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Volumn 22, Issue 25, 2012, Pages 12651-12658

Harnessing Hansen solubility parameters to predict organogel formation

Author keywords

[No Author keywords available]

Indexed keywords

12-HYDROXYSTEARIC ACID; GELATORS; HANSEN SOLUBILITY PARAMETERS; MOLECULAR GELS; ORGANOGEL FORMATION; ORGANOGELS; STATIC RELATIVE PERMITTIVITIES;

EID: 84862187471     PISSN: 09599428     EISSN: 13645501     Source Type: Journal    
DOI: 10.1039/c2jm32056h     Document Type: Article
Times cited : (128)

References (45)
  • 1
    • 80053085599 scopus 로고    scopus 로고
    • Reversible phase transitions within self-assembled fibrillar networks of (R)-18-(n-alkylamino)octadecan-7-ols in their carbon tetrachloride gels
    • V. A. Mallia P. D. Butler B. Sarkar K. T. Holman R. G. Weiss Reversible phase transitions within self-assembled fibrillar networks of (R)-18-(n-alkylamino)octadecan-7-ols in their carbon tetrachloride gels J. Am. Chem. Soc. 2011 133 15045 15054
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 15045-15054
    • Mallia, V.A.1    Butler, P.D.2    Sarkar, B.3    Holman, K.T.4    Weiss, R.G.5
  • 3
    • 33748355395 scopus 로고    scopus 로고
    • Molecular organogels. Soft matter comprised of low-molecular-mass organic gelators and organic liquids
    • M. George R. G. Weiss Molecular organogels. Soft matter comprised of low-molecular-mass organic gelators and organic liquids Acc. Chem. Res. 2006 39 489 497
    • (2006) Acc. Chem. Res. , vol.39 , pp. 489-497
    • George, M.1    Weiss, R.G.2
  • 4
    • 0038782959 scopus 로고    scopus 로고
    • Linear and nonlinear rheological properties of self-assembling tectons in polypropylene matrices
    • M. Fahrländer K. Fuchs R. Mülhaupt C. Friedrich Linear and nonlinear rheological properties of self-assembling tectons in polypropylene matrices Macromolecules 2003 36 3749 3757
    • (2003) Macromolecules , vol.36 , pp. 3749-3757
    • Fahrländer, M.1    Fuchs, K.2    Mülhaupt, R.3    Friedrich, C.4
  • 7
    • 3242683774 scopus 로고    scopus 로고
    • Visible-light-harvesting organogel composed of cholesterol-based perylene derivatives†
    • K. Sugiyasu N. Fujita S. Shinkai Visible-light-harvesting organogel composed of cholesterol-based perylene derivatives† Angew. Chem., Int. Ed. 2004 43 1229 1233
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 1229-1233
    • Sugiyasu, K.1    Fujita, N.2    Shinkai, S.3
  • 8
    • 2942583633 scopus 로고    scopus 로고
    • Entrapment and release of quinoline derivatives using a hydrogel of a low molecular weight gelator
    • A. Friggeri B. L. Feringa J. van Esch Entrapment and release of quinoline derivatives using a hydrogel of a low molecular weight gelator J. Controlled Release 2004 97 241 248
    • (2004) J. Controlled Release , vol.97 , pp. 241-248
    • Friggeri, A.1    Feringa, B.L.2    Van Esch, J.3
  • 9
    • 84862907967 scopus 로고    scopus 로고
    • Solvent effects on structure, photoresponse and speed of gelation of a dicholesterol-linked azobenzene organogel
    • Y. Wu S. Wu G. Zou Q. Zhang Solvent effects on structure, photoresponse and speed of gelation of a dicholesterol-linked azobenzene organogel Soft Matter 2011 7 9177 9183
    • (2011) Soft Matter , vol.7 , pp. 9177-9183
    • Wu, Y.1    Wu, S.2    Zou, G.3    Zhang, Q.4
  • 10
    • 0142216274 scopus 로고    scopus 로고
    • Effects of hydrogen bonding and van der Waals interactions on organogelation using designed low-molecular-weight gelators and gel formation at room temperature
    • M. Suzuki Y. Nakajima M. Yumoto M. Kimura H. Shirai K. Hanabusa Effects of hydrogen bonding and van der Waals interactions on organogelation using designed low-molecular-weight gelators and gel formation at room temperature Langmuir 2003 19 8622 8624
    • (2003) Langmuir , vol.19 , pp. 8622-8624
