Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1302250 | Inorganic Chemistry Communications | 2013 | 5 Pages |
A novel and improved room temperature synthesis of the monohydride catalyst trans-[RuCl(H)(dppe)2] complex (1, dppe (1,2-bis(diphenylphosphino)ethane) = Ph2PCH2CH2PPh2) proceeds through oxidation of methanol (the solvent) by the pentacoordinated cis-[RuCl(dppe)2][PF6] complex and t-BuOK as the base is described. Compound 1 was fully characterized by NMR (1H, 13C, 31P), ESI-MS(TOF +), FTIR and elemental analysis. The X-ray structure of 1 was reported for the first time and unambiguously confirms the trans-configuration of the complex.
Graphical abstractA new and easy way to synthesize the trans-[RuCl(H)(dppe)2], (1) in high-yield was presented and its X-ray structure was reported for the first time.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► A faster way to access the catalyst trans-[RuCl(H)(dppe)2](1) is presented. ► Compound 1 X-ray structure is presented for the first time. ► The synthesis of 1 is a cost effective pathway for the preparation of derivatives. ► Room temp. synthesis of 1 is important in domains beyond catalysis and materials.