Evolution of Dynamic Combinatorial Chemistry

被引:247
作者
Cougnon, Fabien B. L. [1 ]
Sanders, Jeremy K. M. [1 ]
机构
[1] Univ Cambridge, Univ Chem Lab, Cambridge CB2 1EW, England
基金
英国工程与自然科学研究理事会;
关键词
HOST-GUEST BINDING; DONOR-ACCEPTOR; AMPLIFICATION; RECEPTORS; LIBRARIES; SELECTION; DISCOVERY; CATALYST; ACCESS; DRIVEN;
D O I
10.1021/ar200240m
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Since its inception in the mid-1990s, dynamic combinatorial chemistry (DCC), the chemistry of complex systems under thermodynamic control, has proved valuable in identifying unexpected molecules with remarkable binding properties and in providing effective synthetic routes to complex species. Essentially, in this approach, one designs the experiment rather than the molecule. DCC has also provided us with insights Into how some chemical systems respond to external stimuli. Using examples from the work of our laboratory and others, this Account shows how the concept of DCC, inspired by the evolution of living systems, has found an increasing range of applications in diverse areas and has evolved conceptually and experimentally. A dynamic combinatorial library (DCL) is a thermodynamically controlled mixture of interconverting species that can respond to various stimuli. The Cambridge version of dynamic combinatorial chemistry was initially inspired by the mammalian immune system and was conceived as a way to create and identify new unpredictable receptors. For example, an added template can select and stabilize a strongly binding member of the library which is then amplified at the expense of the unsuccessful library members, minimizing the free energy of the system. But researchers have exploited DCC in a variety of other ways: over the past two decades, this technique has contributed to the evolution of chemistry and to applications in the diverse fields of catalysis, fragrance release, and responsive materials. Among these applications, researchers have built intricate and well-defined architectures such as catenanes or hydrogen-bonded nanotubes, using the ability of complex chemical systems to reach a high level of organization. In addition, DCC has proved a powerful tool for the study of complex molecular networks and systems. The use of DCC is improving our understanding of chemical and biological systems. The study of folding or self-replicating macrocycles in DCLs has served as a model for appreciating how complex organisations such as life can emerge from a pool of simple chemicals. Today, DCC is no longer restricted to thermodynamic control, and new systems have recently appeared in which kinetic and thermodynamic control coexist Expanding the realm of DCC to unexplored and promising new territories, these hybrid systems show that the concept of dynamic combinatorial chemistry continues to evolve.
引用
收藏
页码:2211 / 2221
页数:11
相关论文
共 61 条
[1]   Guest-mediated access to a single DNA nanostructure from a library of multiple assemblies [J].
Aldaye, Faisal A. ;
Sleiman, Hanadi F. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (33) :10070-+
[2]  
[Anonymous], 1993, ORIGINS ORDER
[3]   Dynamic Combinatorial Donor-Acceptor Catenanes in Water: Access to Unconventional and Unexpected Structures [J].
Au-Yeung, Ho Yu ;
Pantos, G. Dan ;
Sanders, Jeremy K. M. .
JOURNAL OF ORGANIC CHEMISTRY, 2011, 76 (05) :1257-1268
[4]   A Water Soluble Donor-Acceptor [2]Catenane that Can Switch between a Coplanar and a Gemini-Sign Conformation [J].
Au-Yeung, Ho Yu ;
Pantos, G. Dan ;
Sanders, Jeremy K. M. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2010, 49 (31) :5331-5334
[5]   Amplifying Different [2]Catenanes in an Aqueous Donor-Acceptor Dynamic Combinatorial Library [J].
Au-Yeung, Ho Yu ;
Pantos, G. Dan ;
Sanders, Jeremy K. M. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (44) :16030-+
[6]   Dynamic combinatorial synthesis of a catenane based on donor-acceptor interactions in water [J].
Au-Yeung, Ho Yu ;
Pantos, G. Dan ;
Sanders, Jeremy K. M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (26) :10466-10470
[7]   Ferrocene-amino acid macrocycles as hydrazone-based receptors for anions [J].
Beeren, Sophie R. ;
Sanders, Jeremy K. M. .
CHEMICAL SCIENCE, 2011, 2 (08) :1560-1567
[8]   From static to dynamic: escaping kinetic traps in hydrazone-based dynamic combinatorial libraries [J].
Beeren, Sophie R. ;
Pittelkow, Michael ;
Sanders, Jeremy K. M. .
CHEMICAL COMMUNICATIONS, 2011, 47 (26) :7359-7361
[9]   Discovery of Linear Receptors for Multiple Dihydrogen Phosphate Ions Using Dynamic Combinatorial Chemistry [J].
Beeren, Sophie R. ;
Sanders, Jeremy K. M. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (11) :3804-3807
[10]   Solid-state dynamic combinatorial chemistry: reversibility and thermodynamic product selection in covalent mechanosynthesis [J].
Belenguer, Ana M. ;
Friscic, Tomislav ;
Day, Graeme M. ;
Sanders, Jeremy K. M. .
CHEMICAL SCIENCE, 2011, 2 (04) :696-700