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通过亲核加成-消除策略靶向解锁木质素-碳水化合物酯的一锅法原木质素提取

One-Pot Protolignin Extraction by Targeted Unlocking Lignin-Carbohydrate Esters via Nucleophilic Addition-Elimination Strategy.

作者信息

Lou Yuhan, Sun Xinyue, Yu Yanyan, Zeng Suqing, Li Yilin, Liu Yongzhuang, Yu Haipeng

机构信息

Key Laboratory of Bio-Based Material Science and Technology of Ministry of Education, Northeast Forestry University, Harbin 150040, P. R. China.

出版信息

Research (Wash D C). 2023;6:0069. doi: 10.34133/research.0069. Epub 2023 Mar 9.

Abstract

Protolignin extraction can facilitate structure elucidation and valorization of lignin in biorefinery, but is rather challenging due to the complex chemical bonds present. Here, we developed the in situ generated NH-reline (IGNR) system to realize one-pot protolignin extraction from lignocellulose. In the IGNR system, reline consisting of choline chloride and urea acted as both a solvent and a nucleophile generator, and the nucleophilic addition-elimination mechanism was verified by model compound studies. The in situ generated NH could precisely cleave the lignin-carbohydrate esters in lignocellulose with a near-quantitative retention of carbohydrates. The extracted IGNR-Protolignin exhibited native lignin substructure with high molecular weight and high β-O-4' content (41.5 per 100 aromatic units). In addition, the up-scaled kilogram reaction demonstrated the feasibility of the IGNR system for potential industrial application in a green and sustainable pathway. This work represents a breakthrough toward protolignin extraction in practice with the future goal of achieving total biorefinery.

摘要

原木质素提取有助于生物炼制中木质素的结构解析和价值提升,但由于存在复杂的化学键,这一过程颇具挑战性。在此,我们开发了原位生成的NH-碱体系(IGNR),以实现从木质纤维素中一锅法提取原木质素。在IGNR体系中,由氯化胆碱和尿素组成的碱既作为溶剂又作为亲核试剂生成剂,通过模型化合物研究验证了亲核加成-消除机制。原位生成的NH能够精确切割木质纤维素中的木质素-碳水化合物酯,同时碳水化合物几乎能定量保留。提取的IGNR-原木质素呈现出具有高分子量和高β-O-4'含量(每100个芳香单元中含41.5个)的天然木质素亚结构。此外,扩大到千克级的反应证明了IGNR体系在绿色可持续途径中潜在工业应用的可行性。这项工作代表了原木质素提取在实践中的一项突破,未来目标是实现全生物炼制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3e6/10013968/3ce42ebee1d7/research.0069.fig.001.jpg

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