

Author: Iretskii Alexei García Juventino Picazo Graziela Maitlis Peter
Publisher: Springer Publishing Company
ISSN: 1011-372X
Source: Catalysis Letters, Vol.51, Iss.1-2, 1998-04, pp. : 129-131
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
The thiaplatinacycles, [PtL2(C,S–C12 H8S)] and [PtL2(C,S–C13H10S)] (L = PEt3, PMe3; L2=Ph2PCH2 CH2PPh2), obtained from oxidative insertion of [Pt0Ln] into dibenzothiophene and 4-methyldibenzothiophene are hydrodesulfurized by reaction with hydrogen (toluene, 20 atm, 100°C) to biphenyl and 3-methylbiphenyl, respectively; addition of acidic alumina improves the reaction. These observations link the model systems and the latest generation of commercial second-stage HDS catalysts.
Related content


Inhibition of dibenzothiophene hydrodesulfurization by di-aza heterocycles
Catalysis Letters, Vol. 99, Iss. 3-4, 2005-02 ,pp. :





