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1. |
Studies on microgels, 3. Synthesis using living free radical polymerization |
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Macromolecular Rapid Communications,
Volume 18,
Issue 9,
1997,
Page 755-760
Simmi Abrol,
Peter A. Kambouris,
Mark G. Looney,
David H. Solomon,
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摘要:
AbstractMicrogels which are soluble crosslinked polymer networks have been prepared using the nitroxide living free radical polymerization methodology. When heated in the presence oftert‐butylstyrene and 1,4‐divinylbenzene, the alkoxyamine1derived from 2,2′‐azoisobutyronitrile (AIBN) afforded a high molecular weight soluble polymer which was shown by size exclusion chromatography in conjunction with an on‐line multi angle laser light scattering (MALLS) detector to have microgel p
ISSN:1022-1336
DOI:10.1002/marc.1997.030180901
出版商:Hüthig&Wepf Verlag
年代:1997
数据来源: WILEY
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2. |
Alternative molecularly imprinted polymeric membranes from a tetrapeptide residue consisting ofD‐ orL‐amino acids |
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Macromolecular Rapid Communications,
Volume 18,
Issue 9,
1997,
Page 761-767
Masakazu Yoshikawa,
Jun‐ichiro Izumi,
Toshio Kitao,
Shunji Sakamoto,
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摘要:
AbstractAlternative molecularly imprinted polymeric membranes were prepared from a polystyrene resin bearing tetrapeptides consisting ofD‐amino acids or L‐amino acids. The membrane prepared from a DLDE derivative (H‐Asp(OcHex)‐Leu‐Asp(OcHex)‐Glu(OBzl)CH2) consisting ofD‐amino acids and imprinted by Boc‐D‐Trp recognizes the D‐isomer in preference to the correspondingL‐isomer and vice versa. The amino acid preferentially adsorbed by the membrane was selectively permeated by
ISSN:1022-1336
DOI:10.1002/marc.1997.030180902
出版商:Hüthig&Wepf Verlag
年代:1997
数据来源: WILEY
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3. |
Ring‐opening polymerization of chloromethylthiirane with SO42−/TiO2/Nd3+as initiator |
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Macromolecular Rapid Communications,
Volume 18,
Issue 9,
1997,
Page 769-773
Zhiquan Shen,
Weishi Li,
Fuyao Zhang,
Yifeng Zhang,
Lianfang Shen,
Hanzhen Yuan,
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摘要:
AbstractA new type of solid superacid (SO42−/TiO2/Nd3+) was used for the ring‐opening polymerization of chloromethylthiirane (CMT). TiO2· H2O immersed in a sulfuric acid solution containing Nd3+ions and calcined at 600°C gave the solid superacid for initiating the polymerization of CMT. The effects of polymerization temperature and amount of the initiator on the CMT polymerization were studied. Poly(CMT) obtained has higher molecular weight (M̄w= 52 000) than ever re
ISSN:1022-1336
DOI:10.1002/marc.1997.030180903
出版商:Hüthig&Wepf Verlag
年代:1997
数据来源: WILEY
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4. |
Polymerization of cyclic monomers, 4. Synthesis and radical polymerization of bi‐ and trifunctional 2‐vinylcyclopropanes |
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Macromolecular Rapid Communications,
Volume 18,
Issue 9,
1997,
Page 775-780
Norbert Moszner,
Frank Zeuner,
Volker Rheinberger,
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摘要:
AbstractMultifunctional 2‐vinylcyclopropanes were synthesized by esterification of the 1‐methoxycarbonyl‐2‐vinylcyclopropane‐1‐carboxylic acid with ethylene glycol, 1,1,1‐trimethylolpropane or 1,4‐cyclohexanediol in the presence of 1,3‐dicyclohexylcarbodiimide (DCC). The structure of the new vinylcyclopropanes was confirmed by elemental analysis, IR,1H NMR and13C NMR spectroscopy. The radical polymerization of the 2‐vinylcyclopropanes in bulk with 2,2′‐azoisobutyronitrile (AIBN) results in transparent crosslinked polymers. The polymerization of the liquid monomers is accompanied by a
ISSN:1022-1336
DOI:10.1002/marc.1997.030180904
出版商:Hüthig&Wepf Verlag
年代:1997
数据来源: WILEY
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5. |
Static density gradient centrifugation; extendedHermans‐Endeequation |
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Macromolecular Rapid Communications,
Volume 18,
Issue 9,
1997,
Page 781-786
M. Dieter Lechner,
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摘要:
AbstractAn extendedHermans‐Endeequation for real solutions has been derived in order to calculate the density as a function of the radial distance in a density gradient mixture (light/heavy medium) inside an ultracentrifugal cell. The equation has been tested with equilibrium density gradient measurements of the system water/metrizamide/polystyrene latex where metrizamide is the heavy medium. The solvent compositions were 8 to 15 mass‐% metrizamide (2‐(3‐acetamido‐5‐N‐methylacetamido‐2,4,6‐triiodobenzamido)‐2‐deoxy‐D‐glucose). The latex concentration was 0.03 mass‐%. It is demonstrated that the density gradient is highly influenced due to monideality effects with respect to the solvent composition and due to the pressure grad
ISSN:1022-1336
DOI:10.1002/marc.1997.030180905
出版商:Hüthig&Wepf Verlag
年代:1997
数据来源: WILEY
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6. |
Carboxy‐terminated homo‐ and copolymers of styrene using dicarboxylic acid‐functional azo initiator and 2,2,6,6‐tetramethyl‐1‐piperidyloxyl (TEMPO) |
