메뉴 건너뛰기




Volumn 46, Issue 26, 2007, Pages 5015-5019

One template, multiple rings: Controlled iterative addition of macrocycles onto a single binding site rotaxane thread

Author keywords

Coordination modes; Macrocycles; Palladium; Polyrotaxanes; Rotaxanes; Template synthesis

Indexed keywords

COORDINATION MODES; MACROCYCLES; POLYROTAXANES; ROTAXANES; TEMPLATE SYNTHESIS;

EID: 34447317547     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200700933     Document Type: Article
Times cited : (75)

References (74)
  • 3
    • 2842587248 scopus 로고    scopus 로고
    • For reviews which highlight various aspects of template strategies to mechanically interlocked architectures, see a D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2828;
    • For reviews which highlight various aspects of template strategies to mechanically interlocked architectures, see a) D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2828;
  • 6
    • 0003570337 scopus 로고    scopus 로고
    • Eds, F. Diederich, P. J. Stang, Wiley-VCH, Weinheim
    • d) Templated Organic Synthesis (Eds.: F. Diederich, P. J. Stang), Wiley-VCH, Weinheim, 2000;
    • (2000) Templated Organic Synthesis
  • 17
    • 0030152506 scopus 로고    scopus 로고
    • For examples of [4]rotaxanes (at least three ring-template sites, see a) P. R. Ashton, R. Ballardini, V. Balzani, M. Belohradský, M. T. Gandolfi, D. Philp, L. Prodi, F. M. Raymo, M. V. Reddington, N. Spencer, J. F. Stoddart, M. Venturi, D. J. Williams, J. Am. Chem. Soc. 1996, 118, 4931-4951;
    • For examples of [4]rotaxanes (at least three ring-template sites), see a) P. R. Ashton, R. Ballardini, V. Balzani, M. Belohradský, M. T. Gandolfi, D. Philp, L. Prodi, F. M. Raymo, M. V. Reddington, N. Spencer, J. F. Stoddart, M. Venturi, D. J. Williams, J. Am. Chem. Soc. 1996, 118, 4931-4951;
  • 28
    • 34447328960 scopus 로고    scopus 로고
    • For higher order rotaxanes (at least n-1 ring-template sites for n components), see a) N. Solladié, J.-C. Chambron, C. O. Dietrich-Buchecker, J.-P. Sauvage, Angew. Chem. 1996, 108, 957-960;
    • For higher order rotaxanes (at least n-1 ring-template sites for n components), see a) N. Solladié, J.-C. Chambron, C. O. Dietrich-Buchecker, J.-P. Sauvage, Angew. Chem. 1996, 108, 957-960;
  • 33
    • 0031646421 scopus 로고    scopus 로고
    • for polyrotaxanes, non-monodispersed systems in which several or many rings are threaded onto a polymer chain or a rotaxane monomer are polymerized, see the following reviews e
    • for polyrotaxanes, non-monodispersed systems in which several or many rings are threaded onto a polymer chain or a rotaxane monomer are polymerized, see the following reviews e) A. Harada, Acta. Polymer. 1998, 49, 3-17;
    • (1998) Acta. Polymer , vol.49 , pp. 3-17
    • Harada, A.1
  • 37
    • 34447295596 scopus 로고    scopus 로고
    • For examples of [4]catenanes (at least three ring-template sites, see a) C. O. Dietrich-Buchecker, B. Frommberger, I. Lüer, J.-P Sauvage, F. Vögtle, Angew. Chem. 1993, 105, 1526-1529;
    • For examples of [4]catenanes (at least three ring-template sites), see a) C. O. Dietrich-Buchecker, B. Frommberger, I. Lüer, J.-P Sauvage, F. Vögtle, Angew. Chem. 1993, 105, 1526-1529;
  • 40
    • 34447297501 scopus 로고    scopus 로고
    • For higher order catenanes (at least n-1 ring-template sites for n components), see a) D. B. Amabilino, P. R. Ashton, A. S. Reder, N. Spencer, J. F. Stoddart, Angew. Chem. 1994, 106, 450-453;
