|
1. |
Liquid‐crystalline structure of poly(L‐lysine) containing azobenzene units in the side chain |
|
Macromolecular Rapid Communications,
Volume 17,
Issue 8,
1996,
Page 493-501
Bernard Gallot,
Marc Fafiotte,
Adriano Fissi,
Osvaldo Pieroni,
Preview
|
PDF (490KB)
|
|
摘要:
AbstractThe structure of poly(L‐lysine) containing 44% azobenzene units in the side chain was studied by X‐ray diffraction between room temperature and 150°C. The polymer exhibits a mesomorphic structure of the smectic A1 type. In this structure, stable at least until 150°C, each smectic layer of thicknessdresults from the superposition of two layers: one of thicknessdAcontains the free lysine side chains, the other of thicknessdBcontains the azobenzene modified lysine side chains and the polypeptide main chains, that in their planes are arranged as in the “antiparallel” β‐structure classical for
ISSN:1022-1336
DOI:10.1002/marc.1996.030170801
出版商:Hüthig&Wepf Verlag
年代:1996
数据来源: WILEY
|
2. |
Enzymatic synthesis of a soluble polyphenol derivative from 4,4′‐biphenyldiol |
|
Macromolecular Rapid Communications,
Volume 17,
Issue 8,
1996,
Page 503-508
Shiro Kobayashi,
Hideharu Kurioka,
Hiroshi Uyama,
Preview
|
PDF (295KB)
|
|
摘要:
AbstractEnzymatic oxidative polymerization of 4,4′‐biphenyldiol was performed in an aqueous organic solvent using horseradish peroxidase as catalyst. In the polymerization using a mixture of 1,4‐dioxane and phosphate buffer (pH 7.0) (80:20 vol‐%) as solvent, the monomer was quantitatively consumed to give powdery polymeric materials in a high yield. The resulting polymer is soluble in polar solvents such asN,N‐dimethylformamide, dimethyl sulfoxide, and acetone. The molecular weight of the methylated product is 7.3 × 103. The polymer exhibits high thermal stability unde
ISSN:1022-1336
DOI:10.1002/marc.1996.030170802
出版商:Hüthig&Wepf Verlag
年代:1996
数据来源: WILEY
|
3. |
Thermally switchable polyrotaxane as a model of stimuli‐responsive supramolecules for nano‐scale devices |
|
Macromolecular Rapid Communications,
Volume 17,
Issue 8,
1996,
Page 509-515
Hiroaki Fujita,
Tooru Ooya,
Motoichi Kurisawa,
Hideharu Mori,
Minoru Terano,
Nobuhiko Yui,
Preview
|
PDF (391KB)
|
|
摘要:
AbstractA polyrotaxane consisting of many β‐cyclodextrins (β‐CDs) and a triblock copolymer of poly(ethylene glycol) (PEG) and poly(propylene glycol) (PPG) capped with bulky end‐groups was synthesized as a model of stimuli‐responsive supramolecules for nanoscale devices. The polyrotaxane was reversibly soluble‐insoluble in water in response to temperature. This was achieved through the assembled and dispersed states of β‐CDs along the block copolymer. It is considered that intermolecular hydrogen bondings of β‐CDs, as well as the PEG segment length of the copoloymer, are predominant factors for regulating such thermally switchable behavior of
ISSN:1022-1336
DOI:10.1002/marc.1996.030170803
出版商:Hüthig&Wepf Verlag
年代:1996
数据来源: WILEY
|
4. |
Polymerization of styrenes carrying dendrons of the first, second and third generation |
|
Macromolecular Rapid Communications,
Volume 17,
Issue 8,
1996,
Page 517-527
Ingo Neubert,
Evelin Amoulong‐Kirstein,
A.‐Dieter Schlüter,
Herbert Dautzenberg,
Preview
|
PDF (403KB)
|
|
摘要:
AbstractThe synthesis of styrene monomers5(G‐1,2,3) with Fréchet‐type dendrons of the first, second and third generation, and their radically initiated polymerization to result in high molecular weight dendrimers6(G‐1,2,3) are reported. First light‐scattering investigations using6(G‐2) show that this polymer is best described as a Gaus
ISSN:1022-1336
DOI:10.1002/marc.1996.030170804
出版商:Hüthig&Wepf Verlag
年代:1996
数据来源: WILEY
|
5. |
Polymerization of an azastyrene derivative, 1. 1,6‐addition polymerization of 2,6‐diisopropyl‐N‐methyleneaniline |
|
Macromolecular Rapid Communications,
Volume 17,
Issue 8,
1996,
Page 529-537
Akihito Hashidzume,
Atsushi Kajiwara,
Akira Harada,
Mikiharu Kamachi,
Preview
|
PDF (379KB)
|
|
摘要:
AbstractThe polymerizability of an azastyrene derivative, 2,6‐diisopropyl‐N‐methyleneaniline (DiPMAn), was studied. Although DiPMAn could not be polymerized by radical and anionic initiators, it was polymerized with cationic initiators, such as trifluoroacetic acid (TFA), TiCl4‐TFA, and SnCl4‐TFA. The polymer is formed by 1,6‐addition with electrophilic substitution of an activated monomer inpara‐position of the
ISSN:1022-1336
DOI:10.1002/marc.1996.030170805
