Author
Listed:
- Matías Blanco
(Ciudad Universitaria de Cantoblanco)
- Belén Nieto-Ortega
(Ciudad Universitaria de Cantoblanco)
- Alberto Juan
(Ciudad Universitaria de Cantoblanco)
- Mariano Vera-Hidalgo
(Ciudad Universitaria de Cantoblanco)
- Alejandro López-Moreno
(Ciudad Universitaria de Cantoblanco)
- Santiago Casado
(Ciudad Universitaria de Cantoblanco)
- Luisa R. González
(Universidad Complutense de Madrid)
- Hidetaka Sawada
(JEOL Ltd, 3-1-2 Musashino)
- José M. González-Calbet
(Universidad Complutense de Madrid)
- Emilio M. Pérez
(Ciudad Universitaria de Cantoblanco)
Abstract
One of the most attractive applications of carbon nanomaterials is as catalysts, due to their extreme surface-to-volume ratio. The substitution of C with heteroatoms (typically B and N as p- and n-dopants) has been explored to enhance their catalytic activity. Here we show that encapsulation within weakly doping macrocycles can be used to modify the catalytic properties of the nanotubes towards the reduction of nitroarenes, either enhancing it (n-doping) or slowing it down (p-doping). This artificial regulation strategy presents a unique combination of features found in the natural regulation of enzymes: binding of the effectors (the macrocycles) is noncovalent, yet stable thanks to the mechanical link, and their effect is remote, but not allosteric, since it does not affect the structure of the active site. By careful design of the macrocycles’ structure, we expect that this strategy will contribute to overcome the major hurdles in SWNT-based catalysts: activity, aggregation, and specificity.
Suggested Citation
Matías Blanco & Belén Nieto-Ortega & Alberto Juan & Mariano Vera-Hidalgo & Alejandro López-Moreno & Santiago Casado & Luisa R. González & Hidetaka Sawada & José M. González-Calbet & Emilio M. Pérez, 2018.
"Positive and negative regulation of carbon nanotube catalysts through encapsulation within macrocycles,"
Nature Communications, Nature, vol. 9(1), pages 1-7, December.
Handle:
RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-05183-8
DOI: 10.1038/s41467-018-05183-8
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