메뉴 건너뛰기




Volumn 15, Issue 12, 2011, Pages 2072-2081

Weak interactions: A versatile role in aromatic compounds

Author keywords

Aromatic interaction; Conformation; Intra intermolecular interaction; Self assembly

Indexed keywords

AROMATIC COMPOUNDS; AROMATIZATION; CONFORMATIONS; DRUG INTERACTIONS;

EID: 79960029908     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527211795703667     Document Type: Review
Times cited : (9)

References (99)
  • 2
    • 0030043489 scopus 로고    scopus 로고
    • Cation-π interactions in chemistry and biology: A new view of benzene, Phe, Tyr, and Trp
    • Dougherty, D. A. Cation-π Interactions in Chemistry and Biology: A New View of Benzene, Phe, Tyr, and Trp. Science, 1996, 271, 163-168.
    • (1996) Science , vol.271 , pp. 163-168
    • Dougherty, D.A.1
  • 3
    • 0022419375 scopus 로고
    • Aromatic- aromatic interaction: A mechanism of protein structure stabilization
    • Burley, S. K.; Petsko, G. A. Aromatic- Aromatic interaction: A mechanism of protein structure stabilization. Science, 1985, 229, 23-28.
    • (1985) Science , vol.229 , pp. 23-28
    • Burley, S.K.1    Petsko, G.A.2
  • 4
    • 0035954763 scopus 로고    scopus 로고
    • Chemistry beyond the molecule
    • Desiraju, G. R. Chemistry beyond the molecule. Nature, 2001, 412, 397-400.
    • (2001) Nature , vol.412 , pp. 397-400
    • Desiraju, G.R.1
  • 5
    • 38049030189 scopus 로고    scopus 로고
    • Emerging trends in molecular recognition: Utility of weak aromatic interactions
    • Tewari, A. K.; Dubey, R. Emerging Trends in Molecular Recognition: Utility of Weak Aromatic Interactions. Bio. Med. Chem., 2008, 16, 126-143.
    • (2008) Bio. Med. Chem. , vol.16 , pp. 126-143
    • Tewari, A.K.1    Dubey, R.2
  • 6
    • 0011164114 scopus 로고    scopus 로고
    • Noncovalent interactions: A challenge for experiment and theory
    • Muller, K. D.; Hobza, P. Noncovalent Interactions: A Challenge for Experiment and Theory. Chem. Rev., 2000, 100, 143-167.
    • (2000) Chem. Rev. , vol.100 , pp. 143-167
    • Muller, K.D.1    Hobza, P.2
  • 7
    • 33644850165 scopus 로고    scopus 로고
    • Synthesis and solid state structure for a series of poly(1-pyrrolylmethyl)- benzene derivatives. Control of the interplaying p-p and C-H.π interactions
    • Planas, J. G.; Masalles, C.; Sillanpa, R.; Kivekäs, R.; Teixidora F.; Viñas, C. Synthesis and solid state structure for a series of poly(1-pyrrolylmethyl)- benzene derivatives. Control of the interplaying p-p and C-H.π interactions. Cryst. Eng. Com., 2006, 8, 75-83.
    • (2006) Cryst. Eng. Com. , vol.8 , pp. 75-83
    • Planas, J.G.1    Masalles, C.2    Sillanpa, R.3    Kivekäs, R.4    Teixidora, F.5    Viñas, C.6
  • 8
    • 24144461167 scopus 로고    scopus 로고
    • Off-center oxygen-arene interactions in solution: A quantitative study
    • Gung, B. W.; Xue, X.; Reich, H. J. Off-Center Oxygen-Arene Interactions in Solution: A Quantitative Study. J. Org. Chem. 2005, 70, 7232-7237.
    • (2005) J. Org. Chem. , vol.70 , pp. 7232-7237
    • Gung, B.W.1    Xue, X.2    Reich, H.J.3
  • 9
    • 0033578896 scopus 로고    scopus 로고
    • Influence of perfluoroarene-arene interactions on the phase behavior of liquid crystalline and polymeric materials
    • Weck, M.; Dunn, A. R.; Matsumoto, K.; Coates, G. W.; Lobkovsky, E. B.; Grubbs, R. H. Influence of Perfluoroarene-Arene Interactions on the Phase Behavior of Liquid Crystalline and Polymeric Materials. Angew. Chem. Int. Ed., 1999, 38, 2741-2745.
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 2741-2745
    • Weck, M.1    Dunn, A.R.2    Matsumoto, K.3    Coates, G.W.4    Lobkovsky, E.B.5    Grubbs, R.H.6
  • 10
    • 0037176301 scopus 로고    scopus 로고
    • Aromatic oligomers that form hetero duplexes in aqueous solution
    • Gabriel, G. J.; Iverson, B. L. Aromatic Oligomers that Form Hetero Duplexes in Aqueous Solution. J. Am. Chem. Soc., 2002, 124, 15174-15175.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 15174-15175
    • Gabriel, G.J.1    Iverson, B.L.2
  • 12
    • 0032546782 scopus 로고    scopus 로고
    • π - Stacking interactions. Alive and well in proteins
    • McGaughey, G. B.; Gagne, M.; Rappe, A. K. π - Stacking Interactions. ALIVE AND WELL IN PROTEINS. J. Bio. Chem., 1998, 273, 15458-15463.
    • (1998) J. Bio. Chem. , vol.273 , pp. 15458-15463
    • McGaughey, G.B.1    Gagne, M.2    Rappe, A.K.3
  • 13
    • 33749368925 scopus 로고    scopus 로고
    • Ultrafast carbon-carbon single- bond rotational isomerization in room-temperature solution
    • Zheng, J.; Kwak, K.; Xie, J.; Fayer, M. D. Ultrafast Carbon-Carbon Single- Bond Rotational Isomerization in Room-Temperature Solution. Science, 2006, 313, 1951-1955.
