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Synthesis and characterization of a tert-butyl ester-substituted titanocene dichloride: (t-BuOOC)Cp(2)TiCl(2)
Bis[η(5)-(tert-butoxycarbonyl)cyclopentadienyl]dichloridotitanium(IV), [Ti(C(10)H(13)O(2))(2)Cl(2)], was synthesized from LiCp(COOt-Bu) using TiCl(4), and was characterized by single-crystal X-ray diffraction and (1)H NMR spectroscopy. The distorted tetrahedral geometry about the central tit...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534228/ https://www.ncbi.nlm.nih.gov/pubmed/33117564 http://dx.doi.org/10.1107/S2056989020011834 |
Sumario: | Bis[η(5)-(tert-butoxycarbonyl)cyclopentadienyl]dichloridotitanium(IV), [Ti(C(10)H(13)O(2))(2)Cl(2)], was synthesized from LiCp(COOt-Bu) using TiCl(4), and was characterized by single-crystal X-ray diffraction and (1)H NMR spectroscopy. The distorted tetrahedral geometry about the central titanium atom is relatively unchanged compared to Cp(2)TiCl(2). The complex exhibits elongation of the titanium–cyclopentadienyl centroid distances [2.074 (3) and 2.070 (3) Å] and a contraction of the titanium–chlorine bond lengths [2.3222 (10) Å and 2.3423 (10) Å] relative to Cp(2)TiCl(2). The dihedral angle formed by the planes of the Cp rings [52.56 (13)°] is smaller than seen in Cp(2)TiCl(2). Both ester groups extend from the same side of the Cp rings, and occur on the same side of the complex as the chlorido ligands. The complex may serve as a convenient synthon for titanocene complexes with carboxylate anchoring groups for binding to metal oxide substrates. |
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