کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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69076 | 48529 | 2006 | 6 صفحه PDF | دانلود رایگان |

The behavior of 2-methyl-3-butenenitrile (2M3BN) in the presence of catalytic amount of several cobalt complexes was evaluated. Irrespective of the nature of cobalt complexes and the experimental conditions (presence of ligand [such as P(OPh)3 or pyridine], or/and of Lewis acid [ZnCl2, AlCl3], organic solvent or ionic liquid), the product of isomerization 2-methyl-2-butenenitrile was obtained instead of the expected rearranged product 3-pentenenitrile (3PN). This result was explained by the activation of CH bond instead of CCN bond. With 3PN, the first example of a reversible cleavage of the CCN with complex derived from Co+ was evidenced.
2M3BN in the presence of catalytic amount of several cobalt complexes was mainly isomerized into 2M2BN due to a easier activation of C–H bond instead of CCN bond.With 3PN, the first example of a reversible cleavage of the CCN with complex derived from Co+ was evidenced. Figure optionsDownload as PowerPoint slide
Journal: Journal of Molecular Catalysis A: Chemical - Volume 246, Issues 1–2, 1 March 2006, Pages 242–247