메뉴 건너뛰기




Volumn 3, Issue 3, 2011, Pages 234-238

Controlled folding of synthetic polymer chains through the formation of positionable covalent bridges

Author keywords

[No Author keywords available]

Indexed keywords


EID: 79951998821     PISSN: 17554330     EISSN: 17554349     Source Type: Journal    
DOI: 10.1038/nchem.964     Document Type: Article
Times cited : (218)

References (43)
  • 1
    • 0015859467 scopus 로고
    • Principles that govern the folding of protein chains
    • Anfinsen, C. B. Principles that govern the folding of protein chains. Science 181, 223-230 (1973).
    • (1973) Science , vol.181 , pp. 223-230
    • Anfinsen, C.B.1
  • 2
    • 0347357617 scopus 로고    scopus 로고
    • Protein folding and misfolding
    • Dobson, C. M. Protein folding and misfolding. Nature 426, 884-890 (2003).
    • (2003) Nature , vol.426 , pp. 884-890
    • Dobson, C.M.1
  • 3
    • 0017835737 scopus 로고
    • Molecular morphology in semicrystalline polymers
    • Flory, P. J. & Yoon, D. Y. Molecular morphology in semicrystalline polymers. Nature 272, 226-229 (1978).
    • (1978) Nature , vol.272 , pp. 226-229
    • Flory, P.J.1    Yoon, D.Y.2
  • 4
    • 0000655815 scopus 로고
    • New explanation for chain folding in polymers
    • Sadler, D. M. New explanation for chain folding in polymers. Nature 326, 174-177 (1987).
    • (1987) Nature , vol.326 , pp. 174-177
    • Sadler, D.M.1
  • 5
    • 0542421525 scopus 로고    scopus 로고
    • Foldamers: A manifesto
    • Gellman, S. H. Foldamers: a manifesto. Acc. Chem. Res. 31, 173-180 (1998).
    • (1998) Acc. Chem. Res. , vol.31 , pp. 173-180
    • Gellman, S.H.1
  • 7
    • 58149184505 scopus 로고    scopus 로고
    • Aromatic oligoamide foldamers
    • Huc, I. Aromatic oligoamide foldamers. Eur. J. Org. Chem. 17-29 (2004).
    • (2004) Eur. J. Org. Chem. , pp. 17-29
    • Huc, I.1
  • 8
    • 73249140329 scopus 로고    scopus 로고
    • Helical polymers: Synthesis, structures, and functions
    • Yashima, E., Maeda, K., Iida, H., Furusho, Y. & Nagai, K. Helical polymers: synthesis, structures, and functions. Chem. Rev. 109, 6102-6211 (2009).
    • (2009) Chem. Rev. , vol.109 , pp. 6102-6211
    • Yashima, E.1    Maeda, K.2    Iida, H.3    Furusho, Y.4    Nagai, K.5
  • 9
    • 77952841687 scopus 로고    scopus 로고
    • Ion-triggered spring-like motion of a double helicate accompanied by anisotropic twisting
    • Miwa, K., Furusho, Y. & Yashima, E. Ion-triggered spring-like motion of a double helicate accompanied by anisotropic twisting. Nature Chem. 2, 444-449 (2010).
    • (2010) Nature Chem. , vol.2 , pp. 444-449
    • Miwa, K.1    Furusho, Y.2    Yashima, E.3
  • 10
    • 70450186565 scopus 로고    scopus 로고
    • Sequence control in polymer synthesis
    • Badi, N. & Lutz, J.-F. Sequence control in polymer synthesis. Chem. Soc. Rev. 38, 3383-3390 (2009).
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 3383-3390
    • Badi, N.1    Lutz, J.-F.2
  • 11
    • 76249115928 scopus 로고    scopus 로고
    • Polymer chemistry: A controlled sequence of events
    • Lutz, J.-F. Polymer chemistry: a controlled sequence of events. Nature Chem. 2, 84-85 (2010).
    • (2010) Nature Chem. , vol.2 , pp. 84-85
    • Lutz, J.-F.1
  • 12
    • 77950796120 scopus 로고    scopus 로고
    • Sequence-controlled polymerizations: The next Holy Grail in polymer science?
    • Lutz, J.-F. Sequence-controlled polymerizations: the next Holy Grail in polymer science? Polym. Chem. 1, 55-62 (2010).
    • (2010) Polym. Chem. , vol.1 , pp. 55-62
    • Lutz, J.-F.1
  • 13
    • 1642580697 scopus 로고    scopus 로고
    • Facile synthesis of a chiral polymeric helix; folding by intramolecular hydrogen bonding
    • van Gorp, J. J., Vekemans, J. & Meijer, E. W. Facile synthesis of a chiral polymeric helix; folding by intramolecular hydrogen bonding. Chem. Commun. 60-61 (2004).
    • (2004) Chem. Commun. , pp. 60-61
    • Van Gorp, J.J.1    Vekemans, J.2    Meijer, E.W.3
  • 14
    • 46149101332 scopus 로고    scopus 로고
