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Volumn 278, Issue 1-2, 2006, Pages 365-372

Synthesis of poly(phenylacetylene)-based polydendrons consisting of a phenyleneethynylene repeating unit, and oxygen/nitrogen permeation behavior of their membranes

Author keywords

Dendrimer; Oxygen permselectivity; Polyacetylene; Polydendron; Silyl group

Indexed keywords

CATALYSTS; DENDRIMERS; MECHANICAL PERMEABILITY; ORGANIC POLYMERS; PERMSELECTIVE MEMBRANES; SYNTHESIS (CHEMICAL);

EID: 33646779140     PISSN: 03767388     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.memsci.2005.11.023     Document Type: Article
Times cited : (26)

References (33)
  • 1
    • 0034187550 scopus 로고    scopus 로고
    • Functional dendrimers, hyperbranched and star polymers
    • Inoue K. Functional dendrimers, hyperbranched and star polymers. Prog. Polym. Sci. 25 (2000) 453
    • (2000) Prog. Polym. Sci. , vol.25 , pp. 453
    • Inoue, K.1
  • 2
    • 0037103007 scopus 로고    scopus 로고
    • Discovery of dendrimers and dendritic polymers: a brief historical perspective
    • Tomalia D.A., and Fréchet J.M.J. Discovery of dendrimers and dendritic polymers: a brief historical perspective. J. Polym. Sci. Polym. Chem. Ed. 40 (2002) 2719
    • (2002) J. Polym. Sci. Polym. Chem. Ed. , vol.40 , pp. 2719
    • Tomalia, D.A.1    Fréchet, J.M.J.2
  • 3
    • 0344440704 scopus 로고    scopus 로고
    • Dendrimers and other dendritic macromolecules: form building blocks to functional assemblies in nanoscience and nanotechnology
    • Fréchet J.M.J. Dendrimers and other dendritic macromolecules: form building blocks to functional assemblies in nanoscience and nanotechnology. J. Polym. Sci. Polym. Chem. Ed. 41 (2003) 3713
    • (2003) J. Polym. Sci. Polym. Chem. Ed. , vol.41 , pp. 3713
    • Fréchet, J.M.J.1
  • 4
    • 28144443427 scopus 로고    scopus 로고
    • New macromolecular architecture for permselective membranes
    • Aoki T., and Kaneko T. New macromolecular architecture for permselective membranes. Polym. J. 37 (2005) 717
    • (2005) Polym. J. , vol.37 , pp. 717
    • Aoki, T.1    Kaneko, T.2
  • 5
    • 0031145237 scopus 로고    scopus 로고
    • Polydendron: polymerization of dendritic phenylacetylene monomers
    • Kaneko T., Horie T., Asano M., Aoki T., and Oikawa E. Polydendron: polymerization of dendritic phenylacetylene monomers. Macromolecules 30 (1997) 3118
    • (1997) Macromolecules , vol.30 , pp. 3118
    • Kaneko, T.1    Horie, T.2    Asano, M.3    Aoki, T.4    Oikawa, E.5
  • 6
    • 0030797605 scopus 로고    scopus 로고
    • Enantioselective permeation of amino acids across membranes prepared from 3-helix bundle polyglutamates with oxyethylene chains
    • Inoue K., Miyahara A., and Itaya T. Enantioselective permeation of amino acids across membranes prepared from 3-helix bundle polyglutamates with oxyethylene chains. J. Am. Chem. Soc. 119 (1997) 6191
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 6191
    • Inoue, K.1    Miyahara, A.2    Itaya, T.3
  • 7
    • 0030921683 scopus 로고    scopus 로고
    • pH-switchable, ultrathin permselective membranes prepared from multilayer polymer composites
    • Liu Y., Zhao M., Bergbreiter D.E., and Crooks R.M. pH-switchable, ultrathin permselective membranes prepared from multilayer polymer composites. J. Am. Chem. Soc. 119 (1997) 8720
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 8720
    • Liu, Y.1    Zhao, M.2    Bergbreiter, D.E.3    Crooks, R.M.4
  • 8
    • 0035845776 scopus 로고    scopus 로고
    • Preparation and characterization of dendrimer layers on poly(dimethylsiloxane) films
    • Cha B.J., Kang Y.S., and Won. Preparation and characterization of dendrimer layers on poly(dimethylsiloxane) films. Macromolecules 34 (2001) 6631
