Semicrystalline Poly(azobenzene) with Negative Photochromism for Photochemical Melting of Thick Samples

IF 5.1 Q1 POLYMER SCIENCE
Hantao Zhou, Jesus Guillen Campos, Rishabh Tennankore, Wenwen Xu, Yunfeng Hu, Javier Read de Alaniz, Ryan C. Hayward
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引用次数: 0

Abstract

Photomechanical effects based on photochemical transformations often suffer from challenges of restricted light penetration due to strong light attenuation, limiting their operation to micrometer-scale materials with relatively inefficient bending deformation modes. While recent reports have established semicrystalline poly(azobenzene)s as a promising class of photochemically responsive materials, strong absorption of UV light required to drive trans to cis isomerization has limited switching to within several micrometers of the surface. Negative photochromism offers a possible route to circumvent this limitation, as reversible photobleaching of the ground state absorption upon switching extends the light penetration. Herein, we report the synthesis and characterization of P(Cx-dFdC-azo), a negative photochromic semicrystalline poly(azobenzene) incorporating ortho-difluoro, dichloro-substituted azo photoswitches. These polymers exhibit near-quantitative bidirectional photoisomerization─92% conversion to cis under 617 nm irradiation and 96% conversion to trans under 405 nm irradiation, along with reversible photomelting and crystallization. Photorheological studies demonstrate a significant increase over which photomelting can be achieved, from <10 μm for conventional poly(azobenzene) to at least 300 μm for P(Cx-dFdC-azo), highlighting the potential of these materials for photochemically responsive materials with macroscopic dimensions.

Abstract Image

具有负光致变色的半晶聚偶氮苯用于厚样品的光化学熔化
基于光化学转化的光化学效应经常受到由于强烈的光衰减而限制光穿透的挑战,限制了它们在具有相对低效弯曲变形模式的微米尺度材料上的操作。虽然最近的报道已经建立了半晶聚偶氮苯作为一类有前途的光化学反应材料,但驱动反式到顺式异构化所需的强紫外线吸收限制了在表面几微米内的转换。负光致变色提供了一种可能的途径来规避这一限制,因为开关时基态吸收的可逆光漂白延长了光穿透。在此,我们报道了P(Cx-dFdC-azo)的合成和表征,P(Cx-dFdC-azo)是一种含有邻二氟二氯取代偶氮光开关的负光致变色半晶聚偶氮苯。这些聚合物表现出近定量的双向光异构化,在617 nm照射下92%转化为顺式,在405 nm照射下96%转化为反式,同时发生可逆的光熔化和结晶。光流变学研究表明,光敏化可以从传统聚(偶氮苯)的<;10 μm到P(cx - dfdc -偶氮)的至少300 μm显著增加,突出了这些材料具有宏观尺寸光化学反应材料的潜力。
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来源期刊
CiteScore
10.40
自引率
3.40%
发文量
209
审稿时长
1 months
期刊介绍: ACS Macro Letters publishes research in all areas of contemporary soft matter science in which macromolecules play a key role, including nanotechnology, self-assembly, supramolecular chemistry, biomaterials, energy generation and storage, and renewable/sustainable materials. Submissions to ACS Macro Letters should justify clearly the rapid disclosure of the key elements of the study. The scope of the journal includes high-impact research of broad interest in all areas of polymer science and engineering, including cross-disciplinary research that interfaces with polymer science. With the launch of ACS Macro Letters, all Communications that were formerly published in Macromolecules and Biomacromolecules will be published as Letters in ACS Macro Letters.
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