Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Formation of Rotaxane Dendrimers by Supramolecular Click Chemistry

  • Lee, Jae-Wook (Department of Chemistry, Dong-A University) ;
  • Han, Seung-Choul (Department of Medical Bioscience, Dong-A University) ;
  • Kim, Ji-Hyeon (Department of Chemical & Biochemical Engineering, Dongguk University) ;
  • Ko, Young-Ho (National Creative Research Initiative Center for Smart Supramolecules, Department of Chemistry, Pohang University of Science and Technology) ;
  • Kim, Ki-Moon (National Creative Research Initiative Center for Smart Supramolecules, Department of Chemistry, Pohang University of Science and Technology)
  • Published : 2007.10.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Hahn, U.; Alhabiri, M.; Trabolsi, A.; Herschbach, H.; Leize, E.; Van Dorsselaer, A.; Albrecht-Gary, A.-M.; Nierengarten, J.-F. Angew. Chem., Int. Ed. 2005, 44, 5338 https://doi.org/10.1002/anie.200501249
  2. Hoogenboom, R.; Moore, B. C.; Schubert, U. S. Chem. Commun. 2006, 4010
  3. Kim, J.; Jung, I.-S.; Kim, S.-Y.; Lee, E.; Kang, J.-K.; Sakamoto, S.; Yamaguchi, K.; Kim, K. J. Am. Chem. Soc. 2000, 122, 540
  4. Lee, J. W.; Samal, S.; Selvapalam, N.; Kim, H.-J.; Kim, K. Acc. Chem. Res. 2003, 36, 621 https://doi.org/10.1021/ar020254k
  5. Kim, H.-J.; Heo, J.; Jeon, W. S.; Lee, E.; Kim, J.; Sakamoto, S.; Yamaguchi, K.; Kim, K. Angew. Chem. Int. Ed. 2001, 40, 1526
  6. Ko, Y. H.; Kim, E.; Hwang, I.; Kim, K. Chem. Commun. 2007, 1305
  7. Jeon, Y. J.; Bharadwaj, P. K.; Choi, S. W.; Lee, J. W.; Kim, K. Angew. Chem. Int. Ed. 2002, 41, 4474 https://doi.org/10.1002/1521-3773(20021202)41:23<4474::AID-ANIE4474>3.0.CO;2-S
  8. Lee, J. W.; Kim, K.; Choi, S. W.; Ko, Y. H.; Sakamoto, S.; Yamaguchi, K.; Kim, K. Chem. Commun. 2002, 2692
  9. Kim, K.; Kim, D.; Lee, J. W.; Ko, Y. H.; Kim, K. Chem. Commun. 2004, 848
  10. Ko, Y. H.; Kim, K.; Kang, J.-K.; Chun, H.; Lee, J. W.; Sakamoto, S.; Yamaguchi, K.; Fettinger, J. C.; Kim, K. J. Am. Chem. Soc. 2004, 126, 1932 https://doi.org/10.1021/ja031567t
  11. Jeon, W. S.; Kim, H.-J.; Lee, C.; Kim, K. Chem. Commun. 2002, 1828
  12. Jeon, W. S.; Kim, E.; Ko, Y. H.; Hwang, I.; Lee, J. W.; Kim, S.-Y.; Kim, H.-J.; Kim, K. Angew. Chem. Int. Ed. 2005, 44, 87 https://doi.org/10.1002/anie.200461806
  13. Lee, J. W.; Kim, B. K.; Kim, H. J.; Han, S. C.; Shin, W. S.; Jin, S. H. Macromolecules 2006, 39, 2418 https://doi.org/10.1021/ma052526f
  14. Rostovtsev, V. V.; Green, L. G.; Fokin, V. V.; Sharpless, K. B. Angew. Chem. Int. Ed. 2002, 41, 2596 https://doi.org/10.1002/1521-3773(20020715)41:14<2596::AID-ANIE2596>3.0.CO;2-4
  15. Tornoe, C. W.; Christensen, C.; Meldal, M. J. Org. Chem. 2002, 67, 3057 https://doi.org/10.1021/jo011148j
  16. Lee, J. W.; Kim, B. K.; Jin, S. H. Bull. Korean Chem. Soc. 2005, 26, 833 https://doi.org/10.1007/s11814-009-0139-1
  17. Lee, J. W.; Kim, B. K.; Kim, J. H.; Shin, W. S.; Jin, S. H. Bull. Korean Chem. Soc. 2005, 26, 1790 https://doi.org/10.5012/bkcs.2005.26.11.1790
  18. Lee, J. W.; Kim, B. K. Synthesis 2006, 615
  19. Lee, J. W.; Kim, J. H.; Kim, B. K.; Shin, W. S.; Jin, S. H. Tetrahedron 2006, 62, 894 https://doi.org/10.1016/j.tet.2005.10.039
  20. Lee, J. W.; Kim, J. H.; Kim, B. K. Tetrahedron Lett. 2006, 47, 2683 https://doi.org/10.1016/j.tetlet.2006.02.081
