The DOI matches its Crossref record.
Tuning Azoheteroarene Photoswitch Performance through Heteroaryl Design
Open accessAbstract
Abstract Photoswitchable compounds, which can be reversibly switched between two isomers by light, continue to attract significant attention for a wide array of applications. Azoheteroarenes represent a relatively new but understudied type of photoswitch, where one of the aryl rings from the conventional azobenzene class has been replaced with a five-membered heteroaromatic ring. Initial studies have suggested the azoheteroarenes─the arylazopyrazoles in particular─to have excellent photoswitching properties (quantitative switching and long Z isomer half-life). Here we present a systematic computational and experimental study to elucidate the origin of the long thermal half-lives and excellent addressability of the arylazopyrazoles, and apply this understanding to determine important structure–property relationships for a wide array of comparable azoheteroaryl photoswitches. We identify compounds with Z isomer half-lives ranging from seconds to hours, to days and to years, and variable absorption characteristics, all through tuning of the heteraromatic ring. Conformation perhaps plays the largest role in determining such properties: the compounds with the longest isomerization half-lives adopt a T-shaped ground state Z isomer conformation and proceed through a T-shaped isomerization pathway, whereas the most complete photoswitching is achieved for compounds that have a twisted (rather than T-shaped) Z isomer conformation. By balancing these factors, we report a new azopyrazole 3pzH, which can be quantitatively switched to its Z isomer (>98%) with 355 nm irradiation, near-quantitatively (97%) switched back to the E isomer with 532 nm irradiation, and has a very long half-life for thermal isomerization (t1/2 = 74 d at 25 °C). Given the large tunability of their properties, the predictive nature of their performance, and the other functional opportunities afforded by usage of a heteroaromatic system, we believe the azoheteroaryl photoswitches to have huge potential in a wide range of optically addressable applications.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cited by
Heteroaryl azo dyes as molecular photoswitches
Crespi, S., Simeth, N. A., & König, B. (2019) · Nature Reviews Chemistry · doi:10.1038/s41570-019-0074-6 · Cited by 650
Azobenzene-based solar thermal fuels: design, properties, and applications
Dong, L., Feng, Y., Wang, L., & Feng, W. (2018) · Chemical Society Reviews · doi:10.1039/c8cs00470f · Cited by 474
Recent Implementations of Molecular Photoswitches into Smart Materials and Biological Systems
Pianowski, Z. L. (2019) · Chemistry – A European Journal · doi:10.1002/chem.201805814 · Cited by 328
Expanding the Repertoire of Photoswitchable Unnatural Amino Acids for Enzyme Engineering
Hiefinger, C., Marcon, M., Pape, V., Casadevall, G., Lahmy, R., Haag, C., Nazet, J., Bartl, M., Bruckmann, A., Osuna, S., et al. (2025) · Angewandte Chemie International Edition · doi:10.1002/anie.202508562 · Cited by 5
Expanding the Repertoire of Photoswitchable Unnatural Amino Acids for Enzyme Engineering
Hiefinger, C., Marcon, M., Pape, V., Casadevall, G., Lahmy, R., Nazet, J., Bartl, M., Bruckmann, A., Osuna, S., König, B., et al. (2025) · doi:10.1101/2025.04.17.649278 · Cited by 2
Metadata
- Authors
- Calbo, J., Weston, C. E., White, A. J. P., Rzepa, H. S., Contreras-García, J., & Fuchter, M. J.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2017-01-13
- Volume
- 139
- Issue
- 3
- Pages
- 1261-1274
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W2562071635
- Cited by
- 428
- References
- 0
- FWCI
- 9.46
- Type
- journal article
- Language
- en
- Open access
- hybrid
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Tuning Azoheteroarene Photoswitch Performance through Heteroaryl Design. https://app.cochat.ai/papers/10.1021/jacs.6b11626
- The paper
- Calbo, J., Weston, C. E., White, A. J. P., Rzepa, H. S., Contreras-García, J., & Fuchter, M. J. (2017). Tuning Azoheteroarene Photoswitch Performance through Heteroaryl Design. Journal of the American Chemical Society. https://doi.org/10.1021/jacs.6b11626
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.