메뉴 건너뛰기




Volumn 4, Issue 1, 2012, Pages

The transformation of chiral signals into macroscopic properties of materials using chirality-responsive polymers

Author keywords

chiral materials; chiral recognition; smart polymers

Indexed keywords


EID: 84856064887     PISSN: 18844049     EISSN: 18844057     Source Type: Journal    
DOI: 10.1038/am.2012.6     Document Type: Review
Times cited : (56)

References (88)
  • 1
    • 33645699454 scopus 로고    scopus 로고
    • Chiral recognition mechanisms
    • Berthod, A. Chiral recognition mechanisms. Anal. Chem. 78, 2093 (2006).
    • (2006) Anal. Chem. , vol.78 , pp. 2093
    • Berthod, A.1
  • 2
    • 0042709818 scopus 로고    scopus 로고
    • Chiral selection on inorganic crystalline surfaces
    • Hazen, R. M. & Sholl, D. S. Chiral selection on inorganic crystalline surfaces. Nat. Mater. 2, 367 (2003).
    • (2003) Nat. Mater. , vol.2 , pp. 367
    • Hazen, R.M.1    Sholl, D.S.2
  • 3
    • 31444440235 scopus 로고    scopus 로고
    • Amplification of chirality in two-dimensional enantiomorphous lattices
    • Fasel, R., Parschau, M. & Ernst, K. H. Amplification of chirality in two-dimensional enantiomorphous lattices. Nature 439, 449 (2006).
    • (2006) Nature , vol.439 , pp. 449
    • Fasel, R.1    Parschau, M.2    Ernst, K.H.3
  • 5
    • 60549099164 scopus 로고    scopus 로고
    • Nodal signalling is involved in left-right asymmetry in snails
    • Grande, C. & Patel, N. H. Nodal signalling is involved in left-right asymmetry in snails. Nature 457, 1007 (2009).
    • (2009) Nature , vol.457 , pp. 1007
    • Grande, C.1    Patel, N.H.2
  • 6
    • 0037071838 scopus 로고    scopus 로고
    • Solving the puzzle of mirror-image flowers
    • DOI 10.1038/417707a
    • Jesson, L. K. & Barrett, S. C. H. Enantiostyly: solving the puzzle of mirror-image flowers. Nature 417, 707 (2002). (Pubitemid 34640617)
    • (2002) Nature , vol.417 , Issue.6890 , pp. 707
    • Jesson, L.K.1    Barrett, S.C.H.2
  • 7
    • 0015210110 scopus 로고
    • Odor incongruity and chirality
    • Friedman, L. & Miller, J. G. Odor incongruity and chirality. Science 172, 1044 (1971).
    • (1971) Science , vol.172 , pp. 1044
    • Friedman, L.1    Miller, J.G.2
  • 8
    • 0028198298 scopus 로고
    • Differential adhesion of cells to enantiomorphous crystal surfaces
    • Hanein, D., Geiger, B. & Addadi, L. Differential adhesion of cells to enantiomorphous crystal surfaces. Science 263, 1413 (1994).
    • (1994) Science , vol.263 , pp. 1413
    • Hanein, D.1    Geiger, B.2    Addadi, L.3
  • 9
    • 0043161939 scopus 로고    scopus 로고
    • Liquid crystals for charge transport, luminescence, and photonics
    • O'Neill, M. & Kelly, S. M. Liquid crystals for charge transport, luminescence, and photonics. Adv. Mater. 15, 1135 (2003).
    • (2003) Adv. Mater. , vol.15 , pp. 1135
    • O'neill, M.1    Kelly, S.M.2
  • 10
    • 77951787567 scopus 로고    scopus 로고
    • The road ahead for metamaterials
    • Zheludev, N. I. The road ahead for metamaterials. Science 328, 582 (2010).
    • (2010) Science , vol.328 , pp. 582
    • Zheludev, N.I.1
  • 11
    • 33646468489 scopus 로고    scopus 로고
    • Asymmetric catalysis by chiral hydrogen-bond donors
    • Taylor, M. S. & Jacobsen, E. N. Asymmetric catalysis by chiral hydrogen-bond donors. Angew. Chem. Int. Ed. 45, 1520 (2006).
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 1520
    • Taylor, M.S.1    Jacobsen, E.N.2
  • 12
    • 1842430722 scopus 로고    scopus 로고
    • Fluorescence of organic molecules in chiral recognition
    • Pu, L. Fluorescence of organic molecules in chiral recognition. Chem. Rev. 104, 1687 (2004).
    • (2004) Chem. Rev. , vol.104 , pp. 1687
    • Pu, L.1
  • 13
    • 0035847272 scopus 로고    scopus 로고
    • Separation of enantiomers: Needs, challenges, perspectives
    • Maier, N. M., Franco, P. & Lindner, W. Separation of enantiomers: needs, challenges, perspectives. J. Chromatogr. A. 906, 3 (2001).
