
AbstractNature’s enzymes are an ongoing source of inspiration for scientists. The complex processes behind their selectivity and efficiency is slowly being unraveled, and these findings have spawned many biomimetic catalysts. However, nearly all focus on the conversion of small molecular substrates. Nature itself is replete with inventive catalytic systems which modify, replicate, or decompose entire polymers, often in a processive fashion. Such processivity can, for example, enhance the rate of catalysis by clamping to the polymer substrate, which imparts a large effective molarity. Reviewed herein are the various strategies for processivity in nature’s arsenal and their properties. An overview of what has been achieved by chemists aiming to mimic one of nature’s greatest tricks is also included.
Noncovalent interactions, 1503 Catalysis, Polymers, Scanning Probe Microscopy, Molecular Materials, Processivity, 1600 Chemistry, Catalysis, Enzymes, Substrate Specificity, Host-guest systems, Supramolecular chemistry, Physical Organic Chemistry
Noncovalent interactions, 1503 Catalysis, Polymers, Scanning Probe Microscopy, Molecular Materials, Processivity, 1600 Chemistry, Catalysis, Enzymes, Substrate Specificity, Host-guest systems, Supramolecular chemistry, Physical Organic Chemistry
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 72 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