    • (2006) Science , vol.313 , pp. 1951-1955
    • Zheng, J.1    Kwak, K.2    Xie, J.3    Fayer, M.D.4
  • 17
    • 0347171982 scopus 로고    scopus 로고
    • Theoretical investigations of conformational aspects of polymorphism. Part 1: Oacetamidobenzamide
    • Buttar, D.; Charlton, M. H.; Docherty, R.; Starbuck, J. Theoretical investigations of conformational aspects of polymorphism. Part 1: oacetamidobenzamide. J. Chem. Soc., Perkin Trans. 2, 1998,763-772.
    • (1998) J. Chem. Soc., Perkin Trans. , vol.2 , pp. 763-772
    • Buttar, D.1    Charlton, M.H.2    Docherty, R.3    Starbuck, J.4
  • 20
    • 0037016451 scopus 로고    scopus 로고
    • The hydrogen bond in the solid state
    • Steiner, T. The Hydrogen bond in the Solid State. Angew. Chem. Int. Ed. 2002, 41, 48-76.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 48-76
    • Steiner, T.1
  • 22
    • 0003653494 scopus 로고    scopus 로고
    • The weak hydrogen bond in structural chemistry and biology
    • Oxford: Oxford University Press/International Union of Crystallography
    • Desiraju, G. R.; Steiner, T. The weak hydrogen bond in structural chemistry and biology. IUCr Monographs on Crystallography. Oxford: Oxford University Press/International Union of Crystallography, 1999, 9, xiv+507.
    • (1999) IUCr Monographs on Crystallography , vol.9
    • Desiraju, G.R.1    Steiner, T.2
  • 23
    • 31144447353 scopus 로고    scopus 로고
    • Hydrogen bonding in crystal structures of N,N'-Bis(3-pyridyl)urea. Why is the N-H·O tape synthon absent in diaryl ureas with electron-withdrawing groups?
    • Reddy, L. S.; Basavoju, S.; Vangala, V. R.; Nangia, A. Hydrogen Bonding in Crystal Structures of N,N'-Bis(3-pyridyl)urea. Why Is the N-H·O Tape Synthon Absent in Diaryl Ureas with Electron-Withdrawing Groups?. Cryst. Growth Des., 2006, 6, 161-173.
    • (2006) Cryst. Growth Des. , vol.6 , pp. 161-173
    • Reddy, L.S.1    Basavoju, S.2    Vangala, V.R.3    Nangia, A.4
  • 25
    • 0038615843 scopus 로고    scopus 로고
    • Dual topoisomerase I/II Inhibitors in cancer therapy
    • Denny, W. A.; Baguley, B. C. Dual Topoisomerase I/II Inhibitors in Cancer Therapy. Curr. Top. Med. Chem., 2003, 3, 339-353.
    • (2003) Curr. Top. Med. Chem. , vol.3 , pp. 339-353
    • Denny, W.A.1    Baguley, B.C.2
  • 26
    • 0042265520 scopus 로고    scopus 로고
    • Crystal structure of human cytochrome P450 2C9 with bound warfarin
    • Williams, P. A.; Cosme, J.; Ward, A.; Angove, H. C.; Vinkovic, D. M.; Jhoti, H. Crystal structure of human cytochrome P450 2C9 with bound warfarin. Nature, 2003,424, 464-468.
    • (2003) Nature , vol.424 , pp. 464-468
    • Williams, P.A.1    Cosme, J.2    Ward, A.3    Angove, H.C.4    Vinkovic, D.M.5    Jhoti, H.6
  • 27
    • 0033103478 scopus 로고    scopus 로고
    • Structure of acetylcholinesterase complexed with E2020 (Aricept): Implications for the design of new anti- Alzheimer drugs
    • Kryger, G.; Silman, I.; Sussman, J. L. Structure of acetylcholinesterase complexed with E2020 (Aricept): implications for the design of new anti- Alzheimer drugs. Structure (London), 1999, 7, 297-307.
    • (1999) Structure (London) , vol.7 , pp. 297-307
    • Kryger, G.1    Silman, I.2    Sussman, J.L.3
  • 28
    • 17744399329 scopus 로고    scopus 로고
    • The strength of parallel-displaced arene-arene interactions in chloroform
    • Gung, B. W.; Xue, X.; Reich, H. J. The Strength of Parallel-Displaced Arene-Arene Interactions in Chloroform. J. Org. Chem., 2005, 70, 3641-3644.
    • (2005) J. Org. Chem. , vol.70 , pp. 3641-3644
    • Gung, B.W.1    Xue, X.2    Reich, H.J.3
  • 29
    • 1342306671 scopus 로고    scopus 로고
    • Model systems for flavoenzyme activity: Interplay of hydrogen bonding and aromatic stacking in cofactor redox modulation
    • Gray, M.; Goodman, A. J.; Carroll, J. B.; Bardon, K.; Markey, M.; Cooke, G.; Rotello, V. M. Model Systems for Flavoenzyme Activity: Interplay of Hydrogen Bonding and Aromatic Stacking in Cofactor Redox Modulation. Org. Lett., 2004, 6, 385-388.
    • (2004) Org. Lett. , vol.6 , pp. 385-388
    • Gray, M.1    Goodman, A.J.2    Carroll, J.B.3    Bardon, K.4    Markey, M.5    Cooke, G.6    Rotello, V.M.7
  • 31
    • 0033544354 scopus 로고    scopus 로고
    • Cation π interactions in proteins: Can simple models provide an accurate description?
