on the polymers formed are of minor importance. The most significant method is a core-first process, involving multifunctional poly-DVB cores as the initiating species, made anionically in dilute solution. Although strong association phenomena are occurring during the growth of the branches, star-shaped poly(ethylene oxide)s with a high number of functionalized branches are obtained. The polymers arising from all three methods were characterized accurately.
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  • 283
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    Die Makromolekulare Chemie 189 (1988), S. 2893-2897 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The characteristic ratio and its temperature coefficient were examined for alternating copolymers of ethylene and propylene. The stereochemical composition covers the entire range from racemic through meso. Two different assignments, τ = 0 and σ, were used for the statistical weight employed when a methylene group participates in simultaneous first-order interactions with another methylene group and a methyl group. The best description of the conformational properties of the alternating copolymers is achieved with the larger value for τ. This assignment is the one that would be expected if the first-order interactions were pair-wise additive.
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  • 284
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    Die Makromolekulare Chemie 189 (1988), S. 419-427 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Alternating copolymers of maleic anhydride with vinyl ethers, bearing a 4′-methoxy-4-biphenylyl mesogenic group via an oligo(ethylene oxide) spacer, were synthesized and structurally characterized. From X-ray diffraction observations, a smectic E phase was observed. Smectic layers are single layers of ribbon-like polymer chains, with all pendant groups arranged in a single row and pending on the same side of the backbone. Mesogenic groups are oriented up and down at random, and polymer chains are aligned along the [110] direction of the rectangular lattice describing the packing of the pendant groups.
    Additional Material: 5 Ill.
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  • 285
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    Die Makromolekulare Chemie 189 (1988), S. 523-527 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Photochemical hydrogen peroxide catalyzed degradation of both natural rubber and synthetic cis-polyisoprene is shown to result in the formation of a low-molecular-weight oil functionalised with hydroxyl, carbonyl and epoxide groups. Interestingly, the epoxide groups are shown to be of a trans-configuration. A scheme is proposed to account for the formation of trans-epoxide as well as concomitant mainchain isomerization. The preferential formation of trans-epoxide in free radical oxidations strongly suggests that the naturally occurring cis-epoxide, present in natural rubber, is due to a stereospecific enzymatic process, and is not the byproduct of radical oxidation.
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  • 286
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    Die Makromolekulare Chemie 189 (1988), S. 939-950 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Electron spin resonance (ESR) spectra of styrene/methacrylic acid copolymers neutralized with Cu(II) were observed at room temperature. Three magnetic species were detected; isolated Cu2+, Cu2+-Cu2+ pairs of Cu(II) acetate monohydrate type and anhydrous Cu(II) formate type. One of the absorption patterns due to the Cu2+-Cu2+ pair is the same as that of Cu(II) acetate monohydrate except linewidth. ESR data from the other species are summarized. ESR parameter, effect of the acid and Cu(II) contents, and spectral changes depending on sample preparation procedures or temperatures are discussed.
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  • 287
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    Die Makromolekulare Chemie 189 (1988), S. 969-969 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 288
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    Die Makromolekulare Chemie 189 (1988), S. 1043-1050 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Complementary experiments confirm the recent findings that the rate of propene polymerization is temporary enhanced if a small amount of ethylene is introduced during the polymerization, normalizing after consumption of ethylene by copolymerization. In addition, the study of the sequence distribution of propene monomeric units in the copolymerization carried out under various conditions revealed that the activation by ethylene does not involve the propagation steps, but the re-initiation after deactivation. A similar temporary activation effect was observed after the addition of small amounts of hydrogen. In this case, however, hydrogen is not consumed. Thus, the deactivation observed after the initial rate enhancement is due to another reason. The deactivation could be shown to be reversible after removal of the adsorbed hydrogen when either ethylene or hydrogen was added again to allow re-initiation of the polymerization. One of the important reasons of the continuous decrease of the propene homopolymerization rate may be due to the fact, that, after a transfer step, the re-initiation of polymerization does not take place spontaneously. Small amounts of ethylene or hydrogen allow the reinitiation to take place, at least for some kind of active sites.
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  • 289
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    Die Makromolekulare Chemie 189 (1988), S. 1061-1075 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(dimethylsiloxane) (PDMS) fitted at both chain ends with dimethylsilyl functions was heated at 90 and 110°C in the presence of chloroplatinic acid. A chain-branching reaction was observed yielding very-high-molecular-weight species. The phenomenon, which occurs as well in solution as in the bulk, is temperature dependent. This reaction can exist as a side reaction of the hydrosilylation reaction between PDMS (1) and 1,4-bis(dimethylvinylsilyl)benzene (2) or tetraallyloxyethane (5) when dimethylsilyl functions are in excess. However, it does not take place in hydrosilylations in which mole ratios 1/2 equal to unity or higher are applied.
