Auxiliary Carboxylate-Induced Assembly of Calix[6]arene-Polyoxotitanate Hybrid Systems with Photocatalytic Activity in the Oxidation of Sulfides.

This study used the tert -butylcalix[6]arene (TBC[6]) as the ligand and successfully synthesized six TBC[6]-stabilized titanium-oxo clusters (TOCs) by the one-step solvothermal reaction. These six compounds were [Ti 4 O 2 (TBC[6]) 2 ] ( Ti 4 ), {Ti 2 (TBC[6])(EtO) 2 (SaH 2 ) 2 } ( Ti 2 -SA , H 2 Sa = squaric acid), {Ti 2 (TBC[6]) 2 (EtO) 2 (Oa)} ( Ti 2 -OA , H 2 Oa = oxalic acid), [H 2 Ti 4 (TBC[6])(BA) 2 (EtO) 10 ] ( Ti 4 -BA , HBA = benzoic acid), [Ti 6 O 2 (TBC[6])(BA) 4 (O i Pr) 10 ] ( Ti 6 -BA ), and [Ti 8 (TBC[6]) 2 (Sal) 4 (EtO) 16 ] ( Ti 8 -Sal , H 2 Sal = salicylic acid). These clusters contain one or two TBC[6] ligands, with the biconical or monoconical configuration, greatly increasing the variety of TOCs it could support. The introduction of auxiliary carboxylic ligands can further stimulate the growth of structures, with the cluster core gradually increased from {Ti-TBC[6]-Ti} to {Ti 2 -TBC[6]-Ti 2 }, to {Ti 3 -TBC[6]-Ti 3 }, and finally to {Ti 3 -TBC[6]-Ti 2 -TBC[6]-Ti 3 } with 3.1 nm length. Structural regulation may affect their solution stability, absorption spectra, and photocurrent response. The study of catalytic activities shows that these clusters can be used as recyclable heterogeneous photocatalysts for the oxidation of sulfide to sulfoxide. The catalytic efficiency of the TBC[6]-Ti x system is closely related to the cluster structure, and the exposure of the Ti site on the catalyst surface can significantly enhance the catalytic activity of the clusters.