Utilizing the intramolecular CH–N hydrogen bonding and the bulky substituents at the reactive carbons resulted in the development of photochromic diarylbenzene with both high photoreactivity and fast thermal back reactivity. Click to show full abstract
Utilizing the intramolecular CH–N hydrogen bonding and the bulky substituents at the reactive carbons resulted in the development of photochromic diarylbenzene with both high photoreactivity and fast thermal back reactivity.
               
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