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Volumn 224, Issue 10, 2009, Pages 499-505

Host-guest interaction in propeller-shaped molecules. Part one: Single crystal X-ray analysis of benzylidene-1,1/-bis-2-naphthol solvent cocrystals

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EID: 70449099440     PISSN: 00442968     EISSN: None     Source Type: Journal    
DOI: 10.1524/zkri.2009.1149     Document Type: Article
Times cited : (2)

References (43)
  • 2
    • 33744454651 scopus 로고    scopus 로고
    • Crystal engineering of analogous and homologous organic compounds: Hydrogen bonding patterns in trimethoprim hydrogen phthalate and trimethoprim hydrogen adipate
    • Muthiah, P. T.; Francis, S.; Rychlewska, U.; Warzajtis, B,: Crystal engineering of analogous and homologous organic compounds: hydrogen bonding patterns in trimethoprim hydrogen phthalate and trimethoprim hydrogen adipate. Beilstein J. Org. Chem. 2 (2006) No.8.
    • (2006) Beilstein J. Org. Chem. , vol.2 , Issue.8
    • Muthiah, P.T.1    Francis, S.2    Rychlewska, U.3    Warzajtis, B.4
  • 3
    • 31144447353 scopus 로고    scopus 로고
    • Hydrogen bonding in crystal structures of N,N'-bis(3-pyridyl)urea. why is the N-HO tape synthon absent in diaryl ureas with electron-withdrawing groups, Cryst
    • Reddy, S. L.; Basavoju, S.; Vangala, V. R.; Nangia, A.: Hydrogen bonding in crystal structures of N,N'-bis(3-pyridyl)urea. why is the N-HO tape synthon absent in diaryl ureas with electron-withdrawing groups, Cryst. Growth Des. 6 (2006) 161173.
    • (2006) Growth Des. , vol.6 , pp. 161173
    • Reddy, S.L.1    Basavoju, S.2    Vangala, V.R.3    Nangia, A.4
  • 6
    • 37049103273 scopus 로고
    • Spirans. Part 11. A new method for generating o-quinone methides, and its applications to the synthesis of spirochromans. A note on the autoxidation of a naphthol derivative
    • Bennet, D. J.; Dean, F. M.; Herbin, G. A.; Matkin, D. A.: Spirans. Part 11. A new method for generating o-quinone methides, and its applications to the synthesis of spirochromans. A note on the autoxidation of a naphthol derivative. J. C. S. Perkin Trans. I. 20 (1977) 2289-2294;
    • (1977) J. C. S. Perkin Trans. I. , vol.20 , pp. 2289-2294
    • Bennet, D.J.1    Dean, F.M.2    Herbin, G.A.3    Matkin, D.A.4
  • 7
    • 0000276795 scopus 로고
    • Syntheses of calix[4]naphthalenes derived from 1-naphthol
    • Georghiou, P. E.; Ashram, M.; Li, Z.; Chaulk S. G.: Syntheses of calix[4]naphthalenes derived from 1-naphthol. J. Org. Chem. 60 (1995), 7284-7289.
    • (1995) J. Org. Chem. , vol.60 , pp. 7284-7289
    • Georghiou, P.E.1    Ashram, M.2    Li, Z.3    Chaulk, S.G.4
  • 8
    • 57349196390 scopus 로고    scopus 로고
    • 1-[(2Hydroxy-1-naphthyl)(phenyl)methyl]-2-naphthol ethanol solvate
    • Rashidi-Ranjbar, P.; Abbasi, A.; Vafakish, B.; Fischer A.: 1-[(2Hydroxy-1-naphthyl)(phenyl)methyl]-2-naphthol ethanol solvate. Acta Cryst. E63 (2007) o2093-o2094.
