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Volumn 7, Issue , 2016, Pages

A strategy for sequence control in vinyl polymers via iterative controlled radical cyclization

Author keywords

[No Author keywords available]

Indexed keywords

POLYMER; VINYL DERIVATIVE;

EID: 84962294005     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms11064     Document Type: Article
Times cited : (81)

References (46)
  • 2
    • 0026107795 scopus 로고
    • Living polymerization methods
    • Webster, O. W. Living polymerization methods. Science 251, 887-893 (1991).
    • (1991) Science , vol.251 , pp. 887-893
    • Webster, O.W.1
  • 3
    • 33846841153 scopus 로고    scopus 로고
    • Controlled/living radical polymerization: Features, developments, and perspectives
    • Braunecker, W. A. & Matyjaszewski, K. Controlled/living radical polymerization: features, developments, and perspectives. Prog. Polym. Sci. 32, 93-146 (2007).
    • (2007) Prog. Polym. Sci. , vol.32 , pp. 93-146
    • Braunecker, W.A.1    Matyjaszewski, K.2
  • 4
    • 84985570356 scopus 로고
    • Solid-phase synthesis (nobel lecture)
    • Merrifield, R. B. SOLID-PHASE SYNTHESIS (NOBEL LECTURE). Angew. Chem. Int. Ed. Engl. 24, 799-810 (1985).
    • (1985) Angew. Chem. Int. Ed. Engl. , vol.24 , pp. 799-810
    • Merrifield, R.B.1
  • 5
    • 0015529625 scopus 로고
    • Liquid-phase synthesis of peptides
    • Bayer, E. & Mutter, M. Liquid-phase synthesis of peptides. Nature 237, 512-513 (1972).
    • (1972) Nature , vol.237 , pp. 512-513
    • Bayer, E.1    Mutter, M.2
  • 6
    • 84930225369 scopus 로고    scopus 로고
    • Design and synthesis of digitally encoded polymers that can be decoded and erased
    • Roy, R. K. et al. Design and synthesis of digitally encoded polymers that can be decoded and erased. Nat. Commun. 6, 7237 (2015).
    • (2015) Nat. Commun. , vol.6 , pp. 7237
    • Roy, R.K.1
  • 7
    • 84946073576 scopus 로고    scopus 로고
    • Synthesis of monodisperse sequence-coded polymers with chain lengths above DP100
    • Al Ouahabi, A., Kotera, M., Charles, L. & Lutz, J. F. Synthesis of monodisperse sequence-coded polymers with chain lengths above DP100. ACS Macro Lett. 4, 1077-1080 (2015).
    • (2015) ACS Macro Lett. , vol.4 , pp. 1077-1080
    • Al Ouahabi, A.1    Kotera, M.2    Charles, L.3    Lutz, J.F.4
  • 8
    • 84942080910 scopus 로고    scopus 로고
    • Iterative exponential growth of stereo-and sequencecontrolled polymers
    • Barnes, J. C. et al. Iterative exponential growth of stereo-and sequencecontrolled polymers. Nat. Chem. 7, 810-815 (2015).
    • (2015) Nat. Chem. , vol.7 , pp. 810-815
    • Barnes, J.C.1
  • 9
  • 10
    • 84882782656 scopus 로고    scopus 로고
    • Polypeptoids: A model system to study the effect of monomer sequence on polymer properties and self-assembly
    • Rosales, A. M., Segalman, R. A. & Zuckermann, R. N. Polypeptoids: a model system to study the effect of monomer sequence on polymer properties and self-assembly. Soft Matter 9, 8400-8414 (2013).
    • (2013) Soft Matter , vol.9 , pp. 8400-8414
    • Rosales, A.M.1    Segalman, R.A.2    Zuckermann, R.N.3
  • 11
    • 69249207273 scopus 로고    scopus 로고
    • Precision polymers: Monodisperse, monomersequence-defined segments to target future demands of polymers in medicine
    • Hartmann, L. & Boerner, H. G. Precision polymers: monodisperse, monomersequence-defined segments to target future demands of polymers in medicine. Adv. Mater. 21, 3425-3431 (2009).
