Stoichiometric and catalytic C–F bond activation by the trans-dihydride NHC complex [Ru(IEt2Me2)2(PPh3)2H2] (IEt2Me2 = 1,3-diethyl-4,5-dimethylimidazol-2-ylidene)
Cybulski, Mateusz K., Riddlestone, Ian M., Mahon, Mary F., Woodman, Timothy J. and Whittlesey, Michael K. (2015) Stoichiometric and catalytic C–F bond activation by the trans-dihydride NHC complex [Ru(IEt2Me2)2(PPh3)2H2] (IEt2Me2 = 1,3-diethyl-4,5-dimethylimidazol-2-ylidene) Dalton Transactions, 44 (45). pp. 19597-19605.
Full text not available from this repository.Abstract
The room temperature reaction of C6F6 or C6F5H with [Ru(IEt2Me2)2(PPh3)2H2] (1; IEt2Me2 = 1,3-diethyl-4,5-dimethylimidazol-2-ylidene) generated a mixture of the trans-hydride fluoride complex [Ru(IEt2Me2)2(PPh3)2HF] (2) and the bis-carbene pentafluorophenyl species [Ru(IEt2Me2)2(PPh3)(C6F5)H] (3). The formation of 3 resulted from C–H activation of C6F5H (formed from C6F6via stoichiometric hydrodefluorination), a process which could be reversed by working under 4 atm H2. Upon heating 1 with C6F5H, the bis-phosphine derivative [Ru(IEt2Me2)(PPh3)2(C6F5)H] (4) was isolated. A more efficient route to 2 involved treatment of 1 with 0.33 eq. of TREAT-HF (Et3N·3HF); excess reagent gave instead the [H2F3]− salt (5) of the known cation [Ru(IEt2Me2)2(PPh3)2H]+. Under catalytic conditions, 1 proved to be an active precursor for hydrodefluorination, converting C6F6 to a mixture of tri, di and monofluorobenzenes (TON = 37) at 363 K with 10 mol% 1 and Et3SiH as the reductant.
Item Type: | Article | ||||||||||||||||||
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Divisions : | Faculty of Engineering and Physical Sciences > Chemistry | ||||||||||||||||||
Authors : |
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Date : | 7 December 2015 | ||||||||||||||||||
Funders : | Engineering and Physical Sciences Research Council (EPSRC) | ||||||||||||||||||
DOI : | 10.1039/C5DT01996F | ||||||||||||||||||
Depositing User : | Clive Harris | ||||||||||||||||||
Date Deposited : | 25 Jun 2019 08:13 | ||||||||||||||||||
Last Modified : | 06 Jul 2019 05:27 | ||||||||||||||||||
URI: | http://epubs.surrey.ac.uk/id/eprint/852073 |
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