    • (2001) Macromolecules , vol.34 , pp. 6631
    • Cha, B.J.1    Kang, Y.S.2    Won3
  • 10
    • 0035865834 scopus 로고    scopus 로고
    • Gas permeation properties of hyperbranched polyimide membranes
    • Fang J., Kita H., and Okamoto K. Gas permeation properties of hyperbranched polyimide membranes. J. Membr. Sci. 182 (2001) 245
    • (2001) J. Membr. Sci. , vol.182 , pp. 245
    • Fang, J.1    Kita, H.2    Okamoto, K.3
  • 11
    • 2942620294 scopus 로고    scopus 로고
    • Transport properties of cross-linked polyimide membranes induced by different generations of diaminobutane (DAB) dendrimers
    • Shao L., Chung T.-S., Goh S.H., and Pramoda K.P. Transport properties of cross-linked polyimide membranes induced by different generations of diaminobutane (DAB) dendrimers. J. Membr. Sci. 238 (2004) 153
    • (2004) J. Membr. Sci. , vol.238 , pp. 153
    • Shao, L.1    Chung, T.-S.2    Goh, S.H.3    Pramoda, K.P.4
  • 12
    • 4644308630 scopus 로고    scopus 로고
    • Surface characterization, modification chemistry, and separation performance of polyimide and polyamidoamine dendrimer composite films
    • Xiao Y., Chung T.-S., and Chng. Surface characterization, modification chemistry, and separation performance of polyimide and polyamidoamine dendrimer composite films. Langmuir 20 (2004) 8230
    • (2004) Langmuir , vol.20 , pp. 8230
    • Xiao, Y.1    Chung, T.-S.2    Chng3
  • 13
    • 4644227852 scopus 로고    scopus 로고
    • Gas transport properties of 6FDA-TAPOB hyperbranched polyimide membrane
    • Suzuki T., Yamada Y., and Tsujita Y. Gas transport properties of 6FDA-TAPOB hyperbranched polyimide membrane. Polymer 45 (2004) 7167
    • (2004) Polymer , vol.45 , pp. 7167
    • Suzuki, T.1    Yamada, Y.2    Tsujita, Y.3
  • 14
    • 84989742198 scopus 로고
    • Trimethylsilyl-group containing polyphenylacetylenes for oxygen and ethanol permselective membranes
    • Aoki T., Nakahara H., Hayakawa Y., Kokai M., and Oikawa E. Trimethylsilyl-group containing polyphenylacetylenes for oxygen and ethanol permselective membranes. J. Polym. Sci. Polym. Chem. Ed. 32 (1994) 849
    • (1994) J. Polym. Sci. Polym. Chem. Ed. , vol.32 , pp. 849
    • Aoki, T.1    Nakahara, H.2    Hayakawa, Y.3    Kokai, M.4    Oikawa, E.5
  • 15
    • 0007734978 scopus 로고
    • Oxygen permselective membrane from poly(oligosiloxanyl- or/and trimethylsilyl substituted phenylacetylene)
    • Aoki T., Nakahara H., and Oikawa E. Oxygen permselective membrane from poly(oligosiloxanyl- or/and trimethylsilyl substituted phenylacetylene). Polym. Preprints Jpn. 41 (1992) 4036
    • (1992) Polym. Preprints Jpn. , vol.41 , pp. 4036
    • Aoki, T.1    Nakahara, H.2    Oikawa, E.3
  • 16
    • 0035680834 scopus 로고    scopus 로고
    • Polymerization of phenylacetylene-based monodendrons and structure of the corresponding polydendrons
    • Kaneko T., Asano M., Yamamoto K., and Aoki T. Polymerization of phenylacetylene-based monodendrons and structure of the corresponding polydendrons. Polym. J. 33 (2001) 879
    • (2001) Polym. J. , vol.33 , pp. 879
    • Kaneko, T.1    Asano, M.2    Yamamoto, K.3    Aoki, T.4
  • 17
    • 0022785341 scopus 로고
    • Polymerization using palladium(II) salts: homopolymers and copolymers from phenylethynyl compounds and aromatic bromides
    • Trumbo D.L., and Marvel C.S. Polymerization using palladium(II) salts: homopolymers and copolymers from phenylethynyl compounds and aromatic bromides. J. Polym. Sci. Polym. Chem. Ed. 24 (1986) 2311
    • (1986) J. Polym. Sci. Polym. Chem. Ed. , vol.24 , pp. 2311
    • Trumbo, D.L.1    Marvel, C.S.2
  • 18
    • 0028529234 scopus 로고
