메뉴 건너뛰기




Volumn 23, Issue 12, 2011, Pages 819-828

Microwave-assisted synthesis of novel cyclodextrin-cucurbituril complexes

Author keywords

Cucurbiturils; Cyclodextrins; Microwave irradiation

Indexed keywords


EID: 84856592547     PISSN: 10610278     EISSN: 10290478     Source Type: Journal    
DOI: 10.1080/10610278.2011.636444     Document Type: Article
Times cited : (15)

References (78)
  • 2
    • 0041472445 scopus 로고    scopus 로고
    • Cucurbituril homologues and derivatives: New opportunities in supramolecular chemistry
    • (b) Lee, J.W.; Samal, S.; Selvapalam, N.; Kim, H.-J.; Kim, K. Cucurbituril homologues and derivatives: new opportunities in supramolecular chemistry. Acc. Chem. Res. 2003, 36, 621-630.
    • (2003) Acc. Chem. Res. , vol.36 , pp. 621-630
    • Lee, J.W.1    Samal, S.2    Selvapalam, N.3    Kim, H.-J.4    Kim, K.5
  • 3
    • 0000995482 scopus 로고    scopus 로고
    • Atwood, J.L., Davies, J.E.D., MacNicol, D.D., Vögtle, F. Eds. Elsevier: Oxford
    • (c) Mock, W.L. In Comprehensive Supramolecular Chemistry; Atwood, J.L., Davies, J.E.D., MacNicol, D.D., Vögtle, F. Eds.; Vol. 3, Elsevier: Oxford, 1996; pp. 477-493.
    • (1996) Comprehensive Supramolecular Chemistry , vol.3 , pp. 477-493
    • Mock, W.L.1
  • 5
    • 84933041004 scopus 로고
    • Ueber condensation-sproducte aus glycoluril und formaldehyd
    • Behrend, R.; Meyer, E.; Rusche, F. Ueber condensation-sproducte aus glycoluril und formaldehyd. Justus Liebig Ann. Chem. 1905, 339, 1-37.
    • (1905) Justus Liebig Ann. Chem. , vol.339 , pp. 1-37
    • Behrend, R.1    Meyer, E.2    Rusche, F.3
  • 6
    • 0001482126 scopus 로고    scopus 로고
    • Cucurbit[5]uril, decamethylcucurbit[5]uril and cucurbit[6]uril. Synthesis, solubility and amine complex formation
    • DOI 10.1023/A:1011184725796
    • Jansen, K.; Buschmann, H.-J.; Wego, A.D.; Mayer Döpp, C.; Drexler, H.-J; Holdt, H.-J.; Schollmeyer, E. Cucurbit[5]uril, decamethylcucurbit[5]uril and cucurbit[6]uril. Synthesis, solubility and amine complex formation. J. Incl. Phenom. Macrocycl. Chem. 2001, 39, 357-363. (Pubitemid 33654922)
    • (2001) Journal of Inclusion Phenomena , vol.39 , Issue.3-4 , pp. 357-363
    • Jansen, K.1    Buschmann, H.-J.2    Wego, A.3    Dopp, D.4    Mayer, C.5    Drexler, H.-J.6    Holdt, H.-J.7    Schollmeyer, E.8
  • 7
    • 0041429631 scopus 로고    scopus 로고
    • Facile synthesis of cucurbit[n]uril derivatives via direct functionalization: Expanding utilization of cucurbit[n]uril
    • DOI 10.1021/ja036536c
    • (a) Jon, S.Y.; Selvapalam, N.; Oh, D.H.; Kang, J.-K.; Kim, S.-Y.; Jeon, Y.J.; Lee, J.W.; Kim, K. Facile synthesis of cucurbit[n]uril derivatives via direct functionalization: expanding utilization of cucurbit[n]uril. J. Am. Chem. Soc. 2003, 125, 10186-10187. (Pubitemid 37022225)
    • (2003) Journal of the American Chemical Society , vol.125 , Issue.34 , pp. 10186-10187
    • Jon, S.Y.1    Selvapalam, N.2    Oh, D.H.3    Kang, J.-K.4    Kim, S.-Y.5    Jeon, Y.J.6    Lee, J.W.7    Kim, K.8
  • 8
    • 0035977209 scopus 로고    scopus 로고
    • Controlling factors in the synthesis of cucurbituril and its homologues
    • DOI 10.1021/jo015897c
    • (b) Day, A.; Arnold, A.P.; Blanch, R.J.; Snushall, B. Controlling factors in the synthesis of cucurbituril and its homologues. J. Org. Chem. 2001, 66, 8094-8100. (Pubitemid 34177959)
    • (2001) Journal of Organic Chemistry , vol.66 , Issue.24 , pp. 8094-8100
    • Day, A.1    Arnold, A.P.2    Blanch, R.J.3    Snushall, B.4
  • 9
    • 33645500754 scopus 로고    scopus 로고
    • Host-guest complexation of neutral red with macrocyclic host molecules: Contrasting pK(a) shifts and binding affinities for cucurbit[7]uril and beta-cyclodextrin
    • (a) Mohanty, J.; Bhasikuttan, A.C.; Nau, W.M.; Pal, H. Host-guest complexation of neutral red with macrocyclic host molecules: contrasting pK(a) shifts and binding affinities for cucurbit[7]uril and beta-cyclodextrin. J. Phys. Chem. B 2006, 110, 5132-5138.
