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通过分解为氮化物配合物实现固氮

Nitrogen Fixation via Splitting into Nitrido Complexes.

作者信息

Forrest Sebastian J K, Schluschaß Bastian, Yuzik-Klimova Ekaterina Y, Schneider Sven

机构信息

Institut für Anorganische Chemie, Universität Göttingen, Tammannstrasse 4, D-37077 Göttingen, Germany.

出版信息

Chem Rev. 2021 Jun 9;121(11):6522-6587. doi: 10.1021/acs.chemrev.0c00958. Epub 2021 May 11.

Abstract

The large carbon footprint of the Haber-Bosch process, which provides ammonia for fertilizers but also the feedstock for all nitrogenous commercial products, has fueled the quest for alternative synthetic strategies to nitrogen fixation. Owing to the extraordinarily strong N≡N triple bond, the key step of the Haber-Bosch reaction, i.e., the dissociative adsorption of N, requires high temperatures. Since the first report in 1995, a wide variety of molecular transition metal and f-block compounds have been reported that can fully cleave N at ambient conditions and form well-defined nitrido complexes. We here provide a comprehensive survey of the current state of N splitting reactions in solution and follow-up nitrogen transfer reactivity. Particular emphasis is put on electronic structure requirements for the formation of suitable molecular precursors and their N-N scission reactivity. The prospects of N splitting for the synthesis of nitrogen containing products will be discussed, ranging from ammonia and heterocumulenes to organic amines, amides or nitriles via proton coupled electron transfer, carbonylation, or electrophilic functionalization of N derived nitrido complexes. Accomplishments and challenges for nitrogen fixation via N splitting are presented to offer guidelines for the development of catalytic platforms.

摘要

哈伯-博施(Haber-Bosch)工艺有着巨大的碳足迹,该工艺不仅为肥料提供氨,还为所有含氮商业产品提供原料,这推动了人们寻求固氮的替代合成策略。由于N≡N三键异常牢固,哈伯-博施反应的关键步骤,即N的解离吸附,需要高温。自1995年首次报道以来,已报道了多种分子过渡金属和f区化合物,它们能够在环境条件下完全裂解N并形成结构明确的氮化物配合物。我们在此全面综述了溶液中N裂解反应的现状以及后续的氮转移反应活性。特别强调了形成合适分子前体的电子结构要求及其N-N断裂反应活性。将讨论通过N裂解合成含氮产物的前景,包括通过质子耦合电子转移、羰基化或N衍生氮化物配合物的亲电官能化来合成氨、异累积烯、有机胺、酰胺或腈。本文还介绍了通过N裂解进行固氮的成果与挑战,为催化平台的开发提供指导。

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