Photochromic behavior of diarylbenzene nanoparticles prepared by top-down and bottom-up approaches

The use of photochromic molecules as active elements in aggregates is very important for developing advanced materials in the next generation. Nanoparticle is one of the aggregate forms and has...

Fulgide dyes

This article outlines the general structures and photochromism characteristic of fulgide dyes and their most important related analogues. It provides an overview of synthetic routes to such derivatives in addition to exemplifying how typical structural variations influence photochromic behavior. A brief survey then follows, giving a flavor of the applications that have been – and continue to be – sought for them in the capacity of functional dyes.

Structure and Properties of 1,3,3-Trimethyl-6′-chlorospiro[indoline-2,2′-2H-chromene]

Indoline spiropyran containing an σ-acceptor chlorine atom in 6′ position of the 2H-chromene part of the molecule was synthesized and studied. The use of 1,2,3,3-tetramethyl-3H-indolium perchlorate as a starting compound made it possible to achieve higher product yields as compared to previous studies. The molecular structure of the compound was established by single crystal X-ray diffraction analysis. The features of the crystal structure and intermolecular interactions were investigated using CrystalExplorer17 software package. The photochromic behavior in acetonitrile solution was studied for the first time. It was found that the merocyanine form of spiropyran is characterized by an absorption maximum at 592 nm, which is 37 nm closer to the range of the “biological window” in comparison with the nitro-substituted analog.

Investigating Photochromic Behavior of Organic Dyes in Solution Form using Multilevel Factorial Design

Photochromic compounds, namely spiropyran, spirooxazine, and naphthopyran, have received much attention, because of their high potential applications in various industrial fields. The aim of this study is to understand the behavior of three photochromic dyes in solution form via statistical approach. The types of dyes and solvents were screened using multilevel factorial design. From the analysis of variance results, it was found that the types of dyes and solvents used as well as their interaction have significant effects on the absorbance and photostability. The naphthopyran compound displayed highest change in absorbance intensity, followed by spiropyran and spirooxazine, when dissolved in isopropanol separately. However, the spirooxazine is the most photostable dye compared to naphthopyran and spiropyran, with ethanol as the solvent. Copyright © 2021 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

BioAIEgens derived from rosin: how does molecular motion affect their photophysical processes in solid state?

The exploration of artificial luminogens with bright emission has been fully developed with the advancement of synthetic chemistry. However, many of them face problems like weakened emission in the aggregated state as well as poor renewability and sustainability. Therefore, the development of renewable and sustainable luminogens with anti-quenching function in the solid state, as well as to unveil the key factors that influence their luminescence behavior become highly significant. Herein, a new class of natural rosin-derived luminogens with aggregation-induced emission property (AIEgens) have been facilely obtained with good biocompatibility and targeted organelle imaging capability as well as photochromic behavior in the solid state. Mechanistic study indicates that the introduction of the alicyclic moiety helps suppress the excited-state molecular motion to enhance the solid-state emission. The current work fundamentally elucidates the role of alicyclic moiety in luminogen design and practically demonstrates a new source to large-scalely obtain biocompatible AIEgens.

BioAIEgens Derived from Rosin: How Does Molecular Motion Affect Their Photophysical Processes in Solid State?

<p>The exploration of artificial luminogens with bright emission has been fully developed with the advancement of synthetic chemistry. However, many of them face problems like weakened emission in the aggregated state as well as poor renewability and sustainability. Therefore, the development of renewable and sustainable luminogens with anti-quenching function in the solid state, as well as to unveil the key factors that influence their luminescence behavior become highly significant. Herein, a new class of natural rosin-derived luminogens with aggregation-induced emission property (AIEgens) have been facilely obtained with good biocompatibility and targeted organelle imaging capability as well as photochromic behavior in the solid state. Mechanistic study indicates that the introduction of the alicyclic moiety helps suppress the excited-state molecular motion to enhance the solid-state emission. The current work fundamentally elucidates the role of alicyclic moiety in luminogen design and practically demonstrates a new source to large-scalely obtain biocompatible AIEgens.</p>