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Rapid Photochromic Switching in a Rigid Polymer Matrix Using Living Radical Polymerization

机译:使用活性自由基聚合在刚性聚合物基质中进行快速光致变色转换

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Fast switching of a photochromic dye in a rigid host matrix has been achieved without any modification of electronic nature of the photochromic entity.The method utilizes living radical polymerization (atom transfer radical polymerization (ATRP)) to grow a low glass transition temperature (T_g) poly(n-butyl acrylate) polymer from a spirooxazine core,creating a low-T_g environment to cushion the photochromic dye while keeping the bulk matrix rigid.In these systems,decoloration speed of the photochromic (t_(1/2)) was reduced by 40-75% depending on the molecular weight of the poly(n-butyl acrylate) attached.We have demonstrated with this methodology a controlled tuning of photochromic switching.Coarse and fine tuning can be achieved by adjusting first the choice of polymer and second the molecular weight of the polymer.
机译:无需改变光致变色实体的电子性质即可实现在刚性主体基质中光致变色染料的快速转换。该方法利用活性自由基聚合(原子转移自由基聚合(ATRP))来生长低玻璃化转变温度(T_g)来自螺恶嗪核心的聚丙烯酸正丁酯聚合物,创造了一个低T_g环境以缓冲光致变色染料,同时保持整体基质刚性。在这些系统中,光致变色剂(t_(1/2))的脱色速度降低了取决于所连接的聚丙烯酸正丁酯的分子量,可以调节40-75%。我们已经证明了这种方法可以控制光致变色开关的调节,可以通过首先调节聚合物的选择,然后调节第二个来实现粗调和细调。聚合物的分子量。

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