    • (2006) J. Phys. Chem. B , vol.110 , pp. 5132-5138
    • Mohanty, J.1    Bhasikuttan, A.C.2    Nau, W.M.3    Pal, H.4
  • 12
    • 0037009336 scopus 로고    scopus 로고
    • Rigidity versus flexibility. A review of experimental and theoretical studies pertaining to the cyclodextrin nonrigidity
    • DOI 10.1016/S0022-2860(02)00236-3, PII S0022286002002363
    • (a) Dodziuk, H. Rigidity versus flexibility. A review of experimental and theoretical studies pertaining to the cyclodextrin nonrigidity. J. Mol. Struc. 2002, 614, 33-45. (Pubitemid 34987711)
    • (2002) Journal of Molecular Structure , vol.614 , Issue.1-3 , pp. 33-45
    • Dodziuk, H.1
  • 13
    • 0001092215 scopus 로고    scopus 로고
    • Reconsidering the conformational flexibility of beta-cyclodextrin
    • (b) Kozár, T.; Venanzi, C.A. Reconsidering the conformational flexibility of beta-cyclodextrin. J. Molec. Struc. (THEOCHEM) 1997, 395-396, 451-468.
    • (1997) J. Molec. Struc. (THEOCHEM) , vol.395-396 , pp. 451-468
    • Kozár, T.1    Venanzi, C.A.2
  • 15
    • 33947262994 scopus 로고    scopus 로고
    • Hydration and flexibility of alpha-, beta-, gamma- and delta-cyclodextrin: A molecular dynamics study
    • (d) Raffaini, G.; Ganazzoli, F. Hydration and flexibility of alpha-, beta-, gamma- and delta-cyclodextrin: a molecular dynamics study. Chem. Phys. 2007, 333, 128-134.
    • (2007) Chem. Phys. , vol.333 , pp. 128-134
    • Raffaini, G.1    Ganazzoli, F.2
  • 16
    • 0026603880 scopus 로고
    • Structural and dynamic studies of the hydrate, exchangeable hydrogens, and included molecules in beta-cyclodextrins by powder and single crystal deuterium magnetic-resonance
    • (e) Usha, M.G.; Wittebort, R.J. Structural and dynamic studies of the hydrate, exchangeable hydrogens, and included molecules in beta-cyclodextrins by powder and single crystal deuterium magnetic-resonance. J. Am. Chem. Soc. 1992, 114, 1541-1548.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 1541-1548
    • Usha, M.G.1    Wittebort, R.J.2
  • 17
    • 0010421067 scopus 로고
    • A highresolution C.P.-M.A.S. 13C-N.M.R. study of solid-state cyclomaltohexaose inclusion-complexes: Chemical shifts and structure of the host cyclomaltohexaose
    • (f) Inoue, Y.; Okuda, T.; Chûjô, R. A highresolution c.p.-m.a.s. 13C-n.m.r. study of solid-state cyclomaltohexaose inclusion-complexes: chemical shifts and structure of the host cyclomaltohexaose. Carbohydr. Res. 1985, 141, 179-190.
    • (1985) Carbohydr. Res. , vol.141 , pp. 179-190
    • Inoue, Y.1    Okuda, T.2    Chûjô, R.3
  • 18
    • 0002861777 scopus 로고
    • Determination of the host-guest geometry in the inclusion complexes of cyclomalto-oligosaccharides with p-nitrophenol in solution
    • (g) Yamamoto, Y.; Onda, M.; Takahashi, Y.; Inoue, Y.; Chûjô, R. Determination of the host-guest geometry in the inclusion complexes of cyclomalto-oligosaccharides with p-nitrophenol in solution. Carbohydr. Res. 1988, 182, 41-52.
    • (1988) Carbohydr. Res. , vol.182 , pp. 41-52
    • Yamamoto, Y.1    Onda, M.2    Takahashi, Y.3    Inoue, Y.4    Chûjô, R.5
  • 19
    • 26544432151 scopus 로고
    • 13C-N.M.R. study of the molecular dynamics of some solid-state inclusion-complexes of cyclomaltohexaose and cyclomaltoheptaose
    • 13C-n.m.r. study of the molecular dynamics of some solid-state inclusion-complexes of cyclomaltohexaose and cyclomaltoheptaose. Carbohydr. Res. 1985, 135, C12-C16.
    • (1985) Carbohydr. Res. , vol.135
    • Inoue, Y.1    Kuan, F.H.2    Takahashi, Y.3    Chûjô, R.4
  • 20
    • 0010290203 scopus 로고
    • 13C-N.M.R. study of some solid-state inclusion complexes of cyclomalto-oligosac-charides with para-substituted benzenes
    • 13C-N.M.R. study of some solid-state inclusion complexes of cyclomalto-oligosac-charides with para-substituted benzenes. Carbohydr. Res. 1987, 159, 1-10.
    • (1987) Carbohydr. Res. , vol.159 , pp. 1-10
    • Inoue, Y.1    Kuan, F.H.2    Chûjô, R.3
  • 21
    • 7744228545 scopus 로고
    • Structure of cyclodextrins and their complexes. 2. Do cyclodextrins have a rigid truncated cone structure
    • (j) Dodziuk, H.; Nowiński, K. Structure of cyclodextrins and their complexes. 2. Do cyclodextrins have a rigid truncated cone structure. J. Mol. Struct. (THEOCHEM) 1994, 110, 61-68.
