4.8 Review

Activation of unsaturated small molecules by bio-relevant multinuclear metal-sulfur clusters

Journal

COORDINATION CHEMISTRY REVIEWS
Volume 475, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.ccr.2022.214838

Keywords

Metal-sulfur cluster; Organometallic complex; Small molecules; Nitrogen; Carbon dioxide; Alkynes

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Metal-sulfur (M-S) clusters are a class of multi-metallic compounds with high affinity, forming various compounds with different nuclearities. Recent biochemical studies have elucidated the structures of native M-S clusters, allowing us to develop artificial catalysts superior to enzymes and for biologically inaccessible reactions. This review summarizes the progress in the reaction studies on synthetic M-S clusters for the activation and transformation of small molecules.
The high affinity of sulfur (S) for transition metal ions (M), as well as the flexible M-S bonding and bridging modes, enable the formation of a wide range of multi-metallic compounds called metal-sulfur (M-S) clusters. Even though M-S clusters tolerate various nuclearities in principle, the number of metals in molecular entities, particularly those applicable in catalytic reactions, are typically 4 or lower, while the highest number of 8 has been found in the biological N-2-reducing catalyst. Other than the N-2 reduction, M-S clusters in nature have been found in the conversion of small molecules such as CO2, CO, and H-2. With the detailed structures of these native M-S clusters elucidated by recent biochemical studies, we can take steps toward the development of artificial catalysts superior to enzymes and/or those for biologically inaccessible reactions, while another direction is to deeply understand the enzymatic reactions and their relationship between the M-S structures. Here we review the progress in the reaction studies on synthetic M-S clusters, focusing on their utility in the activation and transformation of small molecules. The main part of this review has been divided into three sections: i) transformations of N-2 and related small molecules, ii) reduction of CO2, and iii) transformations of organic small molecules. Remarkable recent progress includes the development of catalytic N-2-silylation toward N(SiMe3)(3) and CO2 reduction toward C-1-C-4 hydrocarbons. Tandem reduction and N-methylation of nitroarenes have also been accomplished in the last decade. Through the review process, the development of catalytic reactions by M-S clusters was found to be still challenging. Collaborative works among chemists who can synthesize M-S clusters, those who are skilled in developing homogeneous catalytic reactions, those having spectroscopic techniques, and theoretical chemists may provide new insights into this field. (c) 2022 Elsevier B.V. All rights reserved.

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