A Survival Guide for the “Electro-curious”

化学
作者
Cian Kingston,Maximilian D. Palkowitz,Yusuke Takahira,Julien C. Vantourout,Byron K. Peters,Yu Kawamata,Phil S. Baran
出处
期刊:Accounts of Chemical Research [American Chemical Society]
卷期号:53 (1): 72-83 被引量:742
标识
DOI:10.1021/acs.accounts.9b00539
摘要

The appeal and promise of synthetic organic electrochemistry have been appreciated over the past century. In terms of redox chemistry, which is frequently encountered when forging new bonds, it is difficult to conceive of a more economical way to add or remove electrons than electrochemistry. Indeed, many of the largest industrial synthetic chemical processes are achieved in a practical way using electrons as a reagent. Why then, after so many years of the documented benefits of electrochemistry, is it not more widely embraced by mainstream practitioners? Erroneous perceptions that electrochemistry is a "black box" combined with a lack of intuitive and inexpensive standardized equipment likely contributed to this stagnation in interest within the synthetic organic community. This barrier to entry is magnified by the fact that many redox processes can already be accomplished using simple chemical reagents even if they are less atom-economic. Time has proven that sustainability and economics are not strong enough driving forces for the adoption of electrochemical techniques within the broader community. Indeed, like many synthetic organic chemists that have dabbled in this age-old technique, our first foray into this area was not by choice but rather through sheer necessity. The unique reactivity benefits of this old redox-modulating technique must therefore be highlighted and leveraged in order to draw organic chemists into the field. Enabling new bonds to be forged with higher levels of chemo- and regioselectivity will likely accomplish this goal. In doing so, it is envisioned that widespread adoption of electrochemistry will go beyond supplanting unsustainable reagents in mundane redox reactions to the development of exciting reactivity paradigms that enable heretofore unimagined retrosynthetic pathways. Whereas the rigorous physical organic chemical principles of electroorganic synthesis have been reviewed elsewhere, it is often the case that such summaries leave out the pragmatic aspects of designing, optimizing, and scaling up preparative electrochemical reactions. Taken together, the task of setting up an electrochemical reaction, much less inventing a new one, can be vexing for even seasoned organic chemists. This Account therefore features a unique format that focuses on addressing this exact issue within the context of our own studies. The graphically rich presentation style pinpoints basic concepts, typical challenges, and key insights for those "electro-curious" chemists who seek to rapidly explore the power of electrochemistry in their research.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Lucas的应助被负责听云采纳,获得10
1秒前
爱笑的女孩关注了科研通微信公众号
2秒前
2秒前
alice完成签到,获得积分10
2秒前
烟花的应助被ger采纳,获得10
2秒前
bye发布了新的文献求助10
2秒前
CodeCraft的应助被犹豫的大碗采纳,获得10
3秒前
爆米花的应助被yu采纳,获得10
3秒前
执着的枫叶完成签到 ,获得积分10
3秒前
4秒前
岸上牛完成签到,获得积分10
5秒前
寂11发布了新的文献求助10
6秒前
碧蓝千琴发布了新的文献求助10
6秒前
6秒前
Zero完成签到,获得积分10
7秒前
斯文败类的应助被淡然的大雁采纳,获得10
8秒前
添才aaa完成签到 ,获得积分10
9秒前
粥mi发布了新的文献求助10
9秒前
天天快乐的应助被Qim采纳,获得10
9秒前
9秒前
11秒前
ye发布了新的文献求助10
11秒前
寂11完成签到,获得积分10
12秒前
faye完成签到,获得积分10
13秒前
2799完成签到,获得积分10
13秒前
13秒前
CodeCraft的应助被4435采纳,获得10
14秒前
15秒前
汉堡包的应助被胡尾声采纳,获得10
15秒前
aajhajkahna举报李晓北的求助涉嫌违规
15秒前
张日国完成签到,获得积分10
16秒前
222发布了新的文献求助10
16秒前
砺行的应助被gzhoax采纳,获得10
17秒前
18秒前
粥mi完成签到,获得积分10
19秒前
alex完成签到,获得积分10
19秒前
科研通AI6.2的应助被lin采纳,获得10
19秒前
风雨枫完成签到,获得积分10
20秒前
wnan_07发布了新的文献求助10
20秒前
酷波er的应助被流光采纳,获得10
20秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Energie-Contracting 1500
Klimaschutzrecht durch den Energiesektor im Mehrebenensystem – Ein Rechtsvergleich 1000
Stochastic Models in Operations Research,Vol. 2 600
Critical Bildung: Hegel and the Logic of Diremption 500
桑白皮エキスの実験的, 臨床的育毛効果について 500
Qualitative Methodologies in Tourism Studies: Disrupting and Co-creating Critical Research 350
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 工程类 有机化学 化学工程 生物化学 物理 复合材料 内科学 催化作用 光电子学 人工智能 细胞生物学 无机化学 物理化学 数学
热门帖子
关注 科研通微信公众号,转发送积分 8038616
求助须知:如何正确求助?哪些是违规求助? 9473614
关于积分的说明 21267021
捐赠科研通 7607660
什么是DOI,文献DOI怎么找? 3390729
关于科研通互助平台的介绍 2522310
邀请新用户注册赠送积分活动 2428215