Photoinduced transfer hydrogenation of nitrogen to ammonia using a Mo-catalyst and a Hantzsch ester donor is demonstrated with and without an Ir-photoredox co-catalyst

催化作用 光催化 化学 光催化 过电位 光化学 乙腈 氧化还原 背景(考古学) 组合化学 氨生产 氮气 有机化学 电化学 古生物学 电极 物理化学 生物
作者
Christian Johansen,Emily Boyd,Jonas C. Peters
标识
DOI:10.26434/chemrxiv-2022-sn16v
摘要

Whereas photoredox catalysis using molecular systems enjoys considerable utility in small molecule transformations and reactions relevant to organic synthesis, to date there are no related examples of photodriven catalytic nitrogen fixation. We wondered whether a photoinduced transfer hydrogenation strategy might provide a viable pathway toward such a reaction. Hantzsch esters (and related organic structures) offer an opportunity for catalysis design in this context as they can behave as photoreductants, though to our knowledge they had yet to be shown to be compatible with such a redox intensive process (6 e–/6 H+). In the present study we demonstrate that fully reduced Hantzsch esters (abbreviated as HEH2) successively deliver stored H2-equivalents to N2, producing NH3 catalytically, in the presence of a molecular precatalyst (Mo) under blue-light irradiation but otherwise ambient conditions. While not required for the observed photocatalysis, the addition of a photoredox catalyst (Ir) to the reaction mixture enhances both the rate and turnover number of the net transformation. Encouraging with respect to future studies toward recycling the donor, electrochemically or via hydrogenation, other N-heterocycle H2-donors are also compatible with catalysis in the presence of the photoredox catalyst. The reduction of N2 to NH3 by HEH2 or H2 are thermodynamically very similar (ΔΔGf(NH3) = 1.8 kcal mol–1 in acetonitrile). However, whereas the combination of H2 with N2 to produce NH3 is accomplished via high temperature and pressure over a metal catalyst, the needed overpotential to drive the reduction of N2 by HEH2 can instead be derived from light. This study hence illustrates a promising photoredox catalysis approach toward deep reduction of robust small molecule substrates via photoinduced transfer hydrogenation, with the complete reduction of the triple bond of N2 providing a vivid example.

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

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
Owen应助braving采纳,获得10
刚刚
刚刚
sta完成签到,获得积分20
刚刚
1秒前
英勇飞机发布了新的文献求助10
1秒前
2秒前
3秒前
JAJ发布了新的文献求助10
4秒前
嘻嘻应助小金鱼采纳,获得10
4秒前
小芋泥完成签到,获得积分10
5秒前
展锋发布了新的文献求助10
5秒前
呆萌的雁桃完成签到,获得积分10
6秒前
英俊的铭应助ytttt采纳,获得30
6秒前
7秒前
默默采枫完成签到,获得积分20
7秒前
QH完成签到,获得积分10
7秒前
nevermeant发布了新的文献求助30
8秒前
小马甲应助金玉采纳,获得10
8秒前
在水一方应助宋佳珍采纳,获得10
8秒前
Georges-09发布了新的文献求助10
8秒前
8秒前
负责斑马发布了新的文献求助10
9秒前
加百莉发布了新的文献求助10
9秒前
桐桐应助XH采纳,获得10
10秒前
11秒前
11秒前
大维C完成签到,获得积分10
12秒前
小芋泥发布了新的文献求助10
12秒前
12秒前
12秒前
HYC完成签到,获得积分10
13秒前
明亮依波完成签到,获得积分10
13秒前
MAO发布了新的文献求助10
14秒前
爆米花应助正常采纳,获得10
14秒前
14秒前
ZZhou完成签到,获得积分10
14秒前
所所应助炫炫炫采纳,获得10
15秒前
小解发布了新的文献求助10
15秒前
默默采枫发布了新的文献求助10
16秒前
爬坑的良完成签到,获得积分10
16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
On the Angular Distribution in Nuclear Reactions and Coincidence Measurements 1000
Vertébrés continentaux du Crétacé supérieur de Provence (Sud-Est de la France) 600
A complete Carnosaur Skeleton From Zigong, Sichuan- Yangchuanosaurus Hepingensis 四川自贡一完整肉食龙化石-和平永川龙 600
FUNDAMENTAL STUDY OF ADAPTIVE CONTROL SYSTEMS 500
微纳米加工技术及其应用 500
Nanoelectronics and Information Technology: Advanced Electronic Materials and Novel Devices 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 物理化学 基因 遗传学 催化作用 冶金 量子力学 光电子学
热门帖子
关注 科研通微信公众号,转发送积分 5308630
求助须知:如何正确求助?哪些是违规求助? 4453704
关于积分的说明 13857839
捐赠科研通 4341445
什么是DOI,文献DOI怎么找? 2383900
邀请新用户注册赠送积分活动 1378533
关于科研通互助平台的介绍 1346495