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Towards a Series of Design Rules for Homogeneous Catalysis: Synergy Between Experiment and Theory

走向一系列均相催化的设计规则：实验与理论的协同

基本信息

批准号：
EP/H030077/2
负责人：
Gregory Chass
金额：
$ 4.26万
依托单位：
Queen Mary University of London
依托单位国家：
英国
项目类别：
Research Grant
财政年份：
2012
资助国家：
英国
起止时间：
2012 至无数据
项目状态：
已结题

来源：
https://gtr.ukri.org/projects?ref=EP%2FH030077%2F2
关键词：
Towards Series Design Rules Homogeneous

项目摘要

Despite currently shrinking energy supplies and growing industrial environmental impact, demand continues to rise for products manufactured under forcing conditions (eg. high temperature, pressure), often in the presence of toxic solvents. Industry is continually searching for novel means to reducing production expense and environmental impact. The lack of transferability between existing solutions entails starting anew for each class of reactions. Rational design and optimisation of efficient catalysts presents a solution; it also represents one of the ultimate challenges in the molecular sciences, particularly for homogeneous systems. Catalysis has the highest industrial and environmental impact, opening up never-before-possible ways of creating new bonds and compounds besides imparting pollution reduction and energy efficiency to existing processes.A proposal is made to initiate a novel research line to establishing a central methodology towards characterising homogeneous cross-coupling catalysts, by experiment and theory, towards adding to a growing body of 'design rules' thereof. Focus involves the theoretical characterisation of 2 differing cross-coupling mechanisms. Subsequent wavefunction and electronic structure analyses will be carried-out jointly with collaborators. Both the desired product (cross-coupling) and main side-product (arising from beta-hydride elimination) formations will be studied, for selected Ni and Pd-containing systems. Catalyst samples as well as complexes and variations thereof will be synthesised and their reactivities characterised by project collaborators. Results will aid the candidates concurrent pioneering of theory-designed neutron spectroscopy (NS) experiments to quantify substituent alkyl-group dynamics and their coupling to catalyst flexibility, substrate coordination and electronic structure at the catalytic centre.An EPSRC award would be strategic in helping the candidate contribute to the rational optimisation and design of cross-coupling catalysts and to extend the application of NS. The project would be instrumental in establishing the candidate as a world authority in the theoretical and spectroscopic characterisation of existing homogeneous catalysts and design of novel catalysts.This is a demanding project with the objective of advancing the rational design of highly active cross-coupling catalysts, apriori using computation. Therefore, a fundamental understanding at the molecular level of the steric and electronic nature of the ligand and metal centre is essential. Since most organic reactions take place in solvent and not in a vacuum or a static dielectric field, it is pivotal (no matter how challenging!), to develop an accurate method for including the effect of solvent. As the candidate has already co-authored several high-impact publications in this area, this project will focus on the realisation of catalysed reactions in the presence of a reliable explicit solvent model. The findings of the above program of research will be of vast interest to the wider physical, theoretical, synthetic and industrial communities, as witnessed by the recent publicity detailed from ISI Web of Science searches and the candidate's own co-corresponded work highlighted in the September 2009 issue of C&E News.

尽管目前能源供应萎缩，工业对环境的影响日益严重，但对在强制条件下生产的产品的需求仍在继续上升。高温、高压)，常在有毒溶剂中存在。工业一直在寻找新的方法来降低生产成本和环境影响。由于现有溶液之间缺乏可转移性，每一类反应都需要重新开始。合理设计和优化高效催化剂提供了解决方案；它也代表了分子科学的终极挑战之一，特别是对于均相系统。催化对工业和环境的影响最大，除了减少污染和提高现有工艺的能源效率外，还开辟了前所未有的方法来创造新的化学键和化合物。提出了一项新的研究建议，通过实验和理论建立一种描述均质交叉偶联催化剂的中心方法，并将其添加到不断增长的“设计规则”中。重点涉及两种不同交叉耦合机制的理论特征。后续的波函数和电子结构分析将与合作者共同进行。对于选定的含Ni和含pd体系，将研究所需产物（交叉偶联）和主要副产物（由-氢化物消除产生）的形成。催化剂样品以及配合物及其变体将被合成，其反应性由项目合作者表征。这些结果将有助于候选人同时开创理论设计的中子光谱（NS）实验，以量化取代基烷基动力学及其与催化剂柔韧性、底物配位和催化中心电子结构的耦合。EPSRC奖将有助于候选人对交叉偶联催化剂的合理优化和设计做出贡献，并扩大NS的应用范围。该项目将有助于将候选人建立为现有均相催化剂的理论和光谱表征以及新催化剂设计方面的世界权威。这是一个要求很高的项目，目的是通过计算先验地推进高活性交叉偶联催化剂的合理设计。因此，在分子水平上对配体和金属中心的空间和电子性质有一个基本的了解是必不可少的。由于大多数有机反应都是在溶剂中进行的，而不是在真空或静态介质场中进行的，因此开发一种包括溶剂影响的精确方法是至关重要的（无论多么具有挑战性！）。由于候选人已经在该领域共同撰写了几篇高影响力的出版物，因此该项目将侧重于在可靠的显式溶剂模型存在下实现催化反应。上述研究项目的发现将对更广泛的物理、理论、合成和工业社区产生巨大的兴趣，正如ISI Web of Science搜索最近的宣传和候选人自己在2009年9月的C&E News上强调的共同工作所证明的那样。

项目成果

期刊论文数量（10）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

Simplification through complexity: the role of Ni-complexes in catalysed diyne-cyclobutanone [4+2+2] cycloadditions, a comparative DFT study.

DOI：
10.1039/c2cp40067g
发表时间：
2012-04
期刊：
Physical chemistry chemical physics : PCCP
影响因子：
0
作者：
J. Tao;D. Fang;G. Chass
通讯作者：
J. Tao;D. Fang;G. Chass

Atomic and vibrational origins of mechanical toughness in bioactive cement during setting.

DOI：
10.1038/ncomms9631
发表时间：
2015-11-09
期刊：
Nature communications
影响因子：
16.6
作者：
Tian KV;Yang B;Yue Y;Bowron DT;Mayers J;Donnan RS;Dobó-Nagy C;Nicholson JW;Fang DC;Greer AL;Chass GA;Greaves GN
通讯作者：
Greaves GN

Quantum topological resolution of catalyst proficiency

催化剂能力的量子拓扑分辨率