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Volumn 31, Issue 2, 1998, Pages 295-307

Self-assembly of functionalized [2]catenanes bearing a reactive functional group on either one or both macrocyclic components - From monomeric [2]catenanes to polycatenanes

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC POLYMERS; CARBOXYLIC ACIDS; COPOLYMERIZATION; HYDROGEN BONDS; MONOMERS; POLYCONDENSATION; SYNTHESIS (CHEMICAL);

EID: 0031647060     PISSN: 00249297     EISSN: None     Source Type: Journal    
DOI: 10.1021/ma970685w     Document Type: Article
Times cited : (68)

References (58)
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    • For examples of catenanes self-assembled as a result of π-π stacking and edge-to-face interactions and [C-H⋯O] hydrogen bonding, see: (a) Anelli, P. L.; Ashton, P. R.; Ballardini, R.; Balzani, V.; Delgado, M.; Gandolfi, M. T.; Goodnow, T. T.; Kaifer, A. E.; Philp, D.; Pietraszkiewicz, M.; Prodi, L.; Reddington, M. V.; Slawin, A. M. Z.; Spencer, N.; Stoddart, J. F.; Vicent, C.; Williams, D. J. J. Am. Chem. Soc. 1992, 114, 193-218. (b) Ashton, P. R.; Huff, J.; Menzer, S.; Parsons, I. W.; Preece, J. A.; Stoddart, J. F.; Tolley, M. S.; White, A. J. P.; Williams, D J. Chem. Eur. J. 1996, 2, 31-44.
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    • For examples of catenanes self-assembled as a result of hydrogen-bonding interactions, see: (a) Hunter, C. A. J. Am. Chem. Soc. 1992, 114, 5303-5311. (b) Vögtle, F.; Meier, S.; Hoss, R. Angew. Chem., Int. Ed. Engl. 1992, 31, 1619-1622. (c) Leigh, D. A.; Moody, K.; Smart, J. P.; Watson, K. J.; Slawin, A. M.Z. Angew. Chem., Int. Ed. Engl. 1996, 35, 306-310.
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    • 33748631935 scopus 로고
    • For examples of catenanes self-assembled as a result of hydrogen-bonding interactions, see: (a) Hunter, C. A. J. Am. Chem. Soc. 1992, 114, 5303-5311. (b) Vögtle, F.; Meier, S.; Hoss, R. Angew. Chem., Int. Ed. Engl. 1992, 31, 1619-1622. (c) Leigh, D. A.; Moody, K.; Smart, J. P.; Watson, K. J.; Slawin, A. M.Z. Angew. Chem., Int. Ed. Engl. 1996, 35, 306-310.
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    • note
    • 6 are not shifted significantly with respect to the signals for the corresponding protons in the free macrocyclic polyethers 4 or 12. Furthermore, these protons resonate at approximately the same δ values and with the same intensities over the range of temperatures investigated. These observations suggest that the dioxybenzene unit does not reside inside the cavity of the tetracationic cyclophane in any of the [2]-catenanes.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.