    • (1994) J. Mol. Struct. (THEOCHEM) , vol.110 , pp. 61-68
    • Dodziuk, H.1    Nowiński, K.2
  • 22
    • 33749092927 scopus 로고    scopus 로고
    • Molecular modelling of saccharides, 9. On the hydrophobic characteristics of cyclodextrins: Computer-aided visualization of molecular lipophilicity patterns
    • (a) Lichtenthaler, F.W.; Immel, S. Molecular modelling of saccharides. 9. On the hydrophobic characteristics of cyclodextrins: computer-aided visualization of molecular lipophilicity patterns. Liebigs Ann. Chem. 1996, 27-37. (Pubitemid 126808269)
    • (1996) Liebigs Annales , Issue.1 , pp. 27-37
    • Lichtenthaler, F.W.1    Immel, S.2
  • 23
    • 0002775016 scopus 로고    scopus 로고
    • CNDO-electrostatic potential maps for alpha-cyclodextrin
    • (b) Sakurai, M.; Kitagawa, M.; Hoshi, H.; Inoue, Y.; Chûjô, R. CNDO-electrostatic potential maps for alpha-cyclodextrin. Chem. Lett. 1998, 17, 895-898.
    • (1998) Chem. Lett. , vol.17 , pp. 895-898
    • Sakurai, M.1    Kitagawa, M.2    Hoshi, H.3    Inoue, Y.4    Chûjô, R.5
  • 24
    • 33947094519 scopus 로고
    • Approach to the aspects of driving force of inclusion by alpha-cyclodextrin
    • (a) Tabushi, I.; Kiyosuke, Y.; Sugimoto, T.; Yamamura, K.J. Approach to the aspects of driving force of inclusion by alpha-cyclodextrin. J. Am. Chem. Soc. 1978, 100, 916-919.
    • (1978) J. Am. Chem. Soc. , vol.100 , pp. 916-919
    • Tabushi, I.1    Kiyosuke, Y.2    Sugimoto, T.3    Yamamura, K.J.4
  • 25
    • 0000389172 scopus 로고
    • Binding forces contributing to the association of cyclodextrin with alcohol in an aqueous solution
    • (b) Matsui, Y.; Mochida, K. Binding forces contributing to the association of cyclodextrin with alcohol in an aqueous solution. Bull. Chem. Soc. Jpn. 1979, 52, 2808-2814.
    • (1979) Bull. Chem. Soc. Jpn. , vol.52 , pp. 2808-2814
    • Matsui, Y.1    Mochida, K.2
  • 26
    • 0035974348 scopus 로고    scopus 로고
    • Spectrophotometric determinations of binding constants between cyclodextrins and aromatic nitrogen substrates at various pH values
    • DOI 10.1016/S0040-4020(01)00635-4, PII S0040402001006354
    • (c) D'Anna, F.; Lo Meo, P.; Riela, S.; Gruttadauria, M.; Noto, R. Spectrophotometric determinations of binding constants between cyclodextrins and aromatic nitrogen substrates at various pH values. Tetrahedron 2001, 57, 6823-6827. (Pubitemid 32701940)
    • (2001) Tetrahedron , vol.57 , Issue.31 , pp. 6823-6827
    • D'Anna, F.1    Meo, P.L.2    Riela, S.3    Gruttadauria, M.4    Noto, R.5
  • 27
    • 0038185084 scopus 로고    scopus 로고
    • The driving forces in the inclusion complexation of cyclodextrins
    • DOI 10.1023/A:1014520830813
    • (d) Liu, L.; Guo, Q.X. The driving forces in the inclusion complexation of cyclodextrins. J. Incl. Phenom. Macrocycl. Chem. 2002, 42, 1-14. (Pubitemid 38075810)
    • (2002) Journal of Inclusion Phenomena , vol.42 , Issue.1-2 , pp. 1-14
    • Liu, L.1    Guo, Q.-X.2
  • 28
    • 0037008571 scopus 로고    scopus 로고
    • The anatomy of the energetics of molecular recognition by calorimetry: Chiral discrimination of camphor by alpha-cyclodextrin
    • (e) Schmidtchen, F.P. The anatomy of the energetics of molecular recognition by calorimetry: chiral discrimination of camphor by alpha-cyclodextrin. Chem. Eur. J. 2002, 8, 3522-3529.
    • (2002) Chem. Eur. J. , vol.8 , pp. 3522-3529
    • Schmidtchen, F.P.1
  • 29
    • 0141974868 scopus 로고    scopus 로고
    • Spectrophotometric study on the thermodynamics of binding of alpha- and beta-cyclodextrin towards some p-nitrobenzene derivatives
    • (f) Lo Meo, P.; D'Anna, F.; Riela, S.; Gruttadauria, M.; Noto, R. Spectrophotometric study on the thermodynamics of binding of alpha- and beta-cyclodextrin towards some p-nitrobenzene derivatives. Org. Biomol. Chem. 2003, 1, 1584-1590.
    • (2003) Org. Biomol. Chem. , vol.1 , pp. 1584-1590
    • Lo Meo, P.1    D'Anna, F.2    Riela, S.3    Gruttadauria, M.4    Noto, R.5
  • 30
    • 4444325503 scopus 로고    scopus 로고
    • Thermodynamics of binding between α- and β-cyclodextrins and some p-nitro-aniline derivatives: Reconsidering the enthalpy-entropy compensation effect
    • DOI 10.1016/j.tet.2004.07.079, PII S0040402004012542
    • (g) Lo Meo, P.; D'Anna, F.; Gruttadauria, M.; Riela, S.; Noto, R. Thermodynamics of binding between alpha- and beta-cyclodextrins and some p-nitro-aniline derivatives: reconsidering the enthalpy-entropy compensation effect. Tetrahedron 2004, 60, 9099-9111. (Pubitemid 39201186)
    • (2004) Tetrahedron , vol.60 , Issue.41 , pp. 9099-9111
    • Meo, P.L.1    D'Anna, F.2    Gruttadauria, M.3    Riela, S.4    Noto, R.5
  • 31
    • 0030492351 scopus 로고    scopus 로고
    • Chiral discrimination by modified cyclodextrins
    • (h) Easton, C.J.; Lincoln, S.F. Chiral discrimination by modified cyclodextrins. Chem. Soc. Rev. 1996, 25, 163-170.
