posted on 2024-01-02, 11:43authored byKristian
L. Mears, Gia-Ann Nguyen, Bronson Ruiz, Annika Lehmann, Jonah Nelson, James C. Fettinger, Heikki M. Tuononen, Philip P. Power
The bismuth hydride
(2,6-Mes2H3C6)2BiH (1, Mes = 2,4,6-trimethylphenyl), which
has a Bi–H 1H NMR spectroscopic signal at δ
= 19.64 ppm, was reacted with phenylacetylene at 60 °C in toluene
to yield [(2,6-Mes2C6H3)2BiC(Ph)=CH2] (2) after 15 min. Compound 2 was characterized by 1H, 13C NMR,
and UV–vis spectroscopy, single crystal X-ray crystallography,
and calculations employing density functional theory. Compound 2 is the first example of a hydrobismuthation addition product
and displays Markovnikov regioselectivity. Computational methods indicated
that it forms via a radical mechanism with an associated Gibbs energy
of activation of 91 kJ mol–1 and a reaction energy
of −90 kJ mol–1.