Yes / Reactions have been carried out using the titanium(IV) precursors TiCl4 and Ti(OiPr)4, with addition of
two equivalents of a functionalized picolinamide ligand. The reactions with TiCl4 led to the formation
of either a mononuclear titanium species, [Ti(N,O)Cl2X2] or a dinuclear titanium species [Ti(N,O)X3]2[l-
O] (X = OMe or Cl), with incorporation of one picolinamide ligand. The ligand is bound to the titanium
centre as the protonated amide. The reactions with Ti(OiPr)4 resulted in the formation of mononuclear
titanium bis-picolinamide species [Ti(N,O)2(OiPr)2], and also dinuclear and trinuclear products, [(N,O)Ti
(OiPr)2][l-OiPr]2 and [(N,O)Ti(OiPr)2]2[l-OiPr]2[(OiPr)2Ti][l3-O] respectively. In these cases the picolinamide
ligand was found to be deprotonated and bound to the titanium as the iminolate. These molecules
have been characterized by X-ray crystallographic analysis and structural characteristics are
discussed.
| Identifer | oai:union.ndltd.org:BRADFORD/oai:bradscholars.brad.ac.uk:10454/9490 |
| Date | 27 April 2016 |
| Creators | Lord, Rianne M., Lord, S.M., Pask, C.M., McGowan, P.C. |
| Source Sets | Bradford Scholars |
| Language | English |
| Detected Language | English |
| Type | Article, Accepted manuscript |
| Rights | © 2016 Elsevier. Reproduced in accordance with the publisher's self-archiving policy. This manuscript version is made available under the CC-BY-NC-ND 4.0 license., CC-BY-NC-ND |
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