    • Minoux, H.; Chipot, C. Cation π interactions in proteins: can simple models provide an accurate description?. J. Am. Chem. Soc. 1999, 121, 10366-10372.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 10366-10372
    • Minoux, H.1    Chipot, C.2
  • 33
    • 0000382986 scopus 로고    scopus 로고
    • Crystal engineering: Solid state supramolecular synthesis
    • Desiraju, G. R. Crystal engineering: Solid state supramolecular synthesis. Curr. Opi. Solid St. M. Sci, 1997, 2, 451-454.
    • (1997) Curr. Opi. Solid St. M. Sci. , vol.2 , pp. 451-454
    • Desiraju, G.R.1
  • 34
    • 0014422472 scopus 로고
    • Synthetic spectroscopy models related to coenzymes and base pairs.II. Evidence for intramolecular basebase interactions in dinucleotide analogues
    • Browne, D. T.; Eisinger, J.; Leonard, N. J. Synthetic spectroscopy models related to coenzymes and base pairs.II. Evidence for intramolecular basebase interactions in dinucleotide analogues. J. Am. Che. Soc., 1968, 90, 7302-7323.
    • (1968) J. Am. Che. Soc. , vol.90 , pp. 7302-7323
    • Browne, D.T.1    Eisinger, J.2    Leonard, N.J.3
  • 35
    • 0015922272 scopus 로고
    • Synthetic spectroscopic models related to coenzymes and base pairs. XII. Controlled interaction between nucleic acid bases. Intramolecular stacking interactions between two adenine rings
    • Leonard, N. J.; Ito, K. Synthetic spectroscopic models related to coenzymes and base pairs. XII. Controlled interaction between nucleic acid bases. Intramolecular stacking interactions between two adenine rings. J. Am. Chem. Soc., 1973, 95, 4010-4016.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 4010-4016
    • Leonard, N.J.1    Ito, K.2
  • 36
    • 0000687913 scopus 로고
    • Searching for minimum increments of hydrophobic collapse: Flexible Dinaphthyl carboxylates
    • Newcomb, L. F.; Haque, T. S.; Gellman, S. H. Searching for minimum increments of hydrophobic collapse: flexible Dinaphthyl carboxylates. J. Am. Chem. Soc., 1995, 117, 6509-6519.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 6509-6519
    • Newcomb, L.F.1    Haque, T.S.2    Gellman, S.H.3
  • 37
    • 0001543861 scopus 로고
    • Aromatic stacking interactions in aqueous solution: Evidence that neither classical hydrophobic effects nor dispersion forces are important
    • Newcomb, L. F.; Gellman, S. H. Aromatic Stacking Interactions in Aqueous Solution: Evidence That neither Classical Hydrophobic Effects nor Dispersion Forces Are Important. J. Am. Chem. Soc., 1994, 116, 4993-4994.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 4993-4994
    • Newcomb, L.F.1    Gellman, S.H.2
  • 38
    • 0033518870 scopus 로고    scopus 로고
    • Computational and experimental studies of (2,2)-Bis(indol-1-yl-methyl)acetate suggest the importance of the hydrophobic effect in aromatic stacking interactions
    • Pang, Y. P.; Miller, J. L.; Kollman, P. A. Computational and Experimental Studies of (2,2)-Bis(indol-1-yl-methyl)acetate Suggest the Importance of the Hydrophobic Effect in Aromatic Stacking Interactions. J. Am. Chem. Soc. 1999, 121, 1717-1725.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 1717-1725
    • Pang, Y.P.1    Miller, J.L.2    Kollman, P.A.3
  • 39
    • 0000603083 scopus 로고
    • R. 1,3-Bis[4,6- bis(methylthio)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]propane
    • Biswas, G.; Chandra, T.; Avasthi K.; Maulik, P. R. 1,3-Bis[4,6- bis(methylthio)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]propane. Acta Cryst., 1995, C51, 2453-2455.
    • (1995) Acta Cryst , vol.C51 , pp. 2453-2455
    • Biswas, G.1    Chandra, T.2    Avasthi, K.3    Maulik, P.4
  • 40
    • 0035479684 scopus 로고    scopus 로고
    • 1H NMR and X-ray crystallographic analysis of 1,2-bis(4,6- diethylthio-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethane and its 'propylene linker'-analog: Molecular recognition versus crystal engineering
    • 1H NMR and X-ray crystallographic analysis of 1,2-bis(4,6- diethylthio-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethane and its 'propylene linker'-analog: molecular recognition versus crystal engineering. Tetrahedron Lett., 2001, 42, 7115-7117.
    • (2001) Tetrahedron Lett , vol.42 , pp. 7115-7117
    • Avasthi, K.1    Rawat, D.S.2    Maulik, P.R.3    Sarkhel, S.4    Broder, C.5    Howard, J.A.6
  • 41
    • 0141528480 scopus 로고    scopus 로고
    • A stacked pyrazolo [3, 4-d] pyrimidine-based flexible molecule: The effect on stacking of a bulky isopropyl group in comparison with a methyl/ethyl group
    • Avasthi, K.; Farooq, S. M.; Rawat, D. S.; Sharon, A.; Maulik, P. R. A stacked pyrazolo [3, 4-d] pyrimidine-based flexible molecule: the effect on stacking of a bulky isopropyl group in comparison with a methyl/ethyl group. Acta. Crystallogr., 2003, C59, 0523-0524.
    • (2003) Acta. Crystallogr. , vol.C59 , pp. 0523-0524
    • Avasthi, K.1    Farooq, S.M.2    Rawat, D.S.3    Sharon, A.4    Maulik, P.R.5
  • 42
    • 23444450913 scopus 로고    scopus 로고
    • 1H NMR and crystallographic evidence for folded conformation due to arene interactions in pyrazolo [3, 4-d] pyrimidine core based 'propylene linker' compounds
    • 1H NMR and crystallographic evidence for folded conformation due to arene interactions in pyrazolo [3, 4-d] pyrimidine core based 'propylene linker' compounds. J. Mol. Str., 2005, 750, 179-185.
