Author
Listed:
- Alejo M. Lifschitz
(Northwestern University)
- Ryan M. Young
(Northwestern University
Argonne-Northwestern Solar Energy Research (ANSER) Center, Northwestern University)
- Jose Mendez-Arroyo
(Northwestern University)
- Charlotte L. Stern
(Northwestern University)
- C. Michael McGuirk
(Northwestern University)
- Michael R. Wasielewski
(Northwestern University
Argonne-Northwestern Solar Energy Research (ANSER) Center, Northwestern University)
- Chad A. Mirkin
(Northwestern University)
Abstract
Biological photosynthetic machinery allosterically regulate light harvesting via conformational and electronic changes at the antenna protein complexes as a response to specific chemical inputs. Fundamental limitations in current approaches to regulating inorganic light-harvesting mimics prevent their use in catalysis. Here we show that a light-harvesting antenna/reaction centre mimic can be regulated by utilizing a coordination framework incorporating antenna hemilabile ligands and assembled via a high-yielding, modular approach. As in nature, allosteric regulation is afforded by coupling the conformational changes to the disruptions in the electrochemical landscape of the framework upon recognition of specific coordinating analytes. The hemilabile ligands enable switching using remarkably mild and redox-inactive inputs, allowing one to regulate the photoredox catalytic activity of the photosynthetic mimic reversibly and in situ. Thus, we demonstrate that bioinspired regulatory mechanisms can be applied to inorganic light-harvesting arrays displaying switchable catalytic properties and with potential uses in solar energy conversion and photonic devices.
Suggested Citation
Alejo M. Lifschitz & Ryan M. Young & Jose Mendez-Arroyo & Charlotte L. Stern & C. Michael McGuirk & Michael R. Wasielewski & Chad A. Mirkin, 2015.
"An allosteric photoredox catalyst inspired by photosynthetic machinery,"
Nature Communications, Nature, vol. 6(1), pages 1-8, May.
Handle:
RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms7541
DOI: 10.1038/ncomms7541
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