The optimization and modulation of the properties of photochromic compounds, such as their activation wavelengths and thermal relaxation half-lives (), are essential for their adaptation in various applications. In this work, we studied the effect of co-planarization of the rotary fragment of two photochromic hydrazones with the core of the molecule on their switching properties. The and isomers of both compounds exhibit red-shifted absorption bands relative to their twisted versions, allowing for their photoswitching using longer wavelengths of light. Additionally, the thermal half-lives of both hydrazones are drastically shortened from hundreds of years to days.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6996581 | PMC |
http://dx.doi.org/10.1002/open.201900340 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!