Transition Metal Alkane Sigma Complexes by Solid-Gas Synthesis Routes: Defining and Exploiting a New Area of Organometallic Chemistry

固-气合成路线的过渡金属烷烃西格玛配合物：定义和开发有机金属化学的新领域

基本信息

批准号：
EP/K035908/1
负责人：
Andrew Weller
金额：
$ 34.9万
依托单位：
University of Oxford
依托单位国家：
英国
项目类别：
Research Grant
财政年份：
2013
资助国家：
英国
起止时间：
2013 至无数据
项目状态：
已结题

来源：
https://gtr.ukri.org/projects?ref=EP%2FK035908%2F1
关键词：
Transition Metal Alkane Sigma Complexes

项目摘要

Alkanes are cheap and readily available chemicals and a long-term goal of chemical research has been to develop methods to exploit these species directly as chemical feedstocks. This would greatly improve the overall efficiency of chemical synthesis used in the production of commodity and fine chemicals that underpin the chemical and pharmaceutical industries. In order to achieve this goal the means to "activate" (i.e. break) the notoriously unreactive C-H bond is required. While examples of such C-H activation with transition metal complexes have been reported in recent years, much more information on this process is required before the integration of C-H activation into chemical synthesis is fully realised. Much useful insight could be gained by studying the way an alkane interacts with a metal centre prior to actually cleaving the C-H bond. This requires the means to prepare and study such so-called 'transition metal alkane sigma complexes'; however, until recently, examples of such species have been extremely limited due to the lack of straightforward and predictable general methods of preparation. Very recently the Weller (experimental chemistry) and Macgregor (computational modelling) research groups have reported a breakthrough in the synthesis and characterisation of transition metal alkane sigma complexes (see Science 2012, 337, 1648). Our approach was to react a transition metal alkene precursor in the crystalline solid-state with hydrogen gas. This produces the equivalent alkane sigma-complex directly in the crystalline state, allowing for its full characterisation by a variety of experimental and complementary computational techniques. This represents a step-change in current state-of-the-art for the synthesis and characterization of transition metal alkane sigma-complexes, opening up the exciting prospect that, for the first time, such species could be routinely synthesized and their chemistry fully understood.This research proposal seeks support for the Weller and Macgregor groups to fully explore and generalise the new gas-solid synthetic methodology for the synthesis of transition metal alkane sigma-complexes. Our approach will involve experimental synthesis and characterisation allied with the computational modelling; with the latter also providing structural data that are difficult to routinely obtain by experimental means. In addition computational modelling can be used to predict how strong the transition metal-alkane interaction will be. In this way the calculations will be able to target the most promising combinations for further study experimentally, thus significantly enhancing the overall productivity of the project. From our understanding of what makes a transition metal alkane sigma complex stable in the solid state we will then move to develop systems that are also stable in solution in order to provide definitive data on the properties and reactivity (i.e. C-H activation) of such species. Another exciting possibility will be to explore what other chemical transformations occur in the gas-solid regime; for example the commercially important catalytic hydrogenation of alkenes may occur in the solid state, without the need to revert to the use of solvents.The research in this project is fundamental in nature, however it will deliver significant long-term legacy through developing the chemistry of transition metal alkane sigma-complexes and how such species relates to the key C-H activation process. It will also explore the development of solid-state organometallic chemistry, both in terms of making new organometallic supramolecular complexes, but also, more generally, by exploring the potential of new catalytic processes (especially solid-gas reactions) in the solid state.

烷烃是廉价且容易获得的化学品，化学研究的长期目标是开发直接利用这些物质作为化学原料的方法。这将大大提高用于生产支撑化学和制药行业的商品和精细化学品的化学合成的整体效率。为了实现这一目标，需要“激活”（即断裂）众所周知的不活泼的 C-H 键的方法。虽然近年来报道了用过渡金属配合物进行 C-H 活化的例子，但在完全实现 C-H 活化与化学合成的整合之前，还需要更多有关该过程的信息。通过研究烷烃在实际裂解 C-H 键之前与金属中心相互作用的方式，可以获得许多有用的见解。这需要制备和研究这种所谓的“过渡金属烷烃西格玛配合物”的方法；然而，直到最近，由于缺乏直接且可预测的一般制备方法，此类物种的例子还极其有限。最近，Weller（实验化学）和 Macgregor（计算建模）研究小组报告了过渡金属烷烃 σ 配合物的合成和表征方面的突破（参见 Science 2012, 337, 1648）。我们的方法是使结晶固态的过渡金属烯烃前体与氢气反应。这会直接在结晶状态下产生等效的烷烃西格玛复合物，从而可以通过各种实验和补充计算技术对其进行全面表征。这代表了过渡金属烷烃西格玛配合物的合成和表征的当前最先进技术的一个阶段性变化，开辟了令人兴奋的前景，首次可以常规合成此类物质并完全了解其化学性质。该研究计划寻求Weller和Macgregor小组的支持，以充分探索和推广用于合成过渡金属烷烃西格玛络合物的新气固合成方法。我们的方法将涉及与计算建模相结合的实验合成和表征；后者还提供了难以通过实验手段常规获得的结构数据。此外，计算模型可用于预测过渡金属-烷烃相互作用的强度。通过这种方式，计算将能够针对最有希望的组合进行进一步的实验研究，从而显着提高项目的整体生产力。根据我们对过渡金属烷烃西格玛络合物在固态下稳定的原因的理解，我们将着手开发在溶液中也稳定的系统，以便提供有关此类物质的性质和反应性（即 C-H 活化）的明确数据。另一个令人兴奋的可能性是探索气固状态中发生的其他化学转变；例如，商业上重要的烯烃催化氢化可以在固态下进行，而无需重新使用溶剂。该项目的研究本质上是基础性的，但它将通过开发化学技术带来重要的长期遗产过渡金属烷烃西格玛络合物的形成以及此类物质如何与关键的 C-H 活化过程相关。它还将探索固态有机金属化学的发展，不仅在制造新的有机金属超分子配合物方面，而且更广泛地，通过探索固态下新催化过程（特别是固气反应）的潜力。