Please use this identifier to cite or link to this item: https://doi.org/10.1021/om8010849
Title: Palladium(II) pyrazolin-4-ylidenes: Substituent effects on the formation and catalytic activity of pyrazole-based remote NHC complexes
Authors: Han, Y. 
Lee, L.J.
Huynh, H.V. 
Issue Date: 11-May-2009
Source: Han, Y., Lee, L.J., Huynh, H.V. (2009-05-11). Palladium(II) pyrazolin-4-ylidenes: Substituent effects on the formation and catalytic activity of pyrazole-based remote NHC complexes. Organometallics 28 (9) : 2778-2786. ScholarBank@NUS Repository. https://doi.org/10.1021/om8010849
Abstract: Three 4-iodopyrazolium salts with 3,5-dimethyl (3a), 3,5-diphenyl (3b), and 3,5-diisopropyl (3c) substituents, respectively, were synthesized using a modular approach. The oxidative addition of 3a-c to Pd2(dba) 3/PPh3 afforded products (trans-4a, cis-/trans-4b and 4c) of different geometries or connectivities, indicating a dramatic substituent effect on the formation of pyrazolin-4-ylidene complexes. In addition, the reactions of 3a-c with Pd2(dba)3 in the presence of pyridine yielded new mixed pyrazolin-4-ylidene/pyridine complexes (5a-c). All complexes have been fully characterized by multinuclear NMR spectroscopies, ESI mass spectrometry, and X-ray diffraction analyses. Furthermore, an initial catalytic study on Suzuki-Miyaura and Mizoroki-Heck cross-coupling reactions also reveals a significant substituent effect on catalytic activities. © 2009 American Chemical Society.
Source Title: Organometallics
URI: http://scholarbank.nus.edu.sg/handle/10635/94479
ISSN: 02767333
DOI: 10.1021/om8010849
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