    • (2001) J. Chromatogr. A. , vol.906 , pp. 3
    • Maier, N.M.1    Franco, P.2    Lindner, W.3
  • 14
    • 77956241683 scopus 로고    scopus 로고
    • Stimuli-sensitive polymers
    • Lendlein, A. & Shastri, V. P. Stimuli-sensitive polymers. Adv. Mater. 22, 3344 (2010).
    • (2010) Adv. Mater. , vol.22 , pp. 3344
    • Lendlein, A.1    Shastri, V.P.2
  • 16
    • 79953055837 scopus 로고    scopus 로고
    • Biomimetic smart interface materials for biological applications
    • Sun, T. & Qing, G. Biomimetic smart interface materials for biological applications. Adv. Mater. 23, H57 (2011).
    • (2011) Adv. Mater. , vol.23
    • Sun, T.1    Qing, G.2
  • 17
    • 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 (2009).
    • (2009) Chem. Rev. , vol.109 , pp. 6102
    • Yashima, E.1    Maeda, K.2    Iida, H.3    Furusho, Y.4    Nagai, K.5
  • 19
    • 84863116349 scopus 로고    scopus 로고
    • Chiral biointerface materials
    • doi: 10.1039/C1CS15209B
    • Zhang, M. X., Qing, G. Y. & Sun, T. L. Chiral biointerface materials. Chem. Soc. Rev. doi: 10.1039/C1CS15209B (2012).
    • (2012) Chem. Soc. Rev
    • Zhang, M.X.1    Qing, G.Y.2    Sun, T.L.3
  • 20
    • 73749083123 scopus 로고    scopus 로고
    • Recent advances and challenges in designing stimuli-responsive polymers
    • Liu, F. & Urban, M. W. Recent advances and challenges in designing stimuli-responsive polymers. Prog. Polym. Sci. 35, 3 (2010).
    • (2010) Prog. Polym. Sci. , vol.35 , pp. 3
    • Liu, F.1    Urban, M.W.2
  • 21
    • 0038450358 scopus 로고    scopus 로고
    • Chiral conflict. The effect of temperature on the helical sense of a polymer controlled by the competition between structurally different enantiomers: From dilute solution to the lyotropic liquid crystal state
    • Tang, K., Green, M. M., Cheon, K. S., Selinger, J. V. & Garetz, B. A. Chiral conflict. The effect of temperature on the helical sense of a polymer controlled by the competition between structurally different enantiomers: from dilute solution to the lyotropic liquid crystal state. J. Am. Chem. Soc. 125, 7313 (2003).
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 7313
    • Tang, K.1    Green, M.M.2    Cheon, K.S.3    Selinger, J.V.4    Garetz, B.A.5
  • 22
    • 33745798791 scopus 로고    scopus 로고
    • Thermoresponsive on-off switching of chiroptical property induced in poly(4¢-ethynylbenzo-15-crown-5)/aamino acid system
    • Sakai, R., Otsuka, I., Satoh, T., Kakuchi, R., Kaga, H. & Kakuchi, T. Thermoresponsive on-off switching of chiroptical property induced in poly(4¢-ethynylbenzo-15-crown-5)/aamino acid system. Macromolecules 39, 4032 (2006).
    • (2006) Macromolecules , vol.39 , pp. 4032
    • Sakai, R.1    Otsuka, I.2    Satoh, T.3    Kakuchi, R.4    Kaga, H.5    Kakuchi, T.6
  • 23
    • 17144364271 scopus 로고    scopus 로고
    • Dual memory of enantiomeric helices in a polyacetylene induced by a single enantiomer
    • Miyagawa, T., Furuko, A., Maeda, K., Katagiri, H., Furusho, Y. & Yashima, E. Dual memory of enantiomeric helices in a polyacetylene induced by a single enantiomer. J. Am. Chem. Soc. 127, 5018 (2005).
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 5018
    • Miyagawa, T.1    Furuko, A.2    Maeda, K.3    Katagiri, H.4    Furusho, Y.5    Yashima, E.6
  • 24
    • 34548786763 scopus 로고    scopus 로고
    • Dynamic extension-contraction motion in supramolecular springs
    • Kim, H. J., Lee, E., Park, H. S. & Lee, M. Dynamic extension-contraction motion in supramolecular springs. J. Am. Chem. Soc. 129, 10994 (2007).
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 10994
    • Kim, H.J.1    Lee, E.2    Park, H.S.3    Lee, M.4
  • 25
    • 77957314150 scopus 로고    scopus 로고
    • Thermo-and solvent-responsive polymer complex created from supramolecular complexation between a helix-forming polysaccharide and a cationic polythiophene
    • Shiraki, T., Dawn, A., Tsuchiya, Y. & Shinkai, S. Thermo- and solvent-responsive polymer complex created from supramolecular complexation between a helix-forming polysaccharide and a cationic polythiophene. J. Am. Chem. Soc. 132, 13928 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 13928
    • Shiraki, T.1    Dawn, A.2    Tsuchiya, Y.3    Shinkai, S.4
  • 26
    • 27844518927 scopus 로고    scopus 로고
    • A thermal and solvocontrollable cylindrical nanoshutter based on a single screw-sense helical polyguanidine
    • Tang, H. Z., Novak, B. M., He, J. T. & Polavarapu, P. L. A thermal and solvocontrollable cylindrical nanoshutter based on a single screw-sense helical polyguanidine. Angew. Chem. Int. Ed. 44, 7298 (2005).
