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Single-Source Materials for Metal-Doped Titanium Oxide: Syntheses, Structures, and Properties of a Series of Heterometallic Transition-Metal Titanium Oxo Cages.
- Source :
-
Inorganic Chemistry . 12/20/2010, Vol. 49 Issue 24, p11532-11540. 9p. - Publication Year :
- 2010
-
Abstract
- Titanium dioxide (TiO2) doped with transition-metal ions (M) has potentially broad applications in photocatalysis, photovoltaics, and photosensors. One approach to these materials is through controlled hydrolysis of well-defined transition-metal titanium oxo cage compounds. However, to date very few such cages have been unequivocally characterized, a situation which we have sought to address here with the development of a simple synthetic approach which allows the incorporation of a range of metal ions into titanium oxo cage arrangements. The solvothermal reactions of Ti(OEt)4 with transition-metal dichlorides (MIICl2, M = Co, Zn, Fe, Cu) give the heterometallic transition-metal titanium oxo cages [Ti4O(OEt)15(MCl)] [M = Co (2), Zn (3), Fe (4), Cu (5)], having similar MTi4(μ4-O) structural arrangements involving ion pairing of [Ti4O(OEt)15]- anion units with MCl+ fragments. In the case of the reaction of MnCl2, however, two MnII ions are incorporated into this framework, giving the hexanuclear Mn2Ti4(μ4-O) cage [Ti4O(OEt)15(Mn2Cl3)] (6) in which the MCl+ fragments in 2-5 are replaced by a [ClMn(μ-Cl)MnCl]+ unit. Emphasizing that the nature of the heterometallic cage is dependent on the metal ion (M) present, the reaction of Ti(OEt)4 with NiCl2 gives [Ti2(OEt)9(NiCl)]2 (7), which has a dimeric Ni(μ-Cl)2Ni bridged arrangement arising from the association of [Ti2(OEt)9]- ions with NiCl+ units. The syntheses, solid-state structures, spectroscopic and magnetic properties of 2-7 are presented, a first step toward their applications as precursor materials. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00201669
- Volume :
- 49
- Issue :
- 24
- Database :
- Academic Search Index
- Journal :
- Inorganic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 64446779
- Full Text :
- https://doi.org/10.1021/ic101687m