出版商:Hüthig&Wepf Verlag
年代:1996
数据来源: WILEY
|
6. |
Shape memory behaviors of crosslinked copolymers containing stearyl acrylate |
|
Macromolecular Rapid Communications,
Volume 17,
Issue 8,
1996,
Page 539-543
Yoshiharu Kagami,
Jian Ping Gong,
Yoshihito Osada,
Preview
|
PDF (298KB)
|
|
摘要:
AbstractShape memory polymers were prepared by copolymerizing stearyl acrylate and methyl acrylate. The principle of this shape memory effect is based on reversible order‐disorder transition of crystalline aggregates of stearyl moieties. A specific feature of this type of shape memory copolymer is that the transition temperature at which the polymer abruptly becomes soft and deforms can be controlled by changing the monomer composition, which enables one to adjust the shape memory effect at a desired temperature. Mechanism and process of the shape memory behaviors were discusse
ISSN:1022-1336
DOI:10.1002/marc.1996.030170806
出版商:Hüthig&Wepf Verlag
年代:1996
数据来源: WILEY
|
7. |
Command surfaces, 20. Fixation of surface‐assisted homogeneous alignment of nematic liquid crystals by cationic photopolymerization |
|
Macromolecular Rapid Communications,
Volume 17,
Issue 8,
1996,
Page 545-551
Kunihiro Ichimura,
Masatoshi Kidowaki,
Haruhisa Akiyama,
Kazuaki Kudo,
Veronika Strehmel,
Bernd Strehmel,
Preview
|
PDF (347KB)
|
|
摘要:
AbstractThe surface‐assisted alignment of a nematic liquid crystal yields a persistent ordered structure upon cationic photopolymerization of liquid‐crystalline epoxides. Linearly polarized light irradiation of a photocrosslinkable polymer containing azobenzene moieties played a crucial role in this procedure since the photoinduced alignment is not deteriorated by heating for polymerizat
ISSN:1022-1336
DOI:10.1002/marc.1996.030170807
出版商:Hüthig&Wepf Verlag
年代:1996
数据来源: WILEY
|
8. |
Enzymes in polymer chemistry, 9. Polymerizable oligoesters from cholic acid via lipase catalyzed condensation reactions |
|
Macromolecular Rapid Communications,
Volume 17,
Issue 8,
1996,
Page 553-557
Olaf Noll,
Helmut Ritter,
Preview
|
PDF (230KB)
|
|
摘要:
AbstractRegioselective oligocondensation of cholic acid in the 3‐position was achieved in organic solution in the presence of a lipase fromCandida antarctica. Furthermore, a mixture of cholic acid, 11‐methacryloylaminoundecanoic acid and the lipase resulted in the production of a radically polymerizable oligo(cholic acid ester) bearing exactly one methacrylic end group. This new monomer was polymerized radically yielding the corresponding comb‐polymers bearing several cholic acid esters at the end of the side c
ISSN:1022-1336
DOI:10.1002/marc.1996.030170808
出版商:Hüthig&Wepf Verlag
年代:1996
数据来源: WILEY
|
9. |
Ultrahigh molecular weight alternating propene/ethene/carbon monoxide terpolymers with elastic properties |
|
Macromolecular Rapid Communications,
Volume 17,
Issue 8,
1996,
Page 559-565
Adnan S. Abu‐Surrah,
Gabriele Eckert,
Wolfgang Pechhold,
Wolfgang Wilke,
Bernhard Rieger,
Preview
|
PDF (361KB)
|
|
摘要:
AbstractSoluble propene/ethene/CO terpolymers (EPEC) with ultrahigh molecular weight (up to 1.2 × 106g/mol) were prepared by the use of dicationic palladium(II) phosphine catalysts and an optimized amount of water as activator. When the molar ratio of ethene/CO to propene/CO is below 50 mol‐%, the terpolymers are thermoplastic elastomers with excellent properties. Above this ratio the terpolymers are crystalline thermoplastics. The ultrahigh molecular weight elastomers are highly soluble in organic solvents such as CH2Cl2and CHC
ISSN:1022-1336
DOI:10.1002/marc.1996.030170809
出版商:Hüthig&Wepf Verlag
年代:1996
数据来源: WILEY
|
10. |
Evolution of the “knitting pattern” morphology in ABC triblock copolymers |
|
Macromolecular Rapid Communications,
Volume 17,
Issue 8,
1996,
Page 567-575
Ulrike Breiner,
Udo Krappe,
Reimund Stadler,
Preview
|
PDF (1801KB)
|
|
摘要:
AbstractA new morphology of ternary ABC triblock copolymers is presented which results from the asymmetric interaction between a centre block (poly(ethylene‐co‐butene)) to different end blocks (polystyrene and poly(methyl methacrylate)). This morphology with the appearance of a “knitting pattern” can be described as an intermediate of a morphology of A, B and C lamellae and a morphology of A and C lamellae with B cylinders at the A/C in
ISSN:1022-1336
DOI:10.1002/marc.1996.030170810
出版商:Hüthig&Wepf Verlag
年代:1996
数据来源: WILEY
|
|