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| Title: | Highly efficient palladium precatalysts of homoscorpionate bispyrazolyl ligands for the more challenging Suzuki-Miyaura cross-coupling of aryl chlorides |
| Authors: | JOHN, A SHAIKH, MM BUTCHER, RJ GHOSH, P |
| Keywords: | n-heterocyclic-carbene ring-opening polymerization transition-metal compounds mixed aqueous-medium x-ray structures arylboronic acids room-temperature sonogashira reactions heterogeneous catalysis vibrational-spectra |
| Issue Date: | 2010 |
| Publisher: | ROYAL SOC CHEMISTRY |
| Citation: | DALTON TRANSACTIONS, 39(31), 7353-7363 |
| Abstract: | Highly efficient palladium precatalysts {[RN{-(CH(2))(n)-pz(2)(3,5-Me)}(2)]PdCl(2)}(m) [m = n = 1; R = 2,6-Me(2)C(6)H(3) (1), 2,4,6-Me(3)C(6)H(2) (2), CH(2)Ph (3) and m = n = 2; R = CH(2)Ph (4)] of a series of homoscorpionate bispyrazolyl ligands for the Suzuki-Miyaura cross-coupling of the more challenging aryl chloride substrates are reported. In particular, the palladium 1-4 precatalysts carried out the Suzuki-Miyaura cross-coupling of a wide variety of aryl chloride substrates bearing electron withdrawing, electron donating and heteroaryl substituents. Remarkably enough, the molecular structure determination of the 1-4 precatalysts by X-ray diffraction studies revealed the presence of anagostic [C-H center dot center dot center dot Pd] type interactions in the mononuclear 1-3 complexes of methylene bridged bispyrazolyl ligands whereas the ethylene bridged analog 4 yielded an interesting dimeric 20-membered macrometallacyclic complex devoid of any such interaction. |
| URI: | http://dx.doi.org/10.1039/c003174g http://dspace.library.iitb.ac.in/xmlui/handle/10054/11734 http://hdl.handle.net/10054/11734 |
| ISSN: | 1477-9226 |
| Appears in Collections: | Article
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