    • (2007) Acta Cryst. , vol.E63
    • Rashidi-Ranjbar, P.1    Abbasi, A.2    Vafakish, B.3    Fischer, A.4
  • 9
    • 0007116617 scopus 로고
    • The C-H... O hydrogen bond in crystals: What is it
    • Desiraju, G. R.: The C-H ... O hydrogen bond in crystals: what is it. Acc. Chem. Res. 24 (1991) 290-296;
    • (1991) Acc. Chem. Res. , vol.24 , pp. 290-296
    • Desiraju, G.R.1
  • 10
    • 0342580086 scopus 로고
    • 12 coenzyme at 15 K is stabilized by C-H... O hydrogen bonds
    • 12 coenzyme at 15 K is stabilized by C-H... O hydrogen bonds. Acta Cryst. D49 (1993) 592-593;
    • (1993) Acta Cryst. , vol.D49 , pp. 592-593
    • Steiner, T.1    Saenger, W.2
  • 11
    • 0033552238 scopus 로고    scopus 로고
    • Fundamental properties of the CHO interaction: Is it a true hydrogen bond
    • Gu, Y.; Kar, T.; Scheiner S.: Fundamental properties of the CHO interaction: is it a true hydrogen bond. J. Am. Chem. Soc. 121 (1999) 9411-9422;
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 9411-9422
    • Gu, Y.1    Kar, T.2    Scheiner, S.3
  • 13
    • 0003362197 scopus 로고    scopus 로고
    • The Weak Hydrogen Bond
    • International Union of Crystallography, Oxford Science Publication
    • Desiraju, G. R.; Steiner, T.: The Weak Hydrogen Bond, In Structural Chemistry and biology. International Union of Crystallography, Oxford Science Publication 1999.
    • (1999) Structural Chemistry and Biology.
    • Desiraju, G.R.1    Steiner, T.2
  • 14
    • 0029117927 scopus 로고
    • The CH/π interaction: Significance in molecular recognition
    • Nishio, M.; Umezawa, Y.; Hirota, M.; Takeuchi, Y.: The CH/π interaction: significance in molecular recognition. Tetrahedron. 51 (1995) 8665-8701;
    • (1995) Tetrahedron. , vol.51 , pp. 8665-8701
    • Nishio, M.1    Umezawa, Y.2    Hirota, M.3    Takeuchi, Y.4
  • 16
    • 0024260626 scopus 로고
    • Weakly polar interactions in proteins
    • Burley, S. K.; Petsko G. A.: Weakly polar interactions in proteins. Adv Protein Chem. 39 (1988) 125-189;
    • (1988) Adv Protein Chem. , vol.39 , pp. 125-189
    • Burley, S.K.1    Petsko, G.A.2
  • 17
    • 0022419375 scopus 로고
    • Aromtic-aromatic interaction: A mechanism of protein structure stabilization
    • Burley, S. K.; Petsko G. A.: Aromtic-aromatic interaction: a mechanism of protein structure stabilization. Science 229 (1985) 23-28.
    • (1985) Science , vol.229 , pp. 23-28
    • Burley, S.K.1    Petsko, G.A.2
  • 18
    • 0001227655 scopus 로고
    • The nature of ö-ö interactions
    • Hunter, C. A.; Sanders J. K. M.: The nature of ö-ö interactions. J. Am. Chem. Soc. 112 (1990) 5525-5534;
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 5525-5534
    • Hunter, C.A.1    Sanders, J.K.M.2
  • 19
    • 0001894947 scopus 로고
    • The role of aromatic interactions in molecular recognition
    • Hunter, C. A.: The role of aromatic interactions in molecular recognition. Chem. Soc. Rev. 2 (1994) 101-109.
    • (1994) Chem. Soc. Rev. , vol.2 , pp. 101-109
    • Hunter, C.A.1
  • 21
    • 31044447745 scopus 로고    scopus 로고
    • Drug binding interactions in the inner cavity of hERG Channels: Molecular insights from structure-activity relationships of clofilium and ibutilide analogs
    • Perry, M.; Stansfeld, P. J.; Leaney, J.; Wood, C.; Groot, M.; Leishman, D.; Sutcliffe, M. J.; Mitcheson, J. S.: Drug binding interactions in the inner cavity of hERG Channels: molecular insights from structure-activity relationships of clofilium and ibutilide analogs. Mol. Pharmacol. 69 (2006) 509-519.
