Rotaxano (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Rotaxano" in Spanish language version.

refsWebsite

Global rank Spanish rank

18doi.org

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12nih.gov

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1youtube.com

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1nd.edu

2,387^th place

3,261^st place

1web.archive.org

1^st place

1polyacs.org

low place

doi.org

dx.doi.org

J. A. Bravo, F. M. Raymo, J. F. Stoddart, A. J. P. White, D. J. Williams (1998). «High Yielding Template-Directed Syntheses of [2]Rotaxanes». Eur. J. Org. Chem. 1998 (11): 2565-2571. doi:10.1002/(SICI)1099-0690(199811)1998:11<2565::AID-EJOC2565>3.0.CO;2-8.
I. T. Harrison and S. Harrison (1967). «Synthesis of a stable complex of a macrocycle and a threaded chain». J. Am. Chem. Soc. 89 (22): 5723-5724. doi:10.1021/ja00998a052.
F. Aricó, J. D. Badjic, S. J. Cantrill, A. H. Flood, K. C.-F. Leung, Y. Liu, and J. F. Stoddart (2005). «Templated Synthesis of Interlocked Molecules». Topics in Current Chemistry 249: 203-259. doi:10.1007/b104330.
I. Yoon, M. Narita, T. Shimizu, and M. Asakawa (2004). «Threading-Followed-by-Shrinking Protocol for the Synthesis of a [2]Rotaxane Incorporating a Pd(II)-Salophen Moiety». J. Am. Chem. Soc. 126 (51): 16740-16741. PMID 15612709. doi:10.1021/ja0464490.
N. Kameta, K. Hiratani and Y. Nagawa (2004). «A novel synthesis of chiral rotaxanes via covalent bond formation». Chem. Commun. (51): 466-467. PMID 14765261. doi:10.1039/b314744d.
V. Aucagne, J. Berna, J. D. Crowley, S. M. Goldup, K. D. Hänni, D. A. Leigh, P. J. Lusby, V. E. Ronaldson, A. M. Z. Slawin, A. Viterisi, and D. B. Walker (2007). «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. 129 (39): 11950-11963. PMID 17845039. doi:10.1021/ja073513f.
C. A. Stanier, M. J. O Connell, H. L. Anderson and W. Clegg (2001). «Synthesis of fluorescent stilbene and tolan rotaxanes by Suzuki coupling». Chem. Commun. (5): 493-494. doi:10.1039/b010015n.
C. A. Schalley, K. Beizai, and F. Vögtle (2001). «On the Way to Rotaxane-Based Molecular Motors: Studies in Molecular Mobility and Topological Chirality». Acc. Chem. Res. 34 (6): 465-476. PMID 11412083. doi:10.1021/ar000179i.
J. P. Sauvage (1998). «Transition Metal-Containing Rotaxanes and Catenanes in Motion: Toward Molecular Machines and Motors». Acc. Chem. Res. 31 (10): 611-619. doi:10.1021/ar960263r.
F. Coutrot, E. Busseron (2008). «A New Glycorotaxane Molecular Machine Based on an Anilinium and a Triazolium Station». Chem. Eur. J. 14 (16): 4784-4787. PMID 18409178. doi:10.1002/chem.200800480.
V. Serreli, C.-F. Lee, E. R. Kay and D. A. Leigh (2007). «Exercising Demons: A Molecular Information Ratchet». Nature 445 (7127): 523-527. PMID 17268466. doi:10.1038/nature05452.
F. Coutrot, C. Romuald, E. Busseron (2008). «A New pH-Switchable Dimannosyl [c2]Daisy Chain Molecular Machine». Org. Lett. 10 (17): 3741-3744. PMID 18666774. doi:10.1021/ol801390h.
M. Radha Kishan, A. Parham, F. Schelhase, A. Yoneva, G. Silva, Z. Chen, Y. Okamoto, F. Voegtle (2006). «Bridging Rotaxanes' wheels - cyclochiral Bonnanes». Angew. Chem. Int. Ed. 45 (43): 7296-7299. PMID 17029314. doi:10.1002/anie.200602002.
F. Coutrot, E. Busseron (2009). «Controlling the Chair Conformation of a Mannopyranose in a Large-Amplitude [2]Rotaxane Molecular Machine». Chem. Eur. J. 15 (21): 5186-5190. PMID 19229918. doi:10.1002/chem.200900076.
J. E. H. Buston, J. R. Young and H. L. Anderson (2000). «Rotaxane-encapsulated cyanine dyes: enhanced fluorescence efficiency and photostability». Chem. Commun. (11): 905-906. doi:10.1039/b001812k.
M. R. Craig, M. G. Hutchings, T. D. W. Claridge, H. L. Anderson (1998). «Rotaxane-Encapsulation Enhances the Stability of an Azo Dye, in Solution and when Bonded to Cellulose». Angew. Chem. Int. Ed. 40 (6): 1071-1074. PMID 11268077. doi:10.1002/1521-3773(20010316)40:6<1071::AID-ANIE10710>3.0.CO;2-5.
E. Arunkumar, C. C. Forbes, B. C. Noll, and B. D. Smith (2005). «Squaraine-Derived Rotaxanes: Sterically Protected Fluorescent Near-IR Dyes». J. Am. Chem. Soc. 127 (10): 3288-3289. PMID 15755140. doi:10.1021/ja042404n. free copy
M. Feng, X. Guo, X. Lin, X. He, W. Ji, S. Du, D. Zhang, D. Zhu, and H. Gao (2005). «Stable, Reproducible Nanorecording on Rotaxane Thin Films». J. Am. Chem. Soc. 127 (44): 15338-15339. PMID 16262375. doi:10.1021/ja054836j.

