The thermal reactions of the Re(V) dithiolate complex Cp'ReCl2(SCH2CH2S), 1 (where Cp' = EtMe4C5), and related derivatives have been studied. When 1 is heated in toluene in a sealed evacuated tube at 100 degrees C, a dehydrogenation reaction occurs to form a new rhenium complex with a dithiolene ligand, Cp'ReCl2(SCHCHS), 6, in ca. 40% yield. The structure of 6 has been confirmed by an X-ray diffraction study. Under the thermal conditions studied, 1 also undergoes an olefin extrusion reaction. Free ethene is detected in the NMR spectrum of the products, and insoluble rhenium products are also formed. When 1 is reacted with excess ethene under mild conditions, a new organic product, 1,4-dithiane, is formed. Complex 1 is also found to react with oxidants, such as O2 and S8, under mild conditions to form the dehydrogenation product 6. Kinetic studies of the thermal reaction of 1 and related derivatives have been completed, and possible mechanisms for the thermally induced dehydrogenation reaction are discussed.
Ethylene sulfide and propylene sulfide react with the high valent metal complex Cp′ReCl 4 (Cp′ ) EtMe 4 C 5 ) in THF solution to form a product with a chloroalkyl disulfide ligand of the formula Cp′Re(Cl) 3 -S-S-CH(R)CH 2 Cl (R ) H or Me). In contrast, the thietane S(CH 2 ) 3 reacts with Cp′ReCl 4 to form a simple adduct, and no ring-opening reaction has been identified.
The reaction of Cp'ReCl(2)S(3) (Cp' = Me(4)EtC(5)) with slightly less than 2 equiv of a phosphine reagent results in the formation of [Cp'Re(Cl)(2)(mu-S)](2), 2, which has been characterized by an X-ray diffraction study. Reactions of 2 with nucleophiles did not lead to monomeric derivatives of the type Cp'ReS(Cl)(2)(Nuc). The reaction of Cp'ReCl(2)(SC(2)H(4)S) with (Me(3)Si)(2)S resulted in the formation of three new products: Cp'ReS(SC(2)H(4)S), 4; Cp'Re(S(3))(SC(2)H(4)S), 5; and a tetranuclear derivative, [(Cp'Re)(2)(mu-S)(mu,eta(2)-SC(2)H(4)S)(mu,eta(1)-SC(2)H(4)S](2)Cl(2), 6. Complexes 4 and 6 have been characterized by X-ray diffraction studies. The electrochemical properties of the mononuclear Re=S derivative, 4, are compared with those of Re=O and Re=NR analogues.
The syntheses and characterizations of Cp′′ReCl 2 (SC 3 H 6 S), 1, Cp′′ReCl 3 (SCHMe 2 ), 2, and Cp′′ReCl 2 (SCHMe 2 ) 2 , 3, are reported (Cp′′ ) C 5 Me 4 Et). Complex 2 has been characterized by an X-ray diffraction study, which confirms its mononuclear structure. Reactions of 1, 2, and 3 have been studied and compared with those characterized previously for Cp′′ReCl 2 -(SC 2 H 4 S). For example, the thermal reaction of 1 in toluene at 100 °C, results in the elimination of HCl and formation of a complex with a chelated thiolate/thialdehyde ligand, Cp′′ReCl(SCH 2 CH 2 CHdS), 5. Complex 5 can also be synthesized at a lower temperature by the reaction of 1 with excess triethylamine. Spectroscopic characteristics and reactivity of 5 are reported.Supporting Information Available: Tables giving crystal data, positional and thermal parameters, bond distances, and bond angles for 2 and 4, and variable-temperature NMR data for 2. This material is available free of charge via the Internet at http://pubs.acs.org. OM020626T(21) Flack, H. D.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.