Constructing functional molecular systems for solar energy conversion and quantum information science requires a fundamental understanding of electron transfer in donor–bridge–acceptor (D–B–A) systems as well as competitive reaction pathways in acceptor–donor–acceptor (A–D–A) and acceptor–donor–acceptor′ (A–D–A′) systems. Herein we present a supramolecular complex comprising a tetracationic cyclophane having both phenyl-extended viologen (ExV 2+ ) and dipyridylthiazolothiazole (TTz 2+ ) electron acceptors doubly-linked by means of two p -xylylene linkers (TTzExVBox 4+ ), which readily incorporates a perylene (Per) guest in its cavity (Per ⊂ TTzExVBox 4+ ) to establish an A–D–A′ system, in which the ExV 2+ and TTz 2+ units serve as competing electron acceptors with different reduction potentials. Photoexcitation of the Per guest yields both TTz + ˙–Per + ˙–ExV 2+ and TTz 2+ –Per + ˙–ExV + ˙ in <1 ps, while back electron transfer in TTz 2+ –Per + ˙–ExV + ˙ proceeds via the unusual sequence TTz 2+ –Per + ˙–ExV + ˙ → TTz + ˙–Per + ˙–ExV 2+ → TTz 2+ –Per–ExV 2+ . In addition, selective chemical reduction of TTz 2+ gives Per ⊂ TTzExVBox 3+ ˙, turning the complex into a D–B–A system in which photoexcitation of TTz + ˙ results in the reaction sequence 2 *TTz + ˙–Per–ExV 2+ → TTz 2+ –Per–ExV + ˙ → TTz + ˙–Per–ExV 2+ . Both reactions TTz 2+ –Per + ˙–ExV + ˙ → TTz + ˙–Per + ˙–ExV 2+ and TTz 2+ –Per–ExV + ˙ → TTz + ˙–Per–ExV 2+ occur with a (16 ± 1 ps) −1 rate constant irrespective of whether the bridge molecule is Per + ˙ or Per. These results are explained using the superexchange mechanism in which the ionic states of the perylene guest serve as virtual states in each case and demonstrate a novel supramolecular platform for studying the effects of bridge energetics within D–B–A systems.
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Quantum Coherence in Ultrafast Photo-driven Charge Separation
Coherent interactions are prevalent in numerous photodriven processes, ranging from photosynthetic energy transfer to superexchange-mediated electron transfer, resulting in numerous studies aimed towards identifying and understanding these interactions. A key motivator of this interest is the non-statistical scaling laws that result from coherently traversing multiple pathways due to quantum interference. To that end, we employed ultrafast transient absorption spectroscopy to measure electron transfer in two donor-acceptor molecular systems comprising a p-(9-anthryl)-N,N-dimethylaniline chromophore/electron donor and either one or two equivalent naphthalene-1,8:4,5-bis(dicarboximide) electron acceptors at both ambient and cryogenic temperatures. The two-acceptor compound shows a statistical factor of 2.1 0.2 rate enhancement at room temperature and a non-statistical factor of 2.6 0.2 rate enhancement at cryogenic temperatures, suggesting correlated interactions between the two acceptors with the donor and with the bath modes. Comparing the charge recombination rates indicates that the electron is delocalized over both acceptors at low temperature but localized on a single acceptor at room temperature. These results highlight the importance of shielding the system from bath fluctuations to preserve and ultimately exploit the coherent interactions.
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- Award ID(s):
- 1710104
- NSF-PAR ID:
- 10088395
- Date Published:
- Journal Name:
- Faraday Discussions
- ISSN:
- 1359-6640
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Spear, John R. (Ed.)more » « less
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Acidianus sp. DS80 changed its core lipid composition when grown with different electron donor/acceptor pairs. We show that changes in energy and carbon metabolisms significantly affected the relative abundance of rings in the core lipids of DS80. These observations highlight the need to better constrain metabolic parameters, in addition to environmental factors, which may influence changes in membrane physiology in Archaea. Such consideration would be particularly important for studying archaeal lipids from habitats that experience frequent environmental fluctuations and/or where metabolically diverse archaea thrive. -
Electron transfer (ET) in donor–bridge–acceptor (DBA) compounds depends strongly on the structural and electronic properties of the bridge. Among the bridges that support donor–acceptor conjugation, alkyne bridges have attractive and unique properties: they are compact, possess linear structure permitting access to high symmetry DBA molecules, and allow torsional motion of D and A, especially for longer bridges. We report conformation dependent electron transfer dynamics in a set of novel DBA compounds featuring butadiyne (C4) bridge, N -isopropyl-1,8-napthalimide (NAP) acceptors, and donors that span a range of reduction potentials (trimethyl silane (Si-C4-NAP), phenyl (Ph-C4-NAP), and dimethyl aniline (D-C4-NAP)). Transient mid-IR absorption spectra of the CC bridge stretching modes, transient spectra in the visible range, and TD-DFT calculations were used to decipher the ET mechanisms. We found that the electronic excited state energies and, especially, the transition dipoles (S 0 → S n ) depend strongly on the dihedral angle ( θ ) between D and A and the frontier orbital symmetry, offering an opportunity to photo-select particular excited states with specific ranges of dihedral angles by exciting at chosen wavelengths. For example, excitation of D-C4-NAP at 400 nm predominantly prepares an S 1 excited state in the planar conformations ( θ ∼ 0) but selects an S 2 state with θ ∼ 90°, indicating the dominant role of the molecular symmetry in the photophysics. Moreover, the symmetry of the frontier orbitals of such DBA compounds not only defines the photo-selection outcome, but also determines the rate of the S 2 → S 1 charge separation reaction. Unprecedented variation of the S 2 –S 1 electronic coupling with θ by over four orders of magnitude results in slow ET at θ ca. 0° and 90° but extremely fast ET at θ of 20–60°. The unique features of high-symmetry alkyne bridged DBA structures enable frequency dependent ET rate selection and make this family of compounds promising targets for the vibrational excitation control of ET kinetics.more » « less
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1039/C8FD00218E
