2011
DOI: 10.1021/cs200171u
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Biomimetic Catalysis

Abstract: ACKNOWLEDGMENTWe graciously acknowledge the chemistry department at the University of Rhode Island for providing generous funding. Ms. Nicole Cook is also thanked for her editorial suggestions and expertise.

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Cited by 228 publications
(129 citation statements)
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References 267 publications
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“…In this way, NICE complements an ongoing revolution in bioinspired chemistry and materials science [2 ,3 ,4-6], which already sees applications in, for example, enzymemimics and antibody-mimics for catalysis [7][8][9][10] and in artificial photosynthesis [11 ,12 ,13-15]. These applications implement essential mechanistic steps of the biological model system at molecular and supramolecular scales.…”
Section: Q2mentioning
confidence: 99%
See 1 more Smart Citation
“…In this way, NICE complements an ongoing revolution in bioinspired chemistry and materials science [2 ,3 ,4-6], which already sees applications in, for example, enzymemimics and antibody-mimics for catalysis [7][8][9][10] and in artificial photosynthesis [11 ,12 ,13-15]. These applications implement essential mechanistic steps of the biological model system at molecular and supramolecular scales.…”
Section: Q2mentioning
confidence: 99%
“…These mechanisms include: (1) use of optimized, hierarchical networks to bridge scales, minimize transport limitations, and realize efficient, scalable solutions; (2) careful balancing of forces at one or more scales to achieve superior performance, for example, in terms of yield and selectivity; (3) emergence of complex functions from simple components, using dynamics as an organizing mechanism. Figure 1 presents an overview.In this way, NICE complements an ongoing revolution in bioinspired chemistry and materials science [2 ,3 ,4-6], which already sees applications in, for example, enzymemimics and antibody-mimics for catalysis [7][8][9][10] and in artificial photosynthesis [11 ,12 ,13-15]. These applications implement essential mechanistic steps of the biological model system at molecular and supramolecular scales.…”
mentioning
confidence: 99%
“…[49] In combination with host-guest chemistry, binding interactions can be spatially configured to localise organocatalytic events for enhanced catalytic proficiency. [50] Highly functionalised organocatalysts, further developed from the trifunctional prototypes, can be valuable in combining these approaches to access more complex catalysis ( Figure 5). With more organised catalytic functionalities acting in concert, the catalytic cycle may expand to incorporate a higher number of reaction components to approach the catalytic proficiency and complexity shown in biosynthetic assembly lines.…”
Section: Evolution Of Catalytic Proficiency and Complexity: Spatial Amentioning
confidence: 99%
“…It has long been chemists' endeavors to draw inspiration from nature's synthetic processes to design and synthesize enzyme mimics [67], which imitate characteristic features of enzymes that facilitate efficient catalysis, including (1) high enzymesubstrate binding affinities, (2) high catalytic turnovers, (3) excellent selectivity (chemo-, regio-, diastereo-, and enantioselectivity), and (4) substantial rate accelerations as compared to uncatalyzed processes. Investigation of activation models and biosynthetic pathways in Nature offers ample opportunities for synthetic chemists to achieve similar efficient, or even more efficient, transformations.…”
Section: Borrow Ideas From Naturementioning
confidence: 99%