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Volumn 3, Issue 3, 2011, Pages 244-248

An AAAA-DDDD quadruple hydrogen-bond array

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EID: 79951981223     PISSN: 17554330     EISSN: 17554349     Source Type: Journal    
DOI: 10.1038/nchem.987     Document Type: Article
Times cited : (136)

References (33)
  • 1
    • 73249128374 scopus 로고    scopus 로고
    • Supramolecular polymerization
    • de Greef, T. F. A. et al. Supramolecular polymerization. Chem. Rev. 109, 5697-5754 (2009).
    • (2009) Chem. Rev. , vol.109 , pp. 5697-5754
    • De Greef, T.F.A.1
  • 3
    • 43449122456 scopus 로고    scopus 로고
    • Supramolecular polymers
    • de Greef, T. F. A. & Meijer, E. W. Supramolecular polymers. Nature 453, 171-173 (2008).
    • (2008) Nature , vol.453 , pp. 171-173
    • De Greef, T.F.A.1    Meijer, E.W.2
  • 4
    • 33947397298 scopus 로고    scopus 로고
    • Non-covalent polymer assembly using arrays of hydrogen-bonds
    • Wilson, A. J. Non-covalent polymer assembly using arrays of hydrogen-bonds. Soft Matter 3, 409-425 (2007).
    • (2007) Soft Matter , vol.3 , pp. 409-425
    • Wilson, A.J.1
  • 5
    • 0002453698 scopus 로고    scopus 로고
    • Heteroaromatic modules for self-assembly using multiple hydrogen bonds
    • Zimmerman, S. C. & Corbin, P. S. Heteroaromatic modules for self-assembly using multiple hydrogen bonds. Struct. Bonding (Berlin) 96, 63-94 (2000).
    • (2000) Struct. Bonding (Berlin) , vol.96 , pp. 63-94
    • Zimmerman, S.C.1    Corbin, P.S.2
  • 6
    • 0025283298 scopus 로고
    • Importance of secondary interactions in triply hydrogen bonded complexes: Guanine-cytosine vs uracil-2,6-diaminopyridine
    • Jorgensen, W. L. & Pranata, J. Importance of secondary interactions in triply hydrogen bonded complexes: guanine-cytosine vs uracil-2,6- diaminopyridine. J. Am. Chem. Soc. 112, 2008-2010 (1990).
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 2008-2010
    • Jorgensen, W.L.1    Pranata, J.2
  • 7
    • 0037167061 scopus 로고    scopus 로고
    • The elusive atomic rationale for DNA base pair stability
    • Popelier, P. L. A. & Joubert, L. The elusive atomic rationale for DNA base pair stability. J. Am. Chem. Soc. 124, 8725-8729 (2002).
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 8725-8729
    • Popelier, P.L.A.1    Joubert, L.2
  • 8
    • 33846609268 scopus 로고    scopus 로고
    • Does the A•T or G•C base-pair possess enhanced stability? Quantifying the effects of CH...O interactions and secondary interactions on base-pair stability using phenomenological analysis and ab initio calculations
    • Quinn, J. R., Zimmerman, S. C., Del Bene, J. E. & Shavitt, I. Does the A•T or G•C base-pair possess enhanced stability? Quantifying the effects of CH...O interactions and secondary interactions on base-pair stability using phenomenological analysis and ab initio calculations. J. Am. Chem. Soc. 129, 934-941 (2007).
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 934-941
    • Quinn, J.R.1    Zimmerman, S.C.2    Del Bene, J.E.3    Shavitt, I.4
  • 9
    • 0000047118 scopus 로고
    • The effect of substituents on the hydrogen bonding of adenine and uracil derivatives
    • Kyogoku, Y., Lord, R. C. & Rich, A. The effect of substituents on the hydrogen bonding of adenine and uracil derivatives. Proc. Natl Acad. Sci. USA 57, 250-257 (1967).
    • (1967) Proc. Natl Acad. Sci. USA , vol.57 , pp. 250-257
    • Kyogoku, Y.1    Lord, R.C.2    Rich, A.3
  • 10
    • 0014682999 scopus 로고
    • An infrared study of the hydrogen-bonding specificity of hypoxanthine and other nucleic acid derivatives
    • Kyogoku, Y., Lord, R. C. & Rich, A. An infrared study of the hydrogen-bonding specificity of hypoxanthine and other nucleic acid derivatives. Biochim. Biophys. Acta 179, 10-17 (1969).
    • (1969) Biochim. Biophys. Acta , vol.179 , pp. 10-17
    • Kyogoku, Y.1    Lord, R.C.2    Rich, A.3
  • 11
    • 34548328446 scopus 로고
    • New triply hydrogen bonded complexes with highly variable stabilities
    • Murray, T. J. & Zimmerman, S. C. New triply hydrogen bonded complexes with highly variable stabilities. J. Am. Chem. Soc. 114, 4010-4011 (1992).