    • Responsive backbones based on alternating triazole-pyridine/benzene copolymers: From helically folding polymers to metallosupramolecularly crosslinked gels
    • Meudtner, R. M. & Hecht, S. Responsive backbones based on alternating triazole-pyridine/benzene copolymers: from helically folding polymers to metallosupramolecularly crosslinked gels. Macromol. Rapid Commun. 29, 347-351 (2008).
    • (2008) Macromol. Rapid Commun. , vol.29 , pp. 347-351
    • Meudtner, R.M.1    Hecht, S.2
  • 15
    • 59049083255 scopus 로고    scopus 로고
    • Cycloaddition-promoted self-assembly of a polymer into well-defined beta sheets and hierarchical nanofibrils
    • Yu, T. B., Bai, J. Z. & Guan, Z. B. Cycloaddition-promoted self-assembly of a polymer into well-defined beta sheets and hierarchical nanofibrils. Angew. Chem. Int. Ed. 48, 1097-1101 (2009).
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 1097-1101
    • Yu, T.B.1    Bai, J.Z.2    Guan, Z.B.3
  • 16
    • 0037167015 scopus 로고    scopus 로고
    • A facile approach to architecturally defined nanoparticles via intramolecular chain collapse
    • Harth, E. et al. A facile approach to architecturally defined nanoparticles via intramolecular chain collapse. J. Am. Chem. Soc. 124, 8653-8660 (2002).
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 8653-8660
    • Harth, E.1
  • 17
    • 70149083886 scopus 로고    scopus 로고
    • Metastable supramolecular polymer nanoparticles via intramolecular collapse of single polymer chains
    • Foster, E. J., Berda, E. B. & Meijer, E. W. Metastable supramolecular polymer nanoparticles via intramolecular collapse of single polymer chains. J. Am. Chem. Soc. 131, 6964-6966 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 6964-6966
    • Foster, E.J.1    Berda, E.B.2    Meijer, E.W.3
  • 18
    • 76149143425 scopus 로고    scopus 로고
    • Toward controlling folding in synthetic polymers: Fabricating and characterizing supramolecular single-chain nanoparticles
    • Berda, E. B., Foster, E. J. & Meijer, E.W. Toward controlling folding in synthetic polymers: fabricating and characterizing supramolecular single-chain nanoparticles. Macromolecules 43, 1430-1437 (2010).
    • (2010) Macromolecules , vol.43 , pp. 1430-1437
    • Berda, E.B.1    Foster, E.J.2    Meijer, E.W.3
  • 19
    • 67849126439 scopus 로고    scopus 로고
    • Macromolecular chemistry: Polymers kept in the loop
    • Grayson, S. M. Macromolecular chemistry: polymers kept in the loop. Nature Chem. 1, 178-179 (2009).
    • (2009) Nature Chem. , vol.1 , pp. 178-179
    • Grayson, S.M.1
  • 20
    • 33645473133 scopus 로고    scopus 로고
    • An efficient route to well-defined macrocyclic polymers via 'click' cyclization
    • Laurent, B. A. & Grayson, S. M. An efficient route to well-defined macrocyclic polymers via 'click' cyclization. J. Am. Chem. Soc. 128, 4238-4239 (2006).
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 4238-4239
    • Laurent, B.A.1    Grayson, S.M.2
  • 21
    • 40849104871 scopus 로고    scopus 로고
    • Synthesis of macrocyclic copolymer brushes and their self-assembly into supramolecular tubes
    • Schappacher, M. & Deffieux, A. Synthesis of macrocyclic copolymer brushes and their self-assembly into supramolecular tubes. Science 319, 1512-1515 (2008).
    • (2008) Science , vol.319 , pp. 1512-1515
    • Schappacher, M.1    Deffieux, A.2
  • 22
    • 0036643538 scopus 로고    scopus 로고
    • Topological polymer chemistry
    • Tezuka, Y. & Oike, H. Topological polymer chemistry. Prog. Polym. Sci. 27, 1069-1122 (2002).
    • (2002) Prog. Polym. Sci. , vol.27 , pp. 1069-1122
    • Tezuka, Y.1    Oike, H.2
  • 23
    • 77958474335 scopus 로고    scopus 로고
    • Various polystyrene topologies built from tailored cyclic polystyrene via CuAAC reactions
    • Lonsdale, D. E. & Monteiro, M. J. Various polystyrene topologies built from tailored cyclic polystyrene via CuAAC reactions. Chem. Commun. 7945-7947 (2010).
    • (2010) Chem. Commun. , pp. 7945-7947
    • Lonsdale, D.E.1    Monteiro, M.J.2
  • 24
    • 34547770971 scopus 로고    scopus 로고
    • A facile procedure for controlling monomer sequence distribution in radical chain polymerizations
