Table 3.
Photocatalytic activity of the protonated oxides and inorganic−organic derivatives.
| Sample | ω (μmol/h) | ϕ (%) | k Pt | |
|---|---|---|---|---|
| D-glucose | HCN3 | 14 | 0.2 | − |
| HCN3/Pt | 95 | 1.6 | 7 | |
| HCN3/Pt(MeOH) | 140 | 2.4 | 10 | |
| HCN3×BuNH2 | 21 | 0.4 | − | |
| HCN3×BuNH2/Pt | 450 | 7.5 | 21 | |
| HCN3×BuNH2/Pt(MeOH) | 410 | 6.8 | 20 | |
| HCN3×EtOH | 20 | 0.3 | − | |
| HCN3×EtOH/Pt | 200 | 3.3 | 10 | |
| HCN3×EtOH/Pt(MeOH) | 170 | 2.8 | 9 | |
| HLT3 | 4 | 0.1 | − | |
| HLT3/Pt | 61 | 1.0 | 15 | |
| HLT3/Pt(MeOH) | 110 | 1.8 | 28 | |
| HLT3×EtNH2 | 10 | 0.2 | − | |
| HLT3×EtNH2/Pt | 270 | 4.5 | 27 | |
| HLT3×EtNH2/Pt(MeOH) | 240 | 4.0 | 24 | |
| HLT3×EtOH | 30 | 0.5 | − | |
| HLT3×EtOH/Pt | 360 | 6.0 | 12 | |
| HLT3×EtOH/Pt(MeOH) | 120 | 2.0 | 4 | |
| D-xylose | HCN3/Pt | 88 | 1.5 | − |
| HCN3×BuNH2/Pt | 530 | 8.8 | − | |
| HCN3×EtOH/Pt | 140 | 2.3 | − | |
| HLT3/Pt | 48 | 0.80 | − | |
| HLT3×EtNH2/Pt | 380 | 6.3 | − | |
| HLT3×EtOH/Pt | 420 | 7.0 | − |