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 7298
    • Tang, H.Z.1    Novak, B.M.2    He, J.T.3    Polavarapu, P.L.4
  • 27
    • 44949238078 scopus 로고    scopus 로고
    • Nanomechanical function from self-organizable dendronized helical polyphenylacetylenes
    • Percec, V., Rudick, J. G., Peterca, M. & Heiney, P. A. Nanomechanical function from self-organizable dendronized helical polyphenylacetylenes. J. Am. Chem. Soc. 130, 7503 (2008).
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 7503
    • Percec, V.1    Rudick, J.G.2    Peterca, M.3    Heiney, P.A.4
  • 28
    • 31444441391 scopus 로고    scopus 로고
    • Helix-sense controlled polymerization of a single phenyl isocyanide enantiomer leading to diastereomeric helical polyisocyanides with opposite helix-sense and cholesteric liquid crystals with opposite twist-sense
    • Kajitani, T., Okoshi, K., Sakurai, S. I., Kumaki, J. & Yashima, E. Helix-sense controlled polymerization of a single phenyl isocyanide enantiomer leading to diastereomeric helical polyisocyanides with opposite helix-sense and cholesteric liquid crystals with opposite twist-sense. J. Am. Chem. Soc. 128, 708 (2006).
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 708
    • Kajitani, T.1    Okoshi, K.2    Sakurai, S.I.3    Kumaki, J.4    Yashima, E.5
  • 30
    • 33646544017 scopus 로고    scopus 로고
    • Two-dimensional surface chirality control by solvent-induced helicity inversion of a helical polyacetylene on graphite
    • Sakurai, S. I., Okoshi, K., Kumaki, J. & Yashima, E. Two-dimensional surface chirality control by solvent-induced helicity inversion of a helical polyacetylene on graphite. J. Am. Chem. Soc. 128, 5650 (2006).
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 5650
    • Sakurai, S.I.1    Okoshi, K.2    Kumaki, J.3    Yashima, E.4
  • 31
    • 10044283181 scopus 로고    scopus 로고
    • Transformation of helical sense of poly(Npropargylamides) controlled by competition between structurally different enantiomeric amino acids
    • Zhao, H. C., Sanda, F. & Masuda, T. Transformation of helical sense of poly(Npropargylamides) controlled by competition between structurally different enantiomeric amino acids. Macromolecules 37, 8888 (2004).
    • (2004) Macromolecules , vol.37 , pp. 8888
    • Zhao, H.C.1    Sanda, F.2    Masuda, T.3
  • 32
    • 77952219316 scopus 로고    scopus 로고
    • Effect of solvents and temperature on the conformation of poly(b-benzyl-l-aspartate) brushes
    • Yang, C. T., Wang, Y. L. & Chang, Y. C. Effect of solvents and temperature on the conformation of poly(b-benzyl-l-aspartate) brushes. Biomacromolecules 11, 1308 (2010).
    • (2010) Biomacromolecules , vol.11 , pp. 1308
    • Yang, C.T.1    Wang, Y.L.2    Chang, Y.C.3
  • 33
    • 34347248246 scopus 로고    scopus 로고
    • Switching of optical activity in oligosilane through pHresponsive chiral wrapping with amylose
    • Sanji, T., Kato, N. & Tanaka, M. Switching of optical activity in oligosilane through pHresponsive chiral wrapping with amylose. Macromolecules 39, 7508 (2006).
    • (2006) Macromolecules , vol.39 , pp. 7508
    • Sanji, T.1    Kato, N.2    Tanaka, M.3
  • 34
    • 79958205945 scopus 로고    scopus 로고
    • Hierarchical self-assembly of amphiphilic peptide dendrons: Evolution of diverse chiral nanostructures through hydrogel formation over a wide pH range
    • Duan, P. F., Qin, L., Zhu, X. F. & Liu, M. H. Hierarchical self-assembly of amphiphilic peptide dendrons: Evolution of diverse chiral nanostructures through hydrogel formation over a wide pH range. Chem. Eur. J. 17, 6389 (2011).
