Abstract
Reaction of 1,2-bis(diphenylphosphino)benzene (dppbz) with PhpdtFe2(CO)6 (A) in hot acetonitrile yielded a chelated complex, PhpdtFe2(CO)4(κ2-dppbz) (1), in moderate yield. Further treatment using an excess of HBF4·Et2O resulted in the protonation of 1 at room temperature in dichloromethane solution, forming a hydride [Phpdt(μ-H)Fe2(CO)4(κ2-dppbz)]BF4 (2). The chemical structures of both complexes were fully characterized by spectroscopic methods and X-ray crystallography, and the electronic structures were further investigated by UV-vis spectroscopy. The cyclic voltammetry (CV) of 1 in the absence and presence of acetic acid were also investigated.
![](/cms/asset/e61832fe-1c07-4d52-a8be-ba0be019fd9b/gcoo_a_1366997_uf0001_oc.jpg)