重新审视木质素酸解过程中 β-O-4 键裂解的机理。第 9 部分：愈创木酰型化合物的综合结果以及 C6-C3 型和 C6-C2 型化合物中溴阴离子和氯阴离子参与方式的差异

IF 1.7 4区农林科学 Q2 MATERIALS SCIENCE, PAPER & WOOD

Journal of Wood Chemistry and Technology Pub Date : 2024-02-17 DOI:10.1080/02773813.2024.2314477

Qiaoqiao Ye, Kyoko S. Katsumata, Toshihiro Komatsu, Tomoya Yokoyama

{"title":"重新审视木质素酸解过程中 β-O-4 键裂解的机理。第 9 部分：愈创木酰型化合物的综合结果以及 C6-C3 型和 C6-C2 型化合物中溴阴离子和氯阴离子参与方式的差异","authors":"Qiaoqiao Ye, Kyoko S. Katsumata, Toshihiro Komatsu, Tomoya Yokoyama","doi":"10.1080/02773813.2024.2314477","DOIUrl":null,"url":null,"abstract":"A phenolic β-O-4-type lignin model compound with a C6-C3-type side-chain and two guaiacyl nuclei and its derivatives were individually acidolyzed in aqueous 82 vol% 1,4-dioxane containing 0.2 mol/L...","PeriodicalId":17493,"journal":{"name":"Journal of Wood Chemistry and Technology","volume":"2 1","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2024-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Revisiting the mechanism of β-O-4 bond cleavage during acidolysis of lignin. Part 9: Comprehensive results for guaiacyl-type compounds and the difference in participation mode of bromide and chloride anions between C6-C3-type and C6-C2-type compounds\",\"authors\":\"Qiaoqiao Ye, Kyoko S. Katsumata, Toshihiro Komatsu, Tomoya Yokoyama\",\"doi\":\"10.1080/02773813.2024.2314477\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A phenolic β-O-4-type lignin model compound with a C6-C3-type side-chain and two guaiacyl nuclei and its derivatives were individually acidolyzed in aqueous 82 vol% 1,4-dioxane containing 0.2 mol/L...\",\"PeriodicalId\":17493,\"journal\":{\"name\":\"Journal of Wood Chemistry and Technology\",\"volume\":\"2 1\",\"pages\":\"\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2024-02-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Wood Chemistry and Technology\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1080/02773813.2024.2314477\",\"RegionNum\":4,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, PAPER & WOOD\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Wood Chemistry and Technology","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1080/02773813.2024.2314477","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, PAPER & WOOD","Score":null,"Total":0}

引用次数: 0

摘要

一种具有 C6-C3 型侧链和两个愈创木酰基核的酚类 β-O-4 型木质素模型化合物及其衍生物，在含有 0.2 mol/L 的 82 vol% 1,4- 二氧六环水溶液中被单独酸解。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

Revisiting the mechanism of β-O-4 bond cleavage during acidolysis of lignin. Part 9: Comprehensive results for guaiacyl-type compounds and the difference in participation mode of bromide and chloride anions between C6-C3-type and C6-C2-type compounds

A phenolic β-O-4-type lignin model compound with a C6-C3-type side-chain and two guaiacyl nuclei and its derivatives were individually acidolyzed in aqueous 82 vol% 1,4-dioxane containing 0.2 mol/L...

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

Journal of Wood Chemistry and Technology 工程技术-材料科学：纸与木材

CiteScore

3.70

自引率

20.00%

发文量

审稿时长

3 months

期刊介绍： The Journal of Wood Chemistry and Technology (JWCT) is focused on the rapid publication of research advances in the chemistry of bio-based materials and products, including all aspects of wood-based polymers, chemicals, materials, and technology. JWCT provides an international forum for researchers and manufacturers working in wood-based biopolymers and chemicals, synthesis and characterization, as well as the chemistry of biomass conversion and utilization. JWCT primarily publishes original research papers and communications, and occasionally invited review articles and special issues. Special issues must summarize and analyze state-of-the-art developments within the field of biomass chemistry, or be in tribute to the career of a distinguished researcher. If you wish to suggest a special issue for the Journal, please email the Editor-in-Chief a detailed proposal that includes the topic, a list of potential contributors, and a time-line.