Supramolecular gels: Functions and uses

被引:1864
作者
Sangeetha, NM [1 ]
Maitra, U [1 ]
机构
[1] Indian Inst Sci, Dept Organ Chem, Bangalore 560012, Karnataka, India
关键词
D O I
10.1039/b417081b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In recent years there has been immense interest in studying gels derived from low molecular mass gelators (supramolecular, or simply molecular gels). The motivation for this is not only to understand the fundamental aggregate structures in the gels at different length scales, but also to explore their potential for futuristic technological applications. Gels have been made sensitive to external stimuli like light and chemical entities by incorporating a spectroscopically active or a receptor unit as part of the gelator molecule. This makes them suitable for applications such as sensing and actuating. The diversity of gel structural architectures has allowed them to be utilized as templates to prepare novel inorganic superstructures for possible applications in catalysis and separation. Gels derived from liquid crystals (anisotropy gels) that can act as dynamically functional materials have been prepared, for example, for (re-writable) information recording. Supramolecular gels can be important in controlled release applications, in oil recovery, for gelling cryogenic fuels etc. They can also serve as media for a range of applications. This tutorial review highlights some of the instructive work done by various groups to develop smart and functional gels, and covers a wide spectrum of scientific interest ranging from medicine to materials science.
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收藏
页码:821 / 836
页数:16
相关论文
共 62 条
[1]   Multiaddressable self-assembling organogelators based on 2H-chromene and N-acyl-1,ω-amino acid units [J].
Ahmed, SA ;
Sallenave, X ;
Fages, F ;
Mieden-Gundert, G ;
Müller, WM ;
Müller, U ;
Vögtle, F ;
Pozzo, JL .
LANGMUIR, 2002, 18 (19) :7096-7101
[2]   Gelation-assisted light harvesting by selective energy transfer from an oligo(p-phenylenevinylene)-based self-assembly to an organic dye [J].
Ajayaghosh, A ;
George, SJ ;
Praveen, VK .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (03) :332-+
[3]   Binary organogelators which show light and temperature responsiveness [J].
Ayabe, M ;
Kishida, T ;
Fujita, N ;
Sada, K ;
Shinkai, S .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2003, 1 (15) :2744-2747
[4]   Multistimuli, multiresponsive metallo-supramolecular polymers [J].
Beck, JB ;
Rowan, SJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (46) :13922-13923
[5]  
Beginn U, 1998, MACROMOL CHEM PHYSIC, V199, P2379, DOI 10.1002/(SICI)1521-3935(19981101)199:11<2379::AID-MACP2379>3.0.CO
[6]  
2-2
[7]   Reversible optical transcription of supramolecular chirality into molecular chirality [J].
de Jong, JJD ;
Lucas, LN ;
Kellogg, RM ;
van Esch, JH ;
Feringa, BL .
SCIENCE, 2004, 304 (5668) :278-281
[8]   Remarkable stabilization of self-assembled organogels by polymerization [J].
de Loos, M ;
van Esch, J ;
Stokroos, I ;
Kellogg, RM ;
Feringa, BL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (51) :12675-12676
[9]   Water gelation by small organic molecules [J].
Estroff, LA ;
Hamilton, AD .
CHEMICAL REVIEWS, 2004, 104 (03) :1201-1217
[10]   Entrapment and release of quinoline derivatives using a hydrogel of a low molecular weight gelator [J].
Friggeri, A ;
Feringa, BL ;
van Esch, J .
JOURNAL OF CONTROLLED RELEASE, 2004, 97 (02) :241-248