9-BBN hydroborate complexes Ti{(mu-H)(2)BC8H14}(3)(THF)(2) (1), Ti{(mu-H)(2)BC8H14}(3)(OEt2) (2), and [K(OEt2)(4)]-[Ti{(mu-H)(2)BC8H14}(4)] (4) were formed from the reaction of TiCl4 with K[H2BC8H14] in diethyl ether or THF. Ti{(mu-H)(2)BC8H14}(3)(PhNH2) (3) was isolated from the reaction of 2 with aniline in diethyl ether. In the formation of these complexes, Ti(IV) is reduced to Ti(III). The coordinated diethyl ether in 2 can be displaced by the stronger bases THF and aniline, to form 1 and 3, respectively. All of the compounds were characterized by single-crystal X-ray diffraction analysis. In complex 1, which contains two coordinated THF ligands, the titanium possesses a 17 electron configuration and there is no evidence for agostic interaction. Complexes 2 and 3 contain only one coordinated ether or aniline ligand, and the titanium possesses a 15 electron configuration. In these compounds, a C-H hydrogen on an a carbon on the BC8H14 unit of a 9-BBN hydroborate ligand forms an agostic interaction with the titanium. Criteria for assessing the existence of agostic interactions are discussed. As the potassium salt, the anion of complex 4 is more stable than the complexes 1-3. Organometallic anions of the type [ML4](-) for titanium(III) are rare.