    • (1996) Chem. Soc. Rev. , vol.25 , pp. 163-170
    • Easton, C.J.1    Lincoln, S.F.2
  • 32
    • 0345179962 scopus 로고    scopus 로고
    • The stability of cyclodextrin complexes in solution
    • (i) Connors, K.A. The stability of cyclodextrin complexes in solution. Chem. Rev. 1997, 97, 1325-1357. (Pubitemid 127659601)
    • (1997) Chemical Reviews , vol.97 , Issue.5 , pp. 1325-1357
    • Connors, K.A.1
  • 33
    • 4243778369 scopus 로고    scopus 로고
    • Complexation thermodynamics of cyclodextrins
    • (j) Rekharsky, M.V.; Inoue Y. Complexation thermodynamics of cyclodextrins. Chem. Rev. 1998, 98, 1875-1917. (Pubitemid 128633440)
    • (1998) Chemical Reviews , vol.98 , Issue.5 , pp. 1875-1917
    • Rekharsky, M.V.1    Inoue, Y.2
  • 36
    • 1242329836 scopus 로고    scopus 로고
    • Salt effects on the apparent stability of the cucurbit[7]uril 2 methyl viologen inclusion complex
    • DOI 10.1021/jo035030+
    • Ong, W.; Kaifer, A.E. Salt effects on the apparent stability of the cucurbit[7]uril 2 methyl viologen inclusion complex. J. Org. Chem. 2004, 69, 1383-1385. (Pubitemid 38233429)
    • (2004) Journal of Organic Chemistry , vol.69 , Issue.4 , pp. 1383-1385
    • Ong, W.1    Kaifer, A.E.2
  • 37
    • 41049086346 scopus 로고    scopus 로고
    • PH-responsive supramolecular nanovalves based on cucurbit[6]uril pseudorotaxanes
    • Angelos, S.; Yang, Y.-W.; Patel, K.; Stoddart, J.F.; Zink, J.I. pH-responsive supramolecular nanovalves based on cucurbit[6]uril pseudorotaxanes. Angew. Chem. Int. Ed. 2008, 47, 2222-2226.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 2222-2226
    • Angelos, S.1    Yang, Y.-W.2    Patel, K.3    Stoddart, J.F.4    Zink, J.I.5
  • 38
    • 52349091098 scopus 로고    scopus 로고
    • Noncovalent interaction of 5,10,15,20-tetrakis(4-N-methylpyridyl) porphyrin with cucurbit[7]uril: A supramolecular architecture
    • (a) Mohanty, J.; Bhasikuttan, A.C.; Choudhuri, S.D.; Pal, H. Noncovalent interaction of 5,10,15,20-tetrakis(4-N-methylpyridyl)porphyrin with cucurbit[7]uril: a supramolecular architecture J. Phys. Chem. B 2008, 112, 10782-10785.
    • (2008) J. Phys. Chem. B , vol.112 , pp. 10782-10785
    • Mohanty, J.1    Bhasikuttan, A.C.2    Choudhuri, S.D.3    Pal, H.4
  • 39
    • 0000743715 scopus 로고
    • Structure and selectivity in host-guest complexes of cucurbituril
    • (b) Mock, W.L.; Shih, N.-Y. Structure and selectivity in host-guest complexes of cucurbituril. J. Org. Chem. 1986, 51, 4440-4446.
    • (1986) J. Org. Chem. , vol.51 , pp. 4440-4446
    • Mock, W.L.1    Shih, N.-Y.2
  • 41
    • 33645331847 scopus 로고    scopus 로고
    • Cyclodextrin rotaxanes and polyrotaxanes
    • (b) Wenz, G.; Han, B.-H.; Müller, A. Cyclodextrin rotaxanes and polyrotaxanes. Chem. Rev. 2006, 106, 782-817.
    • (2006) Chem. Rev. , vol.106 , pp. 782-817
    • Wenz, G.1    Han, B.-H.2    Müller, A.3
  • 42
    • 35348942810 scopus 로고    scopus 로고
    • Radical cation stabilization in a cucurbituril oligoaniline rotaxane
    • DOI 10.1021/ja074997i
    • (c) Eelkema, R.; Maeda, K.; Odell, B.; Anderson, H.L. Radical cation stabilization in a cucurbituril oligoaniline rotaxane. J. Am. Chem. Soc. 2007, 129, 12384-12385. (Pubitemid 47598225)
    • (2007) Journal of the American Chemical Society , vol.129 , Issue.41 , pp. 12384-12385
    • Eelkema, R.1    Maeda, K.2    Odell, B.3    Anderson, H.L.4
  • 43
    • 34250744240 scopus 로고    scopus 로고
    • Controlled release of guest molecules from mesoporous silica particles based on a pH-responsive polypseudorotaxane motif
    • DOI 10.1002/anie.200603404
    • (a) Park, C.; Oh, K.; Lee, S.C.; Kim, C. Controlled release of guest molecules from mesoporous silica particles based on a pH-responsive polypseudorotaxane motif. Angew. Chem. Int. Ed. 2007, 46, 1455-1457. (Pubitemid 46959995)
    • (2007) Angewandte Chemie - International Edition , vol.46 , Issue.9 , pp. 1455-1457
    • Park, C.1    Oh, K.2    Lee, S.C.3    Kim, C.4
  • 44
    • 48249096729 scopus 로고    scopus 로고
    • Syntheses and self-assembly behaviors of the azobenzenyl modified beta-cyclodextrins isomers
    • (b) Liu, Y.; Yang, Z.-X.; Chen, Y. Syntheses and self-assembly behaviors of the azobenzenyl modified beta-cyclodextrins isomers. J. Org. Chem. 2008, 73, 5298-5304.