    • Suzuki, M.1    Nakajima, Y.2    Yumoto, M.3    Kimura, M.4    Shirai, H.5    Hanabusa, K.6
  • 11
    • 68149129754 scopus 로고    scopus 로고
    • Solvent-modulated nucleation and crystallization kinetics of 12-hydroxystearic acid: A nonisothermal approach
    • M. A. Rogers A. G. Marangoni Solvent-modulated nucleation and crystallization kinetics of 12-hydroxystearic acid: a nonisothermal approach Langmuir 2009 25 8556 8566
    • (2009) Langmuir , vol.25 , pp. 8556-8566
    • Rogers, M.A.1    Marangoni, A.G.2
  • 12
  • 13
    • 33846182909 scopus 로고    scopus 로고
    • Solvent effect on organogel formation by low molecular weight molecules
    • G. Zhu J. S. Dordick Solvent effect on organogel formation by low molecular weight molecules Chem. Mater. 2006 18 5988 5995
    • (2006) Chem. Mater. , vol.18 , pp. 5988-5995
    • Zhu, G.1    Dordick, J.S.2
  • 15
    • 77955604388 scopus 로고    scopus 로고
    • A molecular insight into the nature of crystallographic mismatches in self-assembled fibrillar networks under non-isothermal crystallization conditions
    • R. Lam L. Quaroni T. Pederson M. A. Rogers A molecular insight into the nature of crystallographic mismatches in self-assembled fibrillar networks under non-isothermal crystallization conditions Soft Matter 2010 6 404 408
    • (2010) Soft Matter , vol.6 , pp. 404-408
    • Lam, R.1    Quaroni, L.2    Pederson, T.3    Rogers, M.A.4
  • 16
    • 30344483618 scopus 로고    scopus 로고
    • Arichitecture of a biocompatible supramolecular material by supersaturation-driven fabrication of its network
    • J. L. Li X. Y. Liu R. Y. Wang J. Y. Xiong Arichitecture of a biocompatible supramolecular material by supersaturation-driven fabrication of its network J. Phys. Chem. B 2005 109 24231 24235
    • (2005) J. Phys. Chem. B , vol.109 , pp. 24231-24235
    • Li, J.L.1    Liu, X.Y.2    Wang, R.Y.3    Xiong, J.Y.4
  • 17
    • 77955646139 scopus 로고    scopus 로고
    • Multicomponent hollow tubules formed using phytosterol and γ-oryzanol-based compounds: An understanding of their molecular embrace
    • M. A. Rogers A. Bot R. S. H. Lam T. Pedersen T. May Multicomponent hollow tubules formed using phytosterol and γ-oryzanol-based compounds: an understanding of their molecular embrace J. Phys. Chem. B 2010 114 8278 8295
    • (2010) J. Phys. Chem. B , vol.114 , pp. 8278-8295
    • Rogers, M.A.1    Bot, A.2    Lam, R.S.H.3    Pedersen, T.4    May, T.5
  • 18
    • 84989729992 scopus 로고
    • Photostationary fluorescence emission and time resolved spectroscopy of symmetrically disubstituted anthracenes on the meso and side rings: The unusual behavior of the 1,4 derivative
    • T. Brotin J. P. Devergne F. Fages Photostationary fluorescence emission and time resolved spectroscopy of symmetrically disubstituted anthracenes on the meso and side rings: the unusual behavior of the 1,4 derivative Photochem. Photobiol. 1992 55 349 358
    • (1992) Photochem. Photobiol. , vol.55 , pp. 349-358
    • Brotin, T.1    Devergne, J.P.2    Fages, F.3
  • 19
    • 33751156126 scopus 로고
    • Structures of organogels based upon cholesteryl-4-(2-anthryloxy) butanoate, a highly efficient luminescing gelator - Neutron and X-ray small-angle scattering investigations
    • P. Terech I. Furman R. G. Weiss Structures of organogels based upon cholesteryl-4-(2-anthryloxy)butanoate, a highly efficient luminescing gelator - neutron and X-ray small-angle scattering investigations J. Phys. Chem. 1995 99 9558 9566
    • (1995) J. Phys. Chem. , vol.99 , pp. 9558-9566
    • Terech, P.1    Furman, I.2    Weiss, R.G.3
  • 20
    • 77954540270 scopus 로고    scopus 로고
    • Relationship between molecular structure and thermo-mechanical properties of Candelilla wax and amides derived from (R)-12-hydroxystearic acid as gelators of safflower oil
