In the concerted mechanism, the FLP interacts with H2 in such a way that the H-H bond cleavage occurs simultaneously. The electron-rich amine donates electrons to the H2 molecule, and the electron-deficient borane accepts electrons, causing the H-H bond to break and H2 to release. This mechanism occurs in a single step, with no well-defined intermediates.
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bis[2,4,6-tris(trifluoromethyl)phenyl]borane
4
2,2-Pyrrolidinedicarboxylic acid, 3-(2-ethoxy-2-oxoethyl)-4-(1-methylethenyl)-1-(trifluoroacetyl)-, diethyl ester, trans-
1-[2,4,6-trimethylphenylethynyl]-1,2-benziodoxol-3(1H)-one