    • Pfeifer, S. & Lutz, J.-F. A facile procedure for controlling monomer sequence distribution in radical chain polymerizations. J. Am. Chem. Soc. 129, 9542-9543 (2007).
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 9542-9543
    • Pfeifer, S.1    Lutz, J.-F.2
  • 25
    • 57149131991 scopus 로고    scopus 로고
    • Development of a library of N-substituted maleimides for the local functionalization of linear polymer chains
    • Pfeifer, S. & Lutz, J.-F. Development of a library of N-substituted maleimides for the local functionalization of linear polymer chains. Chem. Eur. J. 14, 10949-10957 (2008).
    • (2008) Chem. Eur. J. , vol.14 , pp. 10949-10957
    • Pfeifer, S.1    Lutz, J.-F.2
  • 26
    • 77955791563 scopus 로고    scopus 로고
    • AAB-sequence living radical chain copolymerization of naturally occurring limonene with maleimide: An end-to-end sequence-regulated copolymer
    • Satoh, K., Matsuda, M., Nagai, K. & Kamigaito, M. AAB-sequence living radical chain copolymerization of naturally occurring limonene with maleimide: an end-to-end sequence-regulated copolymer. J. Am. Chem. Soc. 132, 10003-10005 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 10003-10005
    • Satoh, K.1    Matsuda, M.2    Nagai, K.3    Kamigaito, M.4
  • 27
    • 73649127216 scopus 로고    scopus 로고
    • Facile synthesis of functional periodic copolymers: A step toward polymer-based molecular arrays
    • Berthet, M. A., Zarafshani, Z., Pfeifer, S. & Lutz, J.-F. Facile synthesis of functional periodic copolymers: a step toward polymer-based molecular arrays. Macromolecules 43, 44-50 (2010).
    • (2010) Macromolecules , vol.43 , pp. 44-50
    • Berthet, M.A.1    Zarafshani, Z.2    Pfeifer, S.3    Lutz, J.-F.4
  • 28
    • 68249133592 scopus 로고    scopus 로고
    • Selective radical addition with a designed heterobifunctional halide: A primary study toward sequence-controlled polymerization upon template effect
    • Ida, S., Terashima, T., Ouchi, M. & Sawamoto, M. Selective radical addition with a designed heterobifunctional halide: a primary study toward sequence-controlled polymerization upon template effect. J. Am. Chem. Soc. 131, 10808-10809 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 10808-10809
    • Ida, S.1    Terashima, T.2    Ouchi, M.3    Sawamoto, M.4
  • 29
    • 67649989355 scopus 로고    scopus 로고
    • Liquid-phase synthesis of block copolymers containing sequence-ordered segments
    • Pfeifer, S., Zarafshani, Z., Badi, N. & Lutz, J.-F. Liquid-phase synthesis of block copolymers containing sequence-ordered segments. J. Am. Chem. Soc. 131, 9195-9197 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 9195-9197
    • Pfeifer, S.1    Zarafshani, Z.2    Badi, N.3    Lutz, J.-F.4
  • 30
    • 70450189516 scopus 로고    scopus 로고
    • Polymerization of enantiopure monomers using syndiospecific catalysts: A new approach to sequence control in polymer synthesis
    • Kramer, J. W. et al. Polymerization of enantiopure monomers using syndiospecific catalysts: a new approach to sequence control in polymer synthesis. J. Am. Chem. Soc. 131, 16042-16044 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 16042-16044
    • Kramer, J.W.1
  • 31
    • 84880305872 scopus 로고    scopus 로고
    • Sequence-regulated vinyl copolymers by metal-catalysed step-growth radical polymerization
    • Satoh, K., Ozawa, S., Mizutani, M., Nagai, K. & Kamigaito, M. Sequence-regulated vinyl copolymers by metal-catalysed step-growth radical polymerization. Nature Commun. 1, 6 (2010).
    • (2010) Nature Commun. , vol.1 , pp. 6
    • Satoh, K.1    Ozawa, S.2    Mizutani, M.3    Nagai, K.4    Kamigaito, M.5
  • 32
    • 67949112461 scopus 로고    scopus 로고
    • Nanostructured functional materials prepared by atom transfer radical polymerization
    • Matyjaszewski, K. & Tsarevsky, N. V. Nanostructured functional materials prepared by atom transfer radical polymerization. Nature Chem. 1, 276-288 (2009).
    • (2009) Nature Chem. , vol.1 , pp. 276-288