    • (2006) Mol. Pharmacol. , vol.69 , pp. 509-519
    • Perry, M.1    Stansfeld, P.J.2    Leaney, J.3    Wood, C.4    Groot, M.5    Leishman, D.6    Sutcliffe, M.J.7    Mitcheson, J.S.8
  • 22
    • 0001280906 scopus 로고    scopus 로고
    • Synthetic Supramolecular Chemistry
    • Fyfe, M. C. T.; Stoddart, J. F.: Synthetic Supramolecular Chemistry. Accounts Chem. Res. 30 (1997) 393-401.
    • (1997) Accounts Chem. Res. , vol.30 , pp. 393-401
    • Fyfe, M.C.T.1    Stoddart, J.F.2
  • 23
    • 0035200608 scopus 로고    scopus 로고
    • Attractive intramolecular edge-to-face aromatic interactions in flexible organic molecules
    • Jennings, W. B.; Farrell, B. M.; Malone, J. F.: Attractive intramolecular edge-to-face aromatic interactions in flexible organic molecules. Accounts Chem. Res. 34 (2001) 885-894.
    • (2001) Accounts Chem. Res. , vol.34 , pp. 885-894
    • Jennings, W.B.1    Farrell, B.M.2    Malone, J.F.3
  • 24
    • 0037140729 scopus 로고    scopus 로고
    • Crystalline self-assembly induced by aromatic edge-to-face interactions: The crystal structure of 2,6,6,10tetrabenzyl-2,10-diaza-6-azonia[11] paracyclophane bromide
    • Burguete, M. I.; Bolte, M,; Frias, J.; Garcia-Espana, E.; Luis, S. V; Miravet, J, F.: Crystalline self-assembly induced by aromatic edge-to-face interactions: the crystal structure of 2,6,6,10tetrabenzyl-2,10-diaza-6- azonia[11]paracyclophane bromide. Tetrahedron 58 (2002) 4179-4183.
    • (2002) Tetrahedron 58 , pp. 4179-4183
    • Burguete, M.I.1    Bolte, M.2    Frias, J.3    Garcia-Espana, E.4    Luis, S.V.5    Miravet, J.F.6
  • 25
    • 3843145390 scopus 로고    scopus 로고
    • Conformational and database study on the intramolecular CH...p aromatic bond and its possible influence on the stereochemistry of polypeptide chains
    • Bazzicalupi, C.; Dapporto, P.: Conformational and database study on the intramolecular CH...p aromatic bond and its possible influence on the stereochemistry of polypeptide chains. Struc. Chem. 15 (2004) 259-268.
    • (2004) Struc. Chem. , vol.15 , pp. 259-268
    • Bazzicalupi, C.1    Dapporto, P.2
  • 26
    • 1642519253 scopus 로고    scopus 로고
    • Synthesis of Benzofuro[2,3-b]benzofuran Derivatives under Hoesch Reaction Conditions
    • Kawcki, R.; Mazurek, A. P.; Kozerski, L.; Maurin, J. K.: Synthesis of Benzofuro[2,3-b]benzofuran Derivatives under Hoesch Reaction Conditions. Synthesis. 5 (1999) 751-754;
    • (1999) Synthesis. , vol.5 , pp. 751-754
    • Kawcki, R.1    Mazurek, A.P.2    Kozerski, L.3    Maurin, J.K.4
  • 27
    • 0030450615 scopus 로고    scopus 로고
    • Alkanediyl Bridged Calix[4]arenes: Synthesis, Conformational Analysis, and Rotational Barriers
    • Grüttner, S. C.; Grynszpan, F.; Paulus, E. F.; Thondorf, I.; Vogt, W,: Alkanediyl Bridged Calix[4]arenes: Synthesis, Conformational Analysis, and Rotational Barriers. J. Am. Chem. Soc. 118 (1996) 12938-12949;
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 12938-12949
    • Grüttner, S.C.1    Grynszpan, F.2    Paulus, E.F.3    Thondorf, I.4    Vogt, W.5
  • 28
    • 37049073875 scopus 로고
    • Unusual host-guest -arene H bonding in a hooded cavitand: The first solid-state structure of a calix[4]resorcinarene with underivatised hydroxy groups
    • Leigh, D. A.; Linnane, P.; Pritchard, R. G.; Jackson, G.: Unusual host-guest -arene H bonding in a hooded cavitand: the first solid-state structure of a calix[4]resorcinarene with underivatised hydroxy groups. J. Chem. Soc. Chem. Commun. 4 (1994) 389-390.