    • J. F. Toro-Vazquez J. Morales-Rueda V. A. Mallia R. G. Weiss Relationship between molecular structure and thermo-mechanical properties of Candelilla wax and amides derived from (R)-12-hydroxystearic acid as gelators of safflower oil Food Biophys. 2010 5 193 202
    • (2010) Food Biophys. , vol.5 , pp. 193-202
    • Toro-Vazquez, J.F.1    Morales-Rueda, J.2    Mallia, V.A.3    Weiss, R.G.4
  • 21
    • 0034600775 scopus 로고    scopus 로고
    • New functional materials based on self-assembling organogels: From serendipity towards design
    • J. van Esch B. L. Feringa New functional materials based on self-assembling organogels: from serendipity towards design Angew. Chem., Int. Ed. 2000 39 2263 2266
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 2263-2266
    • Van Esch, J.1    Feringa, B.L.2
  • 22
    • 79960433684 scopus 로고    scopus 로고
    • Organogel formation rationalized by Hansen solubility parameters
    • M. Raynal L. Bouteiller Organogel formation rationalized by Hansen solubility parameters Chem. Commun. 2011 47 8271 8273
    • (2011) Chem. Commun. , vol.47 , pp. 8271-8273
    • Raynal, M.1    Bouteiller, L.2
  • 24
    • 10444269412 scopus 로고    scopus 로고
    • Solvent effects on supramolecular gel-phase materials:two-component dendritic gel
    • A. R. Hirst D. K. Smith Solvent effects on supramolecular gel-phase materials:two-component dendritic gel Langmuir 2004 20 10851 10857
    • (2004) Langmuir , vol.20 , pp. 10851-10857
    • Hirst, A.R.1    Smith, D.K.2
  • 25
    • 0034654663 scopus 로고    scopus 로고
    • Low molecular weight gelators for organic fluids: Gelation using a family of cyclo(dipeptide)s
    • K. Hanabusa M. Matsumoto M. Kimura A. Kakehi H. Shirai Low molecular weight gelators for organic fluids: gelation using a family of cyclo(dipeptide)s J. Colloid Interface Sci. 2000 224 231 244
    • (2000) J. Colloid Interface Sci. , vol.224 , pp. 231-244
    • Hanabusa, K.1    Matsumoto, M.2    Kimura, M.3    Kakehi, A.4    Shirai, H.5
  • 26
    • 34548629850 scopus 로고    scopus 로고
    • ed., John Wiley & Sons: New York, NewYork, 4th edn
    • Solubility Parameter Values, ed., E. A. Grulke, John Wiley & Sons: New York, NewYork, 4th edn, 2005
    • (2005) Solubility Parameter Values
    • Grulke, E.A.1
  • 28
    • 17644376545 scopus 로고    scopus 로고
    • An explanation of dispersion states of single-walled carbon nanotubes in solvents and aqueous surfactant solutions using solubility paramters
    • H. T. Ham Y. S. Choi I. J. Chung An explanation of dispersion states of single-walled carbon nanotubes in solvents and aqueous surfactant solutions using solubility paramters J. Colloid Interface Sci. 2006 286 216 223
    • (2006) J. Colloid Interface Sci. , vol.286 , pp. 216-223
    • Ham, H.T.1    Choi, Y.S.2    Chung, I.J.3
  • 30
    • 0002653985 scopus 로고
    • Equilibrium in nonelectrolyte mixtures
    • G. Scatchard Equilibrium in nonelectrolyte mixtures Chem. Rev. 1949 44 7 35
    • (1949) Chem. Rev. , vol.44 , pp. 7-35
    • Scatchard, G.1
  • 32
    • 0031260410 scopus 로고    scopus 로고
    • A thermodynamic approach using group contribution methods to model the partitioning of semivolatile organic compounds on atmospheric particulate matter
    • M. Jang R. M. MKamens K. B. Leach M. R. Strommen A thermodynamic approach using group contribution methods to model the partitioning of semivolatile organic compounds on atmospheric particulate matter Environ. Sci. Technol. 1997 31 2805 2811
    • (1997) Environ. Sci. Technol. , vol.31 , pp. 2805-2811
    • Jang, M.1    Mkamens, R.M.2    Leach, K.B.3    Strommen, M.R.4
  • 33
    • 0016025821 scopus 로고
    • A method for estimating both the solubility parameters and molar volumes of liquids
    • R. F. Fedors A method for estimating both the solubility parameters and molar volumes of liquids Polym. Eng. Sci. 1974 14 147 154
    • (1974) Polym. Eng. Sci. , vol.14 , pp. 147-154
    • Fedors, R.F.1
