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甲烷的均相功能化。

Homogeneous Functionalization of Methane.

机构信息

The Scripps Energy & Materials Center, The Scripps Research Institute , Jupiter, Florida 33458, United States.

出版信息

Chem Rev. 2017 Jul 12;117(13):8521-8573. doi: 10.1021/acs.chemrev.6b00739. Epub 2017 May 1.

Abstract

One of the remaining "grand challenges" in chemistry is the development of a next generation, less expensive, cleaner process that can allow the vast reserves of methane from natural gas to augment or replace oil as the source of fuels and chemicals. Homogeneous (gas/liquid) systems that convert methane to functionalized products with emphasis on reports after 1995 are reviewed. Gas/solid, bioinorganic, biological, and reaction systems that do not specifically involve methane functionalization are excluded. The various reports are grouped under the main element involved in the direct reactions with methane. Central to the review is classification of the various reports into 12 categories based on both practical considerations and the mechanisms of the elementary reactions with methane. Practical considerations are based on whether or not the system reported can directly or indirectly utilize O as the only net coreactant based only on thermodynamic potentials. Mechanistic classifications are based on whether the elementary reactions with methane proceed by chain or nonchain reactions and with stoichiometric reagents or catalytic species. The nonchain reactions are further classified as CH activation (CHA) or CH oxidation (CHO). The bases for these various classifications are defined. In particular, CHA reactions are defined as elementary reactions with methane that result in a discrete methyl intermediate where the formal oxidation state (FOS) on the carbon remains unchanged at -IV relative to that in methane. In contrast, CHO reactions are defined as elementary reactions with methane where the carbon atom of the product is oxidized and has a FOS less negative than -IV. This review reveals that the bulk of the work in the field is relatively evenly distributed across most of the various areas classified. However, a few areas are only marginally examined, or not examined at all. This review also shows that, while significant scientific progress has been made, greater advances, particularly in developing systems that can utilize O, will be required to develop a practical process that can replace the current energy and capital intensive natural gas conversion process. We believe that this classification scheme will provide the reader with a rapid way to identify systems of interest while providing a deeper appreciation and understanding, both practical and fundamental, of the extensive literature on methane functionalization. The hope is that this could accelerate progress toward meeting this "grand challenge."

摘要

化学领域尚存的“重大挑战”之一是开发新一代、更廉价、更清洁的工艺,使天然气中大量蕴藏的甲烷能够替代或补充石油,成为燃料和化学品的来源。综述了 1995 年后报道的重点强调将甲烷转化为功能化产品的均相(气/液)体系。排除了不专门涉及甲烷功能化的气/固、生物无机、生物和反应体系。各种报告根据与甲烷直接反应涉及的主要元素进行分组。综述的核心是根据与甲烷的基本反应的机制和实际考虑,将各种报告分为 12 类。实际考虑基于所报道的系统是否可以仅基于热力学势直接或间接利用 O 作为唯一净反应剂。基于与甲烷进行链反应或非链反应以及使用计量试剂或催化物种的机制分类。非链反应进一步分为 CH 活化(CHA)或 CH 氧化(CHO)。定义了这些不同分类的依据。特别是,CHA 反应被定义为导致离散甲基中间体的与甲烷的基本反应,其中碳原子的形式氧化态(FOS)相对于甲烷保持不变,仍为- IV。相比之下,CHO 反应被定义为与甲烷的基本反应,其中产物的碳原子被氧化,其 FOS 小于- IV。本综述表明,该领域的大部分工作相对均匀地分布在分类的大多数领域。然而,一些领域仅被轻微检查,或者根本没有检查。本综述还表明,尽管已经取得了重大的科学进展,但要开发能够利用 O 的实用工艺,以取代当前能源和资本密集型的天然气转化工艺,还需要取得更大的进展。我们相信,这种分类方案将为读者提供一种快速识别感兴趣系统的方法,同时对甲烷功能化的广泛文献提供更深入的认识和理解,无论是实际的还是基础的。希望这可以加速实现这一“重大挑战”的进程。

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