    • (2009) Adv. Mater. , vol.21 , pp. 3425-3431
    • Hartmann, L.1    Boerner, H.G.2
  • 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
    • 82055161645 scopus 로고    scopus 로고
    • Single-chain technology using discrete synthetic macromolecules
    • Ouchi, M., Badi, N., Lutz, J. F. & Sawamoto, M. Single-chain technology using discrete synthetic macromolecules. Nat. Chem. 3, 917-924 (2011).
    • (2011) Nat. Chem. , vol.3 , pp. 917-924
    • Ouchi, M.1    Badi, N.2    Lutz, J.F.3    Sawamoto, M.4
  • 15
    • 0025385909 scopus 로고
    • Sequence-regulated oligomers and polymers by living cationic polymerization 1. Synthesis of sequenceregulated trimers and tetramers of functional vinyl ethers
    • Minoda, M., Sawamoto, M. & Higashimura, T. Sequence-regulated oligomers and polymers by living cationic polymerization.1. Synthesis of sequenceregulated trimers and tetramers of functional vinyl ethers. Polym. Bull. 23, 133-139 (1990).
    • (1990) Polym. Bull. , vol.23 , pp. 133-139
    • Minoda, M.1    Sawamoto, M.2    Higashimura, T.3
  • 16
    • 77958491280 scopus 로고    scopus 로고
    • Template-assisted selective radical addition toward sequence-regulated polymerization: Lariat capture of target monomer by template initiator
    • Ida, S., Ouchi, M. & Sawamoto, M. Template-assisted selective radical addition toward sequence-regulated polymerization: Lariat capture of target monomer by template initiator. J. Am. Chem. Soc. 132, 14748-14750 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 14748-14750
    • Ida, S.1    Ouchi, M.2    Sawamoto, M.3
  • 17
    • 79960927307 scopus 로고    scopus 로고
    • Sequence-regulated radical polymerization with a metal-templated monomer: Repetitive ABA sequence by double cyclopolymerization
    • Hibi, Y., Ouchi, M. & Sawamoto, M. Sequence-regulated radical polymerization with a metal-templated monomer: repetitive ABA sequence by double cyclopolymerization. Angew Chem. Int. Ed. 50, 7434-7437 (2011).
    • (2011) Angew Chem. Int. Ed. , vol.50 , pp. 7434-7437
    • Hibi, Y.1    Ouchi, M.2    Sawamoto, M.3
  • 18
    • 78751488442 scopus 로고    scopus 로고
    • Design of AB divinyl 'template monomers'' toward alternating sequence control in metalcatalyzed living radical polymerization
    • Hibi, Y., Tokuoka, S., Terashima, T., Ouchi, M. & Sawamoto, M. Design of AB divinyl 'template monomers'' toward alternating sequence control in metalcatalyzed living radical polymerization. Polym. Chem. 2, 341-347 (2011).
    • (2011) Polym. Chem. , vol.2 , pp. 341-347
    • Hibi, Y.1    Tokuoka, S.2    Terashima, T.3    Ouchi, M.4    Sawamoto, M.5
  • 19
    • 84869429884 scopus 로고    scopus 로고
    • Ultra-precise insertion of functional monomers in chain-growth polymerizations
    • Zamfir, M. & Lutz, J. F. Ultra-precise insertion of functional monomers in chain-growth polymerizations. Nat. Commun. 3, 1138 (2012).
    • (2012) Nat. Commun. , vol.3 , pp. 1138
    • Zamfir, M.1    Lutz, J.F.2
  • 20
    • 84880305872 scopus 로고    scopus 로고
    • Sequenceregulated vinyl copolymers by metal-catalysed step-growth radical polymerization
    • Satoh, K., Ozawa, S., Mizutani, M., Nagai, K. & Kamigaito, M. Sequenceregulated vinyl copolymers by metal-catalysed step-growth radical polymerization. Nat. Commun. 1, 1-6 (2010).
