posted on 2016-01-25, 00:00authored byXiaotian Qi, Ruopeng Bai, Lei Zhu, Rui Jin, Aiwen Lei, Yu Lan
An
in-depth theoretical study of synergistic Cu(II)/Cu(I)-mediated
alkyne coupling was performed to reveal the detailed mechanism for
C–C bond formation, which proceeded via an unusual dinuclear
1,2-reductive elimination. Because the reactant for dinuclear 1,2-reductive
elimination was calculated to be triplet while the products were singlet,
the minimum energy crossing point (MECP) was introduced to the Cu/TMEDA/alkyne
system to clarify the spin crossing between triplet state and singlet
state potential energy surfaces. Computational results suggest that
C–H bond cleavage solely catalyzed by the Cu(I) cation is the
rate-determining step of this reaction and Cu(II)-mediated dinuclear
1,2-reductive elimination after the MECP is a facile process. These
conclusions are in good agreement with our previous experimental results.