Abstract
In this work, Cu-vitamin B5 (pantothenic acid) bonded to 2,4,6-trichloro-1,3,5-triazine produced a bioconjugated dendrimer giving rise to the visible-light photocatalytic activity of nanocrystalline TiO(2). XPS spectra uncovered the coexistence of Cu(II)/Cu(I) oxidation states with a predominant contribution of Cu(I). The new heterogeneous bio-relevant Cu-photocatalyst (Cu(I) Cu(II) [PTAPA G2-B5] @TiO(2)) revealed a band gap value [E(g) = (2.8 eV)] less than those of Cu free components [PTAPA G1-B5]@TiO(2) (3.04) and [PTAPA G2-B5]@TiO(2) (3.06) and particularly the bare TiO(2) (3.15 eV). The reactions showed to be light-dependent with the best performance under room light bulbs. The photocatalytic efficiency of the as-prepared heterojunction photocatalyst was exploited in the aerobic C(sp)(2)-C(sp)(2) homocoupling of phenylboronic acid and C(sp)-C(sp) homocoupling of phenyl acetylenes under visible-light irradiation to prepare structurally and electronically different biaryls. A radical pathway relying on the photogenerated e- and h+ and involving the Cu(I)-Cu(II) synergistic cooperation was postulated. The reusability and stability of the catalyst were verified by the recycling test, FT-IR spectra, and ICP-OES analysis.