    • (2010) Nat. Commun. , vol.1 , pp. 1-6
    • Satoh, K.1    Ozawa, S.2    Mizutani, M.3    Nagai, K.4    Kamigaito, M.5
  • 21
    • 84871399358 scopus 로고    scopus 로고
    • Synthesis of sequence-specific vinyl copolymers by regioselective ROMP of multiply substituted cyclooctenes
    • Zhang, J., Matta, M. E. & Hillmyer, M. A. Synthesis of sequence-specific vinyl copolymers by regioselective ROMP of multiply substituted cyclooctenes. ACS Macro Lett. 1, 1383-1387 (2012).
    • (2012) ACS Macro Lett. , vol.1 , pp. 1383-1387
    • Zhang, J.1    Matta, M.E.2    Hillmyer, M.A.3
  • 22
    • 84934760274 scopus 로고    scopus 로고
    • A general approach to sequence-controlled polymers using macrocyclic ring opening metathesis polymerization
    • Gutekunst, W. R. & Hawker, C. J. A general approach to sequence-controlled polymers using macrocyclic ring opening metathesis polymerization. J. Am. Chem. Soc. 137, 8038-8041 (2015).
    • (2015) J Am Chem. Soc. , vol.137 , pp. 8038-8041
    • Gutekunst, W.R.1    Hawker, C.J.2
  • 23
    • 74349102549 scopus 로고    scopus 로고
    • Polyethylene prodrugs using precisely placed pharmaceutical agents
    • Leonard, J. K., Turek, D., Sloan, K. B. & Wagener, K. B. Polyethylene prodrugs using precisely placed pharmaceutical agents. Macromol. Chem. Phys. 211, 154-165 (2010).
    • (2010) Macromol. Chem. Phys. , vol.211 , pp. 154-165
    • Leonard, J.K.1    Turek, D.2    Sloan, K.B.3    Wagener, K.B.4
  • 25
    • 84874437348 scopus 로고    scopus 로고
    • Sequence matters: Modulating electronic and optical properties of conjugated oligomers via tailored sequence
    • Norris, B. N. et al. Sequence matters: modulating electronic and optical properties of conjugated oligomers via tailored sequence. Macromolecules 46, 1384-1392 (2013).
    • (2013) Macromolecules , vol.46 , pp. 1384-1392
    • Norris, B.N.1
  • 26
    • 84901306371 scopus 로고    scopus 로고
    • Information-containing macromolecules
    • Colquhoun, H. & Lutz, J. F. Information-containing macromolecules. Nat. Chem. 6, 455-456 (2014).
    • (2014) Nat. Chem. , vol.6 , pp. 455-456
    • Colquhoun, H.1    Lutz, J.F.2
  • 27
    • 79955704145 scopus 로고    scopus 로고
    • Exploiting sequence to control the hydrolysis behavior of biodegradable PLGA copolymers
    • Meyer, T. Y., Li, J. & Stayshich, R. M. Exploiting sequence to control the hydrolysis behavior of biodegradable PLGA copolymers. J. Am. Chem. Soc. 133, 6910-6913 (2011).
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 6910-6913
    • Meyer, T.Y.1    Li, J.2    Stayshich, R.M.3
  • 28
    • 48249133981 scopus 로고    scopus 로고
    • Antimicrobial polymers prepared by ROMP with unprecedented selectivity: A molecular construction kit approach
    • Lienkamp, K. et al. Antimicrobial polymers prepared by ROMP with unprecedented selectivity: a molecular construction kit approach. J. Am. Chem. Soc. 130, 9836-9843 (2008).
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 9836-9843
    • Lienkamp, K.1
  • 29
    • 84867830274 scopus 로고    scopus 로고
    • Using EPR to compare peg-branch-nitroxide 'bivalent-brush polymers' and traditional PEG bottle-brush polymers: Branching makes a difference
    • Burts, A. O. et al. Using EPR to compare peg-branch-nitroxide 'bivalent-brush polymers' and traditional PEG bottle-brush polymers: branching makes a difference. Macromolecules 45, 8310-8318 (2012).
