Negative photochromism, in which a thermally stable colored form isomerizes to the transient colorless form by light irradiation and the back reaction occurs thermally, is advantageous in its applications for photoswitching materials because visible light can cause the photochromic color change of the materials. Moreover, the photochromic color change can be induced even on the inside of the materials due to the absence of the reabsorption of the visible excitation light by the photogenerated colorless species. While several negative photochromic compounds have been reported, the time scales of the back reaction are still slower than minutes, and no available fast responsive negative photochromic compounds have been reported. Here, we developed a negative photochromic 1,1'-binaphthyl-bridged phenoxyl-imidazolyl radical complex (BN-PIC) which enables fast photoswitching by visible light. The stable colored BN-PIC shows instantaneous decoloration by visible light irradiation, and the photogenerated colorless form thermally reverts to the initial colored form with a half-life of 1.9 s at room temperature. BN-PIC can also cause the drastic change in the chiroptical properties by the photochromic reaction, and the rate of the thermal back reaction is affected by the chirality of the solvent. Since the negative photochromic reaction can occur on the inside of the materials, the fast negative photochromism is expected to have an impact in the fields of photoresponsive materials of solid states and molecular aggregates.

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A colored hybrid based on a merocyanine adsorbed in a nanoporous-silica-composed dendritic fibrous silica was prepared by adsorption onto the nanoporous silica from a spiropyran solution during UV irradiation (photoinduced adsorption). The obtained red hybrid thus exhibited negative photochromism by visible-light irradiation. The hybrid was further combined with an organophilic clay by a solid-state mixing without using solvent to achieve excellent reversibility of the color change, which was thought to be achieved by molecular diffusion through the two materials, where nanoporous silica and organophilic clay accommodated the colored (merocyanine) and colorless (photogenerated spiropyran) isomers, respectively.

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Anti-1,8-bisTPI-naphthalene in which two imidazole rings are constrained to an anti-conformation leading to the first-formed 1,4'-isomer of the bridged imidazole dimer has been synthesized. The color of the radicals is different from that of the previously reported bridged-imidazolyl radicals because the intramolecular interaction between the radicals becomes weak due to the anti-conformation. This molecular design would be a profitable strategy to control the color of the radicals of the bridged imidazole dimer for application in ophthalmic lenses.

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