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 4010-4011
    • Murray, T.J.1    Zimmerman, S.C.2
  • 12
    • 0029034156 scopus 로고
    • Establishing a cationic AAA-DDD hydrogen bonding complex
    • Bell, D. A. & Anslyn, E. V. Establishing a cationic AAA-DDD hydrogen bonding complex. Tetrahedron 51, 7161-7172 (1995).
    • (1995) Tetrahedron , vol.51 , pp. 7161-7172
    • Bell, D.A.1    Anslyn, E.V.2
  • 13
    • 33846446063 scopus 로고    scopus 로고
    • Extremely strong and readily accessible AAA-DDD triple hydrogen bond complexes
    • Djurdjevic, S. et al. Extremely strong and readily accessible AAA-DDD triple hydrogen bond complexes. J. Am. Chem. Soc. 129, 476-477 (2007).
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 476-477
    • Djurdjevic, S.1
  • 14
    • 70349629965 scopus 로고    scopus 로고
    • AAA-DDD-triple hydrogen bond complexes
    • Blight, B. A. et al. AAA-DDD-triple hydrogen bond complexes. J. Am. Chem. Soc. 131, 14116-14122 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 14116-14122
    • Blight, B.A.1
  • 15
    • 78649328301 scopus 로고    scopus 로고
    • A general scheme based on empirical increments for the prediction of hydrogen-bond associations of nucleobases and of synthetic host-guest complexes
    • Sartorius, J. & Schneider, H.-J. A general scheme based on empirical increments for the prediction of hydrogen-bond associations of nucleobases and of synthetic host-guest complexes. Chem. Eur. J. 2, 1446-1452 (1996).
    • (1996) Chem. Eur. J. , vol.2 , pp. 1446-1452
    • Sartorius, J.1    Schneider, H.-J.2
  • 17
    • 1842332153 scopus 로고    scopus 로고
    • Reversible polymers formed from self-complementary monomers using quadruple hydrogen bonding
    • Sijbesma, R. P. et al. Reversible polymers formed from self-complementary monomers using quadruple hydrogen bonding. Science 278, 1601-1604 (1997).
    • (1997) Science , vol.278 , pp. 1601-1604
    • Sijbesma, R.P.1
  • 18
    • 12444300157 scopus 로고    scopus 로고
    • Complementary quadruple hydrogen bonding in supramolecular copolymers
    • Ligthart, G. B. W. L., Ohkawa, H., Sijbesma, R. P. & Meijer, E. W. Complementary quadruple hydrogen bonding in supramolecular copolymers. J. Am. Chem. Soc. 127, 810-811 (2005).
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 810-811
    • Ligthart, G.B.W.L.1    Ohkawa, H.2    Sijbesma, R.P.3    Meijer, E.W.4
  • 19
    • 33646743972 scopus 로고    scopus 로고
    • Quadruply hydrogen bonded cytosine modules for supramolecular applications
    • Lafitte, V. G. H. et al. Quadruply hydrogen bonded cytosine modules for supramolecular applications. J. Am. Chem. Soc. 128, 6544-6545 (2006).
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 6544-6545
    • Lafitte, V.G.H.1
  • 21
    • 78049277919 scopus 로고    scopus 로고
    • Cytosine modules in quadruple hydrogen bonded arrays
    • Greco, E. et al. Cytosine modules in quadruple hydrogen bonded arrays. New J. Chem. 34, 2634-2642 (1998).
    • (1998) New J. Chem. , vol.34 , pp. 2634-2642
    • Greco, E.1
  • 22
    • 0032561004 scopus 로고    scopus 로고
    • Self-association without regard to prototropy. A heterocycle that forms extremely stable quadruply hydrogen-bonded dimers
    • Corbin, P. S. & Zimmerman, S. C. Self-association without regard to prototropy. A heterocycle that forms extremely stable quadruply hydrogen-bonded dimers. J. Am. Chem. Soc. 120, 9710-9711 (1998).
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 9710-9711
    • Corbin, P.S.1    Zimmerman, S.C.2
  • 23
    • 18644380046 scopus 로고    scopus 로고
    • A highly stable quadruply hydrogen-bonded heterocomplex useful for supramolecular polymer blends
    • Park, T., Zimmerman, S. C. & Nakashima, S. A highly stable quadruply hydrogen-bonded heterocomplex useful for supramolecular polymer blends. J. Am. Chem. Soc. 127, 6520-6521 (2005).