    • (2011) Chem. Eur. J. , vol.17 , pp. 6389
    • Duan, P.F.1    Qin, L.2    Zhu, X.F.3    Liu, M.H.4
  • 36
    • 77957167819 scopus 로고    scopus 로고
    • Oligo(4-aminopiperidine-4-carboxylic acid): An unusual basic oligopeptide with an acid-induced helical conformation
    • Cho, J. I., Tanaka, M., Sato, S., Kinbara, K. & Aida, T. Oligo(4-aminopiperidine-4-carboxylic acid): an unusual basic oligopeptide with an acid-induced helical conformation. J. Am. Chem. Soc. 132, 13176 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 13176
    • Cho, J.I.1    Tanaka, M.2    Sato, S.3    Kinbara, K.4    Aida, T.5
  • 37
    • 41549156500 scopus 로고    scopus 로고
    • Light-controlled supramolecular helicity of a liquid crystalline phase using a helical polymer functionalized with a single chiroptical molecular switch
    • Pijper, D., Jongejan, M. G. M., Meetsmia, A. & Feringa, B. L. Light-controlled supramolecular helicity of a liquid crystalline phase using a helical polymer functionalized with a single chiroptical molecular switch. J. Am. Chem. Soc. 130, 4541 (2008).
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 4541
    • Pijper, D.1    Jongejan, M.G.M.2    Meetsmia, A.3    Feringa, B.L.4
  • 38
    • 33645927311 scopus 로고    scopus 로고
    • Stimuli-responsive conjugated polymers Synthesis and chiroptical properties of polyacetylene carrying L-glutamic acid and Azobenzene in the side chain
    • Zhao, H. C., Sanda, F. & Masuda, T. Stimuli-responsive conjugated polymers. Synthesis and chiroptical properties of polyacetylene carrying L-glutamic acid and Azobenzene in the side chain. Polymer 47, 2596 (2006).
    • (2006) Polymer , vol.47 , pp. 2596
    • Zhao, H.C.1    Sanda, F.2    Masuda, T.3
  • 39
    • 34248169151 scopus 로고    scopus 로고
    • Synthesis of a stimuli-responsive P-chiral polymer with chiral phosphorus atoms and azobenzene moieties in the main chain
    • Ouchi, Y., Morisaki, Y., Ogoshi, T. & Chujo, Y. Synthesis of a stimuli-responsive P-chiral polymer with chiral phosphorus atoms and azobenzene moieties in the main chain. Chem. Asian J. 2, 397 (2007).
    • (2007) Chem. Asian J. , vol.2 , pp. 397
    • Ouchi, Y.1    Morisaki, Y.2    Ogoshi, T.3    Chujo, Y.4
  • 40
    • 34447343572 scopus 로고    scopus 로고
    • Photoinduced chirality in azobenzene-containing polymer systems
    • Choi, S. -W., Kawauchi, S., Ha, N. Y. & Takezoe, H. Photoinduced chirality in azobenzene-containing polymer systems. Phys. Chem. Chem. Phys. 9, 3671 (2007).
    • (2007) Phys. Chem. Chem. Phys. , vol.9 , pp. 3671
    • Choi, S.-W.1    Kawauchi, S.2    Ha, N.Y.3    Takezoe, H.4
  • 41
    • 34249780797 scopus 로고    scopus 로고
    • Photoinduced chirality in achiral liquid crystalline azobenzene polymers containing different polar side groups
    • Zheng, Z., Su, Z., Wang, L., Xua, J., Zhang, Q. & Yang, J. Photoinduced chirality in achiral liquid crystalline azobenzene polymers containing different polar side groups. Euro. Polym. J. 43, 2738 (2007).
    • (2007) Euro. Polym. J. , vol.43 , pp. 2738
    • Zheng, Z.1    Su, Z.2    Wang, L.3    Xua, J.4    Zhang, Q.5    Yang, J.6
  • 43
    • 78650697083 scopus 로고    scopus 로고
    • Supramolecular chirality formation of bisazobenzene-substituted polydiacetylene LB films
    • Pan, X., Jiang, H., Wang, Y., Lei, Z., Zou, G., Zhang, Q. & Wang, K. Supramolecular chirality formation of bisazobenzene-substituted polydiacetylene LB films. J. Colloid Interface Sci. 354, 880 (2011).
    • (2011) J. Colloid Interface Sci. , vol.354 , pp. 880
    • Pan, X.1    Jiang, H.2    Wang, Y.3    Lei, Z.4    Zou, G.5    Zhang, Q.6    Wang, K.7
  • 44
    • 33746047666 scopus 로고    scopus 로고
    • Probing a conjugated polymer's transfer of organization-dependent properties from solutions to films
    • Satrijo, A., Meskers, S. C. J. & Swager, T. M. Probing a conjugated polymer's transfer of organization-dependent properties from solutions to films. J. Am. Chem. Soc. 128, 9030 (2006).
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 9030
    • Satrijo, A.1    Meskers, S.C.J.2    Swager, T.M.3
  • 45
    • 56549090812 scopus 로고    scopus 로고
    • Synthesis and redox-driven chiroptically switching properties of viologen-containing optically active polymer with main-chain axial chirality
    • Deng, J., Zhou, C., Chen, C., Song, N. H. & Su, Z. X. Synthesis and redox-driven chiroptically switching properties of viologen-containing optically active polymer with main-chain axial chirality. Macromolecules 41, 7805 (2008).
