“…Metallacycles have been successfully applied in traditional domains encompassing organic transformations and catalysis, [42][43][44][45][46][47][48] especially the catalytic activation of C-H bonds in unreactive alkanes, [49][50][51] and the stabilization of reactive intermediates. 52,53 In addition, they have been employed in various other domains of materials science, for example as active units in sensors, 54,55 in anticancer agents and for other bioorganometallic applications, [56][57][58][59] as photophysical devices in organometallic light-emitting diodes, [60][61][62] for light harvesting and energy transfer such as in photovoltaic cells, 63 as gelators 64 and birefringents in liquid crystalline materials, 65,66 and as molecular 67,68 or crystalline switches. 69 Of note for the synthetic chemist, a variety of processes other than cyclometalation have been developed in order to prepare metallacycles, especially oxidative addition involving C-X bond activation (X = F, Cl, Br, I, OTf; see eq.…”