    • (2005) J. Mol. Str. , vol.750 , pp. 179-185
    • Avasthi, K.1    Aswal, S.2    Kumar, R.3    Yadav, U.4    Rawat, D.S.5    Maulik, P.R.6
  • 43
    • 33644525024 scopus 로고    scopus 로고
    • 1H NMR and crystallographic evidence for folded conformation due to arene interactions
    • 1H NMR and crystallographic evidence for folded conformation due to arene interactions. J. Mol. Str., 2006, 785, 106-113.
    • (2006) J. Mol. Str. , vol.785 , pp. 106-113
    • Avasthi, K.1    Farooq, S.M.2    Raghunandan, R.3    Maulik, P.R.4
  • 45
    • 0035200608 scopus 로고    scopus 로고
    • Attractive intramolecular edge to face aromatic interactions in flexible organic molecules
    • Jennings, W. B.; Farrell, B. M.; Malone, J. M. Attractive intramolecular edge to face aromatic interactions in flexible organic molecules. Acc. Chem. Res., 2001, 34, 885-894.
    • (2001) Acc. Chem. Res. , vol.34 , pp. 885-894
    • Jennings, W.B.1    Farrell, B.M.2    Malone, J.M.3
  • 46
    • 16244393370 scopus 로고    scopus 로고
    • 12-containing infinite chain encapsulated in supramolecular open framework built of cadmium(II), 1,3-di(4- pyridyl)propane and 5-sulfoisophthalic acid monosodium salt
    • 12-containing infinite chain encapsulated in supramolecular open framework built of cadmium(II), 1,3-di(4- pyridyl)propane and 5-sulfoisophthalic acid monosodium salt. Cryst. Eng. Commun., 2005, 7, 87-89.
    • (2005) Cryst. Eng. Commun. , vol.7 , pp. 87-89
    • Liu, Q.Y.1    Xu, L.2
  • 47
    • 17744399329 scopus 로고    scopus 로고
    • The strength of parallel-displaced arene-Arene Interactions in Chloroform
    • Gung, B. W.; Xue, X.; Reich, H. J. The Strength of Parallel-Displaced Arene-Arene Interactions in Chloroform. J. Org. Chem., 2005, 70, 3641-3644.
    • (2005) J. Org. Chem. , vol.70 , pp. 3641-3644
    • Gung, B.W.1    Xue, X.2    Reich, H.J.3
  • 48
    • 33745394944 scopus 로고
    • Supramolecular synthons in crystal engineering - a new organic synthesis
    • Desiraju, G. R. Supramolecular Synthons in Crystal Engineering - A New Organic Synthesis. Ang. Chem. Int. Ed. Eng., 1995, 34, 2311-2327.
    • (1995) Ang. Chem. Int. Ed. Eng. , vol.34 , pp. 2311-2327
    • Desiraju, G.R.1
  • 49
    • 0037164009 scopus 로고    scopus 로고
    • Acridinylresorcinol as a Self- Complementary Building Block of Robust Hydrogen-Bonded 2D Nets with Coordinative Saturation. Preservation of Crystal Structures upon Guest Alteration, Guest Removal, and Host Modification
    • Tanaka, T.; Tassaki, T.; Aoyama, Y. Acridinylresorcinol as a Self- Complementary Building Block of Robust Hydrogen-Bonded 2D Nets with Coordinative Saturation. Preservation of Crystal Structures upon Guest Alteration, Guest Removal, and Host Modification. J. Am. Chem. Soc., 2002, 124, 12453-12462.
    • J. Am. Chem. Soc. , vol.124 , pp. 12453-12462
    • Tanaka, T.1    Tassaki, T.2    Aoyama, Y.3
  • 50
    • 4544344125 scopus 로고    scopus 로고
    • CH/π hydrogen bonds in crystals
    • Nishio, M. CH/π hydrogen bonds in crystals. Cryst. Eng. Comm., 2004, 6, 130-158.
    • (2004) Cryst. Eng. Comm. , vol.6 , pp. 130-158
    • Nishio, M.1
  • 51
    • 0002462375 scopus 로고    scopus 로고
    • A critical account on π- π stacking in metal complexes with aromatic nitrogen-containing ligands
    • Janiak, C. A critical account on π- π stacking in metal complexes with aromatic nitrogen-containing ligands. J. Chem. Soc. Dalton Trans, 2000, 3885-3896.
    • (2000) J. Chem. Soc. Dalton Trans. , pp. 3885-3896
    • Janiak, C.1
  • 52
    • 0032696761 scopus 로고    scopus 로고
    • Derivatives of N-Benzyl-2-phenylpyridinium bromide, minimalist models for face-to-face, center-to-edge π-Stacking in water
    • Martin, C. B.; Muller, H. R.; Willis, P. G.; Cammers-Goodwin, P. A. Derivatives of N-Benzyl-2-phenylpyridinium Bromide, Minimalist Models for Face-to-Face, Center-to-Edge π-Stacking in Water. J. Org. Chem., 1999, 64, 7802-7806.
    • (1999) J. Org. Chem. , vol.64 , pp. 7802-7806
    • Martin, C.B.1    Muller, H.R.2    Willis, P.G.3    Cammers-Goodwin, P.A.4
  • 53
    • 29844448114 scopus 로고    scopus 로고
    • Recognition and activation by ureas and thioureas stereoselective reaction using ureas and thioureas as hydrogen donors
    • Takemoto, Y. Recognition and activation by ureas and thioureas stereoselective reaction using ureas and thioureas as hydrogen donors. Org. Biomol. Chem., 2005, 3, 4299-4306.