    • Supramolecular tubular structures of a polymethacrylate with tapered side groups in aligned hexagonal phases
    • Kwon Y.K., Chvalun S., Schneider A.-I., Blackwell J., Percec V., and Heck J.A. Supramolecular tubular structures of a polymethacrylate with tapered side groups in aligned hexagonal phases. Macromolecules 27 (1994) 6129
    • (1994) Macromolecules , vol.27 , pp. 6129
    • Kwon, Y.K.1    Chvalun, S.2    Schneider, A.-I.3    Blackwell, J.4    Percec, V.5    Heck, J.A.6
  • 19
    • 0025627113 scopus 로고
    • 2-triethylamine catalyst containing long-lived propagation species
    • 2-triethylamine catalyst containing long-lived propagation species. Polym. J. 22 (1990) 1105
    • (1990) Polym. J. , vol.22 , pp. 1105
    • Tabata, M.1    Yang, W.2    Yokota, K.3
  • 20
    • 0028416964 scopus 로고
    • 1H NMR and UV studies of Rh complexes as a stereoregular polymerization catalysts for phenylacetylenes: effects of ligands and solvents on its catalyst activity
    • 1H NMR and UV studies of Rh complexes as a stereoregular polymerization catalysts for phenylacetylenes: effects of ligands and solvents on its catalyst activity. J. Polym. Sci. Polym. Chem. Ed. 32 (1994) 1113
    • (1994) J. Polym. Sci. Polym. Chem. Ed. , vol.32 , pp. 1113
    • Tabata, M.1    Yang, W.2    Yokota, K.3
  • 21
    • 0033616111 scopus 로고    scopus 로고
    • Well-controlled polymerization of phenylacetylenes with organorhodium(I) complexes: mechanism and structure of the polyenes
    • Kishimoto Y., Eckerle P., Miyatake T., Kainosho M., Ono A., Ikariya T., and Noyori R. Well-controlled polymerization of phenylacetylenes with organorhodium(I) complexes: mechanism and structure of the polyenes. J. Am. Chem. Soc. 121 (1999) 12035
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 12035
    • Kishimoto, Y.1    Eckerle, P.2    Miyatake, T.3    Kainosho, M.4    Ono, A.5    Ikariya, T.6    Noyori, R.7
  • 22
    • 0032182223 scopus 로고    scopus 로고
    • Living polymerization of phenylacetylene by novel rhodium catalysts. Quantitative initiation and introduction of functional groups at the initiating chain end
    • Misumi Y., and Masuda T. Living polymerization of phenylacetylene by novel rhodium catalysts. Quantitative initiation and introduction of functional groups at the initiating chain end. Macromolecules 31 (1998) 7572
    • (1998) Macromolecules , vol.31 , pp. 7572
    • Misumi, Y.1    Masuda, T.2
  • 23
    • 0001441909 scopus 로고    scopus 로고
    • Living polymerization of phenylacetylene by rhodium-based ternary catalysts, (diene)Rh(I) complex/vinyllithium/phosphorus ligand. Effects of catalyst components
    • Misumi Y., Kanki K., Miyake M., and Masuda T. Living polymerization of phenylacetylene by rhodium-based ternary catalysts, (diene)Rh(I) complex/vinyllithium/phosphorus ligand. Effects of catalyst components. Macromol. Chem. Phys. 201 (2000) 2239
    • (2000) Macromol. Chem. Phys. , vol.201 , pp. 2239
    • Misumi, Y.1    Kanki, K.2    Miyake, M.3    Masuda, T.4
  • 25
    • 0017542596 scopus 로고
    • Polymerization of acetylenic derivatives. XXX. Isomers of polyphenylacetylene
    • Simionescu C.I., Percec V., and Dumitrescu S. Polymerization of acetylenic derivatives. XXX. Isomers of polyphenylacetylene. J. Polym. Sci. Polym. Chem. Ed. 15 (1977) 2497
    • (1977) J. Polym. Sci. Polym. Chem. Ed. , vol.15 , pp. 2497
    • Simionescu, C.I.1    Percec, V.2    Dumitrescu, S.3
  • 26
    • 24944584172 scopus 로고    scopus 로고
    • Independent electrocyclization and oxidative chain cleavage along the backbone of cis-poly(phenylacetylene)
