Abstract
Titanium tert-butoxide (Ti(OC(CH3)3)4; Ti(OtBu)4) was chemically modified with catechol (C6H4(OH)2) and hydrolysis and condensation behavior of a resultant modified alkoxide was studied. Spectroscopic results revealed that the reaction between titanium tert-butoxide and catechol resulted in the formation of catecholate groups (C6H4O22-) bound to titanium and corresponding release of tert-butanol. The mass spectrometry and cryoscopy indicated that main species was a dimer [(C6H4O2)2Ti2 (OtBu)4]. The hydrolysis of the modified alkoxide in the system with Ti:tetrahydrofuran (THF):H2O = 1:10:x (x = 0.5-10) resulted in the partial hydrolysis, and all the hydrolyzed products after the drying under reduced pressure were soluble in THF and chloroform.
Original language | English |
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Pages (from-to) | 133-138 |
Number of pages | 6 |
Journal | Journal of Sol-Gel Science and Technology |
Volume | 22 |
Issue number | 1-2 |
DOIs | |
Publication status | Published - 2001 Sept |
Keywords
- Catechol
- Chemical modification
- Hydrolysis
- Titanium tert-butoxide
ASJC Scopus subject areas
- Electronic, Optical and Magnetic Materials
- Ceramics and Composites
- Chemistry(all)
- Biomaterials
- Condensed Matter Physics
- Materials Chemistry