    • (2008) J. Org. Chem. , vol.73 , pp. 5298-5304
    • Liu, Y.1    Yang, Z.-X.2    Chen, Y.3
  • 45
    • 0347949889 scopus 로고    scopus 로고
    • Poly(polyrotaxane): Photoreactions of 9-anthracene-capped polyrotaxane
    • (c) Okada, M.; Harada, A. Poly(polyrotaxane): photoreactions of 9-anthracene-capped polyrotaxane. Macromolecules 2003, 36, 9701-9703.
    • (2003) Macromolecules , vol.36 , pp. 9701-9703
    • Okada, M.1    Harada, A.2
  • 46
    • 0033806536 scopus 로고    scopus 로고
    • A novel experimental method for the study of complex formation between alpha-, beta- and gamma-cyclodextrin and nearly insoluble cucurbituril-[2] rotaxanes in aqueous solution
    • (a) Buschmann, H.-J.; Cleve, E.; Schollmeyer, E. A novel experimental method for the study of complex formation between alpha-, beta- and gamma-cyclodextrin and nearly insoluble cucurbituril-[2]rotaxanes in aqueous solution. Microchemical J. 2000, 64, 99-103.
    • (2000) Microchemical J. , vol.64 , pp. 99-103
    • Buschmann, H.-J.1    Cleve, E.2    Schollmeyer, E.3
  • 47
    • 33746911942 scopus 로고    scopus 로고
    • PH-responsive movement of cucurbit[7]uril in a diblock polypseudorotaxane containing dimethyl β-cyclodextrin and cucurbit[7]uril
    • DOI 10.1021/ol060697e
    • (b) Ooya, T.; Inoue, D., Choi, H.S.; Kobayashi, Y.; Loethen, S.; Thompson, D.H.; Ko, Y.H.; Kim, M.; Yui, N. pH-responsive movement of cucurbit[7]uril in a diblock polypseudorotaxane containing dimethyl beta-cyclodextrin and cucurbit[7]uril. Org. Lett. 2006, 8, 3159-3162. (Pubitemid 44187405)
    • (2006) Organic Letters , vol.8 , Issue.15 , pp. 3159-3162
    • Ooya, T.1    Inoue, D.2    Choi, H.S.3    Kobayashi, Y.4    Loethen, S.5    Thompson, D.H.6    Ko, Y.H.7    Kim, K.8    Yui, N.9
  • 48
    • 0037161453 scopus 로고    scopus 로고
    • Pseudopolyrotaxanes made to order: Cucurbituril threaded on polyviologen
    • DOI 10.1021/ma011759d
    • (c) Choi, S.W., Lee, J.W.; Ko, Y.H.; Kim, K. Pseudopolyrotaxanes made to order: cucurbituril threaded on polyviologen. Macromolecules 2002, 35, 3526-3531. (Pubitemid 34593506)
    • (2002) Macromolecules , vol.35 , Issue.9 , pp. 3526-3531
    • Choi, S.W.1    Lee, J.W.2    Ko, Y.H.3    Kim, K.4
  • 49
    • 33846046536 scopus 로고    scopus 로고
    • Reversible 2D pseudopolyrotaxanes based on cyclodextrins and cucurbit[6]uril
    • DOI 10.1021/jo0617159
    • Liu, Y.; Ke, C.-F.; Zhang, H.-Y.; Wu, W.-Y.; Shi, J. Reversible 2D pseudopolyrotaxanes based on cyclodextrins and cucurbit[6]uril. J. Org. Chem. 2007, 72, 280-283. (Pubitemid 46068231)
    • (2007) Journal of Organic Chemistry , vol.72 , Issue.1 , pp. 280-283
    • Liu, Y.1    Ke, C.-F.2    Zhang, H.-Y.3    Wu, W.-J.4    Shi, J.5
  • 50
    • 33644964660 scopus 로고    scopus 로고
    • Sequential formation of a ternary complex among dihexylammonium, cucurbit[6]uril, and cyclodextrin with positive cooperativity
    • DOI 10.1021/ol0528742
    • Rekharsky, M.V.; Yamamura, H.; Kawai, M.; Osaka, I.; Arakawa, R.; Sato, A.; Ko, Y.H.; Selvapalam, N.; Kim, K.; Inoue, Y. Sequential formation of a ternary complex among dihexylammonium, cucurbit[6]uril, and cyclodextrin with positive cooperativity. Org. Lett. 2006, 8, 815-818. (Pubitemid 43411972)
    • (2006) Organic Letters , vol.8 , Issue.5 , pp. 815-818
    • Rekharsky, M.V.1    Yamamura, H.2    Kawai, M.3    Osaka, I.4    Arakawa, R.5    Sato, A.6    Ko, Y.H.7    Selvapalam, N.8    Kim, K.9    Inoue, Y.10
  • 51
    • 70350057489 scopus 로고    scopus 로고
    • The formation of homogeneous and heterogeneous 2:1 complexes between dialkyl- and diarylammonium ions and alpha-cyclodextrin and cucurbit[6]uril in aqueous formic acid
    • Buschmann, H.-J.; Mutihac, L.; Schollmeyer, E. The formation of homogeneous and heterogeneous 2:1 complexes between dialkyl- and diarylammonium ions and alpha-cyclodextrin and cucurbit[6]uril in aqueous formic acid. Thermochim. Acta 2009, 495, 28-32.
