Oligomerisation and stereoselective polymerisation of alkenes and alkynes using pyridyl-based Al(iii) catalysts
Dipanjana Choudhury, Richard Danylyuk, Alexandros Terzopoulos, Natalie S. Potter, Oren A. Scherman, Jonathan M. Goodman, Dominic S. Wright

TL;DR
Scientists created new aluminum-based catalysts that can efficiently polymerize alkenes and cyclotrimerize alkynes with high stereocontrol.
Contribution
This is the first report of stereoselective Al(iii) polymerization and alkyne cyclotrimerization using static main group metal catalysis.
Findings
The Al(iii) cationic catalysts polymerize alkenes with high stereoregularity, including syndiotactic polystyrene.
The catalysts cyclotrimerize terminal alkynes to form trisubstituted benzenes and fulvene.
Abstract
Dealkylation of the dimers [R2Al(2-py′)]2 (2-py′ = 6-substituted pyridyl, R = Me, iBu) with [Ph3C][B(C6F5)4] gives the putative cations [RAl(2-py′)2(µ-R)AlR]+ which can polymerise a range of alkenes with a high degree of stereoregularity (syndiotacticity in the case of polystyrene) and which cylotrimerise terminal alkynes to trisubstituted benzenes and a fulvene. This is the first report of stereoslective Al(iii) polymerisation and of the cyclotrimerisation of alkynes by static catalysis using a main group metal. The putative Al(iii) cationic catalysts [RAl(2-py′)2(µ-R)AlR]+ (2-py′ = 6-substituted pyridyl, R = Me, iBu) can polymerise terminal alkenes with a high degree of stereocontrol and cyclotrimerise terminal alkynes.
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Taxonomy
TopicsOrganoboron and organosilicon chemistry · Organometallic Complex Synthesis and Catalysis · Synthesis and characterization of novel inorganic/organometallic compounds
