期刊
ORGANOMETALLICS
卷 29, 期 7, 页码 1712-1716出版社
AMER CHEMICAL SOC
DOI: 10.1021/om901101f
关键词
-
资金
- NSF [CHE-0748312]
- University of California, Irvine
The relative kinetic basicities of a series of differentially substituted and hybridized neutral organogold compounds were examined through competitive protodeauration experiments and were found to span 2.2 orders of magnitude. The effect of electron-withdrawing and electron-donating substituents on the rate of protodeauration of alkenylgold and arylgold compounds was explored. An acid counterion effect indicated the presence of a gold-mediated substrate preequilibrium before protodemetalation, and hybridization effects and a Hammett correlation with rho(+) = -0.41 indicated the involvement of the C-C pi system in the protodeauration of vinylgold, alkynylgold, and arylgold complexes.
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