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Rationally designed molecular D-A-D triad for piezochromic and acidochromic fluorescence on-off switching

机译:合理设计的分子D-A-D三元组,用于压变色和酸性变色荧光开关

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We report herein a new class of piezochromic luminescence (PCL) material with an acid stimulus response based on a donor (D)-acceptor (A)-donor (D) molecular triad, m-BHHDCS (1), synthesized via a rational design strategy. Acid-responsive harmane derivatives were rationally introduced into the unique D-A-D platform to obtain dual-stimuli responsive properties, i.e. acidochromic and piezochromic behaviors. Upon exposure to mechanical force and/or acid treatment, the pristine powders of 1 showed rapid and instant fluorescence turn-on with discernible intensity (Φ_(1B) = 9% and Φ_(1C) = 5%, respectively). In order to test more practical applications, we utilized light as a stimulus source using a photo-acid generator (PAG) instead of acid, and thus successfully demonstrated an intriguing optical recording medium orthogonally activated by mechanical force and light. Moreover, based on the in-depth combined experimental and computational studies, we could conclude that the dual-stimuli responsive properties of 1 originated from a structurally controlled photo-induced electron transfer (PET) process in the molecular assemblies, that is inhibited by mechanical force and acid. Mechanical force destroys the characteristic stacked structure, so that the ultrafast PET is inhibited and fluorescence is recovered. In contrast, acid covalently binds to the harmane appendages in the specific stacked arrangement of 1, which efficiently blocks PET. We believe that this system will inspire the development of a new class of smart PCL materials, and furthermore provide important insights into solid-state emission and stimuli-response behaviors.
机译:我们在这里报告了一种新型的压致变色发光(PCL)材料,其基于通过合理设计合成的供体(D)-受体(A)-供体(D)分子三元组m-BHHDCS(1)具有酸刺激响应战略。将对酸有响应的harmane衍生物合理地引入独特的D-A-D平台中,以获得双重刺激的响应特性,即酸致变色和压致变色行为。受到机械力和/或酸处理后,原始粉末1的荧光强度迅速且立即打开(可分辨强度分别为Φ_(1B)= 9%和Φ_(1C)= 5%)。为了测试更实际的应用,我们使用光作为光致酸产生剂(PAG)代替酸的刺激源,从而成功地展示了一种由机械力和光正交激活的有趣的光学记录介质。此外,基于深入的实验和计算研究,我们可以得出结论,1的双重刺激响应特性源自分子组件中结构受控的光诱导电子传递(PET)过程,该过程受机械抑制。力和酸。机械力破坏了特有的堆叠结构,因此超快PET被抑制并恢复了荧光。相比之下,酸以1的特定堆叠结构共价结合到harmane附属物上,从而有效地阻断了PET。我们相信,该系统将激发新型智能PCL材料的开发,并进一步提供对固态发射和刺激响应行为的重要见解。

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