    • (1994) J. Chem. Soc. Chem. Commun. , vol.4 , pp. 389-390
    • Leigh, D.A.1    Linnane, P.2    Pritchard, R.G.3    Jackson, G.4
  • 29
    • 0001412059 scopus 로고
    • Conformational properties of cis.cis1,4-cyclooctadiene. Dynamic nuclear magnetic resonance spectroscopy and iterative strain-energy calculations
    • Anet, F. A. L.; Yavari I.: Conformational properties of cis.cis1,4-cyclooctadiene. Dynamic nuclear magnetic resonance spectroscopy and iterative strain-energy calculations. J. Am. Chem. Soc. 99 (1977) 6986-6991.
    • (1977) J. Am. Chem. Soc. , vol.99 , pp. 6986-6991
    • Anet, F.A.L.1    Yavari, I.2
  • 30
    • 33845469636 scopus 로고
    • Conformation of seven- And eight-membered organosilicon heterocycles in solution
    • Pastor, S. D.; Spivack, J. D.; Rodebaugh, R. K.; Bini, D.: Conformation of seven- and eight-membered organosilicon heterocycles in solution. J. Org. Chem. 49 (1984) 1297-1300;
    • (1984) J. Org. Chem. , vol.49 , pp. 1297-1300
    • Pastor, S.D.1    Spivack, J.D.2    Rodebaugh, R.K.3    Bini, D.4
  • 31
    • 0030794823 scopus 로고    scopus 로고
    • Steric consequences on the conformation of medium-sized rings: Solution NMR, solid-state crystallographic, ab-Initio molecular orbital calculations, and molecular mechanics studies on substituted eight-membered organosilicon ring systems
    • Burke, L. P.; DeBellis, A. D.; Fuhrer, H.; Meier, H.; Pastor, S. D.; Rihs, G.; Rist, G.; Rodebaugh, R. K.; Shum, S. P.: Steric consequences on the conformation of medium-sized rings: solution NMR, solid-state crystallographic, ab-Initio molecular orbital calculations, and molecular mechanics studies on substituted eight-membered organosilicon ring systems. J. Am. Chem. Soc. 119 (1997) 8313-8323.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 8313-8323
    • Burke, L.P.1    Debellis, A.D.2    Fuhrer, H.3    Meier, H.4    Pastor, S.D.5    Rihs, G.6    Rist, G.7    Rodebaugh, R.K.8    Shum, S.P.9
  • 33
    • 84962476487 scopus 로고    scopus 로고
    • Characterization of lowbarrier hydrogen bonds. 7. relationship between strength and geometry of short-strong hydrogen bonds, the formic acid-formate anion model system, An ab-Initio and DFT investigation
    • Smallwood, C. J.; McAllister, M. A.: Characterization of lowbarrier hydrogen bonds. 7. relationship between strength and geometry of short-strong hydrogen bonds, the formic acid-formate anion model system, An ab-Initio and DFT investigation, J. Am. Chem. Soc. 119 (1997) 11277-11281;
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 11277-11281
    • Smallwood, C.J.1    McAllister, M.A.2
  • 34
    • 36949041474 scopus 로고
    • Distribution of hydrogen bond angles in molecular crystals
    • Hasegawa, M.; Noda, H.: Distribution of hydrogen bond angles in molecular crystals. Nature. 254 (1975) 212-212
    • (1975) Nature. , vol.254 , pp. 212-212
    • Hasegawa, M.1    Noda, H.2
