Gandhi, Thirumanavelan and Jagirdar, Balaji R (2005) Utilization of $CS_2$ as a Source of $C_1$ Synthetic Units for the Preparation of Bis(alkylthio)methanes and Alkyl Dithioformates. In: Inorganic Chemistry, 44 (4). pp. 1118-1124.
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Abstract
Double insertion of $CS_2$ into two Ru-H bonds of $[(dppm)_2Ru(H)_2] (dppm = Ph_2PCH_2PPh_2)$ affords the methanedithiolate complex $[(dppm)_2Ru( 2-S_2CH_2)]$. The methanedithiolate moiety has been functionalized using 2 equiv of RX resulting in bis(alkylthio)methane derivatives $[(dppm)_2Ru(RSCH_2SR)][X]_2$. The bis(alkylthio)methane complex loses the bis(alkylthio)methane moiety under very mild conditions and in turn affords the $[(dppm)_2RuX\$2]$ complex from which the starting dihydride $[(dppm)_2Ru(H)_2]$ has been regenerated via reaction with KOH/EtOH. On the other hand, insertion of $CS_2$ into one Ru-H bond of $[(dppe)_2Ru(H)_2] (dppe = Ph_2PCH_2CH_2PPh_2)$ followed by functionalization using RX results in alkyl dithioformate complex trans- $[(dppe)_2Ru(H)(SC(SR)H)][X]$. In this case also, the alkyl dithioformate moiety gets eliminated under very mild conditions to afford the $[(dppe)_2Ru(H)(X)]$ derivative from which the starting dihydride has been regenerated via reaction with $NaBH_4$. The reactions presented here constitute utilization of $CS_2$ as a $C_1$ synthetic source for the generation of useful organic compounds.
Item Type: | Journal Article |
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Publication: | Inorganic Chemistry |
Publisher: | American Chemical Society |
Additional Information: | The copyright for this article belongs to American Chemical Society. |
Department/Centre: | Division of Chemical Sciences > Inorganic & Physical Chemistry |
Date Deposited: | 15 Apr 2005 |
Last Modified: | 20 Jan 2012 09:19 |
URI: | http://eprints.iisc.ac.in/id/eprint/3024 |
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