    • (2008) Macromolecules , vol.41 , pp. 7805
    • Deng, J.1    Zhou, C.2    Chen, C.3    Song, N.H.4    Su, Z.X.5
  • 46
    • 70349908121 scopus 로고    scopus 로고
    • Chiroptically active photonics polymers: Synthesis and chiroptically switching properties of helical polyacetylene bearing electrochromic viologens in the side chains
    • Deng, J., Zhou, C. & Song, N. H. Chiroptically active photonics polymers: synthesis and chiroptically switching properties of helical polyacetylene bearing electrochromic viologens in the side chains. Macromolecules 42, 6865 (2009).
    • (2009) Macromolecules , vol.42 , pp. 6865
    • Deng, J.1    Zhou, C.2    Song, N.H.3
  • 48
    • 33646540522 scopus 로고    scopus 로고
    • Two-dimensional hierarchical selfassembly of one-handed helical polymers on graphite
    • Sakurai, S. I., Okoshi, K., Kumaki, J. & Yashima, E. Two-dimensional hierarchical selfassembly of one-handed helical polymers on graphite. Angew. Chem. Int. Ed. 45, 1245 (2006).
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 1245
    • Sakurai, S.I.1    Okoshi, K.2    Kumaki, J.3    Yashima, E.4
  • 49
    • 34447580111 scopus 로고    scopus 로고
    • Supramolecular helical structure of the stereocomplex composed of complementary isotactic and syndiotactic poly(methyl methacrylate)s as revealed by atomic force microscopy
    • Kumaki, J., Kawauchi, T., Okoshi, K., Kusanagi, H. & Yashima, F. Supramolecular helical structure of the stereocomplex composed of complementary isotactic and syndiotactic poly(methyl methacrylate)s as revealed by atomic force microscopy. Angew. Chem. Int. Ed. 46, 5348 (2007).
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 5348
    • Kumaki, J.1    Kawauchi, T.2    Okoshi, K.3    Kusanagi, H.4    Yashima, F.5
  • 50
    • 51549108741 scopus 로고    scopus 로고
    • Synthesis, chain helicity, assembling structure, and biological compatibility of poly(phenylacetylene)s containing l-alanine moieties
    • Cheuk, K. K. L., Li, B. S., Lam, J. W. Y., Xie, Y. & Tang, B. Z. Synthesis, chain helicity, assembling structure, and biological compatibility of poly(phenylacetylene)s containing l-alanine moieties. Macromolecules 41, 5997 (2008).
    • (2008) Macromolecules , vol.41 , pp. 5997
    • Cheuk, K.K.L.1    Li, B.S.2    Lam, J.W.Y.3    Xie, Y.4    Tang, B.Z.5
  • 51
    • 34447525379 scopus 로고    scopus 로고
    • Highly twisted helical polyacetylene with morphology free from the bundle of fibrils synthesized in chiral nematic liquid crystal reaction field
    • Goh, M., Kyotani, M. & Akagi, K. Highly twisted helical polyacetylene with morphology free from the bundle of fibrils synthesized in chiral nematic liquid crystal reaction field. J. Am. Chem. Soc. 129, 8519 (2007).
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 8519
    • Goh, M.1    Kyotani, M.2    Akagi, K.3
  • 53
    • 35748961695 scopus 로고    scopus 로고
    • Helical polyaniline nanofibers induced by chiral dopants by a polymerization process
    • Yan, Y., Yu, Z., Huang, Y. W., Yuan, W. X. & Wei, Z. X. Helical polyaniline nanofibers induced by chiral dopants by a polymerization process. Adv. Mater. 19, 3353 (2007).
    • (2007) Adv. Mater. , vol.19 , pp. 3353
    • Yan, Y.1    Yu, Z.2    Huang, Y.W.3    Yuan, W.X.4    Wei, Z.X.5
  • 54
    • 33748309472 scopus 로고    scopus 로고
    • Hierarchical amplification of macromolecular helicity in a lyotropic liquid crystalline charged poly(phenylacetylene) by nonracemic dopants in water and its helical structure
    • Nagai, K., Sakajiri, K., Maeda, K., Okoshi, K., Sato, T. & Yashima, E. Hierarchical amplification of macromolecular helicity in a lyotropic liquid crystalline charged poly(phenylacetylene) by nonracemic dopants in water and its helical structure. Macromolecules 39, 5371 (2006).
    • (2006) Macromolecules , vol.39 , pp. 5371
    • Nagai, K.1    Sakajiri, K.2    Maeda, K.3    Okoshi, K.4    Sato, T.5    Yashima, E.6
  • 55
    • 34547448298 scopus 로고    scopus 로고
    • Double helical oligoresorcinols specifically recognize oligosaccharides via heteroduplex formation through noncovalent interactions in water
    • Goto, H., Furusho, Y. & Yashima, E. Double helical oligoresorcinols specifically recognize oligosaccharides via heteroduplex formation through noncovalent interactions in water. J. Am. Chem. Soc. 129, 9168 (2007).