    • 1H NMR of the polydendrons, the peak at δ 5.9 assignable to the cis proton of poly(phenylacetylene) main-chain was similar to the 1H integral value. However, the precision was diminished with each subsequent generation due to the relative decrease of the main-chain's proton against all protons. Intramolecular electrocyclization, an expected reaction, was not detected for the same reason. The reference for intramolecular electrocyclization:
    • 1H NMR of the polydendrons, the peak at δ 5.9 assignable to the cis proton of poly(phenylacetylene) main-chain was similar to the 1H integral value. However, the precision was diminished with each subsequent generation due to the relative decrease of the main-chain's proton against all protons. Intramolecular electrocyclization, an expected reaction, was not detected for the same reason. The reference for intramolecular electrocyclization:. Percec V., and Rudick J.G. Independent electrocyclization and oxidative chain cleavage along the backbone of cis-poly(phenylacetylene). Macromolecules 38 (2005) 7241
    • (2005) Macromolecules , vol.38 , pp. 7241
    • Percec, V.1    Rudick, J.G.2
  • 27
    • 0000906251 scopus 로고
    • Polyacetylene with substituents: their synthesis and properties
    • Masuda T., and Higashimura T. Polyacetylene with substituents: their synthesis and properties. Adv. Polym. Sci. 81 (1987) 121
    • (1987) Adv. Polym. Sci. , vol.81 , pp. 121
    • Masuda, T.1    Higashimura, T.2
  • 29
    • 84963275124 scopus 로고
    • Polyacetylene derivatives with chain-sided phenoxy and galvinoxyl radicals
    • Nishide H., Kaneko T., Gotoh R., and Tsuchida E. Polyacetylene derivatives with chain-sided phenoxy and galvinoxyl radicals. Mol. Cryst. Liq. Cryst. 233 (1993) 89
    • (1993) Mol. Cryst. Liq. Cryst. , vol.233 , pp. 89
    • Nishide, H.1    Kaneko, T.2    Gotoh, R.3    Tsuchida, E.4
  • 30
    • 0000859385 scopus 로고
    • Synthesis of poly(ethynylbenzene) with pendant nitroxide radicals by rhodium-catalyzed polymerization of ethynylphenyl nitroxide
    • Miura Y., Matsumoto M., and Ushitani Y. Synthesis of poly(ethynylbenzene) with pendant nitroxide radicals by rhodium-catalyzed polymerization of ethynylphenyl nitroxide. Macromolecules 26 (1993) 2628
    • (1993) Macromolecules , vol.26 , pp. 2628
    • Miura, Y.1    Matsumoto, M.2    Ushitani, Y.3
  • 31
    • 0029882334 scopus 로고    scopus 로고
    • Living polymerization of (o-(trimethylsilyl)phenyl)acetylene by molybdenum imido alkylidene complexes
    • Schrock R.R., Luo S., Lee J.C., Zanetti N.C., and Davis W.M. Living polymerization of (o-(trimethylsilyl)phenyl)acetylene by molybdenum imido alkylidene complexes. J. Am. Chem. Soc. 118 (1996) 3883
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 3883
    • Schrock, R.R.1    Luo, S.2    Lee, J.C.3    Zanetti, N.C.4    Davis, W.M.5
  • 32
    • 0001141337 scopus 로고
    • Pressure-induced cis to trans isomerization of poly(o-methoxyphenylacetylene) polymerized by Rh complex catalyst. A Ramman, X-ray, and ESR study
    • Tabata M., Takamura H., Yokota K., Nozaki Y., Hoshina T., Minakawa H., and Kodaira K. Pressure-induced cis to trans isomerization of poly(o-methoxyphenylacetylene) polymerized by Rh complex catalyst. A Ramman, X-ray, and ESR study. Macromolecules 27 (1994) 6234
    • (1994) Macromolecules , vol.27 , pp. 6234
    • Tabata, M.1    Takamura, H.2    Yokota, K.3    Nozaki, Y.4    Hoshina, T.5    Minakawa, H.6    Kodaira, K.7
  • 33
    • 33646803904 scopus 로고    scopus 로고
    • The molecular modeling was performed on the assumption of a fully extended conformation for side-chain monodendrons, and distorted cis-transoid main-chain conformations, as described in Ref. [16].


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