Design of Multicatalytic Systems Through Self-Assembly

被引:0
作者
Fernandes, Antony E. [1 ]
Jonas, Alain M. [2 ]
机构
[1] Certech, Rue Jules Bordet 45,Zone Ind C, B-7180 Seneffe, Belgium
[2] Univ Catholique Louvain UCLouvain, Inst Condensed Matter & Nanosci IMCN, Bio & Soft Matter BSMA, Croix Sud 1-L7-04-02, B-1348 Louvain La Neuve, Belgium
关键词
multicatalysis; self-assembly; non-covalent; cooperative; supramolecular; enzyme mimics; COMBINATORIAL HOMOGENEOUS CATALYSIS; FRIEDEL-CRAFTS ALKYLATION; SULFA-MICHAEL ADDITION; BIDENTATE LIGANDS; BIFUNCTIONAL ORGANOCATALYST; SUPRAMOLECULAR CATALYSIS; ASYMMETRIC CATALYSIS; MONODENTATE LIGANDS; SUPPORTED CATALYSTS; AEROBIC OXIDATION;
D O I
10.3390/catal15030265
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 development of self-assembled multicatalytic systems has emerged as a promising strategy for mimicking enzymatic catalysis in synthetic systems. This approach leverages the use of non-covalent interactions, such as hydrophobic interactions, hydrogen bonding, metal-ligand coordination, and aromatic stacking, to organize multiple catalytic centers within a defined, cooperative framework, allowing for enhanced reactivity, selectivity and efficiency, akin to the behavior of natural enzymes. The versatility of this approach enables the modular design, preparation, screening and optimization of systems capable of concerted catalysis and dynamic adaptation, making them suitable for a wide range of reactions, including asymmetric synthesis. The potential of these systems to emulate the precision and functionality of natural enzymes opens new avenues for the development of artificial multicatalytic systems with tailored and adaptable functions.
引用
收藏
页数:21
相关论文
共 104 条
[1]   Aromatic donor-acceptor interaction promoted catalyst assemblies for hydrolytic kinetic resolution of epichlorohydrin [J].
Blechschmidt, Daniel R. ;
Woodhouse, Matthew D. ;
Inagaki, Sebastien ;
Whitfield, Melita ;
Ogunsanya, Ayokunnumi ;
Yoder, Aaron ;
Lilly, Daniel ;
Heim, Eric W. ;
Soucie, Luke N. ;
Liang, Jian ;
Liu, Yu .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2019, 17 (01) :172-180
[2]   Self-assembly of bidentate ligands for combinatorial homogeneous catalysis based on an A-T base-pair model [J].
Breit, B ;
Seiche, W .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (11) :1640-1643
[3]   Hydrogen bonding as a construction element for bidentate donor ligands in homogeneous catalysis: Regioselective hydroformylation of terminal alkenes [J].
Breit, B ;
Seiche, W .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (22) :6608-6609
[4]   From nature to industry: Harnessing enzymes for biocatalysis [J].
Buller, R. ;
Lutz, S. ;
Kazlauskas, R. J. ;
Snajdrova, R. ;
Moore, J. C. ;
Bornscheuer, U. T. .
SCIENCE, 2023, 382 (6673)
[5]   Synthesis of discrete catalytic oligomers and their potential in silica-supported cooperative catalysis [J].
Chandra, Prakash ;
Jonas, AlainM. ;
Fernandes, Antony E. .
RSC ADVANCES, 2019, 9 (25) :14194-14197
[6]   Spatial Coordination of Cooperativity in Silica-Supported Cu/TEMPO/Imidazole Catalytic Triad [J].
Chandra, Prakash ;
Jonas, Alain M. ;
Fernandes, Antony E. .
ACS CATALYSIS, 2018, 8 (07) :6006-6011
[7]   Sequence and Surface Confinement Direct Cooperativity in Catalytic Precision Oligomers [J].
Chandra, Prakash ;
Jonas, Alain M. ;
Fernandes, Antony E. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2018, 140 (15) :5179-5184
[8]   Simulation of Intermediate Channeling by Nanoscale Confinement [J].
Chavan, Kanchan Suklal ;
Barton, Scott Calabrese .
JOURNAL OF PHYSICAL CHEMISTRY C, 2018, 122 (26) :14474-14480
[9]   Engineering new catalytic activities in enzymes [J].
Chen, Kai ;
Arnold, Frances H. .
NATURE CATALYSIS, 2020, 3 (03) :203-213
[10]   Chiral-at-Metal Octahedral Iridium Catalyst for the Asymmetric Construction of an All-Carbon Quaternary Stereocenter [J].
Chen, Liang-An ;
Tang, Xiaojuan ;
Xi, Jianwei ;
Xu, Weici ;
Gong, Lei ;
Meggers, Eric .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2013, 52 (52) :14021-14025