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 9168
    • Goto, H.1    Furusho, Y.2    Yashima, E.3
  • 56
    • 67650519810 scopus 로고    scopus 로고
    • Enantiomerselective and helix-sense-selective living block copolymerization of isocyanide enantiomers initiated by single-handed helical poly(phenyl isocyanide)s
    • Wu, Z. Q., Nagai, K., Banno, M., Okoshi, K., Onitsuka, K. & Yashima, E. Enantiomerselective and helix-sense-selective living block copolymerization of isocyanide enantiomers initiated by single-handed helical poly(phenyl isocyanide)s. J. Am. Chem. Soc. 131, 6708 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 6708
    • Wu, Z.Q.1    Nagai, K.2    Banno, M.3    Okoshi, K.4    Onitsuka, K.5    Yashima, E.6
  • 60
    • 33947628580 scopus 로고    scopus 로고
    • Supramolecular helical assembly of an achiral cyanine dye in an induced helical amphiphilic poly(-phenylacetylene) interior in water
    • Miyagawa, T., Yamamoto, M., Muraki, R., Onouchi, H. & Yashima, E. Supramolecular helical assembly of an achiral cyanine dye in an induced helical amphiphilic poly(-phenylacetylene) interior in water. J. Am. Chem. Soc. 129, 3676 (2007).
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 3676
    • Miyagawa, T.1    Yamamoto, M.2    Muraki, R.3    Onouchi, H.4    Yashima, E.5
  • 61
    • 33746310020 scopus 로고    scopus 로고
    • Assisted formation of chiral porphyrin homoaggregates by an induced helical poly(phenylacetylene) template and their chiral memory
    • Onouchi, H., Miyagawa, T., Morino, K. & Yashima, E. Assisted formation of chiral porphyrin homoaggregates by an induced helical poly(phenylacetylene) template and their chiral memory. Angew. Chem. Int. Ed. 45, 2381 (2006).
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 2381
    • Onouchi, H.1    Miyagawa, T.2    Morino, K.3    Yashima, E.4
  • 63
    • 38349181456 scopus 로고    scopus 로고
    • Syntheses and chiroptical properties of optically active helical poly(phenylacetylene)s bearing [60]fullerene pendants
    • Ohsawa, S., Maeda, K. & Yashima, E. Syntheses and chiroptical properties of optically active helical poly(phenylacetylene)s bearing [60]fullerene pendants. Macromolecules 40, 9244 (2007).
    • (2007) Macromolecules , vol.40 , pp. 9244
    • Ohsawa, S.1    Maeda, K.2    Yashima, E.3
  • 64
    • 1842588623 scopus 로고    scopus 로고
    • A helical array of pendant fullerenes on a helical poly(phenylacetylene) induced by non-covalent chiral interactions
    • Nishimura, T., Ohsawa, S., Maeda, K. & Yashima, E. A helical array of pendant fullerenes on a helical poly(phenylacetylene) induced by non-covalent chiral interactions. Chem. Commun. 646 (2004).
    • (2004) Chem. Commun. , vol.646
    • Nishimura, T.1    Ohsawa, S.2    Maeda, K.3    Yashima, E.4
  • 65
    • 0037419845 scopus 로고    scopus 로고
    • Detection and amplification of a small enantiomeric imbalance in a-amino acids by a helical poly(phenylacetylene) with crown ether pendants
    • Nonokawa, R. & Yashima, E. Detection and amplification of a small enantiomeric imbalance in a-amino acids by a helical poly(phenylacetylene) with crown ether pendants. J. Am. Chem. Soc. 125, 1278 (2003).
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 1278
    • Nonokawa, R.1    Yashima, E.2
  • 67
    • 33745037692 scopus 로고    scopus 로고
    • Switching of macromolecular helicity of optically active poly(phenylacetylene)s bearing cyclodextrin pendants induced by various external stimuli
    • Maeda, K., Mochizuki, H., Watanabe, M. & Yashima, E. Switching of macromolecular helicity of optically active poly(phenylacetylene)s bearing cyclodextrin pendants induced by various external stimuli. J. Am. Chem. Soc. 128, 7639 (2006).
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 7639
    • Maeda, K.1    Mochizuki, H.2    Watanabe, M.3    Yashima, E.4
  • 68
    • 61349133046 scopus 로고    scopus 로고
    • Lost in translation? Chirality effects in the self-assembly of nanostructured gel-phase materials
    • Smith, D. K. Lost in translation? Chirality effects in the self-assembly of nanostructured gel-phase materials. Chem. Soc. Rev. 38, 684 (2009).
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 684
    • Smith, D.K.1
  • 69
    • 0037420325 scopus 로고    scopus 로고
    • Chiral stimuli-responsive gels: Helicity induction in poly(phenylacetylene) gels bearing a carboxyl group with chiral amines
    • Goto, H., Zhang, H. Q. & Yashima, E. Chiral stimuli-responsive gels: Helicity induction in poly(phenylacetylene) gels bearing a carboxyl group with chiral amines. J. Am. Chem. Soc. 125, 2516 (2003).