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 6520-6521
    • Park, T.1    Zimmerman, S.C.2    Nakashima, S.3
  • 24
    • 59649105964 scopus 로고    scopus 로고
    • Hydrogen-bonded DeUG.DAN heterocomplex: Structure and stability and a scalable synthesis of DeUG with reactive functionality
    • Kuykendall, D. W., Anderson, C. A. & Zimmerman, S. C. Hydrogen-bonded DeUG.DAN heterocomplex: structure and stability and a scalable synthesis of DeUG with reactive functionality. Org. Lett. 11, 61-64 (2009).
    • (2009) Org. Lett. , vol.11 , pp. 61-64
    • Kuykendall, D.W.1    Anderson, C.A.2    Zimmerman, S.C.3
  • 25
    • 0036900513 scopus 로고    scopus 로고
    • A new quadruply bound heterodimer DDAD.AADA and investigations into the association process
    • Brammer, S., Lüning, U. & Kühl, C. A new quadruply bound heterodimer DDAD.AADA and investigations into the association process. Eur. J. Org. Chem. 4054-4062 (2002).
    • (2002) Eur. J. Org. Chem. , pp. 4054-4062
    • Brammer, S.1    Lüning, U.2    Kühl, C.3
  • 26
    • 70749121025 scopus 로고    scopus 로고
    • The AAAA•DDDD hydrogen bond dimer. Synthesis of a soluble sulfurane as AAAA domain and generation of a DDDD counterpart
    • Taubitz, J. & Lüning, U. The AAAA•DDDD hydrogen bond dimer. Synthesis of a soluble sulfurane as AAAA domain and generation of a DDDD counterpart. Aust. J. Chem. 62, 1550-1555 (2009).
    • (2009) Aust. J. Chem. , vol.62 , pp. 1550-1555
    • Taubitz, J.1    Lüning, U.2
  • 27
    • 77951190510 scopus 로고    scopus 로고
    • A new quadruple hydrogen-bonding module based on five-membered heterocyclic urea structure
    • Hisamatsu, Y., Shirai, N., Ikeda, S.-i. & Odashima, K. A new quadruple hydrogen-bonding module based on five-membered heterocyclic urea structure. Org. Lett. 12, 1776-1779 (2010).
    • (2010) Org. Lett. , vol.12 , pp. 1776-1779
    • Hisamatsu, Y.1    Shirai, N.2    Ikeda, S.-I.3    Odashima, K.4
  • 28
    • 37749050931 scopus 로고    scopus 로고
    • Conformer independent heterodimerisation of linear arrays using three hydrogen bonds
    • McGhee, A. M., Kilner, C. & Wilson, A. J. Conformer independent heterodimerisation of linear arrays using three hydrogen bonds. Chem. Commun. 344-346 (2008).
    • (2008) Chem. Commun. , pp. 344-346
    • McGhee, A.M.1    Kilner, C.2    Wilson, A.J.3
  • 30
    • 7244258931 scopus 로고    scopus 로고
    • Quantifying intermolecular interactions: Guidelines for the molecular recognition toolbox
    • Hunter, C. A. Quantifying intermolecular interactions: guidelines for the molecular recognition toolbox. Angew. Chem. Int. Ed. 43, 5310-5324 (2004).
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 5310-5324
    • Hunter, C.A.1
  • 31
    • 17044362699 scopus 로고    scopus 로고
    • Ureidopyrimidones incorporating a functionalizable p-aminophenyl electron-donating group at C-6
    • Lafitte, V. G. H., Aliev, A. E., Hailes, H. C., Bala, K. & Golding, P. Ureidopyrimidones incorporating a functionalizable p-aminophenyl electron-donating group at C-6. J. Org. Chem. 70, 2701-2707 (2005).
    • (2005) J. Org. Chem. , vol.70 , pp. 2701-2707
    • Lafitte, V.G.H.1    Aliev, A.E.2    Hailes, H.C.3    Bala, K.4    Golding, P.5
  • 32
    • 0000639741 scopus 로고
    • A remarkable effect of solvent size on the stability of a molecular complex
    • Chapman, K. T. & Still, W. C. A remarkable effect of solvent size on the stability of a molecular complex. J. Am. Chem. Soc. 111, 3075-3077 (1989).
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 3075-3077
    • Chapman, K.T.1    Still, W.C.2
  • 33
    • 0031832791 scopus 로고    scopus 로고
    • The 55% solution: A formula for molecular recognition in the liquid state
    • Mecozzi, S. & Rebek, J. Jr. The 55% solution: a formula for molecular recognition in the liquid state. Chem. Eur. J. 4, 1016-1022 (1998).
    • (1998) Chem. Eur. J. , vol.4 , pp. 1016-1022
    • Mecozzi, S.1    Rebek Jr., J.2


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