    • Matyjaszewski, K.1    Tsarevsky, N.V.2
  • 33
    • 72949114189 scopus 로고    scopus 로고
    • Transition metal-catalyzed living radical polymerization: Toward perfection in catalysis and precision polymer synthesis
    • Ouchi, M., Terashima, T. & Sawamoto, M. Transition metal-catalyzed living radical polymerization: toward perfection in catalysis and precision polymer synthesis. Chem. Rev. 109, 4963-5050 (2009).
    • (2009) Chem. Rev. , vol.109 , pp. 4963-5050
    • Ouchi, M.1    Terashima, T.2    Sawamoto, M.3
  • 34
    • 0034604562 scopus 로고    scopus 로고
    • Acetylenic coupling: A powerful tool in molecular construction
    • Siemsen, P., Livingston, R. C. & Diederich, F. Acetylenic coupling: a powerful tool in molecular construction. Angew. Chem. Int. Ed. 39, 2633-2657 (2000).
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 2633-2657
    • Siemsen, P.1    Livingston, R.C.2    Diederich, F.3
  • 35
    • 11844255741 scopus 로고    scopus 로고
    • Copper(I)-catalyzed synthesis of azoles. DFT study predicts unprecedented reactivity and intermediates
    • Himo, F. et al. Copper(I)-catalyzed synthesis of azoles. DFT study predicts unprecedented reactivity and intermediates. J. Am. Chem. Soc. 127, 210-216 (2004).
    • (2004) J. Am. Chem. Soc. , vol.127 , pp. 210-216
    • Himo, F.1
  • 36
    • 23844451374 scopus 로고    scopus 로고
    • The convergence of synthetic organic and polymer chemistries
    • Hawker, C. J. &Wooley, K. L. The convergence of synthetic organic and polymer chemistries. Science 309, 1200-1205 (2005).
    • (2005) Science , vol.309 , pp. 1200-1205
    • Hawker, C.J.1    Wooley, K.L.2
  • 37
    • 34247237682 scopus 로고    scopus 로고
    • 1,3-Dipolar cycloadditions of azides and alkynes: A universal ligation tool in polymer and materials science
    • Lutz, J.-F. 1,3-Dipolar cycloadditions of azides and alkynes: a universal ligation tool in polymer and materials science. Angew. Chem. Int. Ed. 46, 1018-1025 (2007).
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 1018-1025
    • Lutz, J.-F.1
  • 38
    • 77949810836 scopus 로고    scopus 로고
    • The application of CuAAC 'click' chemistry to catenane and rotaxane synthesis
    • Hanni, K. D. & Leigh, D. A. The application of CuAAC 'click' chemistry to catenane and rotaxane synthesis. Chem. Soc. Rev. 39, 1240-1251 (2010).
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 1240-1251
    • Hanni, K.D.1    Leigh, D.A.2
  • 39
    • 72949117217 scopus 로고    scopus 로고
    • Cyclic polymers: Synthetic strategies and physical properties
    • Kricheldorf, H. R. Cyclic polymers: synthetic strategies and physical properties. J. Polym. Sci. A 48, 251-284 (2010).
    • (2010) J. Polym. Sci. A , vol.48 , pp. 251-284
    • Kricheldorf, H.R.1
  • 40
    • 0000003753 scopus 로고
    • Synthesis of high molecular weight ring polystyrenes
    • Roovers, J. & Toporowski, P. M. Synthesis of high molecular weight ring polystyrenes. Macromolecules 16, 843-849 (1983).
    • (1983) Macromolecules , vol.16 , pp. 843-849
    • Roovers, J.1    Toporowski, P.M.2
  • 41
    • 20444381375 scopus 로고    scopus 로고
    • Synthesis and characterization of macrocyclic vinyl-aromatic polymers. Molecular weight-dependent glass transition temperatures and emission of macrocyclic polystyrene
    • Alberty, K. A., Hogen-Esch, T. E. & Carlotti, S. Synthesis and characterization of macrocyclic vinyl-aromatic polymers. Molecular weight-dependent glass transition temperatures and emission of macrocyclic polystyrene. Macromol. Chem. Phys. 206, 1035-1042 (2005).
    • (2005) Macromol. Chem. Phys. , vol.206 , pp. 1035-1042
    • Alberty, K.A.1    Hogen-Esch, T.E.2    Carlotti, S.3
  • 43
    • 0000760733 scopus 로고
    • Synthesis and characterization of 'eight-shaped' polystyrene
    • Antonietti, M. & Fölsch, K. J. Synthesis and characterization of 'eight-shaped' polystyrene. Makromol. Chem. Rapid Commun. 9, 423-430 (1988).
    • (1988) Makromol. Chem. Rapid Commun. , vol.9 , pp. 423-430
    • Antonietti, M.1    Fölsch, K.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.