The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.
Contemporary Issues in Electron Transfer Research
Abstract
This is an overview of some of the important, challenging, and problematic issues in contemporary electron transfer research. After a qualitative discussion of electron transfer, its time and distance scales, energy curves, and basic parabolic energy models are introduced to define the electron transfer process. Application of transition state theory leads to the standard Marcus formulation of electron transfer rate constants. Electron transfer in solution is coupled to solvent polarization effects, and relaxation processes can contribute to and even control electron transfer. The inverted region, in which electron transfer rate constants decrease with increasing exoergicity, is one of the most striking phenomena in electron transfer chemistry. It is predicted by both semiclassical and quantum mechanical models, with the latter appropriate if there are coupled high- or medium-frequency vibrations. The intramolecular reorganizational energy has different contributions from different vibrational modes, which, in favorable cases, can be measured on a mode-by-mode basis by resonance Raman spectroscopy. Alternatively, mode-averaging procedures are available for including multimode contributions based on absorption or emission spectra. Rate constants for intramolecular electron transfer depend on electronic coupling and orbital overlap and, therefore, on distance. Mixed-valence systems have provided an important experimental platform for investigating solvent and structural effects and the transition between localized and delocalized behavior. One of the important developments in electron transfer is the use of absorption and emission measurements to calculate electron transfer rate constants. Ultrafast electron transfer measurements have been used to uncover nonequilibrium relaxation effects, an area that presents special challenges to the understanding of the dynamics and relaxation of the coupled processes. Electron transfer in the gas phase offers substantial insights into the nature of the electron transfer process. Similarly, electron transport in conductive polymers and synthetic metals depends on the basic principles of electron transfer, with some special nuances of their own.
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Cites
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Jiao, Y., Zheng, Y., Jaroniec, M., & Qiao, S. Z. (2015) · Chemical Society Reviews · doi:10.1039/c4cs00470a · Cited by 5,388
Proton-coupled electron transfer
Huynh, M. H. V., & Meyer, T. J. (2007) · Chemical Reviews · doi:10.1021/cr0500030 · Cited by 1,659
Self-citationMolecular electronics: Some views on transport junctions and beyond
Joachim, C., & Ratner, M. A. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0500075102 · Cited by 522
Self-citationTay, N. E. S., Lehnherr, D., & Rovis, T. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00384 · Cited by 518
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Metadata
- Authors
- Barbara, P. F., Meyer, T. J., & Ratner, M. A.
- Venue
- The Journal of Physical Chemistry
- Publisher
- American Chemical Society (ACS)
- Published
- 1996-01-01
- Volume
- 100
- Issue
- 31
- Pages
- 13148-13168
- ISSN
- 0022-3654 (ISSN-L)
- 1541-5740
- OpenAlex
- W2022205840
- Cited by
- 1,558
- References
- 6
- FWCI
- 28.40
- Type
- journal article
- Language
- en
- Open access
- closed
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