M. Paneque et al., C-H AND C-S ACTIVATION OF THIOPHENE BY RHODIUM COMPLEXES - INFLUENCE OF THE ANCILLARY LIGANDS ON THE THERMODYNAMIC STABILITY OF THE PRODUCTS, Organometallics, 15(12), 1996, pp. 2678-2679
The reaction of thiophene with the rhodium compound [TpRh(C2H4)(PMe(3
))] (1a; Tp = hydrotris-(3,5-dimethyl-1-pyrazolyl)borate) leads to a
mixture of the C-H an C-S activation products [TpRh(H)(2-C4H3S)(PMe(3
))] (2a) and [TpRh(CHCHCHCHS)(PMe(3))] (3a), respectively. In contras
t to previous observations, the former is the thermodynamically prefer
red isomer. For the PEt(3) derivative [TpRh(C2H4)(PEt(3))] (1b), an e
ven higher selectively toward C-H activation is observed.