875-29-6Relevant academic research and scientific papers
Mechanism of trialkylborane promoted adhesion to low surface energy plastics
Sonnenschein, Mark F.,Webb, Steven P.,Kastl, Patrick E.,Arriola, Daniel J.,Wendt, Benjamin L.,Harrington, Daniel R.,Rondan, Nelson G.
, p. 7974 - 7978 (2004)
Excellent adhesion to low surface energy substrates such as polypropylene, polyethylene, poly(vinyl difluoride), and poly(tetrafluoroethylene) is obtained with acrylic polymerization initiated by trialkylboranes at room temperature and without need for surface pretreatment. The mechanism of adhesion is a consequence of a series of radical processes resulting from the initial oxidation of the trialkylborane followed by the production of alkoxy and alkyl radicals. This paper will elucidate the mechanism of adhesion using both experiment and theory.
Catalytic double carbonylation of epoxides to succinic anhydrides: Catalyst discovery, reaction scope, and mechanism
Rowley, John M.,Lobkovsky, Emil B.,Coates, Geoffrey W.
, p. 4948 - 4960 (2008/02/03)
The first catalytic method for the efficient conversion of epoxides to succinic anhydrides via one-pot double carbonylation is reported. This reaction occurs in two stages: first, the epoxide is carbonylated to a β-lactone, and then the β-lactone is subsequently carbonylated to a succinic anhydride. This reaction is made possible by the bimetallic catalyst [(CITPP)Al(THF)2]+[Co(CO)4]- (1; CITPP = meso-tetra(4-chlorophenyl)porphyrinato; THF = tetrahydrofuran), which is highly active and selective for both epoxide and lactone carbonylation, and by the identification of a solvent that facilitates both stages. The catalysis is compatible with substituted epoxides having aliphatic, aromatic, alkene, ether, ester, alcohol, nitrile, and amide functional groups. Disubstituted and enantiomerically pure anhydrides are synthesized from epoxides with excellent retention of stereochemical purity. The mechanism of epoxide double carbonylation with 1 was investigated by in situ IR spectroscopy, which reveals that the two carbonylation stages are sequential and non-overlapping, such that epoxide carbonylation goes to completion before any of the intermediate β-lactone is consumed. The rates of both epoxide and lactone carbonylation are independent of carbon monoxide pressure and are first-order in the concentration of 1. The stages differ in that the rate of epoxide carbonylation is independent of substrate concentration and first-order in donor solvent, whereas the rate of lactone carbonylation is first-order in lactone and inversely dependent on the concentration of donor solvent. The opposite solvent effects and substrate order for these two stages are rationalized in terms of different resting states and rate-determining steps for each carbonylation reaction.
