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Updated: May 29, 2025

Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes
Published on: April 1, 2013
Naphthalenediimide-Based Hybrid Material with Eu-Substituted Polyoxometalate: Photochromism, Near-Infrared
Silang Chen1,2, Qiuting Yang1,2, Xiang Shen1
1Yunnan Key Laboratory of Crystalline Porous Organic Functional Materials, College of Chemical and Materials Engineering, Qujing Normal University, Qujing 655011, China.
Abstract:
Designing and developing novel photochromic materials with additional functions such as photothermal conversion and photocatalysis are challenging but meaningful objectives. Crystalline naphthalenediimide (NDI)-based hybrids are an attractive class of multifunctional materials with fast-response photoinduced electron transfer and charge separation properties. They are promising photothermal conversion materials and photocatalysts. Herein, a novel hybrid material, EuPMo11O39(L)1.5(H2O)2]·DMA (EuMo-NDI) (L = N,N'-di(1-oxido-4-pyridyl)-1,4,5,8-naphthalenediimide), was prepared with a solvothermal method, integrating a photoactive NDI derivative and an Eu-substituted polyoxometalate. EuMo-NDI exhibits 0D structure with sensitive photochromic behavior under UV-vis light irradiation due to fast-response photoinduced electron transfer between its components. The colored EuMo-NDI sample demonstrated efficient near-infrared photothermal conversion due to the strong absorption of the photogenerated radical anion NDI•- and mixed valence heteropoly blue in the near-infrared region. Meanwhile, EuMo-NDI is easily excited in the presence of electron donors to form the radical species, which can activate inert O2 to superoxide radical O2•-. EuMo-NDI exhibited high photocatalytic activity for C-3 thiocyanation of indoles under mild conditions using white light as a driving force. This work provides an effective avenue to design novel photothermal conversion materials and photocatalysts using photochromic materials as platforms.
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