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1. |
New synthesis of polyaromatics through oxidative polymerization by using metal complexes with air |
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Makromolekulare Chemie. Macromolecular Symposia,
Volume 59,
Issue 1,
1992,
Page 1-16
Eishun Tsuchida,
Kimihisa Yamamoto,
Hiroyuki Nishide,
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摘要:
AbstractThe oxidative polymerization provides a new synthetic route to polyaromatics. Poly(p‐phenylene sulfide) (PPS) is produced by oxidative polymerization of thiophenol with a vanadyl complex catalyst. The metal complexes act as an efficient catalyst of oxygen oxidative polymerization. The polymerization to yield PPS is discussed especially focusing on the catalytic mechanism of the complexe
ISSN:0258-0322
DOI:10.1002/masy.19920590103
出版商:Hüthig&Wepf Verlag
年代:1992
数据来源: WILEY
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2. |
Polymeric porphyrins as new photocatalysts in photodynamic therapy of cancer |
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Makromolekulare Chemie. Macromolecular Symposia,
Volume 59,
Issue 1,
1992,
Page 17-33
D. Wöhrle,
A. Ardeshirpur,
A. Heuermann,
S. Müller,
G. Graschew,
H. Rinneberg,
M. Kohl,
J. Neukammer,
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摘要:
AbstractPhotodynamic therapy and diagnosis (PDT) is described as an efficient clinical method for the treatment of cancer patients using hematoporphyrin derivative (Hpd) as sensitizer. Newly developed metal‐containing porphyrin type compounds are potential agents for PDT. A concept for covalently bound polymeric metal‐containing or metal‐free sensitizers is discussed. First results of these polymeric sensitizers are reported from in vivo experiments. High tumor accumulation up to 30% was observed. Results of fluorescence diagnosis are
ISSN:0258-0322
DOI:10.1002/masy.19920590104
出版商:Hüthig&Wepf Verlag
年代:1992
数据来源: WILEY
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3. |
Applications of highly luminescent transition metal complexes in polymer systems |
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Makromolekulare Chemie. Macromolecular Symposia,
Volume 59,
Issue 1,
1992,
Page 35-51
J. N. Demas,
B. A. Degraff,
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摘要:
AbstractAdvances in understanding the photophysics and photochemistry of transition metal complexes offer opportunities to utilize these materials as luminescence sensors and probes. However, heterogeneity has an enormous effect on luminescence, quenching, and photochemistry. An intimate understanding of the detailed interactions between the complexes and their environment will be necessary before the rational design of new high performance sensors and probes can be achieved. Such understanding is fairly well established for homogeneous media, but it is still in its infancy in solid supports (surfaces and polymers). We present case studies involving luminescent metal complexes bound to a variety of polymer systems. Both their potential and the difficulties inherent in these composite systems are presented. We discuss tools that have proved useful or are likely to be valuable in unraveling these complex systems.
ISSN:0258-0322
DOI:10.1002/masy.19920590105
出版商:Hüthig&Wepf Verlag
年代:1992
数据来源: WILEY
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4. |
Hydroformylation of vinyl acetate to α‐acetoxypropanal catalyzed by a silica‐supported polyalumazane‐rhodium complex |
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Makromolekulare Chemie. Macromolecular Symposia,
Volume 59,
Issue 1,
1992,
Page 53-58
Shi‐You Guan,
Mei‐Yu Huang,
Ying‐Yan Jiang,
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摘要:
AbstractHydroformylation of vinyl acetate was catalyzed by silica‐supported polyalumazane‐rhodium complex to give α‐acetoxypropanal in higher than 90% yield. The product was only α‐acetoxypropanal, isoaldehyde, and no β‐acetoxypropanal, normal aldehyde, or any other by‐product was observed. The catalyst was very stable in the hydroformylation, and it could be reused several times without any remarkable change of cata
ISSN:0258-0322
DOI:10.1002/masy.19920590106
出版商:Hüthig&Wepf Verlag
年代:1992
数据来源: WILEY
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5. |
Oxidative phenol coupling catalyzed by polymer‐bound copper‐imidazole complexes |
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Makromolekulare Chemie. Macromolecular Symposia,
Volume 59,
Issue 1,
1992,
Page 59-74
G. Challa,
W. Chen,
J. Reedijk,
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摘要:
AbstractPolymer‐bound imidazole‐copper(II) complexes were investigated and applied as catalysts for oxidative coupling (polymerization) of 2,6‐dialkylphenols. These polymeric catalysts were also immobilized on silica particles through adsorption, quaternization and grafting. Especially, the grafted catalysts showed interesting catalytic properties, e.g. good specificity for C‐O coupling and very good stability during prolonged use in continuous processes. This stability furnished new information about the mechanism of the oxidative coupling polymerization. Finally, this reaction was optimized for the preparation of PPO‐type te
ISSN:0258-0322
DOI:10.1002/masy.19920590107
出版商:Hüthig&Wepf Verlag
年代:1992
数据来源: WILEY
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6. |
Activation and copolymerization of CO2by macromolecule‐metal complexes |
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Makromolekulare Chemie. Macromolecular Symposia,
