Related Experiment Video
Updated: Aug 6, 2026

Developing Photosensitizer-Cobaloxime Hybrids for Solar-Driven H2 Production in Aqueous Aerobic Conditions
Published on: October 5, 2019
Effect of the anchoring group (carboxylate vs phosphonate) in Ru-complex-sensitized TiO2 on hydrogen production under
1School of Environmental Science and Engineering, Pohang University of Science and Technology (POSTECH), Pohang 790-784, Korea.
Abstract:
We synthesized six Ru-bipyridyl complexes having di-, tetra-, and hexacarboxylate (C2, C4, and C6) and di-, tetra-, and hexaphosphonate (P2, P4, and P6) as the anchoring group, prepared six different sensitized TiO2 samples by using them, and then systematically tested their visible light reactivity for hydrogen production in aqueous suspension (with EDTA as an electron donor) under lambda > 420 nm illumination. The properties and efficiencies of C- and P-complexes as a sensitizer depended on the number and kind of anchoring groups in very different ways. The adsorption of P-complexes on TiO2 is strong enough not to be hampered by the presence of competing adsorbates (EDTA), whereas that of C-complexes is significantly inhibited. As a result, P-TiO2 exhibited much higher activity for the hydrogen production than C-TiO2, although the visible light absorbing capabilities are comparable among C- and P-complexes. Among the six sensitizers, P2 was the most active one for the H2 production. The hydrogen production activities of C-TiO2 and P-TiO2 depended on the concentration of sensitizers and electron donors in different ways as well. How the sensitizing activity for hydrogen production is influenced by the anchoring group and the experimental conditions was investigated and discussed in detail. It is also notable that the effects of the anchoring group on the sensitized production of hydrogen were drastically different from those on the dye-sensitized solar cell we recently reported for the same set of six sensitizers.
Related Concept Videos
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
ortho–para-Directing Activators: –CH3, –OH, –⁠NH2, –OCH3
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation reactions,...
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
Acid Halides to Carboxylic Acids: Hydrolysis
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic acid...

