Supramolecular chirality of self-assembled systems in solution

被引:394
作者
Mateos-Timoneda, MA [1 ]
Crego-Calama, M [1 ]
Reinhoudt, DN [1 ]
机构
[1] Univ Twente, MESA Res Inst, Lab Supramol Chem & Technol, NL-7500 AE Enschede, Netherlands
关键词
D O I
10.1039/b305550g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Self-assembly plays an important role in the formation of many ( chiral) biological structures, such as DNA, alpha-helices or beta-sheets of proteins. This process, which is the main tool of Supramolecular Chemistry (i.e. the chemistry of the molecular assemblies and of the intermolecular bonds), starts to play a significant role in nanotechnology for the construction of functional synthetic structures of nanometer size. The control of chirality in synthetic self-assembled systems is very important for applications of these systems e. g. in molecular recognition or mimicking of the catalytic activity of enzymes. This tutorial review deals with the most representative contributions in the field of supramolecular chirality. Specifically, the discussion centers on several examples that represent the control over chirality for self-assembled systems in solution.
引用
收藏
页码:363 / 372
页数:10
相关论文
共 77 条
[1]   Let's twist again - Double-stranded, triple-stranded, and circular helicates [J].
Albrecht, M .
CHEMICAL REVIEWS, 2001, 101 (11) :3457-3497
[2]   Chiral recognition of lactic acid derivatives with chromenone-benzoxazole receptors [J].
Almaraz, M ;
Raposo, C ;
Martín, M ;
Caballero, MC ;
Morán, JR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (14) :3516-3517
[3]   A synthetic receptor for choline and carnitine [J].
Ballester, P ;
Shivanyuk, A ;
Far, AR ;
Rebek, J .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (47) :14014-14016
[4]   Supramolecular helical stacking of metallomesogens derived from enantiopure and racemic polycatenar oxazolines [J].
Barberá, J ;
Cavero, E ;
Lehmann, M ;
Serrano, JL ;
Sierra, T ;
Vázquez, JT .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (15) :4527-4533
[5]  
Borovkov VV, 2002, ANGEW CHEM INT EDIT, V41, P1378, DOI 10.1002/1521-3773(20020415)41:8<1378::AID-ANIE1378>3.0.CO
[6]  
2-L
[7]   Configurationally homogeneous diastereomers of a linear hexa(tertiary phosphine):: Enantioselective self-assembly of a double-stranded parallel helicate of the type (P)-[Cu3(hexaphos)2](PF6)3 [J].
Bowyer, PK ;
Cook, VC ;
Gharib-Naseri, N ;
Gugger, PA ;
Rae, AD ;
Swiegers, GF ;
Willis, AC ;
Zank, J ;
Wild, SB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (08) :4877-4882
[8]  
Bruice PY., 2001, ORGANIC CHEM, VThird
[9]   Supramolecular polymers [J].
Brunsveld, L ;
Folmer, BJB ;
Meijer, EW ;
Sijbesma, RP .
CHEMICAL REVIEWS, 2001, 101 (12) :4071-4097
[10]   Recognition of neutral species with synthetic receptors [J].
Chen, HD ;
Weiner, WS ;
Hamilton, AD .
CURRENT OPINION IN CHEMICAL BIOLOGY, 1997, 1 (04) :458-466