Volume 59,
Issue 1,
1992,
Page 75-82
Li‐Ban Chen,
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摘要:
AbstractThe activation of CO2and relevant comonomers can be promoted by using catalysts consisting of appropriate chelating polymers, suitable bimetallic combinations, and prepared by appropriate procedures. In this way, aliphatic polycarbonates, polycarbonate‐polyurethanes, saturated and unsaturated polycarbonate‐polyesters, as well as some other copolymers were synthesized in high yie
ISSN:0258-0322
DOI:10.1002/masy.19920590108
出版商:Hüthig&Wepf Verlag
年代:1992
数据来源: WILEY
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7. |
Lanthanide metal polymer complexes. Synthesis, characterization and application |
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Makromolekulare Chemie. Macromolecular Symposia,
Volume 59,
Issue 1,
1992,
Page 83-98
Yoshi Okamoto,
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摘要:
AbstractOur recent results on the investigation of lanthanide metal polymer complexes were presented. Luminescence properties of Tb3+or Eu3+‐polycarboxylate complexes in aqueous solution were investigated. The excitation band near 300 nm for Tb or Eu(polyacrylate) solutions were drastically enhanced by the addition of hydroxy radical generating reagents as well as ultrasonic irradiation. These spectral changes were attributed to the energy transfer from chromophore molecules formed by generated hydroxy radicals in both systems. Since the increase in the luminescence intensity was proportional to the hydroxy radical concentration, the Eu3+or Tb3+(PAA) system can provide a convenient method for the determination of hydroxy radical concentration in aqueous solution. We have also utilized lanthanide metal ion complexes as a luminescent emitter in electroluminescence (EL) devices. The configuration of the EL cell and experimental results were discusse
ISSN:0258-0322
DOI:10.1002/masy.19920590109
出版商:Hüthig&Wepf Verlag
年代:1992
数据来源: WILEY
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8. |
Effects of chemical modification of supports on properties of tertiary amino resin dispersed palladium catalysts for the hydrogenation of methyl acrylate |
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Makromolekulare Chemie. Macromolecular Symposia,
Volume 59,
Issue 1,
1992,
Page 99-111
Chunfu Chen,
Juntan Sun,
Hong Li,
Binglin He,
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摘要:
AbstractTertiary amino resins (TAR) were chemically modified by quaternization with methyl iodide. By this route six partly quaternized tertiary amino resins (PQTAR) with different I/N mole ratio were synthesized. Four different reducing agents, i.e., NaH, LiAlH4, CH3OH‐NaOH and NaBH4, were tested for the preparation of palladium catalysts dispersed on TAR or PQTAR. The rate of hydrogenation of methyl acrylate and the amount of Pd leached from the catalysts during the hydrogenation reaction were found to be dependent not only on the type of reducing agent but also on the structure of polymer support. Both the rate of hydrogenation and the amount of Pd eluted closely relate to the I/N mole ratio of the polymer support
ISSN:0258-0322
DOI:10.1002/masy.19920590110
出版商:Hüthig&Wepf Verlag
年代:1992
数据来源: WILEY
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9. |
Hydrogenation catalytic behaviors of palladium complexes of chitin and chitosan |
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Makromolekulare Chemie. Macromolecular Symposia,
Volume 59,
Issue 1,
1992,
Page 113-121
Xin‐Xin Wang,
Mei‐Yu Huang,
Ying‐Yan Jiang,
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摘要:
AbstractPalladium complexes of chitin and chitosan have been shown to have catalytic activities for hydrogenation at room temperature and under atmospheric pressure. They could catalyze not only reduction of olefines but also aromatic nitro‐compounds and acrylic acid. And they are very active, stable and selective. They also show different catalytic behaviors in different pH solutions. It is noteworthy that the catalytic activities of the two polymer‐supported metal complexes in the cycle of pH 11 → pH 2 → pH 11 are rev
ISSN:0258-0322
DOI:10.1002/masy.19920590111
出版商:Hüthig&Wepf Verlag
年代:1992
数据来源: WILEY
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10. |
Novel synthesis of electroconducting polymers from simple monomers with transition metal complex catalysts |
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Makromolekulare Chemie. Macromolecular Symposia,
Volume 59,
Issue 1,
1992,
Page 123-134
Naoki Toshima,
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摘要:
AbstractElectroconductive polyaromatics or polyarylenes have been successfully prepared by the oxidative polymerization of the corresponding simple monomers over the transition metal complex catalyst. For example, poly(1,4‐phenylene) was prepared from benzene by using oxygen as an oxidant and a copper(I) chloride‐aluminum chloride double complex as the catalyst. The same catalytic system was applied to the preparation of poly(2,5‐pyrrolylene) and poly(2,5‐thienylene) from pyrrole and 2,2′‐bithiophen, respectively. The electrochemical oxidative polymerization was also carried out for the preparation of the poly(1,4‐phenylene) and poly(1,4‐naphthylene) films in the presence of copper(I) chloride and al
ISSN:0258-0322
DOI:10.1002/masy.19920590112
出版商:Hüthig&Wepf Verlag
年代:1992
数据来源: WILEY
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