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  • 290
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    Die Makromolekulare Chemie 189 (1988), S. 1051-1060 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new method for the synthesis of compact, multifunctional star-shaped polystyrenes was designed. A plurifunctional metalorganic initiator is obtained upon reaction of potassium naphthalene with commercial divinylbenzene. The resulting polymeric “core” exhibits a number of metalorganic sites. In a subsequent step, these sites initiate the polymerization of styrene to yield a star-shaped polymer. High numbers of branches can be obtained, thus rendering these molecules extremely compact. However, the major advantage of the “core first” method is that it allows functionalization of the branches at their outer end, thus providing the possibility of further reaction or selective adsorption. This “core first” method was also applied to the preparation of star-block copolymers formed of a polystyrene block and a poly(ethylene oxide) block.
    Additional Material: 2 Ill.
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  • 291
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Copolyesters of 3-hydroxybutyric acid (HB) and 3-hydroxyvaleric acid (HV), P(HB-co-HV), were isolated from Alcaligenes eutrophus and characterized by solution NMR, solid-state 13C CP/MAS NMR, and differential scanning calorimetry. The 13C CP/MAS NMR analysis was compatible with that of a random copolyester of oxy-(1-methyl-3-oxotrimethylene) (B) and oxy-(1-ethyl-3-oxotrimethylene) (V) units which adopts a regular conformation of a 21 -helix in the solid state throughout a wide range of compositions varying from 0 to 90 mol-% V units. The chain dynamics of P(HB-co-HV) in chloroform was studied by analysis of the 13C and 1H NMR spectra. The carbon-13 spin-lattice relaxation times (T1) and nuclear Overhauser enhancements (NOE) indicated that the copolyester molecules in chloroform are not rigid but rather flexible. The conformational preferences of the copolyester molecules were determined by analysis of the 1H NMR spectra.
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  • 292
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    Die Makromolekulare Chemie 189 (1988), S. 1087-1095 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polystyrene-block-poly(styrene-ran-isoprene)-block-polyisoprene characterized by a morphology of spherical rubbery microdomains in a continuous polystyrene matrix is considered as a model for rubber-toughened thermoplastics in which the volume fraction of the interfacial layer can be varied by varying the volume fraction of the interblock. Stress-strain measurements of these systems are presented in relation to their morphology, interblock volume fraction and molecular weight of the polystyrene block. The results indicate that the energy of fracture is increased with increasing width of the interfacial layer without change of Young's modulus.
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  • 293
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    Die Makromolekulare Chemie 189 (1988), S. 1117-1131 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A general reexamination of the configurational statistics of polymers obtained by ringopening polymerization of heterocyclic monomers is presented. The polymers under study involve one or two asymmetric centres in the main chain per monomeric unit. Sequence probabilities are calculated for Bernoullian, and first- and second-order Markov propagation models. The analyses of two polymers [poly(styrene oxide) and poly(tert-butyloxirane)] for which tacticity data are available in the literature are given as examples.
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  • 294
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    Die Makromolekulare Chemie 189 (1988), S. 1133-1140 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of ethylene/propylene/1-octene terpolymers with different composition is examined by 13C NMR. Assignments of the various carbon resonances are accomplished by comparison with spectra of ethylene/propylene, ethylene/1-octene, and propylene/1-octene copolymers and by INEPT multi-pulse technique. The polymers obtained with a high-mileage titanium-magnesium catalyst contain no inverted propylene sequences. The intensities of all the lines are used in the calculation, and this approach allows the terpolymer composition and the sequence distribution to be determined.
    Additional Material: 2 Ill.
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  • 295
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Pairs of chains taken from ensembles of five-way cubic lattice chains (athermal or theta) were analysed for the (relative) probability of contact formation between specified segments belonging to different chains within this pair. This probability may be taken as a measure of the rate constant which characterizes bimolecular polymer-polymer reactions which occur between active sites attached to or localized at these segments, relative to the reaction between the same active sites, if these were not bound to the polymer chains. It turns out that the (expected) effect which results from the interaction between the chains as a whole (external shielding) is of comparatively small extent and is fairly independent of chain length. The much more important contribution, however, is made by a novel phenomenon which  -  exhibiting a strong dependence on chain length n  -  is responsible for an “internal” shielding: the compatible pair configurations (i. e. those which are free of intermolecular intersections) are characterized by largely increased segment-segment distances. As a consequence, the probability of contact formation is much lower than it would be expected from a convolution of the (mutually independent) radial distributions of the segments participating in contact formation. The overall shielding factor K can be represented as a product of the fairly independent contributions of external (KG) and internal (Kw) shielding. The overall chain length dependence is described by a power law K = Dnd, where the exponent d depends on whether two (Type I contacts), one (Type II) or no endsegment at all (Type III) is involved in contact formation. For athermal chains the exponents are d = -0,16 (Type I), d = -0,30 (Type II), and d = -0,50 (Type III), the pre-factor being of the order of unity throughout. Θ-systems roughly show the same general characteristics as the athermal ones, however, to a lesser extent. Thus, neither shielding nor its chain length dependence vanish, the exponents being about -0,06 (Type I), -0,1 (Type II), and -0,2 (Type III), respectively.
