Small-angle X-ray scattering from a dual-component organogel to exhibit a charge transfer interaction

被引:23
作者
Jeong, Y
Friggeri, A
Akiba, I
Masunaga, H
Sakurai, K
Sakurai, S
Okamoto, S
Inoue, K
Shinkai, S
机构
[1] Univ Kitakyushu, Dept Chem Proc & Environm, Wakamatsu Ku, Kitakyushu, Fukuoka 8080135, Japan
[2] Japan Sci & Technol, Chemotransfigurat Project, Kurume, Fukuoka 8390861, Japan
[3] Kyoto Inst Technol, Dept Polymer Sci & Engn, Kyoto 6068585, Japan
[4] Nagoya Inst Technol, Nagoya, Aichi 4668555, Japan
[5] Japan Synchrotron Radiat Res Inst, SPring 8, Sayo, Hyogo 6795198, Japan
[6] Kyushu Univ, Grad Sch Engn, Dept Chem & Biochem, Higashi Ku, Fukuoka 8128581, Japan
基金
日本科学技术振兴机构;
关键词
small-angle X-ray scattering (SAXS); dual-component organogel; cross-sectional radius of gyration; radial electron density distribution;
D O I
10.1016/j.jcis.2004.08.179
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The structure of a dual-component organogel consisting of methyl 4,6-O-(p-aminobenzylidene)-alpha-D-glucopyranoside and methyl 4,6-O-(p-nitrobenzylidene)-alpha-D-glucopyranoside in diphenyl ether was investigated with small-angle X-ray scattering (SAXS). The individual components gelatinized the solvent to yield a colorless gel and the gel fiber consisted of the crystal, providing the crystalline peaks at the same diffraction angles as those of the solid samples. When the components were mixed in equimolar ratio and dissolved in diphenyl ether, a yellow gel was formed and the crystalline peaks disappeared. For all compositions, the SAXS profiles were well fitted by a cylinder model. The cross-sectional radius of gyration, r(c), was determined from the cross-sectional Guinier plot (qI vs q(2), where I and q are the scattering intensity and the magnitude of the scattering vector). The value of rc reached a minimum of 3.0 nm at the equimolar composition. By correcting the data for the thermal scattering background, we obtained the entire SAXS profile for the equimolar dual-component gel. From this profile, the radial electron density distribution was determined and the radius of the cylinder was estimated to be 2.6 nm. The electron density distribution thus obtained revealed that four gelator molecules are packed in the sectional direction. This model was consistent with the size of the gelator molecules. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:113 / 122
页数:10
相关论文
共 52 条
[11]   'Bifunctional' sugar-integrated gelators for organic solvents and water-on the role of nitro-substituents in 1-O-methyl-4,6-O-(nitro benzylidene)-monosaccharides for the improvement of gelation ability [J].
Gronwald, O ;
Shinkai, S .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 2001, (10) :1933-1937
[12]   Further evidence for the gelation ability-structure correlation in sugar-based gelators [J].
Gronwald, O ;
Sakurai, K ;
Luboradzki, R ;
Kimura, T ;
Shinkai, S .
CARBOHYDRATE RESEARCH, 2001, 331 (03) :307-318
[13]   Organogel formation and molecular imprinting by functionalized gluconamides and their metal complexes [J].
Hafkamp, RJH ;
Kokke, BPA ;
Danke, IM ;
Geurts, HPM ;
Rowan, AE ;
Feiters, MC ;
Nolte, RJM .
CHEMICAL COMMUNICATIONS, 1997, (06) :545-546
[14]   A SMALL MOLECULAR GELLING AGENT FOR ORGANIC LIQUIDS - N-BENZYLOXYCARBONYL-L-ALANINE 4-HEXADECANOYL-2-NITROPHENYL ESTER [J].
HANABUSA, K ;
OKUI, K ;
KARAKI, K ;
KOYAMA, T ;
SHIRAI, H .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1992, (18) :1371-1373
[15]   Prominent gelation and chiral aggregation of alkylamides derived from trans-1,2-diaminocyclohexane [J].
Hanabusa, K ;
Yamada, M ;
Kimura, M ;
Shirai, H .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1996, 35 (17) :1949-1951
[16]   Formation of organogels by intermolecular hydrogen bonding between ureylene segment [J].
Hanabusa, K ;
Shimura, K ;
Hirose, K ;
Kimura, M ;
Shirai, H .
CHEMISTRY LETTERS, 1996, (10) :885-886
[17]   Small molecular gelling agents to harden organic liquids: Trialkyl cis-1,3,5-cyclohexanetricarboxamides [J].
Hanabusa, K ;
Kawakami, A ;
Kimura, M ;
Shirai, H .
CHEMISTRY LETTERS, 1997, (03) :191-192
[18]   CHIRAL DISCRIMINATION OF MONOSACCHARIDES THROUGH GEL FORMATION [J].
JAMES, TD ;
MURATA, K ;
HARADA, T ;
UEDA, K ;
SHINKAI, S .
CHEMISTRY LETTERS, 1994, (02) :273-276
[19]   Novel vesicular aggregates of crown-appended cholesterol derivatives which act as gelators of organic solvents and as templates for silica transcription [J].
Jung, JH ;
Ono, Y ;
Sakurai, K ;
Sano, M ;
Shinkai, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (36) :8648-8653
[20]  
Jung JH, 2000, CHEM-EUR J, V6, P4552, DOI 10.1002/1521-3765(20001215)6:24<4552::AID-CHEM4552>3.3.CO