    • (2009) Thermochim. Acta , vol.495 , pp. 28-32
    • Buschmann, H.-J.1    Mutihac, L.2    Schollmeyer, E.3
  • 53
    • 0347868932 scopus 로고    scopus 로고
    • The determination of complex stabilities between different cyclodextrins and dibenzo-18-crown-6, cucurbit[6]uril, decamethylcucurbit[5]uril, cucurbit[5]uril, p-tert-butylcalix[4]arene and p-tert-butylcalix[6]arene in aqueous solutions using a spectrophotometric method
    • PII S0928493101002065
    • Buschmann, H.-J.; Cleve, E.; Jensen, K.; Wego, A.; Schollmeyer, E. The determination of complex stabilities between different cyclodextrins and dibenzo-18-crown-6, cucurbit[6]uril, decamethylcucurbit[5]uril, cucurbit[5]uril, p-tert-butylcalix[4]arene and p-tert-butylcalix[6]arene in aqueous solutions using a spectrophotometric method. Mat. Sci. Eng. C 2001, 14, 35-39. (Pubitemid 32835993)
    • (2001) Materials Science and Engineering C , vol.14 , Issue.1-2 , pp. 35-39
    • Buschmann, H.-J.1    Cleve, E.2    Jansen, K.3    Wego, A.4    Schollmeyer, E.5
  • 54
    • 0001119930 scopus 로고    scopus 로고
    • Methods for selective modifications of cyclodextrins
    • Khan, A.R.; Forgo, P.; Stine, K.J.; D'Souza, V.T. Methods for selective modifications of cyclodextrins. Chem. Rev. 1998, 98, 1977-1996. (Pubitemid 128633443)
    • (1998) Chemical Reviews , vol.98 , Issue.5 , pp. 1977-1996
    • Khan, A.R.1    Forgo, P.2    Stine, K.J.3    D'Souza, V.T.4
  • 56
    • 0037157798 scopus 로고    scopus 로고
    • Spectrophotometric determination of binding constants between some aminocyclodextrins and nitrobenzene derivatives at various pH values
    • DOI 10.1016/S0040-4020(02)00579-3, PII S0040402002005793
    • (a) Lo Meo, P.; D'Anna, F.; Riela, S.; Gruttadauria, M.; Noto, R. Spectrophotometric determination of binding constants between some aminocyclodextrins and nitrobenzene derivatives at various pH values. Tetrahedron 2002, 58, 6039-6045. (Pubitemid 35245185)
    • (2002) Tetrahedron , vol.58 , Issue.30 , pp. 6039-6045
    • Lo Meo, P.1    D'Anna, F.2    Riela, S.3    Gruttadauria, M.4    Noto, R.5
  • 57
    • 0037183384 scopus 로고    scopus 로고
    • The binary pyrene/heptakis-(6-amino-6-deoxy)-β-cyclodextrin complex: A suitable chiral discriminator. Spectrofluorimetric study of the effect of some α-amino acids and esters on the stability of the binary complex
    • DOI 10.1016/S0957-4166(02)00418-4, PII S0957416602004184
    • (b) D'Anna, F.; Riela, S.; Lo Meo, P.; Gruttadauria, M.; Noto, R. The binary pyrene/heptakis-(6-amino-6-deoxy)-beta-cyclodextrin complex: a suitable chiral discriminator. Spectrofluorimetric study of the effect of some alpha-amino acids and esters on the stability of the binary complex. Tetrahedron: Asymm. 2002, 13, 1755-1760. (Pubitemid 35247850)
    • (2002) Tetrahedron Asymmetry , vol.13 , Issue.16 , pp. 1755-1760
    • D'Anna, F.1    Riela, S.2    Lo Meo, P.3    Gruttadauria, M.4    Noto, R.5
  • 58
    • 71049135293 scopus 로고    scopus 로고
    • Binding properties of mono-(6-deoxy-6-amino)-beta-cyclodextrin towards p-nitroaniline derivatives: A polarimetric study
    • Lo Meo, P.; D'Anna, F.; Gruttadauria, M.; Riela, S.; Noto, R. Binding properties of mono-(6-deoxy-6-amino)-beta-cyclodextrin towards p-nitroaniline derivatives: a polarimetric study. Tetrahedron. 2009, 65, 10413-10417.
