烷烃官能化:最新进展

IF 20.3 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
{"title":"烷烃官能化:最新进展","authors":"","doi":"10.1016/j.ccr.2024.216175","DOIUrl":null,"url":null,"abstract":"<div><p>Despite the progress of alternative/renewable energy technologies (solar, wind, hydroelectric, geothermal, nuclear, hydrogen, bio, tidal and wave), still the fossil raw materials such as petroleum (crude oil), natural gas and coal remain the main source of energy. The major constituents of crude oil (<em>ca.</em> 20–50 %) and natural gas (<em>ca.</em> 95 % methane, 4 % ethane, 0.2 % propane and 0.02 % butane) are alkanes, which are stable molecules due to high bond dissociation enthalpy of C<sub>sp3</sub> − H (96–105 kcal/mol) and C<sub>sp3</sub> – C<sub>sp3</sub> (83–90 kcal/mol) bonds. Due to the low cost and high richness in carbon, alkanes are fundamental feedstocks in chemical industry and starting materials in the synthesis of value-added products. In contrast to unselective classic radical mechanism, the metal complex catalysed direct activation of chemical inert C<sub>sp3</sub> − H and C<sub>sp3</sub> – C<sub>sp3</sub> bonds in alkanes concerns extremely important synthetic transformations with high economic impact. This review is aimed to provide an overview on recent (2019–2023) advances in homogenous metal free and metal complex catalysed activation and functionalization of alkanes leading to C<img>C or C<sub>sp3</sub> − Element bonds. Instead of a comprehensive review, herein a special attention is focused on selected new synthetic strategies and reaction mechanisms in C<sub>sp3</sub> − H functionalization in alkanes.</p></div>","PeriodicalId":289,"journal":{"name":"Coordination Chemistry Reviews","volume":null,"pages":null},"PeriodicalIF":20.3000,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Alkane functionalization: Recent advances\",\"authors\":\"\",\"doi\":\"10.1016/j.ccr.2024.216175\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Despite the progress of alternative/renewable energy technologies (solar, wind, hydroelectric, geothermal, nuclear, hydrogen, bio, tidal and wave), still the fossil raw materials such as petroleum (crude oil), natural gas and coal remain the main source of energy. The major constituents of crude oil (<em>ca.</em> 20–50 %) and natural gas (<em>ca.</em> 95 % methane, 4 % ethane, 0.2 % propane and 0.02 % butane) are alkanes, which are stable molecules due to high bond dissociation enthalpy of C<sub>sp3</sub> − H (96–105 kcal/mol) and C<sub>sp3</sub> – C<sub>sp3</sub> (83–90 kcal/mol) bonds. Due to the low cost and high richness in carbon, alkanes are fundamental feedstocks in chemical industry and starting materials in the synthesis of value-added products. In contrast to unselective classic radical mechanism, the metal complex catalysed direct activation of chemical inert C<sub>sp3</sub> − H and C<sub>sp3</sub> – C<sub>sp3</sub> bonds in alkanes concerns extremely important synthetic transformations with high economic impact. This review is aimed to provide an overview on recent (2019–2023) advances in homogenous metal free and metal complex catalysed activation and functionalization of alkanes leading to C<img>C or C<sub>sp3</sub> − Element bonds. Instead of a comprehensive review, herein a special attention is focused on selected new synthetic strategies and reaction mechanisms in C<sub>sp3</sub> − H functionalization in alkanes.</p></div>\",\"PeriodicalId\":289,\"journal\":{\"name\":\"Coordination Chemistry Reviews\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":20.3000,\"publicationDate\":\"2024-09-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Coordination Chemistry Reviews\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0010854524005216\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Coordination Chemistry Reviews","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0010854524005216","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0

摘要

尽管替代/可再生能源技术(太阳能、风能、水能、地热能、核能、氢能、生物能、潮汐能和波浪能)不断进步,但石油(原油)、天然气和煤炭等化石原料仍然是主要的能源来源。原油(约占 20-50%)和天然气(约占 95%的甲烷、4%的乙烷、0.2%的丙烷和 0.02%的丁烷)的主要成分是烷烃,由于 Csp3 - H(96-105 kcal/mol)和 Csp3 - Csp3(83-90 kcal/mol)键的键离焓高,因此是稳定的分子。由于成本低、含碳量高,烷烃是化学工业的基本原料,也是合成高附加值产品的起始原料。与无选择性的经典自由基机理不同,金属复合物催化直接活化烷烃中的化学惰性 Csp3 - H 和 Csp3 - Csp3 键涉及极其重要的合成转化,具有很高的经济效益。本综述旨在概述最近(2019-2023 年)在均质无金属和金属络合物催化活化和官能化烷烃以形成 CC 或 Csp3 - 元键方面取得的进展。本文没有进行全面综述,而是特别关注烷烃中 Csp3 - H 功能化的部分新合成策略和反应机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Alkane functionalization: Recent advances

Alkane functionalization: Recent advances

Despite the progress of alternative/renewable energy technologies (solar, wind, hydroelectric, geothermal, nuclear, hydrogen, bio, tidal and wave), still the fossil raw materials such as petroleum (crude oil), natural gas and coal remain the main source of energy. The major constituents of crude oil (ca. 20–50 %) and natural gas (ca. 95 % methane, 4 % ethane, 0.2 % propane and 0.02 % butane) are alkanes, which are stable molecules due to high bond dissociation enthalpy of Csp3 − H (96–105 kcal/mol) and Csp3 – Csp3 (83–90 kcal/mol) bonds. Due to the low cost and high richness in carbon, alkanes are fundamental feedstocks in chemical industry and starting materials in the synthesis of value-added products. In contrast to unselective classic radical mechanism, the metal complex catalysed direct activation of chemical inert Csp3 − H and Csp3 – Csp3 bonds in alkanes concerns extremely important synthetic transformations with high economic impact. This review is aimed to provide an overview on recent (2019–2023) advances in homogenous metal free and metal complex catalysed activation and functionalization of alkanes leading to CC or Csp3 − Element bonds. Instead of a comprehensive review, herein a special attention is focused on selected new synthetic strategies and reaction mechanisms in Csp3 − H functionalization in alkanes.

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
Coordination Chemistry Reviews
Coordination Chemistry Reviews 化学-无机化学与核化学
CiteScore
34.30
自引率
5.30%
发文量
457
审稿时长
54 days
期刊介绍: Coordination Chemistry Reviews offers rapid publication of review articles on current and significant topics in coordination chemistry, encompassing organometallic, supramolecular, theoretical, and bioinorganic chemistry. It also covers catalysis, materials chemistry, and metal-organic frameworks from a coordination chemistry perspective. Reviews summarize recent developments or discuss specific techniques, welcoming contributions from both established and emerging researchers. The journal releases special issues on timely subjects, including those featuring contributions from specific regions or conferences. Occasional full-length book articles are also featured. Additionally, special volumes cover annual reviews of main group chemistry, transition metal group chemistry, and organometallic chemistry. These comprehensive reviews are vital resources for those engaged in coordination chemistry, further establishing Coordination Chemistry Reviews as a hub for insightful surveys in inorganic and physical inorganic chemistry.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信