    • For higher order catenanes (at least n-1 ring-template sites for n components), see a) D. B. Amabilino, P. R. Ashton, A. S. Reder, N. Spencer, J. F. Stoddart, Angew. Chem. 1994, 106, 450-453;
  • 47
    • 0033104834 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1999, 38, 637-641;
    • (1999) Chem. Int. Ed , vol.38 , pp. 637-641
    • Angew1
  • 56
    • 33746282221 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 4099-4104.
    • (2006) Chem. Int. Ed , vol.45 , pp. 4099-4104
    • Angew1
  • 57
    • 0001413546 scopus 로고    scopus 로고
    • Higher interlocked oligomers, up to a [7]catenane [a F. Bitsch, C. O. Dietrich-Buchecker, A.-K. Khémiss, J.-P. Sauvage, A. Van Dorsselaer, J. Am. Chem. Soc. 1991, 113, 4023-4025]
    • Higher interlocked oligomers, up to a [7]catenane [a) F. Bitsch, C. O. Dietrich-Buchecker, A.-K. Khémiss, J.-P. Sauvage, A. Van Dorsselaer, J. Am. Chem. Soc. 1991, 113, 4023-4025]
  • 58
    • 34447339898 scopus 로고    scopus 로고
    • and a [6]rotaxane [b A. H. Parham, R. Schmeider, F. Vögtle, Synlett 1999, 1887-1890], have been detected in various reaction mixtures by mass spectrometry. The latter example, which features six template sites on the thread for up to five macrocycles, was termed an iterative rotaxane synthesis by the authors but is essentially a standard one-pot threading-and-stoppering strategy; for high order catenanes and rotaxanes in which the threaded rings are covalently connected together,
    • and a [6]rotaxane [b) A. H. Parham, R. Schmeider, F. Vögtle, Synlett 1999, 1887-1890], have been detected in various reaction mixtures by mass spectrometry. The latter example, which features six template sites on the thread for up to five macrocycles, was termed an "iterative rotaxane synthesis" by the authors but is essentially a standard one-pot "threading-and-stoppering" strategy; for high order catenanes and rotaxanes in which the threaded rings are covalently connected together,
  • 64
    • 33845474499 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 8051-8055.
    • (2006) Chem. Int. Ed , vol.45 , pp. 8051-8055
    • Angew1
  • 66
    • 4644265484 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 3914-3918;
    • (2004) Chem. Int. Ed , vol.43 , pp. 3914-3918
    • Angew1
  • 69
    • 9744235833 scopus 로고    scopus 로고
    • II template has also been described: Y. Furusho, T. Matsuyama, T. Takata, T, Moriuchi, T. Hirao, Tetrahedron Lett. 2004, 45, 9593-9597.
    • II template has also been described: Y. Furusho, T. Matsuyama, T. Takata, T, Moriuchi, T. Hirao, Tetrahedron Lett. 2004, 45, 9593-9597.
  • 70
    • 84892620357 scopus 로고    scopus 로고
    • [9] Various alternative reagents and conditions were investigated of which ortho-nitrobenzenesulfonylhydrazide (NBSH) proved the most efficacious [see A. G. Myers, B. Zheng, M. Movassaghi, J. Org. Chem. 1997, 62, 7507].
    • [9] Various alternative reagents and conditions were investigated of which ortho-nitrobenzenesulfonylhydrazide (NBSH) proved the most efficacious [see A. G. Myers, B. Zheng, M. Movassaghi, J. Org. Chem. 1997, 62, 7507].
  • 72
    • 22844442238 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 4557-4564.
    • (2005) Chem. Int. Ed , vol.44 , pp. 4557-4564
    • Angew1
  • 74
    • 4544231480 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 3260-3264.
    • (2004) Chem. Int. Ed , vol.43 , pp. 3260-3264
    • Angew1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.