    • (2009) Tetrahedron , vol.65 , pp. 10413-10417
    • Lo Meo, P.1    D'Anna, F.2    Gruttadauria, M.3    Riela, S.4    Noto, R.5
  • 59
    • 0347025932 scopus 로고    scopus 로고
    • Study of the supramolecular inclusion of β-cyclodextrin with andrographolide
    • DOI 10.1023/A:1021223407297
    • Zhao, D.; Liao, K.; Ma, X.; Yan, X. Study of the supramolecular inclusion of β-cyclodextrin with androgra-pholide. J. Incl. Phenom. Macrocycl. Chem. 2002, 43, 259-264. (Pubitemid 38075757)
    • (2002) Journal of Inclusion Phenomena , vol.43 , Issue.3-4 , pp. 259-264
    • Zhao, D.1    Liao, K.2    Ma, X.3    Yan, X.4
  • 60
    • 33750030185 scopus 로고    scopus 로고
    • Preparation and biological activity of novel cucurbit[8]uril-fullerene complex
    • DOI 10.1016/j.jphotobiol.2006.08.001, PII S1011134406001904
    • Jiang, G.; Li, G. Preparation and biological activity of novel cucurbit[8]uril-fullerene complex. J. Photochem. Photobiol. B 2006, 85, 223-227. (Pubitemid 44567379)
    • (2006) Journal of Photochemistry and Photobiology B: Biology , vol.85 , Issue.3 , pp. 223-227
    • Jiang, G.1    Li, G.2
  • 61
    • 53849113988 scopus 로고    scopus 로고
    • Copolymer-cyclodextrin inclusion complexes in water and in the solid state. A physico-chemical study
    • (a) Lazzara, G.; Milioto, S. Copolymer-cyclodextrin inclusion complexes in water and in the solid state. A physico-chemical study. J. Phys. Chem. B 2008, 112, 11887-11895.
    • (2008) J. Phys. Chem. B , vol.112 , pp. 11887-11895
    • Lazzara, G.1    Milioto, S.2
  • 62
    • 70350362304 scopus 로고    scopus 로고
    • Aggregation in aqueous media of tri-block copolymers tuned by the molecular selectivity of cyclodextrins
    • (b) De Lisi, R.; Lazzara, G. Aggregation in aqueous media of tri-block copolymers tuned by the molecular selectivity of cyclodextrins. J. Therm. Anal. Calorim. 2009, 97, 797-803.
    • (2009) J. Therm. Anal. Calorim. , vol.97 , pp. 797-803
    • De Lisi, R.1    Lazzara, G.2
  • 64
    • 41549122784 scopus 로고    scopus 로고
    • Thermal decomposition behaviors of β-cyclodextrin, its inclusion complexes of alkyl amines, and complexed β-cyclodextrin at different heating rates
    • (b) Song, L.X.; Teng, C.F.; Wang, H.M.; Zhang, Z.Q.; Liu, Q.Q. Thermal decomposition behaviors of β-cyclodextrin, its inclusion complexes of alkyl amines, and complexed β-cyclodextrin at different heating rates. J. Incl. Phenom. Macrocycl. Chem. 2008, 60, 223-233.
    • (2008) J. Incl. Phenom. Macrocycl. Chem. , vol.60 , pp. 223-233
    • Song, L.X.1    Teng, C.F.2    Wang, H.M.3    Zhang, Z.Q.4    Liu, Q.Q.5
  • 65
    • 41549083307 scopus 로고    scopus 로고
    • Synthesis and characterization of inclusion complex of the vasodilator drug minoxidil with β-cyclodextrin
    • (c) Calderini, A.; Pessini, F.B.T. Synthesis and characterization of inclusion complex of the vasodilator drug minoxidil with β-cyclodextrin. J. Incl. Phenom. Macrocycl. Chem. 2008, 60, 369-377.
    • (2008) J. Incl. Phenom. Macrocycl. Chem. , vol.60 , pp. 369-377
    • Calderini, A.1    Pessini, F.B.T.2
  • 66
    • 0002555296 scopus 로고    scopus 로고
    • Thermal behaviour of hydrated and anhydrous Cucurbituril : A DSC, T.G. and calorimetric study in temperature range from 100 to 800 K
    • PII S0040603198002524
    • (a) Germain, P.; Létoffé, J.M.; Merlin, M.P.; Buschmann, H.-J. Thermal behaviour of hydrated and anhydrous cucurbituril - A DSC, TG and calorimetric study in temperature range from 100 to 800 K. Thermochim. Acta 1998, 315, 87-92. (Pubitemid 128349536)
    • (1998) Thermochimica Acta , vol.315 , Issue.2 , pp. 87-92
    • Germain, P.1    Letoffe, J.M.2    Merlin, M.P.3    Buschmann, H.J.4
  • 67
    • 0002107773 scopus 로고    scopus 로고
    • The formation of cucurbituril complexes with amino acids and amino alcohols in aqueous formic acid studied by calorimetric titrations
    • PII S0040603198003773
    • (b) Buschmann, H.-J.; Jansen, K.; Schollmeyer, E. The formation of cucurbituril complexes with amino acids and amino alcohols in aqueous formic acid studied by calorimetric titrations. Thermochim. Acta 1998, 317, 95-98. (Pubitemid 128349578)
    • (1998) Thermochimica Acta , vol.317 , Issue.1 , pp. 95-98
    • Buschmann, H.-J.1    Jansen, K.2    Schollmeyer, E.3
  • 68
    • 55249099317 scopus 로고    scopus 로고
    • A comparative study on the binding behaviors of β-cyclodextrin and its two derivatives to four fanlike organic guests
    • Song, L.X.; Wang, H.M.; Guo, X.Q.; Bai, L. A comparative study on the binding behaviors of β-cyclodextrin and its two derivatives to four fanlike organic guests. J. Org. Chem. 2008, 73, 8305-8316.