    • (2012) Macromolecules , vol.45 , pp. 8310-8318
    • Burts, A.O.1
  • 30
    • 4544357020 scopus 로고    scopus 로고
    • DNA-templated organic synthesis: Nature's strategy for controlling chemical reactivity applied to synthetic molecules
    • Li, X. Y. & Liu, D. R. DNA-templated organic synthesis: nature's strategy for controlling chemical reactivity applied to synthetic molecules. Angew. Chem. Int. Ed. 43, 4848-4870 (2004).
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 4848-4870
    • Li, X.Y.1    Liu, D.R.2
  • 31
    • 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
  • 32
    • 78651436778 scopus 로고    scopus 로고
    • Designer template initiator for sequence regulated polymerization: Systems design for substrate-selective metal-catalyzed radical addition and living radical polymerization
    • Ida, S., Ouchi, M. & Sawamoto, M. Designer template initiator for sequence regulated polymerization: systems design for substrate-selective metal-catalyzed radical addition and living radical polymerization. Macromol. Rapid Commun. 32, 209-214 (2011).
    • (2011) Macromol. Rapid Commun. , vol.32 , pp. 209-214
    • Ida, S.1    Ouchi, M.2    Sawamoto, M.3
  • 33
    • 0035781198 scopus 로고    scopus 로고
    • Metal-catalyzed living radical polymerization
    • Kamigaito, M., Ando, T. & Sawamoto, M. Metal-catalyzed living radical polymerization. Chem. Rev. 101, 3689-3745 (2001).
    • (2001) Chem. Rev. , vol.101 , pp. 3689-3745
    • Kamigaito, M.1    Ando, T.2    Sawamoto, M.3
  • 34
    • 0035470133 scopus 로고    scopus 로고
    • Atom transfer radical polymerization
    • Matyjaszewski, K. & Xia, J. H. Atom transfer radical polymerization. Chem. Rev. 101, 2921-2990 (2001).
    • (2001) Chem. Rev. , vol.101 , pp. 2921-2990
    • Matyjaszewski, K.1    Xia, J.H.2
  • 35
    • 33947464489 scopus 로고
    • Homolytic addition to olefins-chain termination by metal halides
    • Kochi, J. K. Homolytic addition to olefins-chain termination by metal halides. J. Am. Chem. Soc. 78, 4815-4815 (1956).
    • (1956) J. Am. Chem. Soc. , vol.78 , pp. 4815
    • Kochi, J.K.1
  • 36
    • 78751558601 scopus 로고    scopus 로고
    • Toward the synthesis of sequencecontrolled vinyl copolymers
    • Tong, X. M., Guo, B. H. & Huang, Y. B. Toward the synthesis of sequencecontrolled vinyl copolymers. Chem. Commun. 47, 1455-1457 (2011).
    • (2011) Chem. Commun. , vol.47 , pp. 1455-1457
    • Tong, X.M.1    Guo, B.H.2    Huang, Y.B.3
  • 37
    • 76249131765 scopus 로고    scopus 로고
    • A synthetic small molecule that can walk down a track
    • von Delius, M., Geertsema, E. M. & Leigh, D. A. A synthetic small molecule that can walk down a track. Nat. Chem. 2, 96-101 (2010).
    • (2010) Nat Chem. , vol.2 , pp. 96-101
    • Von Delius, M.1    Geertsema, E.M.2    Leigh, D.A.3
  • 38
    • 33947488929 scopus 로고
    • Use of esters of N-hydroxysuccinimide in peptide synthesis
    • Anderson, G. W., Callahan, F. M. & Zimmerman, J. E. Use of esters of N-hydroxysuccinimide in peptide synthesis. J. Am. Chem. Soc. 86, 1839-1840 (1964).
    • (1964) J. Am. Chem. Soc. , vol.86 , pp. 1839-1840
    • Anderson, G.W.1    Callahan, F.M.2    Zimmerman, J.E.3
  • 39
    • 0002778807 scopus 로고
    • New synthetic concepts in organosulfur chemistry I. New pathway to unsymmetrical disulfides. The thiol-induced fragmentation of sulfenyl thiocarbonates
    • Breis, S. J., Pilot, J. F. & Barnum, H. W. New synthetic concepts in organosulfur chemistry. I. new pathway to unsymmetrical disulfides. The thiol-induced fragmentation of sulfenyl thiocarbonates. J. Am. Chem. Soc. 92, 7629-7631 (1970).