    • (2005) Org. Biomol. Chem. , vol.3 , pp. 4299-4306
    • Takemoto, Y.1
  • 55
    • 0033873950 scopus 로고    scopus 로고
    • Circularly Polarized Electroluminescence from Liquid-Crystalline Chiral Polyfluorenes
    • Oda, M.; Nothofer, H. G.; Lieser, G.; Scherf, U.; Meskers, S. C. J.; Neher, D. Circularly Polarized Electroluminescence from Liquid-Crystalline Chiral Polyfluorenes. Adv. Matter., 2000, 12, 362-363.
    • (2000) Adv. Matter. , vol.12 , pp. 362-363
    • Oda, M.1    Nothofer, H.G.2    Lieser, G.3    Scherf, U.4    Meskers, S.C.J.5    Neher, D.6
  • 56
    • 0000768284 scopus 로고
    • Preference for cisamide structure in N-acyl-N-methylanilines
    • Itai, A.; Toriumi, Y.; Saito, S.; Kagechika, H.; Shudo, K. Preference for cisamide structure in N-acyl-N-methylanilines. J. Am. Chem. Soc., 1992, 114, 10649-10650.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 10649-10650
    • Itai, A.1    Toriumi, Y.2    Saito, S.3    Kagechika, H.4    Shudo, K.5
  • 57
    • 0038298140 scopus 로고    scopus 로고
    • Synthesis, structure, and evaluation of the effect of multiple stacking on the electron-donor properties of -stacked polyfluorenes
    • Rathore, R.; Abdeiwashed, S. H.; Guzei, I. A. Synthesis, Structure, and Evaluation of the Effect of Multiple Stacking on the Electron-Donor Properties of -Stacked Polyfluorenes. J. Am. Chem. Soc., 2003, 125, 8712-8713.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 8712-8713
    • Rathore, R.1    Abdeiwashed, S.H.2    Guzei, I.A.3
  • 58
    • 0001195982 scopus 로고
    • Trimethylene bridges as synthetic spacers for the detection of intramolecular interaction
    • Leonard, N. J. Trimethylene Bridges as synthetic spacers for the detection of intramolecular interaction. Acc. Chem. Res., 1979, 12, 423-429.
    • (1979) Acc. Chem. Res. , vol.12 , pp. 423-429
    • Leonard, N.J.1
  • 59
    • 0037028989 scopus 로고    scopus 로고
    • Unexpected substituent effects in offset π-π stacked interactions in water
    • Rashkin, M. J.; Waters, M. L. Unexpected substituent effects in offset π-π stacked interactions in water. J. Am. Chem. Soc., 2002, 124, 1860-1861.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 1860-1861
    • Rashkin, M.J.1    Waters, M.L.2
  • 60
    • 0025698613 scopus 로고
    • Transient folding intermediates characterized by protein engineering
    • Matouschek, A.; Kellis, J. T. Jr:; Serrano, L.; Bycroft, M.; Fersht, A. R. Transient folding intermediates characterized by protein engineering. Nature, 1990, 346, 440-445.
    • (1990) Nature , vol.346 , pp. 440-445
    • Matouschek, A.1    Kellis Jr., J.T.2    Serrano, L.3    Bycroft, M.4    Fersht, A.R.5
  • 61
    • 0032483756 scopus 로고    scopus 로고
    • Measurement of molecular electrostatic field effects in edge to face aromatic interactions and CH-π interactions with implications for protein folding and molecular recognition
    • Kim, E.; Paliwal, S.; Wilcox, C. S. Measurement of molecular electrostatic field effects in edge to face aromatic interactions and CH-π interactions with implications for protein folding and molecular recognition. J. Am. Chem. Soc., 1998, 120, 11192-11193.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 11192-11193
    • Kim, E.1    Paliwal, S.2    Wilcox, C.S.3
  • 62
    • 0029144713 scopus 로고
    • Preparations, crystal structures, and unusual proton NMR characteristics of some phthalimides
    • Baarrett, D. M. Y.; Kahwa, I. A.; Mague, J. T.; Mcpherson, G. L. Preparations, Crystal Structures, and Unusual Proton NMR Characteristics of Some Phthalimides. J. Org. Chem., 1995, 60, 5946-5953.
    • (1995) J. Org. Chem. , vol.60 , pp. 5946-5953
    • Baarrett, D.M.Y.1    Kahwa, I.A.2    Mague, J.T.3    McPherson, G.L.4
  • 63
    • 0010425738 scopus 로고    scopus 로고
    • Hydrolytic products of diphthalimidodiethylamine and temperature independent sensitized luminescence of their lanthanide(III) complexes
    • Baarrett, D. M. Y.; Kahwa, I. A.; Raduchel, B.; White, A. J. P.; Williams, D. J. Hydrolytic products of diphthalimidodiethylamine and temperature independent sensitized luminescence of their lanthanide(III) complexes. J. Chem. Soc. Perkin. Trans.2, 1998, 1851-1856.
    • (1998) J. Chem. Soc. Perkin. Trans. , vol.2 , pp. 1851-1856
    • Baarrett, D.M.Y.1    Kahwa, I.A.2    Raduchel, B.3    White, A.J.P.4    Williams, D.J.5
  • 64
    • 33745213179 scopus 로고    scopus 로고
    • Polyamines. I. Spectroscopic properties of N,N-bis-(phthalimidopropyl)-N-propylamine and supramolecular interactions in its crystals
    • Brycki, B.; Kowalczy, I.; Werner, J.; Borowiak, T.; Wolska, I.; Polyamines. I. Spectroscopic properties of N,N-bis-(phthalimidopropyl)-N-propylamine and supramolecular interactions in its crystals. J. Mol. Str., 2006, 791, 137-143.
