Salicylaldiminato derivatives of cyclotriveratrylene: Flexible strategy for new rim-metalated CTV complexes

Citation
Ds. Bohle et Dj. Stasko, Salicylaldiminato derivatives of cyclotriveratrylene: Flexible strategy for new rim-metalated CTV complexes, INORG CHEM, 39(25), 2000, pp. 5768-5770
Citations number
19
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
INORGANIC CHEMISTRY
ISSN journal
00201669 → ACNP
Volume
39
Issue
25
Year of publication
2000
Pages
5768 - 5770
Database
ISI
SICI code
0020-1669(200012)39:25<5768:SDOCFS>2.0.ZU;2-3
Abstract
The amino-derivatized cyclotriveratrylene analogue, triaminotrimethoxytribe nzocyclononene [CTV(NH2)(3)(OMe)(3)], 1, is readily converted into triply s ubstituted imine compounds [CTV(sal)(3)(OMe)(3)], 2, in high yield by treat ment of the acid salt of 1 with a variety of substituted salicylaldehydes. Cleavage of the protecting methoxy group generates the tristridentate chela te CTV(sal)(3)(OH)(3), 3, which is readily converted into new rim-metalated species CTV(sal)(3)(ONiL)(3), 4a (a, L = pyrrolidine; b, L = 1-n-butyl-imi dazole). Taken together, these results illustrate the remarkable synthetic flexibility that is possible for the CTV-based metal complexes by alteratio n of the metal, the salicylaldehyde component of the CTV ligand, or the anc illary ligands coordinated to the metal.