US EPA

6927497 

Journal Article 

Iridium complexes of N-heterocyclic carbenes in C-H borylation using energy efficient microwave technology: influence of structure, ligand donor strength and counter ion on catalytic activity 

Rentzsch, CF; Tosh, E; Herrmann, WA; Kuehn, FE; , 

2009 

Yes 

Green Chemistry
ISSN: 1463-9262
EISSN: 1463-9270 

ROYAL SOC CHEMISTRY 

CAMBRIDGE 

11 

10 

1610-1617 

English 

10.1039/b913055c 

WOS:000270542400021 

https://www.proquest.com/docview/2327974731?accountid=171501&bdid=64564&_bd=MSXIDaYbmgi5TH41tipex2kRN%2Bo%3D
Exit
 

Bridged and unbridged N-heterocyclic carbene (NHC) ligands were metalated with [Ir(COD)Cl](2) to give iridium(I) mono-and biscarbene substituted catalysts [Ir(COD)NHC(Cl)] and [Ir(COD)(NHC)(2)][X] (X: I, PF6, BF4, CF3COO, OTf). The prepared NHC-complexes were tested in the C-H borylation reaction of aromatic carbons with bis(pinacolato) diboron (B(2)pin(2)) and pinacolborane (HBpin). The use of microwave technology in this study not only facilitates a time efficient screening of a wide range of influences such as ligand sigma-donor strength and structural motif as well as the effects of the complex counter ion, but also provides an energy efficient heating source. Catalyst 6(TFA), which features a chelating NHC ligand, proved to be most effective catalyst and further investigations with this complex in the borylation of mono-and disubstituted benzene derivatives exploring chemo-and regioselectivity were undertaken.