    • (2006) J. Mol. Str. , vol.791 , pp. 137-143
    • Brycki, B.1    Kowalczy, I.2    Werner, J.3    Borowiak, T.4    Wolska, I.5
  • 65
    • 0001894947 scopus 로고
    • Meldola lecture. The role of aromatic interactions in molecular recognition
    • Hunter, C. A. Meldola Lecture. The role of aromatic interactions in molecular recognition. Chem. Soc. Rev., 1994, 2, 101-109.
    • (1994) Chem. Soc. Rev. , vol.2 , pp. 101-109
    • Hunter, C.A.1
  • 66
    • 0001227655 scopus 로고
    • The Nature of π-π interaction
    • Hunter, C. A.; Sanders, J. K. M. The Nature of π-π interaction. J. Am. Chem. Soc., 1990, 112, 5525-5534.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 5525-5534
    • Hunter, C.A.1    Sanders, J.K.M.2
  • 68
    • 0036897848 scopus 로고    scopus 로고
    • Aromatic interactions in model systems
    • Waters, M. L. Aromatic interactions in model systems. Current Opion. Chem. Biol., 2002, 6, 736-741.
    • (2002) Current Opion.Chem. Biol. , vol.6 , pp. 736-741
    • Waters, M.L.1
  • 69
    • 0000213148 scopus 로고
    • Structure and properties of Benzenecontaining molecular clusters: Nonemperical ab initio calculations and experiments
    • Hobza, P.; Selzel, H. L.; Schlag, E. W. Structure and properties of Benzenecontaining molecular clusters: Nonemperical ab initio calculations and experiments. Chem. Rev., 1994, 94, 1767-1785.
    • (1994) Chem. Rev. , vol.94 , pp. 1767-1785
    • Hobza, P.1    Selzel, H.L.2    Schlag, E.W.3
  • 70
    • 0037918475 scopus 로고    scopus 로고
    • Substituent effects on the stability of arene-arene complexes: An AM1 study of the conformational equilibria of cis-1,3-diphenylcyclohexanes
    • Williams, V. E.; Lemieux, R. P.; Thatcher, G. R. J. Substituent Effects on the Stability of Arene-Arene Complexes: An AM1 Study of the Conformational Equilibria of cis-1,3-Diphenylcyclohexanes. J. Org. Chem., 1996, 61, 1927-1933.
    • (1996) J. Org. Chem. , vol.61 , pp. 1927-1933
    • Williams, V.E.1    Lemieux, R.P.2    Thatcher, G.R.J.3
  • 72
    • 0001390955 scopus 로고    scopus 로고
    • The supramolecular concept as a bridge between organic, inorganic and organometallic crystal chemistry
    • Desiraju, G. R. The supramolecular concept as a bridge between organic, inorganic and organometallic crystal chemistry. J. Mol. Str., 1996, 374, 191-198.
    • (1996) J. Mol. Str. , vol.374 , pp. 191-198
    • Desiraju, G.R.1
  • 73
    • 77952621354 scopus 로고    scopus 로고
    • Studies of inter/ intramolecular weak interactions with CH.S and S.arene interaction in symmetrical and dissymmetrical models
    • Dubey, R.; Tewari, A. K.; Ravikumar, K.; Sridhar, B. Studies of Inter/ intramolecular Weak Interactions with CH.S and S.arene Interaction in Symmetrical and Dissymmetrical Models. Bull. Korean Chem. Soc., 2010, 31, 1326-1330.
    • (2010) Bull. Korean Chem. Soc. , vol.31 , pp. 1326-1330
    • Dubey, R.1    Tewari, A.K.2    Ravikumar, K.3    Sridhar, B.4
  • 74
    • 0036588037 scopus 로고    scopus 로고
    • 4-amino-6-benzloxy-2-(methylsulfanyl)-5-nitropyrimidine: Hydrogen bonded dimers linked into π stacked chains
    • Low, J. N.; Quesada, A.; Marchal, A.; Nogueras, M.; Sanchez, A.; Glidewell, C. 4-amino-6-benzloxy-2-(methylsulfanyl)-5-nitropyrimidine: Hydrogen bonded dimers linked into π stacked chains. Acta. Cryst., 2002, C58, 0284-0286.
    • (2002) Acta. Cryst. , vol.C58 , pp. 0284-0286
    • Low, J.N.1    Quesada, A.2    Marchal, A.3    Nogueras, M.4    Sanchez, A.5    Glidewell, C.6
  • 75
    • 44349192729 scopus 로고    scopus 로고
    • OH-π and halogen-π interactions as driving forces in the crystal organisations of tribromo and tri-iodo trityl alcohols
    • Schollmeyer, D.; Shishkin, O. V.; Ruhl, T.; Vysotsky, M. O. OH-π and halogen-π interactions as driving forces in the crystal organisations of tribromo and tri-iodo trityl alcohols. Cryst. Eng. Commun., 2008, 10, 715-723.
    • (2008) Cryst. Eng. Commun. , vol.10 , pp. 715-723
    • Schollmeyer, D.1    Shishkin, O.V.2    Ruhl, T.3    Vysotsky, M.O.4
  • 77
    • 0031043017 scopus 로고    scopus 로고
    • Molecular symmetry and the design of molecular solids: The oxalamide functionality as persistent hydrogen bonding unit
    • Coe, S.; Kane, J. J.; Nguyen, T. L.; Toledo, L. M.; Wininger, E.; Fowler, F. W.; Lauher, J. W. Molecular Symmetry and the Design of Molecular Solids: The Oxalamide Functionality as Persistent Hydrogen Bonding Unit. J. Am. Chem. Soc., 1997, 119, 86-93.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 86-93
    • Coe, S.1    Kane, J.J.2    Nguyen, T.L.3    Toledo, L.M.4    Wininger, E.5    Fowler, F.W.6    Lauher, J.W.7
  • 78
    • 33646722467 scopus 로고    scopus 로고
    • Preparation of poly(diiododiacetylene), an ordered conjugated polymer of carbon and iodine
    • Sun, A.; Lauher, J. W.; Goroff, N. S. Preparation of Poly(diiododiacetylene), an Ordered Conjugated Polymer of Carbon and Iodine. Science, 2006, 312, 1030-1034.
