Systematic design of amide- and urea-type gelators with tailored properties

被引:140
作者
Fages, F
Vögtle, F
Zinic, M
机构
[1] Univ Aix Marseille 2, Fac Sci Luminy, F-13288 Marseille 9, France
[2] Univ Bonn, Kekule Inst Organ Chem & Biochem, D-53121 Bonn, Germany
[3] Rudjer Boskovic Inst, Zagreb 10002, Croatia
来源
LOW MOLECULAR MASS GELATORS: DESIGN, SELF-ASSEMBLY, FUNCTION | 2005年 / 256卷
关键词
hydrogen bonding; self-assembly; supramolecular chemistry; amide gelators; urea gelators;
D O I
10.1007/b107172
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The formation of gels by structurally highly diverse low molecular weight organic molecules is paradigmatically a supramolecular phenomenon. It is based on the self-assembly of certain organic molecules and involves highly specific noncovalent intermolecular interactions, in particular those inducing predominantly unidirectional aggregation. in this chapter, the design of low molecular weight gelators that incorporate single or multiple amide units as intermolecular hydrogen-bonding functionalities and methods of their preparation are given. Many efficient gelators of organic solvents and water could be prepared by the structural combination of amidic, carbamate, urea, or oxalamide groups and long aliphatic chains or aromatic groups with a large surface. The numerous potential applications in slow drug-delivery systems, the fabrication of templated materials, and in sensing devices are also discussed.
引用
收藏
页码:77 / 131
页数:55
相关论文
共 133 条
[1]   Self-assembling peptide polyelectrolyte β-sheet complexes form nematic hydrogels [J].
Aggeli, A ;
Bell, M ;
Boden, N ;
Carrick, LM ;
Strong, AE .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (45) :5603-5606
[2]   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
[3]  
ANGELLI A, 2001, P NATL ACAD SCI USA, V98, P11857
[4]  
ANGELLI A, 1997, NATURE, V386, P259
[5]  
[Anonymous], 1994, MONOGRAPHS SUPRAMOLE
[6]   Modulated supramolecular assemblies composed of tripeptide derivatives: Formation of micrometer-scale rods, nanometer-size needles, and regular patterns with molecular-level flatness from the same compound [J].
Ariga, K ;
Kikuchi, J ;
Naito, M ;
Koyama, E ;
Yamada, N .
LANGMUIR, 2000, 16 (11) :4929-4939
[7]   Pyrene-derived novel one- and two-component organogelators [J].
Babu, P ;
Sangeetha, NM ;
Vijaykumar, P ;
Maitra, U ;
Rissanen, K ;
Raju, AR .
CHEMISTRY-A EUROPEAN JOURNAL, 2003, 9 (09) :1922-1932
[8]   Self-assembly of small peptidomimetic cyclophanes [J].
Becerril, J ;
Burguete, MI ;
Escuder, B ;
Galindo, F ;
Gavara, R ;
Miravet, JF ;
Luis, SV ;
Peris, G .
CHEMISTRY-A EUROPEAN JOURNAL, 2004, 10 (16) :3879-3890
[9]   Minimalist peptidomimetic cyclophanes as strong organogelators [J].
Becerril, J ;
Burguete, MI ;
Escuder, B ;
Luis, SV ;
Miravet, JF ;
Querol, M .
CHEMICAL COMMUNICATIONS, 2002, (07) :738-739
[10]  
Beginn U, 2000, MACROMOL CHEM PHYSIC, V201, P1008, DOI 10.1002/1521-3935(20000601)201:10<1008::AID-MACP1008>3.3.CO