Enhanced reactivities toward amines by introducing an imine arm to the pincer ligand: Direct coupling of two amines to form an imine without oxidant
Type
ArticleKAUST Department
Advanced Membranes and Porous Materials Research CenterBiological and Environmental Sciences and Engineering (BESE) Division
Chemical Engineering Program
Chemical Science Program
Homogeneous Catalysis Laboratory (HCL)
KAUST Catalysis Center (KCC)
Numerical Porous Media SRI Center (NumPor)
Physical Science and Engineering (PSE) Division
Date
2012-07-09Online Publication Date
2012-07-09Print Publication Date
2012-07-23Permanent link to this record
http://hdl.handle.net/10754/562245
Metadata
Show full item recordAbstract
Dehydrogenative homocoupling of primary alcohols to form esters and coupling of amines to form imines was accomplished using a class of novel pincer ruthenium complexes. The reactivities of the ruthenium pincer complexes for the direct coupling of amines to form imines were enhanced by introducing an imine arm to the pincer ligand. Selective oxidation of benzylamines to imines was achieved using aniline derivatives as the substrate and solvent. © 2012 American Chemical Society.Citation
He, L.-P., Chen, T., Gong, D., Lai, Z., & Huang, K.-W. (2012). Enhanced Reactivities toward Amines by Introducing an Imine Arm to the Pincer Ligand: Direct Coupling of Two Amines To Form an Imine Without Oxidant. Organometallics, 31(14), 5208–5211. doi:10.1021/om300422vSponsors
We are grateful for generous financial support from King Abdullah University of Science and Technology. We thank Prof. Hsiao-hua Yu (RIKEN) for useful discussions.Publisher
American Chemical Society (ACS)Journal
Organometallicsae974a485f413a2113503eed53cd6c53
10.1021/om300422v