Abstract
Artificial photosynthetic systems for solar energy conversion exploit both covalent and supramolecular chemistry to produce favorable arrangements of light-harvesting and redox-active chromophores in space. An understanding of the interplay between key processes for photosynthesis, namely light-harvesting, energy transfer, and photoinduced charge separation and the design of novel, self-assembling components capable of these processes are imperative for the realization of multifunctional integrated systems. We report our investigations on the potential of extended tetracationic cyclophane/perylene diimide systems as components for artificial photosynthetic applications. We show how the selection of appropriate heterocycles, as extending units, allows for tuning of the electron accumulation and photophysical properties of the extended tetracationic cyclophanes. Spectroscopic techniques confirm energy transfer between the extended tetracationic cyclophanes and perylene diimide is ultrafast and quantitative, while the heterocycle specifically influences the energy transfer related parameters and the acceptor excited state.
| Original language | English |
|---|---|
| Pages (from-to) | 15299-15307 |
| Number of pages | 9 |
| Journal | Journal of the American Chemical Society |
| Volume | 137 |
| Issue number | 48 |
| DOIs | |
| Publication status | Published - Dec 9 2015 |
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ASJC Scopus subject areas
- Chemistry(all)
- Catalysis
- Biochemistry
- Colloid and Surface Chemistry
Cite this
Energy and Electron Transfer Dynamics within a Series of Perylene Diimide/Cyclophane Systems. / Ryan, Seán T J; Young, Ryan M.; Henkelis, James J.; Hafezi, Nema; Vermeulen, Nicolaas A.; Hennig, Andreas; Dale, Edward J.; Wu, Yilei; Krzyaniak, Matthew D.; Fox, Athan; Nau, Werner M.; Wasielewski, Michael R; Stoddart, J. Fraser; Scherman, Oren A.
In: Journal of the American Chemical Society, Vol. 137, No. 48, 09.12.2015, p. 15299-15307.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Energy and Electron Transfer Dynamics within a Series of Perylene Diimide/Cyclophane Systems
AU - Ryan, Seán T J
AU - Young, Ryan M.
AU - Henkelis, James J.
AU - Hafezi, Nema
AU - Vermeulen, Nicolaas A.
AU - Hennig, Andreas
AU - Dale, Edward J.
AU - Wu, Yilei
AU - Krzyaniak, Matthew D.
AU - Fox, Athan
AU - Nau, Werner M.
AU - Wasielewski, Michael R
AU - Stoddart, J. Fraser
AU - Scherman, Oren A.
PY - 2015/12/9
Y1 - 2015/12/9
N2 - Artificial photosynthetic systems for solar energy conversion exploit both covalent and supramolecular chemistry to produce favorable arrangements of light-harvesting and redox-active chromophores in space. An understanding of the interplay between key processes for photosynthesis, namely light-harvesting, energy transfer, and photoinduced charge separation and the design of novel, self-assembling components capable of these processes are imperative for the realization of multifunctional integrated systems. We report our investigations on the potential of extended tetracationic cyclophane/perylene diimide systems as components for artificial photosynthetic applications. We show how the selection of appropriate heterocycles, as extending units, allows for tuning of the electron accumulation and photophysical properties of the extended tetracationic cyclophanes. Spectroscopic techniques confirm energy transfer between the extended tetracationic cyclophanes and perylene diimide is ultrafast and quantitative, while the heterocycle specifically influences the energy transfer related parameters and the acceptor excited state.
AB - Artificial photosynthetic systems for solar energy conversion exploit both covalent and supramolecular chemistry to produce favorable arrangements of light-harvesting and redox-active chromophores in space. An understanding of the interplay between key processes for photosynthesis, namely light-harvesting, energy transfer, and photoinduced charge separation and the design of novel, self-assembling components capable of these processes are imperative for the realization of multifunctional integrated systems. We report our investigations on the potential of extended tetracationic cyclophane/perylene diimide systems as components for artificial photosynthetic applications. We show how the selection of appropriate heterocycles, as extending units, allows for tuning of the electron accumulation and photophysical properties of the extended tetracationic cyclophanes. Spectroscopic techniques confirm energy transfer between the extended tetracationic cyclophanes and perylene diimide is ultrafast and quantitative, while the heterocycle specifically influences the energy transfer related parameters and the acceptor excited state.
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UR - http://www.scopus.com/inward/citedby.url?scp=84949571112&partnerID=8YFLogxK
U2 - 10.1021/jacs.5b10329
DO - 10.1021/jacs.5b10329
M3 - Article
AN - SCOPUS:84949571112
VL - 137
SP - 15299
EP - 15307
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
SN - 0002-7863
IS - 48
ER -