Transition Metal Chain Complexes Supported by Soft Donor Assembling Ligands

• Published in: Chemical reviews 2021-07, Vol.121 (13), p.7346-7397
• Main Authors: Braunstein, Pierre, Danopoulos, Andreas A
• Format: Article
• Language: English
• Subjects: Atomic properties; Bites; Chemical Sciences; Classification; Coordination chemistry; Coordination compounds; Ligands; Metals; Molecular chains; Oxidation; Periodic table; Phosphides; Phosphines; Transition metals
• ISSN: 0009-2665; 1520-6890
• DOI: 10.1021/acs.chemrev.0c01197

The chemistry of discrete molecular chains constituted by metals in low oxidation states, displaying metal–metal proximity and stabilized by suitable metal-bridging, assembling ligands comprising at least one soft donor atom is comprehensively reviewed; complexes with a single (hard or soft) bridging atom (e.g., μ-halide, μ-sulfide, or μ-PR2 etc.) as well as “closed” metal arrays (that fall in the realm of cluster chemistry) are excluded. The focus is on transition metal-based systems, with few excursions to cases combining transition and post-transition elements. Most relevant supporting ligands have neutral C, P, O, or S donor (mainly, N-heterocyclic carbene, phosphine, ether, thioether) or anionic donor (mainly phenyl, ylide, silyl, phosphide, thiolate) groups. A supporting-ligand-based classification of the metal chains is introduced, using as the classifying parameter the number of “bites” (i.e., ligand bridges) subtending each intermetallic separation. The ligands are further grouped according to the number of donor atoms interacting with the metal chain (called denticity in the following) and the column of the Periodic Table to which the set of donor atoms belongs (in ascending order). A complementary metal-based compilation of the complexes discussed is also provided in a concise tabular form.