    • (2006) Science , vol.312 , pp. 1030-1034
    • Sun, A.1    Lauher, J.W.2    Goroff, N.S.3
  • 79
    • 35148864770 scopus 로고    scopus 로고
    • Arylperfluoroaryl stackinginteraction, hydrogen bonding and steric effect controlling the structure of supramolecular assemblies of N, N'- diaryloxalamides
    • Piotrkowska, B.; Gdaniec, M.; Milewska, M. J.; Polonski, T. Arylperfluoroaryl stackinginteraction, hydrogen bonding and steric effect controlling the structure of supramolecular assemblies of N, N'- diaryloxalamides. Cryst. Eng. Commun., 2007, 9, 868-872.
    • (2007) Cryst. Eng. Commun. , vol.9 , pp. 868-872
    • Piotrkowska, B.1    Gdaniec, M.2    Milewska, M.J.3    Polonski, T.4
  • 80
    • 0000437845 scopus 로고    scopus 로고
    • Status and perspective for molecular nonlinear optics: From crystals to polymers and fundamentals to applications
    • Zyss, J.; Nicoud, J. F. Status and perspective for molecular nonlinear optics: from crystals to polymers and fundamentals to applications. Curr. Opin. Solid State M. Sci., 1996, 1, 533-546.
    • (1996) Curr. Opin. Solid State M. Sci. , vol.1 , pp. 533-546
    • Zyss, J.1    Nicoud, J.F.2
  • 81
    • 0033667212 scopus 로고    scopus 로고
    • C-H·O and C-H·N hydrogen bond networks in the crystal structure of some 1, 2-dihydro-N-aryl-4,6-dimethyl pyrimidin-2-ones
    • Muthuraman, M.; Fur, Y. L.; Beucher, M. B.; Masse, R.; Nicoud, J. F.; George, S.; Nangia, A.; Desiraju, G. R. C-H·O and C-H·N hydrogen bond networks in the crystal structure of some 1, 2-dihydro-N-aryl-4,6-dimethyl pyrimidin-2-ones. J. Solid. State. Chem., 2000, 152, 221-228.
    • (2000) J. Solid. State. Chem. , vol.152 , pp. 221-228
    • Muthuraman, M.1    Fur, Y.L.2    Beucher, M.B.3    Masse, R.4    Nicoud, J.F.5    George, S.6    Nangia, A.7    Desiraju, G.R.8
  • 82
    • 0000670508 scopus 로고    scopus 로고
    • Donor and acceptor strength in CH·O hydrogen bonds quantified from crystallographic data of small solvent molecules
    • Steiner, T. Donor and acceptor strength in CH·O hydrogen bonds quantified from crystallographic data of small solvent molecules. New. J. Chem., 1998, 1099-1103.
    • (1998) New. J. Chem. , pp. 1099-1103
    • Steiner, T.1
  • 83
    • 1542686181 scopus 로고    scopus 로고
    • Designer crystals: Intermolecular interactions, network structures and supramolecular synthons
    • Desiraju, G. R. Designer crystals: Intermolecular interactions, network structures and supramolecular synthons. Chem. Comm., 1997, 1475-1482.
    • (1997) Chem. Comm. , pp. 1475-1482
    • Desiraju, G.R.1
  • 84
    • 0034741002 scopus 로고    scopus 로고
    • Solid state coordination chemistry of the copper(I)-cyano-organodiimine system. Two- and three-dimensional copper cyanide phases incorporating linear dipodal ligands
    • Chesnut, D. J.; Plewak, D.; Zubieta, J. Solid state coordination chemistry of the copper(I)-cyano-organodiimine system. Two- and three-dimensional copper cyanide phases incorporating linear dipodal ligands. J. Chem. Soc. Dalton Trans., 2001, 2567-2570.
    • (2001) J. Chem. Soc. Dalton Trans. , pp. 2567-2570
    • Chesnut, D.J.1    Plewak, D.2    Zubieta, J.3
  • 85
    • 25844451233 scopus 로고    scopus 로고
    • One-dimensional supramolecular tapes in the cocrystals of 2,5-dibromo-3,6-dihydroxy-1,4-benzoquinone (bromanilic acid) with heterocyclic compounds containing a pyrazine ring unit
    • Tomura, M.; Yamashita, Y. One-dimensional supramolecular tapes in the cocrystals of 2,5-dibromo-3,6-dihydroxy-1,4-benzoquinone (bromanilic acid) with heterocyclic compounds containing a pyrazine ring unit. Cryst. Eng. Commun., 2000, 2, 92-95.
    • (2000) Cryst. Eng. Commun. , vol.2 , pp. 92-95
    • Tomura, M.1    Yamashita, Y.2
  • 86
    • 0034103003 scopus 로고    scopus 로고
    • Role of weak hydrogen bonds in the crystal structures of phenazine, 5,10- dihydrophenazine and their 1:1 and 3:1 molecular complexes
    • Thalladi, V. R.; Smolka, T.; Gehrke, A.; Boese, R.; Sustmann, R. Role of weak hydrogen bonds in the crystal structures of phenazine, 5,10- dihydrophenazine and their 1:1 and 3:1 molecular complexes. New. J. Chem., 2000, 24, 143-147.
