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. 2018 Nov 17;23(11):3006. doi: 10.3390/molecules23113006

Table 1.

Reaction conditions for the synthesis of the different TiO2 samples.

Sample Precursor (amount) O-donor a Solvent Temperature (time) Calc. yield b/%
TiO2-E-NS TiCl4 (12.5 mmol) iPr2O none 110 °C (72 h) 93
TiO2-E-Tol TiCl4 (12.5 mmol) iPr2O toluene (5 mL) 110 °C (72 h) 94
TiO2-E-Squ TiCl4 (12.5 mmol) iPr2O squalane (5 mL) 110 °C (72 h) 96
TiO2-E-CH TiCl4 (12.5 mmol) iPr2O cyclohexane (5 mL) 110 °C (72 h) 93
TiO2-A-NS Ti(OiPr)4 (4.4 mmol) PhCOCH3 none 200 °C (12 h) 92
TiO2-A-Tol Ti(OiPr)4 (4.4 mmol) PhCOCH3 toluene (10 mL) 200 °C (12 h) 95
TiO2-A-Squ Ti(OiPr)4 (4.4 mmol) PhCOCH3 squalane (10 mL) 200 °C (12 h) 96
TiO2-B-NS Ti(OiPr)4 (4.4 mmol) (PhCO)2O none 200 °C (12 h) 56
TiO2-B-Tol Ti(OiPr)4 (4.4 mmol) (PhCO)2O toluene (10 mL) 200 °C (12 h) 53
TiO2-B-Squ Ti(OiPr)4 (4.4 mmol) (PhCO)2O squalane (10 mL) 200 °C (12 h) 78

a 2 equivalents relative to the precursor; b calcination yield (500 °C, 5 h, in air).