791124-86-2Relevant academic research and scientific papers
Amine attack on coordinated alkenes: An interconversion from anti-Markovnikoff to Markovnikoff products
Pryadun, Ruslan,Sukumaran, Dinesh,Bogadi, Robert,Atwood, Jim D.
, p. 12414 - 12420 (2007/10/03)
A sequence of alkene complexes of platinum, PtCl2(PPh 3)(alkene) (alkene = ethylene, propene, 1-butene, cis-2-butene, 1-hexene, 1-octene, and 1-decene), has been prepared. These complexes are characterized by NMR spectroscopy, including assignment of each proton, and X-ray crystal structures of the 1-propene and 1-hexene complexes. Each complex was reacted with diethylamine. For the 1-hexene, 1-octene, and 1-decene complexes, the amine displaces the alkene. For the smaller alkenes, the diethylamine nucleophilically attacks the coordinated alkene. For propene and 1-butene, the low-temperature addition leads to the anti-Markovnikoff nucleophilic attack, which slowly converts at room temperature to the Markovnikoff product. The transformation from anti-Markovnikoff to Markovnikoff addition occurs without diethylamine dissociation.