    • (2008) J. Org. Chem. , vol.73 , pp. 8305-8316
    • Song, L.X.1    Wang, H.M.2    Guo, X.Q.3    Bai, L.4
  • 69
    • 33751113279 scopus 로고    scopus 로고
    • Polarimetry as a useful tool for the determination of binding constants between cyclodextrins and organic guest molecules
    • DOI 10.1016/j.tetlet.2006.10.078, PII S0040403906020715
    • (a) Lo Meo, P.; D'Anna, F.; Riela, S.; Gruttadauria, M.; Noto, R. Polarimetry as a useful tool for the determination of binding constants between cyclodextrins and organic guest molecules. Tetrahedron Lett. 2006, 47, 9099-9102. (Pubitemid 44768027)
    • (2006) Tetrahedron Letters , vol.47 , Issue.51 , pp. 9099-9102
    • Lo Meo, P.1    D'Anna, F.2    Riela, S.3    Gruttadauria, M.4    Noto, R.5
  • 70
    • 34547569028 scopus 로고    scopus 로고
    • Host-guest interactions involving cyclodextrins: Useful complementary insights achieved by polarimetry
    • DOI 10.1016/j.tet.2007.06.065, PII S0040402007011180
    • (b) Lo Meo, P.; D'Anna, F.; Riela, S.; Gruttadauria, M.; Noto, R. Host-guest interactions involving cyclodextrins: useful complementary insights achieved by polarimetry. Tetrahedron 2007, 63, 9163-9171. (Pubitemid 47189664)
    • (2007) Tetrahedron , vol.63 , Issue.37 , pp. 9163-9171
    • Lo Meo, P.1    D'Anna, F.2    Riela, S.3    Gruttadauria, M.4    Noto, R.5
  • 71
    • 59449093667 scopus 로고    scopus 로고
    • Binding equilibria between b-cyclodextrin and p-nitro-aniline derivatives: The first systematic study in mixed water-methanol solvent systems
    • (c) Lo Meo, P.; D'Anna, F.; Riela, S.; Gruttadauria, M.; Noto, R. Binding equilibria between b-cyclodextrin and p-nitro-aniline derivatives: the first systematic study in mixed water-methanol solvent systems. Tetrahedron 2009, 65, 2037-2042.
    • (2009) Tetrahedron , vol.65 , pp. 2037-2042
    • Lo Meo, P.1    D'Anna, F.2    Riela, S.3    Gruttadauria, M.4    Noto, R.5
  • 72
    • 0346408626 scopus 로고    scopus 로고
    • Chiral recognition of α-amino acids by charged cyclodextrins through cooperative effects of Coulomb interaction and inclusion
    • Kitae, T.; Nakayama, T.; Kano, K. Chiral recognition of alpha-amino acids by charged cyclodextrins through cooperative effects of Coulomb interaction and inclusion. J. Chem. Soc., Perkin Trans. 2 1998, 207-212. (Pubitemid 128434878)
    • (1998) Journal of the Chemical Society. Perkin Transactions 2 , Issue.2 , pp. 207-212
    • Kitae, T.1    Nakayama, T.2    Kano, K.3
  • 74
    • 0141450234 scopus 로고    scopus 로고
    • Efficient determination and evaluation of model cyclodextrin complex binding constants by electrospray mass spectrometry
    • DOI 10.1016/S1044-0305(03)00451-3
    • Dotsikas, Y.; Lonkas, Y.L. Efficient determination and evaluation of model cyclodextrin complex binding constants by electrospray mass spectrometry. J. Am. Soc. Mass Spectrom. 2003, 14, 1123-1129. (Pubitemid 37204964)
    • (2003) Journal of the American Society for Mass Spectrometry , vol.14 , Issue.10 , pp. 1123-1129
    • Dotsikas, Y.1    Loukas, Y.L.2
  • 75
    • 34548321400 scopus 로고    scopus 로고
    • Mononuclear rearrangements of heterocycles in water/β-CD: Information on the real site of reaction from structural modifications of substrates and from proton concentration dependence of the reactivity
    • DOI 10.1016/j.tet.2007.07.084, PII S0040402007013348
    • Guernelli, S.; Lo Meo, P.; Morganti, S.; Noto, R.; Spinelli, D. Mononuclear rearrangements of heterocycles in water/beta-CD: information on the real site of reaction from structural modifications of substrates and from proton concentration dependence of the reactivity. Tetrahedron 2007, 63, 10260-10268. (Pubitemid 47334831)
    • (2007) Tetrahedron , vol.63 , Issue.41 , pp. 10260-10268
    • Guernelli, S.1    Lo Meo, P.2    Morganti, S.3    Noto, R.4    Spinelli, D.5
  • 77
    • 32944473828 scopus 로고    scopus 로고
    • Characterization of host-guest complexes of cucurbit[n]uril (n = 6, 7) by electrospray ionization mass spectrometry
    • DOI 10.1002/jms.978
    • (a) Osaka, I.; Kondou, M.; Selvapalam, N.; Samal, S.; Kim, K.; Rekharsky, M.V.; Inoue, Y.; Arakawa, R. Characterization of host-guest complexes of cucurbit[-n]uril (n=6, 7) by electrospray ionization mass spectrometry. J. Mass Spectrom. 2006, 41, 202-207. (Pubitemid 43260161)
    • (2006) Journal of Mass Spectrometry , vol.41 , Issue.2 , pp. 202-207
    • Osaka, I.1    Kondou, M.2    Selvapalam, N.3    Samal, S.4    Kim, K.5    Rekharsky, M.V.6    Inoue, Y.7    Arakawa, R.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.