RESUMEN
Over the past decade, significant research efforts have focused on osmapentalyne, characterized by the more reactive Os≡C7 (Carbon atoms numbered in a clockwise direction on the osmapentalyne skeleton), across areas encompassing electrophilic, nucleophilic, and addition reactions. Nevertheless, the reactivity of osmapentalyne featuring Os≡C1 remains ripe for further exploration. In this investigation, we effectively synthesized a lineage of osmapentalenofurans through the nucleophilic reaction of osmapentalyne incorporating Os≡C1 with phenols. These resulting complexes demonstrate near-infrared luminescence traits in both solid and liquid states. Particularly noteworthy is the osmapentalenofuran derived from tetraphenylethane (TPE) unit, which showcases remarkable aggregation-induced emission ( AIE) property in the aggregated state. These osmapentalenofurans are also able to further extend their range of reactions, including reactions with base and isonitrile. This study not only broadens the scope of applications for metal aromatics but also furnishes valuable insights into the realm of specialized functional materials.