  21. Lee, J. W.; Kim, B. K.; Kim, J. H.; Shin, W. S.; Jin, S. H. J. Org. Chem. 2006, 71, 4988 https://doi.org/10.1021/jo0605905
  22. Lee, J. W.; Kim, J. H.; Kim, B. K.; Kim, J. H.; Shin, W. S.; Jin, S. H. Tetrahedron 2006, 62, 894 https://doi.org/10.1016/j.tet.2005.10.039
  23. Lee, J. W.; Kim, J. H.; Kim, B. K.; Kim, J. H.; Shin, W. S.; Jin, S. H.; Kim, M. Bull. Korean Chem. Soc. 2006, 27, 1795 https://doi.org/10.5012/bkcs.2006.27.11.1795
  24. Wang, W.; Kaifer, A. E. Angew. Chem. Int. Ed. 2006, 45, 7042 https://doi.org/10.1002/anie.200602220

Cited by

  1. Pharmacological significance of triazole scaffold vol.26, pp.1, 2011, https://doi.org/10.3109/14756360903524304
  2. Supramolecular Assemblies Constructed by Cucurbituril-Catalyzed Click Reaction vol.51, pp.5-6, 2011, https://doi.org/10.1002/ijch.201100034
  3. Synthesis of dendrimers via Staudinger/aza-Wittig reaction of Fréchet-type dendritic benzyl azides and Fréchet-type dendritic benzaldehydes vol.20, pp.10, 2012, https://doi.org/10.1007/s13233-012-0149-4
  4. Synthesis of Dendrimer Containing Dialkylated-fluorene Unit as a Core Chromophore via Click Chemistry vol.33, pp.1, 2012, https://doi.org/10.5012/bkcs.2012.33.1.137
  5. Organometallic rotaxane dendrimers with fourth-generation mechanically interlocked branches vol.112, pp.18, 2015, https://doi.org/10.1073/pnas.1500489112
  6. Our Expedition in Linear Neutral Platinum-Acetylide Complexes: The Preparation of Micro/nanostructure Materials, Complicated Topologies, and Dye-Sensitized Solar Cells vol.16, pp.3, 2016, https://doi.org/10.1002/tcr.201500271
  7. Observation of Supramolecular Chirality in a Hierarchically Self-Assembled Mixed-Stack Charge-Transfer Complex vol.23, pp.40, 2017, https://doi.org/10.1002/chem.201701123
  8. Dual stimuli-responsive rotaxane-branched dendrimers with reversible dimension modulation vol.9, pp.1, 2018, https://doi.org/10.1038/s41467-018-05670-y
  9. A Review on Thornless Roses vol.6, pp.19, 2003, https://doi.org/10.3923/pjbs.2003.1712.1719
  10. ChemInform Abstract: Formation of Rotaxane Dendrimers by Supramolecular Click Chemistry. vol.39, pp.6, 2008, https://doi.org/10.1002/chin.200806048
  11. Synthetic Molecular Machine Based on Reversible End-to-Interior and End-to-End Loop Formation Triggered by Electrochemical Stimuli vol.3, pp.8-9, 2008, https://doi.org/10.1002/asia.200800054
  12. Redox-driven switching in pseudorotaxanes vol.33, pp.2, 2009, https://doi.org/10.1039/b819466a
  13. Complexation of Aliphatic Ammonium Ions with a Water-Soluble Cucurbit[6]uril Derivative in Pure Water: Isothermal Calorimetric, NMR, and X-ray Crystallographic Study vol.15, pp.25, 2009, https://doi.org/10.1002/chem.200900305
  14. Self-assembly and thermodynamic synthesis of rotaxane dendrimers and related structures vol.1, pp.7, 2010, https://doi.org/10.1039/b9py00380k
  15. Unconventional U-shaped conformation of a bolaamphiphile embedded in a synthetic host vol.46, pp.23, 2010, https://doi.org/10.1039/c0cc00752h
  16. Binding Modes of a trans-Vinylbipyridinium Surfactant Bearing a Hexadecyl Chain to Cucurbit[n]uril (n = 6-8) in Aqueous Solution vol.29, pp.10, 2007, https://doi.org/10.5012/bkcs.2008.29.10.2043
  17. One-Pot Synthesis of 1,2,3-Triazoles from Michael Reaction vol.29, pp.4, 2008, https://doi.org/10.5012/bkcs.2008.29.4.723
