碱化氮化碳上 TEMPO 介导的葡萄糖氧化选择性光催化生产葡萄糖酸

Jiu Wang, Qi Zhao, Zheng Li, Yejun Xiao, Xianwen Zhang, Na Zhong, Heng Zhao, Liquan Jing, Devis Di Tommaso, Rachel Crespo-Otero, Md Golam Kibria, Jinguang Hu
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引用次数: 0

摘要

生物质光提炼是一种很有前景的可持续清洁能源和高价值化学品生产方法。然而,由于难以将末端羟基转化为羧基,选择性地将葡萄糖转化为最有价值的衍生物--葡萄糖酸仍是一项重大挑战。在这里,我们证明了通过将聚合物氮化碳(CN)的碱化改性与 2,2,6,6- 四甲基哌啶-1-氧代(TEMPO)介导协同耦合,可实现高选择性葡萄糖光致再精制成葡萄糖酸,TEMPO 介导可促进葡萄糖酸 C6 位点上的伯醇基团氧化。密度泛函理论(DFT)计算证实了改性氯化萘在葡萄糖酸生产中性能的提高。当加入 TEMPO 时,优化后的光催化技术实现了 ∼ 100 % 的葡萄糖转化率和 > 30 % 的葡萄糖酸产量,创下了光催化葡萄糖酸生产的记录。这项工作展示了将光催化剂改性和氧化还原调解结合起来,为生物质光催化的高效光催化系统提供灵感的重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Selective photocatalytic glucaric acid production from TEMPO-mediated glucose oxidation on alkalized carbon nitride
Biomass photorefining is a promising approach for sustainable clean energy and high-value chemical production. However, selectively converting glucose into glucaric acid, the most valuable derivative, still poses a significant challenge due to the difficulty in transforming the terminal hydroxyl group into a carboxy group. Here, we demonstrate that highly selective glucose photorefining into glucaric acid can be achieved by synergistically coupling alkalizing modification of polymeric carbon nitride (CN) with 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) mediation, which promotes the oxidation of the primary alcohol group attached to the C6 site of gluconic acid. Density functional theory (DFT) calculations affirm the enhanced performance of modified CN in glucaric acid production. When medicated with TEMPO, the optimized photocatalysis achieves ∼ 100 % glucose conversion and > 30 % glucaric acid yield, setting a record for photocatalytic glucaric acid production. This work showcases the significance of combining photocatalyst modification and redox mediation for inspiring high-efficiency photocatalysis systems for biomass photorefining.
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