Speed-controlled molecular shuttles

Collection of Czechoslovak Chemical Communications

Volumn 67, Issue 11, 2002, Pages 1719-1728

  Bělohradský, Martin ^a   Elizarov, Arkadij M ^b   Stoddart, J Fraser ^b  

^a INSTITUTE OF ORGANIC CHEMISTRY AND BIOCHEMISTRY   (Czech Republic)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Bipyridinium salts; Crown ethers; Dynamic NMR spectroscopy; Molecular machines; Molecular recognition; Molecular shuttle; Post assembly covalent modification; Rotaxanes

Indexed keywords

BENZENE DERIVATIVE; BIS 1,4 PHENYLENE[34]CROWN 10; METHANE; ROTAXANE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL MODIFICATION; MOLECULAR RECOGNITION; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 0036881064     PISSN: 00100765     EISSN: None     Source Type: Journal    
DOI: 10.1135/cccc20021719     Document Type: Article

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43. The slippage methodology was exploited early on when rotaxanes were prepared in a statistical manner. For examples, see: a) Harrison I. T.: J. Chem. Soc., Chem. Commun. 1972, 231; b) Schill G., Beckmann W., Schweikert N., Fritz H.: Chem. Ber. 1986, 119, 2647. The first successful template-directed synthesis of rotaxanes by slippage was reported in 1993, see: c) Ashton P. R., Belohradsky M., Philp D., Stoddart J. F.: J. Chem. Soc., Chem. Commun. 1993, 1269. For a discussion of the phenomenon, see: d) Fyfe M. C. T., Raymo F. M., Stoddart J. F. in: Stimulating Concepts in Chemistry (M. Shibasaki, J. F. Stoddart and F. Vögtle, Eds), p. 211. VCH-Wiley, Weinheim 2000. For recent examples, see: e) Sohgawa Y. H., Fujimori H., Shoji J., Furusho Y., Kihara N., Takata T.: Chem. Lett. 2001, 8, 774; f) Jeppesen J. O., Becher J., Stoddart J. F.: Org. Lett. 2002, 4, 557.
44. The slippage methodology was exploited early on when rotaxanes were prepared in a statistical manner. For examples, see: a) Harrison I. T.: J. Chem. Soc., Chem. Commun. 1972, 231; b) Schill G., Beckmann W., Schweikert N., Fritz H.: Chem. Ber. 1986, 119, 2647. The first successful template-directed synthesis of rotaxanes by slippage was reported in 1993, see: c) Ashton P. R., Belohradsky M., Philp D., Stoddart J. F.: J. Chem. Soc., Chem. Commun. 1993, 1269. For a discussion of the phenomenon, see: d) Fyfe M. C. T., Raymo F. M., Stoddart J. F. in: Stimulating Concepts in Chemistry (M. Shibasaki, J. F. Stoddart and F. Vögtle, Eds), p. 211. VCH-Wiley, Weinheim 2000. For recent examples, see: e) Sohgawa Y. H., Fujimori H., Shoji J., Furusho Y., Kihara N., Takata T.: Chem. Lett. 2001, 8, 774; f) Jeppesen J. O., Becher J., Stoddart J. F.: Org. Lett. 2002, 4, 557.
45. The slippage methodology was exploited early on when rotaxanes were prepared in a statistical manner. For examples, see: a) Harrison I. T.: J. Chem. Soc., Chem. Commun. 1972, 231; b) Schill G., Beckmann W., Schweikert N., Fritz H.: Chem. Ber. 1986, 119, 2647. The first successful template-directed synthesis of rotaxanes by slippage was reported in 1993, see: c) Ashton P. R., Belohradsky M., Philp D., Stoddart J. F.: J. Chem. Soc., Chem. Commun. 1993, 1269. For a discussion of the phenomenon, see: d) Fyfe M. C. T., Raymo F. M., Stoddart J. F. in: Stimulating Concepts in Chemistry (M. Shibasaki, J. F. Stoddart and F. Vögtle, Eds), p. 211. VCH-Wiley, Weinheim 2000. For recent examples, see: e) Sohgawa Y. H., Fujimori H., Shoji J., Furusho Y., Kihara N., Takata T.: Chem. Lett. 2001, 8, 774; f) Jeppesen J. O., Becher J., Stoddart J. F.: Org. Lett. 2002, 4, 557.
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