Autonomous reaction Pareto-front mapping with a self-driving catalysis laboratory

氢甲酰化 催化作用 吞吐量 标杆管理 计算机科学 化学 工艺工程 工程类 有机化学 电信 营销 业务 无线
作者
Jeffrey A. Bennett,Negin Orouji,Muhammad Babar Khan,Sina Sadeghi,Jordan Rodgers,Milad Abolhasani
出处
期刊: 卷期号:1 (3): 240-250 被引量:50
标识
DOI:10.1038/s44286-024-00033-5
摘要

Ligands play a crucial role in enabling challenging chemical transformations with transition metal-mediated homogeneous catalysts. Despite their undisputed role in homogeneous catalysis, discovery and development of ligands have proven to be a challenging and resource-intensive undertaking. Here, in response, we present a self-driving catalysis laboratory, Fast-Cat, for autonomous and resource-efficient parameter space navigation and Pareto-front mapping of high-temperature, high-pressure, gas–liquid reactions. Fast-Cat enables autonomous ligand benchmarking and multi-objective catalyst performance evaluation with minimal human intervention. Specifically, we utilize Fast-Cat to perform rapid Pareto-front identification of the hydroformylation reaction between syngas (CO and H2) and olefin (1-octene) in the presence of rhodium and various classes of phosphorus-based ligands. By reactor benchmarking, we demonstrate Fast-Cat's knowledge scalability, essential to fine/specialty chemical industries. We report the details of the modular flow chemistry platform of Fast-Cat and its autonomous experiment-selection strategy for the rapid generation of optimized experimental conditions and in-house data required for supplying machine-learning approaches to reaction and ligand investigations. A self-driving catalysis laboratory, Fast-Cat, is presented for efficient high-throughput screening of high-pressure, high-temperature, gas–liquid reaction conditions using rhodium-catalyzed hydroformylation as a case study. Fast-Cat is used to Pareto map the reaction space and investigate the varying performance of several phosphorus-based hydroformylation ligands.
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
天天快乐应助6and1采纳,获得10
刚刚
刚刚
斯文败类应助dmm采纳,获得10
刚刚
刚刚
刚刚
csu_zs完成签到,获得积分10
刚刚
1秒前
lancet完成签到,获得积分10
1秒前
积极璎完成签到,获得积分10
1秒前
嘟嘟发布了新的文献求助20
1秒前
烟花应助郭嘉仪采纳,获得10
1秒前
儒雅傲之发布了新的文献求助10
1秒前
打打应助星辰采纳,获得10
1秒前
小柯发布了新的文献求助10
2秒前
2秒前
漾漾的羊完成签到 ,获得积分10
2秒前
深情安青应助喵喵采纳,获得10
2秒前
风晓人情完成签到 ,获得积分10
2秒前
3秒前
ZY完成签到,获得积分10
3秒前
3秒前
meikoo完成签到 ,获得积分10
3秒前
4秒前
4秒前
马少洋发布了新的文献求助10
4秒前
4秒前
4秒前
4秒前
kevinarnett完成签到,获得积分10
5秒前
李xq完成签到,获得积分10
5秒前
喻白玉完成签到,获得积分10
5秒前
bingo完成签到,获得积分20
5秒前
5秒前
6秒前
Lucky牛发布了新的文献求助10
6秒前
向中恶发布了新的文献求助10
6秒前
6秒前
6秒前
6秒前
月晓风清发布了新的文献求助10
6秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(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
Matrix Methods in Data Mining and Pattern Recognition 510
Social Skills Improvement System-Rating Scales--Chinese Version 500
Dynamische Polarisation von H-1 und B-11 in (CH-3)-3NBH-3 500
CLSI M07 2024 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7248141
求助须知:如何正确求助?哪些是违规求助? 8871083
关于积分的说明 18715513
捐赠科研通 6927189
什么是DOI,文献DOI怎么找? 3198137
关于科研通互助平台的介绍 2373857
邀请新用户注册赠送积分活动 2172991