nd.edu

E. Arunkumar, C. C. Forbes, B. C. Noll, and B. D. Smith (2005). «Squaraine-Derived Rotaxanes: Sterically Protected Fluorescent Near-IR Dyes». J. Am. Chem. Soc. 127 (10): 3288-3289. PMID 15755140. doi:10.1021/ja042404n. free copy

nih.gov

ncbi.nlm.nih.gov

I. Yoon, M. Narita, T. Shimizu, and M. Asakawa (2004). «Threading-Followed-by-Shrinking Protocol for the Synthesis of a [2]Rotaxane Incorporating a Pd(II)-Salophen Moiety». J. Am. Chem. Soc. 126 (51): 16740-16741. PMID 15612709. doi:10.1021/ja0464490.
N. Kameta, K. Hiratani and Y. Nagawa (2004). «A novel synthesis of chiral rotaxanes via covalent bond formation». Chem. Commun. (51): 466-467. PMID 14765261. doi:10.1039/b314744d.
V. Aucagne, J. Berna, J. D. Crowley, S. M. Goldup, K. D. Hänni, D. A. Leigh, P. J. Lusby, V. E. Ronaldson, A. M. Z. Slawin, A. Viterisi, and D. B. Walker (2007). «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. 129 (39): 11950-11963. PMID 17845039. doi:10.1021/ja073513f.
C. A. Schalley, K. Beizai, and F. Vögtle (2001). «On the Way to Rotaxane-Based Molecular Motors: Studies in Molecular Mobility and Topological Chirality». Acc. Chem. Res. 34 (6): 465-476. PMID 11412083. doi:10.1021/ar000179i.
F. Coutrot, E. Busseron (2008). «A New Glycorotaxane Molecular Machine Based on an Anilinium and a Triazolium Station». Chem. Eur. J. 14 (16): 4784-4787. PMID 18409178. doi:10.1002/chem.200800480.
V. Serreli, C.-F. Lee, E. R. Kay and D. A. Leigh (2007). «Exercising Demons: A Molecular Information Ratchet». Nature 445 (7127): 523-527. PMID 17268466. doi:10.1038/nature05452.
F. Coutrot, C. Romuald, E. Busseron (2008). «A New pH-Switchable Dimannosyl [c2]Daisy Chain Molecular Machine». Org. Lett. 10 (17): 3741-3744. PMID 18666774. doi:10.1021/ol801390h.
M. Radha Kishan, A. Parham, F. Schelhase, A. Yoneva, G. Silva, Z. Chen, Y. Okamoto, F. Voegtle (2006). «Bridging Rotaxanes' wheels - cyclochiral Bonnanes». Angew. Chem. Int. Ed. 45 (43): 7296-7299. PMID 17029314. doi:10.1002/anie.200602002.
F. Coutrot, E. Busseron (2009). «Controlling the Chair Conformation of a Mannopyranose in a Large-Amplitude [2]Rotaxane Molecular Machine». Chem. Eur. J. 15 (21): 5186-5190. PMID 19229918. doi:10.1002/chem.200900076.
M. R. Craig, M. G. Hutchings, T. D. W. Claridge, H. L. Anderson (1998). «Rotaxane-Encapsulation Enhances the Stability of an Azo Dye, in Solution and when Bonded to Cellulose». Angew. Chem. Int. Ed. 40 (6): 1071-1074. PMID 11268077. doi:10.1002/1521-3773(20010316)40:6<1071::AID-ANIE10710>3.0.CO;2-5.
E. Arunkumar, C. C. Forbes, B. C. Noll, and B. D. Smith (2005). «Squaraine-Derived Rotaxanes: Sterically Protected Fluorescent Near-IR Dyes». J. Am. Chem. Soc. 127 (10): 3288-3289. PMID 15755140. doi:10.1021/ja042404n. free copy
M. Feng, X. Guo, X. Lin, X. He, W. Ji, S. Du, D. Zhang, D. Zhu, and H. Gao (2005). «Stable, Reproducible Nanorecording on Rotaxane Thin Films». J. Am. Chem. Soc. 127 (44): 15338-15339. PMID 16262375. doi:10.1021/ja054836j.

polyacs.org

«E. S. Wilks Macromolecular Nomenclature Note No. 24». Archivado desde el original el 11 de octubre de 2008. Consultado el 12 de diciembre de 2011.

web.archive.org

«E. S. Wilks Macromolecular Nomenclature Note No. 24». Archivado desde el original el 11 de octubre de 2008. Consultado el 12 de diciembre de 2011.

youtube.com

Antonio Romero Carrasco (28 de junio de 2011), Rotaxane by clipping, consultado el 8 de marzo de 2017 .