  • 35
    • 0037202193 scopus 로고    scopus 로고
    • The role of hydrogen bonding on the H-atom-donating abilities of catechols and naphthalene diols and on a previously overlooked aspect of their infrared spectra
    • Mairo, C. F.; Barclay, L. R. C.; Ingold, K. U.: The role of hydrogen bonding on the H-atom-donating abilities of catechols and naphthalene diols and on a previously overlooked aspect of their infrared spectra. J. Am. Chem. Soc. 124 (2002) 12881-12888.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 12881-12888
    • Mairo, C.F.1    Barclay, L.R.C.2    Ingold, K.U.3
  • 36
    • 34547645015 scopus 로고    scopus 로고
    • Inclusion Compounds of Dehydrocholic Acid with Solvents
    • Fogagnolo, M.; Fantin, G.; Bortolini, O.: Inclusion Compounds of Dehydrocholic Acid with Solvents. Int. J. Mol. Sci. 8 (2007) 662-669.
    • (2007) Int. J. Mol. Sci. , vol.8 , pp. 662-669
    • Fogagnolo, M.1    Fantin, G.2    Bortolini, O.3
  • 37
    • 0041474874 scopus 로고    scopus 로고
    • Physicochemical aspects of host-guest compounds
    • Nassimbeni, L. R.: Physicochemical aspects of host-guest compounds. Accounts Chem. Res. 36 (2003) 631-637.
    • (2003) Accounts Chem. Res. , vol.36 , pp. 631-637
    • Nassimbeni, L.R.1
  • 39
    • 0034605425 scopus 로고    scopus 로고
    • Inclusion of aminobenzonitrile isomers by a diol host compound: Structure and selectivity
    • Caira, M. R.; Nassimbeni, L. R; Toda, F.; Vujovic, D.: Inclusion of aminobenzonitrile isomers by a diol host compound: structure and selectivity. J. Am. Chem. Soc. 122 (2000) 9367-9372;
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 9367-9372
    • Caira, M.R.1    Nassimbeni, L.R.2    Toda, F.3    Vujovic, D.4
  • 40
    • 1642456511 scopus 로고    scopus 로고
    • Structures of 4,4'-bis(diphenylhydroxymethyl)diphenyl with picolines: Selectivity and phase transformation
    • Nassimbeni, L. R, Su, H.; Weber, E.; Skobridis, K.: Structures of 4,4'-bis(diphenylhydroxymethyl)diphenyl with picolines: selectivity and phase transformation. Cryst. Growth Des. 4 (2004) 85-88;
    • (2004) Cryst. Growth Des. , vol.4 , pp. 85-88
    • Nassimbeni, L.R.1    Su, H.2    Weber, E.3    Skobridis, K.4
  • 41
    • 0036346434 scopus 로고    scopus 로고
    • Inclusion compounds of binaphthol with volatile guests: Structures, selectivity and kinetics of desolvation
    • Nassimbeni, L. R; Hong, S.: Inclusion compounds of binaphthol with volatile guests: structures, selectivity and kinetics of desolvation. New. J. Chem. 26 (2002) 989-995.
    • (2002) New. J. Chem. , vol.26 , pp. 989-995
    • Nassimbeni, L.R.1    Hong, S.2
  • 43
    • 0004078505 scopus 로고    scopus 로고
    • Release 3.1d. Crystal Impact GbR, Bonn, Germany.
    • Brandenburg, K.: DIAMOND. Release 3.1d. Crystal Impact GbR, Bonn, Germany.
    • DIAMOND.
    • Brandenburg, K.1


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