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 2516
    • Goto, H.1    Zhang, H.Q.2    Yashima, E.3
  • 70
    • 9644310405 scopus 로고    scopus 로고
    • Two component dendritic gel: Effect of stereochemistry on the on the supramolecular chiral assembly
    • Hirst, A. R., Smith, D. K., Feiters, M. C. & Geurts, H. P. M. Two component dendritic gel: effect of stereochemistry on the on the supramolecular chiral assembly. Chem. Eur. J. 10, 5901 (2004).
    • (2004) Chem. Eur. J. , vol.10 , pp. 5901
    • Hirst, A.R.1    Smith, D.K.2    Feiters, M.C.3    Geurts, H.P.M.4
  • 71
    • 34248551763 scopus 로고    scopus 로고
    • Self-organisation in the assembly of gels from mixtures of different dendritic peptide building blocks
    • Hirst, A. R., Huang, B. Q., Castelletto, V., Hamley, I.W. & Smith, D. K. Self-organisation in the assembly of gels from mixtures of different dendritic peptide building blocks. Chem. Eur. J. 13, 2180 (2007).
    • (2007) Chem. Eur. J. , vol.13 , pp. 2180
    • Hirst, A.R.1    Huang, B.Q.2    Castelletto, V.3    Hamley, I.W.4    Smith, D.K.5
  • 72
    • 17444403549 scopus 로고    scopus 로고
    • Helicity induction in a poly(phenylacetylene) bearing Aza-18-crown-6 ether pendants with optically active bis(amino acid)s and its chiral stimuli-responsive gelation
    • Morino, K., Oobo, M. & Yashima, E. Helicity induction in a poly(phenylacetylene) bearing Aza-18-crown-6 ether pendants with optically active bis(amino acid)s and its chiral stimuli-responsive gelation. Macromolecules 38, 3461 (2005).
    • (2005) Macromolecules , vol.38 , pp. 3461
    • Morino, K.1    Oobo, M.2    Yashima, E.3
  • 73
    • 77952832456 scopus 로고    scopus 로고
    • Smart supramolecular hydrogel of Na-(4-n-Alkyloxybenzoyl)-l-histidine exhibiting pH-modulated properties
    • Patra, T., Pal, A. & Dey, J. Smart supramolecular hydrogel of Na-(4-n-Alkyloxybenzoyl)-l-histidine exhibiting pH-modulated properties. Langmuir 26, 7761 (2010).
    • (2010) Langmuir , vol.26 , pp. 7761
    • Patra, T.1    Pal, A.2    Dey, J.3
  • 74
    • 78651431026 scopus 로고    scopus 로고
    • Fabrication of self-assembling d-form peptide nanofiber scaffold d-EAK16 for rapid hemostasis
    • Luo, Z. L., Wang, S. K. & Zhang, S. G. Fabrication of self-assembling d-form peptide nanofiber scaffold d-EAK16 for rapid hemostasis. Biomaterials 32, 2013 (2011).
    • (2011) Biomaterials , vol.32 , pp. 2013
    • Luo, Z.L.1    Wang, S.K.2    Zhang, S.G.3
  • 75
    • 79551558448 scopus 로고    scopus 로고
    • Applications of bio-inspired special wettable surfaces
    • Yao, X., Song, Y. L. & Jiang, L. Applications of bio-inspired special wettable surfaces. Adv. Mater. 23, 719 (2011).
    • (2011) Adv. Mater. , vol.23 , pp. 719
    • Yao, X.1    Song, Y.L.2    Jiang, L.3
  • 76
    • 79953785038 scopus 로고    scopus 로고
    • Chirality-triggered wettability switching on a smart polymer surface
    • Qing, G. & Sun, T. Chirality-triggered wettability switching on a smart polymer surface. Adv. Mater. 23, 1615 (2011).
    • (2011) Adv. Mater. , vol.23 , pp. 1615
    • Qing, G.1    Sun, T.2
  • 77
    • 33947361084 scopus 로고    scopus 로고
    • DNA-protein interactions as the source of largelength-scale chirality evident in the liquid crystal behavior of filamentous bacteriophages
    • Tomar, S., Green, M. M. & Day, L. A. DNA-protein interactions as the source of largelength-scale chirality evident in the liquid crystal behavior of filamentous bacteriophages. J. Am. Chem. Soc. 129, 3367 (2007).
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 3367
    • Tomar, S.1    Green, M.M.2    Day, L.A.3
  • 78
    • 70349290626 scopus 로고    scopus 로고
    • A model liquid crystalline system based on rodlike viruses with variable chirality and persistence length
    • Barry, E., Beller, D. & Dogic, Z. A model liquid crystalline system based on rodlike viruses with variable chirality and persistence length. Soft Matter 5, 2563 (2009).