  • 34
  • 37
    • 0034188189 scopus 로고    scopus 로고
    • Rheological properties and structural correlations in molecular gels
    • P. Terech D. Pasquier V. Bordas C. Rossat Rheological properties and structural correlations in molecular gels Langmuir 2000 16 4485 4494
    • (2000) Langmuir , vol.16 , pp. 4485-4494
    • Terech, P.1    Pasquier, D.2    Bordas, V.3    Rossat, C.4
  • 38
    • 0031146846 scopus 로고    scopus 로고
    • Effect of lecithin on organogel formation of 12-hydroxystearic acid
    • T. Tamura M. Ichikawa Effect of lecithin on organogel formation of 12-hydroxystearic acid J. Am. Oil Chem. Soc. 1997 74 491 495
    • (1997) J. Am. Oil Chem. Soc. , vol.74 , pp. 491-495
    • Tamura, T.1    Ichikawa, M.2
  • 39
    • 84863338387 scopus 로고    scopus 로고
    • Influence of positional isomers on the macroscale and nanoscale architectures of aggregates of racemic hydroxyoctadecanoic acids in their molecular gel, dispersion, and solid states
    • S. Abraham Y. Lan R. S. H. Lam D. A. S. Grahame J. J. H. Kim R. G. Weiss M. A. Rogers Influence of positional isomers on the macroscale and nanoscale architectures of aggregates of racemic hydroxyoctadecanoic acids in their molecular gel, dispersion, and solid states Langmuir 2012 4955 4964
    • (2012) Langmuir , pp. 4955-4964
    • Abraham, S.1    Lan, Y.2    Lam, R.S.H.3    Grahame, D.A.S.4    Kim, J.J.H.5    Weiss, R.G.6    Rogers, M.A.7
  • 40
    • 61549095783 scopus 로고    scopus 로고
    • Non-isothermal nucleation and crystallization of 12-hydroxystearic acid in vegetable oils
    • M. A. Rogers A. G. Marangoni Non-isothermal nucleation and crystallization of 12-hydroxystearic acid in vegetable oils Cryst. Growth Des. 2008 8 4596 4601
    • (2008) Cryst. Growth Des. , vol.8 , pp. 4596-4601
    • Rogers, M.A.1    Marangoni, A.G.2
  • 41
    • 45749103299 scopus 로고    scopus 로고
    • Engineering the oil binding capacity and crystallinity of self-assembled fibrillar networks of 12-hydroxystearic acid in edible oils
    • M. A. Rogers A. J. Wright A. G. Marangoni Engineering the oil binding capacity and crystallinity of self-assembled fibrillar networks of 12-hydroxystearic acid in edible oils Soft Matter 2008 4 1483 1490
    • (2008) Soft Matter , vol.4 , pp. 1483-1490
    • Rogers, M.A.1    Wright, A.J.2    Marangoni, A.G.3
  • 42
    • 63749122745 scopus 로고    scopus 로고
    • Nanostructuring fiber morphology and solvent inclusions in 12-hydroxystearic acid/canola oil organogels
    • M. A. Rogers A. J. Wright A. G. Marangoni Nanostructuring fiber morphology and solvent inclusions in 12-hydroxystearic acid/canola oil organogels Curr. Opin. Colloid Interface Sci. 2009 14 223
    • (2009) Curr. Opin. Colloid Interface Sci. , vol.14 , pp. 223
    • Rogers, M.A.1    Wright, A.J.2    Marangoni, A.G.3
  • 43
    • 0004766673 scopus 로고
    • 12-d-Hydroxyoctadecanoic acid organogels - A small-angle neutron-scattering study
    • P. Terech 12-d-Hydroxyoctadecanoic acid organogels - a small-angle neutron-scattering study J. Phys. II 1992 2 2181 2195
    • (1992) J. Phys. II , vol.2 , pp. 2181-2195
    • Terech, P.1
  • 44
    • 0028521711 scopus 로고
    • Organogels and areogels of racemic and chiral 12-hydroxyoctadecanoic acid
    • P. Terech V. Rodriguez J. D. Barnes G. B. McKenna Organogels and areogels of racemic and chiral 12-hydroxyoctadecanoic acid Langmuir 1994 10 3406 3418
    • (1994) Langmuir , vol.10 , pp. 3406-3418
    • Terech, P.1    Rodriguez, V.2    Barnes, J.D.3    McKenna, G.B.4
  • 45
    • 0034275888 scopus 로고    scopus 로고
    • Organogels and low molecular mass organic gelators
    • A. J. Abdallah R. G. Weiss Organogels and low molecular mass organic gelators Adv. Mater. 2000 12 1237 1247
    • (2000) Adv. Mater. , vol.12 , pp. 1237-1247
    • Abdallah, A.J.1    Weiss, R.G.2


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