    • (1970) J. Am. Chem. Soc. , vol.92 , pp. 7629-7631
    • Breis, S.J.1    Pilot, J.F.2    Barnum, H.W.3
  • 40
    • 0036128645 scopus 로고    scopus 로고
    • Atom transfer radical cyclisation reactions mediated by copper complexes
    • Clark, A. J. Atom transfer radical cyclisation reactions mediated by copper complexes. Chem. Soc. Rev. 31, 1-11 (2002).
    • (2002) Chem. Soc. Rev. , vol.31 , pp. 1-11
    • Clark, A.J.1
  • 41
    • 33745054093 scopus 로고    scopus 로고
    • Highly efficient atom transfer radical addition reactions with a Ru-III complex as a catalyst precursor
    • Quebatte, L., Thommes, K. & Severin, K. Highly efficient atom transfer radical addition reactions with a Ru-III complex as a catalyst precursor. J. Am. Chem. Soc. 128, 7440-7441 (2006).
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 7440-7441
    • Quebatte, L.1    Thommes, K.2    Severin, K.3
  • 42
    • 0032652705 scopus 로고    scopus 로고
    • Half-metallocenetype ruthenium complexes as active catalysts for living radical polymerization of methyl methacrylate and styrene
    • Takahashi, H., Ando, T., Kamigaito, M. & Sawamoto, M. Half-metallocenetype ruthenium complexes as active catalysts for living radical polymerization of methyl methacrylate and styrene. Macromolecules 32, 3820-3823 (1999).
    • (1999) Macromolecules , vol.32 , pp. 3820-3823
    • Takahashi, H.1    Ando, T.2    Kamigaito, M.3    Sawamoto, M.4
  • 43
    • 0035912976 scopus 로고    scopus 로고
    • Ru(Cp∗)Cl(PPh3)2: A versatile catalyst for living radical polymerization of methacrylates, acrylates, and styrene
    • Watanabe, Y., Ando, T., Kamigaito, M. & Sawamoto, M. Ru(Cp∗)Cl(PPh3)2: A versatile catalyst for living radical polymerization of methacrylates, acrylates, and styrene. Macromolecules 34, 4370-4374 (2001).
    • (2001) Macromolecules , vol.34 , pp. 4370-4374
    • Watanabe, Y.1    Ando, T.2    Kamigaito, M.3    Sawamoto, M.4
  • 44
    • 9644254051 scopus 로고    scopus 로고
    • Cysteine-reactive polymers synthesized by atom transfer radical polymerization for conjugation to proteins
    • Bontempo, D., Heredia, K. L., Fish, B. A. & Maynard, H. D. Cysteine-reactive polymers synthesized by atom transfer radical polymerization for conjugation to proteins. J. Am. Chem. Soc. 126, 15372-15373 (2004).
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 15372-15373
    • Bontempo, D.1    Heredia, K.L.2    Fish, B.A.3    Maynard, H.D.4
  • 45
    • 84861401896 scopus 로고    scopus 로고
    • Highly active bipyridine-based ligands for atom transfer radical polymerization
    • Magenau, A. J. D., Kwak, Y., Schroder, K. & Matyjaszewski, K. Highly active bipyridine-based ligands for atom transfer radical polymerization. ACS Macro Lett. 1, 508-512 (2012).
    • (2012) ACS Macro Lett. , vol.1 , pp. 508-512
    • Magenau, A.J.D.1    Kwak, Y.2    Schroder, K.3    Matyjaszewski, K.4
  • 46
    • 84878323351 scopus 로고    scopus 로고
    • Reversible-deactivation radical polymerization in the presence of metallic copper activation of alkyl halides by Cu(0)
    • Peng, C. H. et al. Reversible-deactivation radical polymerization in the presence of metallic copper. activation of alkyl halides by Cu(0). Macromolecules 46, 3803-3815 (2013).
    • (2013) Macromolecules , vol.46 , pp. 3803-3815
    • Peng, C.H.1


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