    • (2009) Soft Matter , vol.5 , pp. 2563
    • Barry, E.1    Beller, D.2    Dogic, Z.3
  • 80
    • 0037460136 scopus 로고    scopus 로고
    • Antibody recognition of chiral surfaces. enantiomorphous crystals of leucine-leucine-tyrosine
    • Geva, M., Frolow, F., Eisenstein, M. & Addadi, L. Antibody recognition of chiral surfaces. enantiomorphous crystals of leucine-leucine- tyrosine. J. Am. Chem. Soc. 125, 696 (2003).
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 696
    • Geva, M.1    Frolow, F.2    Eisenstein, M.3    Addadi, L.4
  • 81
    • 2542575545 scopus 로고    scopus 로고
    • Antibody recognition of chiral surfaces Structural models of antibody complexes with leucine-leucine-tyrosine crystal surfaces
    • Geva, M., Eisenstein, M. & Addadi, L. Antibody recognition of chiral surfaces. Structural models of antibody complexes with leucine-leucine-tyrosine crystal surfaces. Proteins 55, 862 (2004).
    • (2004) Proteins , vol.55 , pp. 862
    • Geva, M.1    Eisenstein, M.2    Addadi, L.3
  • 82
    • 33847002367 scopus 로고    scopus 로고
    • Stereospecific interaction between immune cells and chiral surfaces
    • Sun, T., Han, D., Riehemann, K., Chi, L. & Fuchs, H. Stereospecific interaction between immune cells and chiral surfaces. J. Am. Chem. Soc. 129, 1496 (2007).
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 1496
    • Sun, T.1    Han, D.2    Riehemann, K.3    Chi, L.4    Fuchs, H.5
  • 83
    • 50249184122 scopus 로고    scopus 로고
    • Stereoselective interaction between DNA and chiral surfaces
    • Tang, K., Gan, H., Li, Y., Chi, L., Sun, T. & Fuchs, H. Stereoselective interaction between DNA and chiral surfaces. J. Am. Chem. Soc. 130, 11284 (2008).
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 11284
    • Tang, K.1    Gan, H.2    Li, Y.3    Chi, L.4    Sun, T.5    Fuchs, H.6
  • 84
    • 70349932190 scopus 로고    scopus 로고
    • Selective adsorption of DNA on chiral surfaces: Supercoiled or relaxed conformation
    • Gan, H., Tang, K., Sun, T., Hirtz, M., Li, Y., Chi, L., Butz, S. & Fuchs, H. Selective adsorption of DNA on chiral surfaces: supercoiled or relaxed conformation. Angew. Chem. Int. Ed. 48, 5282 (2009).
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 5282
    • Gan, H.1    Tang, K.2    Sun, T.3    Hirtz, M.4    Li, Y.5    Chi, L.6    Butz, S.7    Fuchs, H.8
  • 85
    • 79959232185 scopus 로고    scopus 로고
    • Chirality of glutathione surface coating affects the cytotoxicity of quantum dots
    • Li, Y., Zhou, Y., Wang, H. Y., Perrett, S., Zhao, Y., Tang, Z. & Nie, G. Chirality of glutathione surface coating affects the cytotoxicity of quantum dots. Angew. Chem. Int. Ed. 50, 5860 (2011).
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 5860
    • Li, Y.1    Zhou, Y.2    Wang, H.Y.3    Perrett, S.4    Zhao, Y.5    Tang, Z.6    Nie, G.7
  • 86
    • 77955354452 scopus 로고    scopus 로고
    • Stereochemistry triggered differential cell behaviours on chiral polymer surfaces
    • Wang, X., Gan, H., Sun, T., Su, B., Fuchs, H., Vestweber, D. & Butz, S. Stereochemistry triggered differential cell behaviours on chiral polymer surfaces. Soft Matter 6, 3851 (2010).
    • (2010) Soft Matter , vol.6 , pp. 3851
    • Wang, X.1    Gan, H.2    Sun, T.3    Su, B.4    Fuchs, H.5    Vestweber, D.6    Butz, S.7
  • 87
    • 80052418711 scopus 로고    scopus 로고
    • Chiral design for polymeric biointerface: The influence of surface chirality on protein adsorption
    • Wang, X., Gan, H. & Sun, T. Chiral design for polymeric biointerface: the influence of surface chirality on protein adsorption. Adv. Funct. Mater. 21, 3276 (2011).
    • (2011) Adv. Funct. Mater. , vol.21 , pp. 3276
    • Wang, X.1    Gan, H.2    Sun, T.3
  • 88
    • 66949136654 scopus 로고    scopus 로고
    • The chiral effects on the responses of osteoblastic cells to the polymeric substrates
    • Yi, Q., Wen, X., Li, L., He, B., Nie, Y., Wu, Y., Zhang, Z. & Gu, Z. The chiral effects on the responses of osteoblastic cells to the polymeric substrates. Euro. Polym. J. 45, 1970 (2009).
    • (2009) Euro. Polym. J. , vol.45 , pp. 1970
    • Yi, Q.1    Wen, X.2    Li, L.3    He, B.4    Nie, Y.5    Wu, Y.6    Zhang, Z.7    Gu, Z.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.