Rotaxane (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "Rotaxane" in French language version.

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865th place
633rd place
2,343rd place
4,329th place
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acs.org (Global: 865th place; French: 633rd place)

pubs.acs.org

doi.org (Global: 2nd place; French: 3rd place)

dx.doi.org

  • (en) J. A. Bravo, F. M. Raymo, J. F. Stoddart, A. J. P. White, D. J. Williams, « High Yielding Template-Directed Syntheses of [2]Rotaxanes », European Journal of Organic Chemistry, vol. 1998, no 11, , p. 2565–2571 (DOI 10.1002/(SICI)1099-0690(199811)1998:11<2565::AID-EJOC2565>3.0.CO;2-8)
  • (en) I. T. Harrison and S. Harrison, « Synthesis of a stable complex of a macrocycle and a threaded chain », J. Am. Chem. Soc., vol. 89, no 22, , p. 5723–5724 (DOI 10.1021/ja00998a052)
  • (en) F. Aricó, J. D. Badjic, S. J. Cantrill, A. H. Flood, K. C.-F. Leung, Y. Liu, and J. F. Stoddart, « Templated Synthesis of Interlocked Molecules », Topics in Current Chemistry, vol. 249, , p. 203–259 (DOI 10.1007/b104330)
  • (en) I. Yoon, M. Narita, T. Shimizu, and M. Asakawa, « Threading-Followed-by-Shrinking Protocol for the Synthesis of a [2]Rotaxane Incorporating a Pd(II)-Salophen Moiety », J. Am. Chem. Soc., vol. 126, no 51, , p. 16740–16741 (DOI 10.1021/ja0464490)
  • (en) N. Kameta, K. Hiratani and Y. Nagawa, « A novel synthesis of chiral rotaxanes via covalent bond formation », Chem. Commun., no 51, , p. 466–467 (DOI 10.1039/b314744d)
  • (en) V. Aucagne, J. Berna, J. D. Crowley, S. M. Goldup, K. D. Hanni, D. A. Leigh, P. J. Lusby, V. E. Ronaldson, A. M. Z. Slawin, A. Viterisi, and D. B. Walker, « Catalytic "active-metal" template synthesis of [2]rotaxanes, [3]rotaxanes, and molecular shuttles, and some observations on the mechanism of the Cu(I)-catalyzed azide-alkyne 1,3-cycloaddition », J. Am. Chem. Soc., vol. 129, , p. 11950–11963 (DOI 10.1021/ja073513f)
  • (en) C. A. Schalley, K. Beizai, and F. Vögtle, « On the Way to Rotaxane-Based Molecular Motors: Studies in Molecular Mobility and Topological Chirality », Acc. Chem. Res., vol. 34, no 6, , p. 465–476 (DOI 10.1021/ar000179i)
  • (en) J. P. Sauvage, « Transition Metal-Containing Rotaxanes and Catenanes in Motion: Toward Molecular Machines and Motors », Acc. Chem. Res., vol. 31, no 10, , p. 611–619 (DOI 10.1021/ar960263r)
  • (en) F. Coutrot, E. Busseron, « A New Glycorotaxane Molecular Machine Based on an Anilinium and a Triazolium Station », Chem. Eur. J., vol. 14, , p. 4784-4787 (DOI 10.1002/chem.200800480)
  • (en) V. Serreli, C.-F. Lee, E. R. Kay and D. A. Leigh, « Exercising Demons: A Molecular Information Ratchet », Nature, vol. 445, , p. 523–527 (DOI 10.1038/nature05452)
  • (en) F. Coutrot, C. Romuald, E. Busseron, « A New pH-Switchable Dimannosyl [c2]Daisy Chain Molecular Machine », Org. Lett., vol. 10, , p. 3741-3744 (DOI 10.1021/ol801390h)
