Isomerization, Protonation, and Hydrolysis Properties of Naphthalimide-Containing Spiropyran in Aqueous Media-Reference-Cited by-同舟云学术

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Isomerization, Protonation, and Hydrolysis Properties of Naphthalimide-Containing Spiropyran in Aqueous Media

Published:2024-08-31 Issue:36 Volume:128 Page:8797-8806
ISSN:1520-6106
Container-title:The Journal of Physical Chemistry B
language:en
Short-container-title:J. Phys. Chem. B

Author:

Shiraishi Yasuhiro¹²^ORCID,Oshima Taku¹,Hirai Takayuki¹

Affiliation:

1. Research Center for Solar Energy Chemistry and Division of Chemical Engineering, Graduate School of Engineering Science, Osaka University, Toyonaka 560-8531, Japan

2. Innovative Catalysis Science Division, Institute for Open and Transdisciplinary Research Initiatives (ICS-OTRI), Osaka University, Suita 565-0871, Japan

Funder

Ministry of Education, Culture, Sports, Science and Technology

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jpcb.4c03894

Reference42 articles.

1. Photochromism and reversible multiple internal transitions in some spiropyrans at low temperatures. Part I

2. Spiropyrans and Spirooxazines for Memories and Switches

3. Reversibly Photoswitchable Dual-Color Fluorescent Nanoparticles as New Tools for Live-Cell Imaging

4. Design of rewritable and read-only non-volatile optical memory elements using photochromic spiropyran-based salts as light-sensitive materials

5. Spiropyran as a Selective, Sensitive, and Reproducible Cyanide Anion Receptor

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