  18. Efficient One-pot Synthesis of Dendritic Benzyl Azides from Their Alcohols vol.29, pp.5, 2008, https://doi.org/10.5012/bkcs.2008.29.5.1055
  19. Staudinger /Aza-Wittig Click Chemistry for Synthesis of Dendrimers Using Frechet Type Dendritic Benzyl Azides vol.30, pp.5, 2007, https://doi.org/10.5012/bkcs.2009.30.5.1001
  20. Synthesis of Poly(benzyl ether) Dendrimers Containing Core Diversitiesby Click Chemistry vol.30, pp.1, 2007, https://doi.org/10.5012/bkcs.2009.30.1.157
  21. Synthesis of Dendrimers by Homocoupling of Alkyne-focal Frechet Type Dendrons vol.30, pp.9, 2007, https://doi.org/10.5012/bkcs.2009.30.9.1925
  22. Molecular recognition of organic ammonium ions in solution using synthetic receptors vol.6, pp.None, 2007, https://doi.org/10.3762/bjoc.6.32
  23. Azide/Alkyne Resins for Quick Preparation of 1,4-Disubstituted 1,2,3-Triazoles vol.31, pp.7, 2007, https://doi.org/10.5012/bkcs.2010.31.7.1843
  24. Synthesis of Dendrimers from Alkyne-focal Dendrons by Oxidative Homo-coupling of Terminal Acetylene vol.32, pp.11, 2011, https://doi.org/10.5012/bkcs.2011.32.11.3899
  25. Convergent Synthesis and Characterization of Dumbbell Type Dendritic Materials by Click Chemistry vol.32, pp.11, 2011, https://doi.org/10.5012/bkcs.2011.32.11.3933
  26. Synthesis of Dendrimers via Sonogashira Coupling Reaction of Alkyne-focal Fréchet Type Dendrons vol.32, pp.9, 2007, https://doi.org/10.5012/bkcs.2011.32.9.3211
  27. Facile Synthesis of Aldehyde-focal Fréchet Type Dendrons and Dendrimers via Staudinger/Aza-Wittig Reactions vol.32, pp.10, 2007, https://doi.org/10.5012/bkcs.2011.32.10.3624
  28. Synthesis of [3]-Rotaxane Dendrimers by Host-mediated Click Chemistry vol.32, pp.10, 2007, https://doi.org/10.5012/bkcs.2011.32.10.3809
  29. Charge Transfer Based Colorimetric Detection of Silver Ion vol.35, pp.5, 2014, https://doi.org/10.5012/bkcs.2014.35.5.1541
  30. Comprehensive Synthesis of Monohydroxy–Cucurbit[n]urils (n = 5, 6, 7, 8): High Purity and High Conversions vol.137, pp.32, 2007, https://doi.org/10.1021/jacs.5b04553
  31. Hierarchical Self‐Assembly of Pyrene‐Linked Cyclodextrin and Adamantane‐Linked Naphthalene Diimide System: A Case of Inclusion‐Binding‐Assisted Charge‐Transfe vol.4, pp.2, 2019, https://doi.org/10.1002/slct.201803166
  32. Fulleren‐gefüllte Flüssigkristall‐Sterne: Ein supramolekularer Klick‐Mechanismus zur Bildung von maßgeschneiderten Donor‐Akzeptor‐Strukturen vol.131, pp.11, 2007, https://doi.org/10.1002/ange.201812465
  33. Fullerene‐Filled Liquid‐Crystal Stars: A Supramolecular Click Mechanism for the Generation of Tailored Donor–Acceptor Assemblies vol.58, pp.11, 2019, https://doi.org/10.1002/anie.201812465
  34. Supramolecular click procedures in liquid crystals vol.46, pp.13, 2019, https://doi.org/10.1080/02678292.2019.1618936
  35. Rotaxane-Branched Dendrimers with Enhanced Photosensitization vol.142, pp.39, 2007, https://doi.org/10.1021/jacs.0c07292
  36. Development and advancement of rotaxane dendrimers as switchable macromolecular machines vol.4, pp.10, 2007, https://doi.org/10.1039/d0qm00368a
  37. Oligomeric Cucurbituril Complexes: from Peculiar Assemblies to Emerging Applications vol.132, pp.48, 2007, https://doi.org/10.1002/ange.202004622
  38. Oligomeric Cucurbituril Complexes: from Peculiar Assemblies to Emerging Applications vol.59, pp.48, 2007, https://doi.org/10.1002/anie.202004622