  • (en) M. Radha Kishan, A. Parham, F. Schelhase, A. Yoneva, G. Silva, Z. Chen, Y. Okamoto, F. Voegtle, « Bridging Rotaxanes' wheels - cyclochiral Bonnanes », Angew. Chem. Int. Ed., vol. 45, , p. 7296-7299 (DOI 10.1002/anie.200602002)
  • (en) F. Coutrot, E. Busseron, « Controlling the Chair Conformation of a Mannopyranose in a Large-Amplitude [2]Rotaxane Molecular Machine », Chem. Eur. J., vol. 15, , p. 5186-5190 (DOI 10.1002/chem.200900076)
  • (en) E. Busseron, C. Romuald, F. Coutrot,, « Bistable or Oscillating State Depending on Station and Temperature in Three-Station Glycorotaxane Molecular Machines », Chem. Eur. J., vol. 16, , p. 10062-10073 (DOI 10.1002/chem.201000777)
  • (en) C. Romuald, E. Busseron, F. Coutrot,, « Very Contracted to Extended co-Conformations with or without Oscillations in Two- and Three-Station [c2]Daisy Chains », J. Org. Chem., vol. 75, , p. 6516-6531 (DOI 10.1021/jo101234u)
  • (en) C. Clavel, C. Romuald, E. Brabet, F. Coutrot,, « A pH-Sensitive Lasso-Based Rotaxane Molecular Switch », Chem. Eur. J., vol. 19, , p. 2982-2989 (DOI 10.1002/chem.201203597)
  • (en) C. Romuald, A. Arda, C. Clavel, J. Jimenez-Barbero, F. Coutrot,, « Tightening or loosening a pH-sensitive double-lasso molecular machine readily synthesized from an ends-activated [c2]daisy chain », Chem. Sci., vol. 3, , p. 1851-1857 (DOI 10.1039/C2SC20072D)
  • (en) C. Romuald, G. Cazals, C. Enjalbal, F. Coutrot,, « Straightforward Synthesis of a Double-Lasso Macrocycle from a Nonsymmetrical [c2]Daisy Chain », Org. Lett., vol. 15, , p. 184-187 (DOI 10.1021/ol303186j)
  • (en) J. E. H. Buston, J. R. Young and H. L. Anderson, « Rotaxane-encapsulated cyanine dyes: enhanced fluorescence efficiency and photostability », Chem. Commun., no 11, , p. 905–906 (DOI 10.1039/b001812k)
  • (en) M. R. Craig, M. G. Hutchings, T. D. W. Claridge, H. L. Anderson, « Rotaxane-Encapsulation Enhances the Stability of an Azo Dye, in Solution and when Bonded to Cellulose », Angew. Chem. Int. Ed., vol. 40, no 6, , p. 1071–1074 (DOI 10.1002/1521-3773)
  • (en) E. Arunkumar, C. C. Forbes, B. C. Noll, and B. D. Smith, « Squaraine-Derived Rotaxanes: Sterically Protected Fluorescent Near-IR Dyes », J. Am. Chem. Soc., vol. 127, no 10, , p. 3288–3289 (DOI 10.1021/ja042404n) free copy
  • (en) M. Feng, X. Guo, X. Lin, X. He, W. Ji, S. Du, D. Zhang, D. Zhu, and H. Gao, « Stable, Reproducible Nanorecording on Rotaxane Thin Films », J. Am. Chem. Soc., vol. 127, no 44, , p. 15338–15339 (DOI 10.1021/ja054836j)

nd.edu (Global: 2,343rd place; French: 4,329th place)

  • (en) E. Arunkumar, C. C. Forbes, B. C. Noll, and B. D. Smith, « Squaraine-Derived Rotaxanes: Sterically Protected Fluorescent Near-IR Dyes », J. Am. Chem. Soc., vol. 127, no 10, , p. 3288–3289 (DOI 10.1021/ja042404n) free copy

polyacs.org (Global: low place; French: low place)

  • E. S. Wilks Macromolecular Nomenclature Note No. 24