    Additional Material: 8 Ill.
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  • 296
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The synthesis and characterization of poly[trans-11-{4-[5-(4-methoxyphenyl)-1,3-dioxan-2-yl]-2,6-dimethylphenoxy}undecyl methacrylate] and poly[trans-11-{4-[5-(4-methoxyphenyl)-1,3-dioxan-2-yl]-2,6-dimethylphenoxy}undecyl acrylate] is presented. Both polymers exhibit nematic mesophases and do not present side-chain crystallization. At temperatures higher than 160°C the 1,3-dioxane-2,5-diyl groups undergo a thermally induced trans-cis isomerization. A radical mechanism is proposed for this isomerization.
    Additional Material: 3 Ill.
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  • 297
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    Die Makromolekulare Chemie 189 (1988), S. 1155-1165 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The radical heterophase copolymerization of maleic anhydride (1) with isobutene (2), 1-butene (3) or with a petrochemical C4-fraction free from butadiene (C4) yielded copolymers with a molecular weight of 424 · 103, 291 · 103 and 190 · 103 g/mol, respectively. The structures of poly(1-co-2), poly(1-co-3) and poly(1-co-C4) obtained were elucidated by 13C NMR, 1H NMR and IR spectroscopy. Irrespective of whether 2, 3 or C4 was used as comonomer, the appropriate 13C NMR, 1H NMR and IR spectra proved to be essentially identical. These spectra confirm the presence of the 1,1-dimethylethylene structural units in the repeating units of each of the copolymers investigated. Thus, the radical copolymerization of 1-butene with maleic anhydride is accompanied by a rearrangement within the 1-butene molecule due to hydrogen and methyl shift.
    Additional Material: 7 Ill.
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  • 298
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Phthalocyanine moieties containing polymers 3 a - e were prepared by the reaction of several oxy- and arylenedioxy-bridged diphthalonitriles 2 a - e in the absence or the presence of metal salts or metals. The structure of the polymers was thoroughly discussed on the basis of their IR and UV/VIS spectra. According to the nitrile end groups determined by IR spectroscopy, the structurally uniform polymers consist of phthalocyanine moieties. Saponification of the nitrile end groups of 3 a - e leads to polymeric phthalocyanines with carboxylic acid end groups with a lower degree of annulation than that of the polymers before saponification. The low-molecular-weight phthalocyanines 5a, b were prepared as model compounds for the polymers.
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  • 299
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    Die Makromolekulare Chemie 189 (1988), S. 1207-1217 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dynamic mechanical relaxations of poly(ethylene terephthalate) (PET), poly(1,4-cyclo-hexylenedimethylene terephthalate) (PCHDMT), and a copolymer of them (COP) were measured in the temperature range from -150 to 150°C by use of a dynamic viscoelastometer. The viscoelastic relaxations of COP are studied and compared with those of PET and PCHDMT. The anisotropy of the viscoelastic properties of stretched COP samples was also studied in order to distinguish between main and secondary relaxations.
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  • 300
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    Die Makromolekulare Chemie 189 (1988), S. 1189-1197 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Based on polarisation microscopic observation of polymers with mesogenic side groups at the phase transition isotropic-smectic, a domain-like structure has to be assumed for smectic phases. Two different regular-shaped nuclei are formed at the phase transition on slightly different conditions which grow after twinning into bǎtonnets. The Avrami equation can be applied for a quantitative description of the growth of the anisotropic areas as shown for one form of the nuclei. Unoriented and sheared samples maintain their morphology when cooled from the liquid-crystalline to the partially crystalline phase. The crystalline phase of polymers with mesogenic side groups was investigated by X-ray diffraction on differently oriented samples. It was found that the crystallites have the same internal structure despite the fact that they exhibit different uniaxial fibre axes. Optical investigations provide helpful supplementary information for deciding what kind of layered structure is present in the crystalline and smectic phase.
    Additional Material: 9 Ill.
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