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Macromolecular Rapid Communications,
Volume 18,
Issue 9,
1997,
Page 787-794
Martin Baumert,
Rolf Mülhaupt,
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摘要:
AbstractCarboxy‐terminated polystyrene, poly(styrene‐co‐acrylonitrile), and polystyrene‐block‐poly(styrene‐co‐acrylonitrile) with ratios of weight‐ to number‐average molar massesM̄w/M̄nbelow 1.3 were synthesized via a controlled radical polymerization mechanism. The polymerizations were initiated with 4,4′‐azobis(4‐cyanopentane‐carboxylic acid) and 2,2,6,6‐tetramethyl‐1‐piperidyloxyl radical and conducted in bulk at elevated temperatures. The polymerization was monitored by nuclear magnetic resonance, size‐exclusion chromatography, end‐group titration
ISSN:1022-1336
DOI:10.1002/marc.1997.030180906
出版商:Hüthig&Wepf Verlag
年代:1997
数据来源: WILEY
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7. |
[η3‐methallyl‐nickel‐dad]PF6complex: new catalyst precursor for ethylene polymerization |
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Macromolecular Rapid Communications,
Volume 18,
Issue 9,
1997,
Page 795-800
Roberto‐F. De Souza,
Raquel S. Mauler,
Leonardo C. Simon,
Fernanda F. Nunes,
Daniela V. S. Vescia,
Alessandro Cavagnolli,
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摘要:
AbstractThe complex [η3‐methallyl‐nickel‐dad]PF6is a new catalyst precursor for ethylene polymerization. The system is active in the presence of usual organoaluminium compounds like diethylaluminium chloride, at low Al/Ni ratios and under mild reaction conditions (temperatures between −10°C and 25°C, ethylene partial pressure from 1 to 15 atm). The polymers show extensive methyl branching, whose content is controlled by reaction parameters like temperature and ethylen
ISSN:1022-1336
DOI:10.1002/marc.1997.030180907
出版商:Hüthig&Wepf Verlag
年代:1997
数据来源: WILEY
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8. |
Polymerization of styrene to isotactic polymer with MAO‐Ni(acac)2. Examination of the factors that influence activity and stereospecificity |
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Macromolecular Rapid Communications,
Volume 18,
Issue 9,
1997,
Page 801-808
Geraldo Lopes Crossetti,
Carlotta Bormioli,
Alberto Ripa,
Antonino Giarrusso,
Lido Porri,
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摘要:
AbstractThe soluble catalyst system methylaluminoxane (MAO)‐Ni(acac), (acac: acetylacetonate) gives polystyrene consisting of an amorphous (aPS) and a crystalline isotactic (ips) fraction. Al(CH3)3, which is always present in commercial samples of MAO, decreases both polymer yield and stereospecificity. The polymer yield increases with increasing the MAO/Ni ratio but, at the same time, the iPS/aPS ratio decreases. Addition of N(C2H5)3(mole ratio N/Ni = 1) increases the proportion of the isotactic fraction, while it decreases the polymer yield. A tentative interpretation of the stereospecificity is reporte
ISSN:1022-1336
DOI:10.1002/marc.1997.030180908
出版商:Hüthig&Wepf Verlag
年代:1997
数据来源: WILEY
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9. |
Polymerization of ϵ‐caprolactone using heterobimetallic lanthanocene complexes |
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Macromolecular Rapid Communications,
Volume 18,
Issue 9,
1997,
Page 809-815
Kai C. Hultzsch,
Jun Okuda,
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摘要:
AbstractThe chiral heterobimetallic complexes Li[Ln(η5: η1‐C5R41SiMe2NCH2CH2R2)2] (Ln = Y, Lu; C5R41= C5Me4, C5H4, 3‐C5H3tBu; R2= OMe, NMe2; Me: methyl;tBu:tert‐butyl) have been found to polymerize ϵ‐caprolactone to give a polymer of high molecular weight (M̄n<20 000) and moderate polydispersity (M̄w/M̄n<2.0). Failure to observe a correlation between monomer/initiator ratio and molecular weight suggests a polymerization mechanism different from a pseudo‐an
ISSN:1022-1336
DOI:10.1002/marc.1997.030180909
出版商:Hüthig&Wepf Verlag
年代:1997
数据来源: WILEY
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10. |
Oligo(ether‐sulfones), 2. Synthesis of a novel macrocyclic aromatic ether sulfone bearing two carboxylic groups and the corresponding polyamide via direct condensation of the macrocycle with 4,4′‐diaminodiphenylmethane |
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Macromolecular Rapid Communications,
Volume 18,
Issue 9,
1997,
Page 817-825
Barbara Rodewald,
Helmut Ritter,
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摘要:
AbstractA new macrocyclic arylene ether sulfone bearing two carboxylic groups,4, was prepared by use of pseudo high dilution techniques. In a first step, 4,4‐bis[4‐(4‐(4‐chlorophenylsulfonyl)phenoxy)phenyl]pentanoic acid (3) was prepared from bis(4‐chlorophenyl)sulfone (1) and an excess of 4,4‐bis(4‐hydroxyphenyl)pentanoic acid (2). Then, the purified trimer3was cyclocondensed with 4,4‐bis(4‐hydroxyphenyl)pentanoic acid (2), yielding the bifunctionalized macrocycle4. The existence of the ring‐shaped molecule was proved by use of MALDI‐TOF, NMR‐ and IR‐spectroscopy. The free carboxylic groups of4were used to build up polyamides that contain the macrocycle in the main chain and 4,4′‐diaminodiphenylmetha
ISSN:1022-1336
DOI:10.1002/marc.1997.030180910
出版商:Hüthig&Wepf Verlag
年代:1997
数据来源: WILEY
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