    • (2000) New. J. Chem. , vol.24 , pp. 143-147
    • Thalladi, V.R.1    Smolka, T.2    Gehrke, A.3    Boese, R.4    Sustmann, R.5
  • 87
    • 25844530818 scopus 로고    scopus 로고
    • Interplay of hydrogen bonding and aromatic ring interaction in supramolecular complexs of phenazine with N, N'- bis (2-pyridyl) aryldiamines
    • Gdaniec, M.; Bensemann, I.; Polonski, T. Interplay of hydrogen bonding and aromatic ring interaction in supramolecular complexs of phenazine with N, N'- bis (2-pyridyl) aryldiamines. Crys. Eng. Comm., 2005, 7, 433-438.
    • (2005) Crys. Eng. Comm. , vol.7 , pp. 433-438
    • Gdaniec, M.1    Bensemann, I.2    Polonski, T.3
  • 88
    • 0344276611 scopus 로고
    • Intermolecular carbonyl carbon-oxygen interactions in organic crystal structures
    • Bolton, W. Intermolecular Carbonyl Carbon-oxygen Interactions in Organic Crystal Structures. Nature (London), 1964, 201, 987-989.
    • (1964) Nature (London) , vol.201 , pp. 987-989
    • Bolton, W.1
  • 89
    • 0032907157 scopus 로고    scopus 로고
    • Axial and equatorial conformations of penicillins, their sulphoxides and sulphones: The role of N---H·S and C---H·O hydrogen bonds
    • Nangia, A.; Desiraju, G. R. Axial and equatorial conformations of penicillins, their sulphoxides and sulphones: the role of N---H·S and C---H·O hydrogen bonds. J. Mol. Str.,1999,474, 65-79.
    • (1999) J. Mol. Str. , vol.474 , pp. 65-79
    • Nangia, A.1    Desiraju, G.R.2
  • 90
    • 16244385598 scopus 로고    scopus 로고
    • Short C=O·C intermoleculr contacts for molecular assembly
    • Bhattachariya, G.; Savitha, G.; Ramanathan, G. Short C=O·C intermoleculr contacts for molecular assembly. Cryst. Eng. Comm., 2004, 6, 233-235.
    • (2004) Cryst. Eng. Comm. , vol.6 , pp. 233-235
    • Bhattachariya, G.1    Savitha, G.2    Ramanathan, G.3
  • 92
    • 0242417008 scopus 로고    scopus 로고
    • Interactions with aromatic rings in chemical and biological recognition
    • Castellano, R. K.; Diederich, F.; Meyer, E. A. Interactions with Aromatic Rings in Chemical and Biological Recognition. Angew. Chem. Int. Ed., 2003, 42, 1210-1250.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 1210-1250
    • Castellano, R.K.1    Diederich, F.2    Meyer, E.A.3
  • 93
    • 0742325413 scopus 로고    scopus 로고
    • CH-π interactions in ethynylbenzenes; the crystal structure of ethynylbenzene and 1, 3, 5-triethynylbenzene and a redetermination of the structure of 1, 4- diethynylbenzene
    • Weiss, H. C.; Blaser, D.; Boese, R.; Doughan, B. M.; Haley, M. M. CH-π interactions in ethynylbenzenes; the crystal structure of ethynylbenzene and 1, 3, 5-triethynylbenzene and a redetermination of the structure of 1, 4- diethynylbenzene. Chem. Commun., 1997, 1703-1704.
    • (1997) Chem. Commun. , pp. 1703-1704
    • Weiss, H.C.1    Blaser, D.2    Boese, R.3    Doughan, B.M.4    Haley, M.M.5
  • 94
    • 0032054015 scopus 로고    scopus 로고
    • CH/π Interactions as demonstrated in the crystal structure of guanine-nucleotide binding proteins, Src homology-2 domains and human growth hormone in complex with their specific ligands
    • Umezawa, Y.; Nishio, M. CH/π Interactions as demonstrated in the crystal structure of guanine-nucleotide binding proteins, Src homology-2 domains and human growth hormone in complex with their specific ligands. Bio. Med. Chem., 1998, 6, 493-504.
    • (1998) Bio. Med. Chem. , vol.6 , pp. 493-504
    • Umezawa, Y.1    Nishio, M.2
  • 97
    • 0033798257 scopus 로고    scopus 로고
    • CH/π interactions in the crystal structure of TATA-box binding protein/DNA complexes
    • Umezawa, Y.; Nishio, M. CH/π interactions in the crystal structure of TATA-box binding protein/DNA complexes. Bio. Med. Chem., 2000, 8, 2643-2650.
    • (2000) Bio. Med. Chem. , vol.8 , pp. 2643-2650
    • Umezawa, Y.1    Nishio, M.2
  • 98
    • 42449124902 scopus 로고    scopus 로고
    • Strength from weakness: CH-π stabilized conformational tuning of benzyl ethers and a consequent cooperative edge to face CH-π network
    • Sureshan, K. M.; Uchimaru, T.; Yao, Y.; Watanabe, Y. Strength from weakness: CH-π stabilized conformational tuning of benzyl ethers and a consequent cooperative edge to face CH-π network. Cryst. Eng. Commun., 2008, 10, 493-496.
    • (2008) Cryst. Eng. Commun. , vol.10 , pp. 493-496
    • Sureshan, K.M.1    Uchimaru, T.2    Yao, Y.3    Watanabe, Y.4
  • 99
    • 79957507211 scopus 로고    scopus 로고
    • Weak interactions: Potency for stabilization of molecule in solid state
    • DOI 10.1002/jhet.601 (In press)
    • Dubey, R.; Tewari, A. K.; Ravikumar, K.; Sridhar, B. Weak interactions: potency for stabilization of molecule in solid state. J. Het. Chem. 2010. DOI 10.1002/jhet.601 (In press).
    • (2010) J. Het. Chem.
    • Dubey, R.1    Tewari, A.K.2    Ravikumar, K.3    Sridhar, B.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.