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1. |
Mechanism of anionic polymerization of (meth)acrylates in the presence of aluminium alkyls, 2.Kinetic investigations with methyl methacrylate in toluene |
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Macromolecular Rapid Communications,
Volume 16,
Issue 6,
1995,
Page 399-406
Helmut Schlaad,
Axel H. E. Müller,
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摘要:
AbstractThe kinetics of the polymerization of methyl methacrylate initiated by lithium alkyls (tert‐butyllithium or ethyl α‐lithiobutyrate) was investigated in the presence of aluminium alkyls (triethylaluminium or triisobutylaluminium) in toluene at −78°C. The rate of polymerization decreases considerably once the living dimer is formed. This suggests that the aluminate end‐group coordinates with the penultimate ester group of the polymer chain, thus decreasing reactivity. The results are at variance with an activated monomer
ISSN:1022-1336
DOI:10.1002/marc.1995.030160601
出版商:Hüthig&Wepf Verlag
年代:1995
数据来源: WILEY
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2. |
Polymerizable mesoions, 2.Radical polymerization and 1,4‐dipolar polycycloaddition of a 4‐vinylphenyl‐modified mesoionic 4,6‐dioxo‐1,3‐diazine |
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Macromolecular Rapid Communications,
Volume 16,
Issue 6,
1995,
Page 407-415
Helmut Ritter,
Rolf Sperber,
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摘要:
AbstractMesoionic 5‐methyl‐4,6‐dioxo‐3‐phenyl‐1‐(4‐vinylphenyl)‐1,3‐diazine (5) was obtained by condensation of 3‐phenyl‐1‐(4‐vinylphenyl)formamidine (3) with methylmalonic acid (4). This vinyl‐substituted mesoionic heterocyclic compound was polymerized by usual radical initiation and, additionally, by thermally controlled polycycloaddition in solution, yielding two different types of polymers,6, 7. According to the X‐ray diffraction analysis, the structure of a low molecular weight model proves the regioselec
ISSN:1022-1336
DOI:10.1002/marc.1995.030160602
出版商:Hüthig&Wepf Verlag
年代:1995
数据来源: WILEY
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3. |
The effect of mixing time on the morphology and physical properties of liquid crystalline polymer based blends |
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Macromolecular Rapid Communications,
Volume 16,
Issue 6,
1995,
Page 417-424
Ane M. Zaldua,
M. Eugenia Muñoz,
Juan J. Peña,
Anton Santamaría,
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摘要:
AbstractRheological and thermal analysis results of blends of a thermotropic copolyesteramide and polyarylate of bisphenol A depend on the thermo‐mechanical treatment during mixing. The changes observed as mixing time increases are the following: (a) melt viscosity and loss factor increase, (b) glass transition temperature decreases. The morphological analysis of the blends shows the inability of the treated blends to form an oriented liquid crystalline polymer (LCP) phase, which explains the observed viscoelastic propertie
ISSN:1022-1336
DOI:10.1002/marc.1995.030160603
出版商:Hüthig&Wepf Verlag
年代:1995
数据来源: WILEY
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4. |
Effect of photoinitiator on the molar mass distribution obtained from a pulsed laser polymerization |
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Macromolecular Rapid Communications,
Volume 16,
Issue 6,
1995,
Page 425-434
Ute Bergert,
Sabine Beuermann,
Michael Buback,
Caroline H. Kurz,
Gregory T. Russell,
Claudia Schmaltz,
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摘要:
AbstractThe choice of the photoinitiator is not usually regarded as being as important consideration in attempting to determine the value of the propagation rate coefficientkpfrom a pulsed laser‐initiated polymerization (PLP). It is shown that in fact the choice of the photoinitiator can profoundly influence the success of such experiments. Specially, for a number of monomers it was found that the successful determination ofkpis essentially impossible when 1,1‐azodicyclohexanecarbonitrile is employed as a photoinitiator. The likely reason for this phenomenon is discussed from which it would seem appropriate to be wary in using any azo compound as a PLP photoinitiator. From PLP experiments with a non‐azo photoinitiator, ambient pressurekphas been determined for bulk polymerization of methyl methacrylate over an extended temperature
ISSN:1022-1336
DOI:10.1002/marc.1995.030160604
出版商:Hüthig&Wepf Verlag
年代:1995
数据来源: WILEY
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5. |
Amphiphilic liquid‐crystalline networks — phase behavior and alignment by mechanical fields |
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Macromolecular Rapid Communications,
Volume 16,
Issue 6,
1995,
Page 435-447
Peter Fischer,
Claudia Schmidt,
Heino Finkelmann,
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摘要:
AbstractA cross‐linked polysiloxane carrying non‐ionic amphiphilic side‐groups attached with their hydrophobic end to the polymer backbone is synthesized. The amphiphilic groups are selectively deuterated at the α‐position of the hydrophobic alkyl chains. The phase behavior with water is studied by deuterium nuclear magnetic resonance spectroscopy. A lamellar phase (La) is observed on the low‐water‐concentration side of the liquid‐crystalline regime. The domains of the La‐phase can be aligned macroscopically by uniaxial compressi
ISSN:1022-1336
DOI:10.1002/marc.1995.030160605
出版商:Hüthig&Wepf Verlag
年代:1995
数据来源: WILEY
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6. |
A fast catalyst system for the ring‐opening polymerization of cyclosiloxanes |
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Macromolecular Rapid Communications,
Volume 16,
Issue 6,
1995,
Page 449-453
Aart Molenberg,
Martin Möller,
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摘要:
AbstractMethanol, in combination with a non‐ionic phosphazene base, was used to initiate the polymerization of octamethylcyclotetrasiloxane. In bulk, an instantaneous and large increase in viscosity was observed upon addition of the initiator. In toluene solution, the equilibrium state was reached in approximately 1 min. In addition to its high polymerization rate, another advantage of this system, as compared with e.g. alkali metal hydroxides, is that it is homogeneou
ISSN:1022-1336
DOI:10.1002/marc.1995.030160606
出版商:Hüthig&Wepf Verlag
年代:1995
数据来源: WILEY
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