This is the authors' abstract. We don't add key points for this paper.
2-(1,3-Bis-3'-butylimidazol-1'-yl-2'-ylidene)phenylene)bis(dimethylamido) iodo zirconium(iv) (3) and 2-(1,3-bis-3'-butylimidazol-1'-yl-2'-ylidene)phenylene)bis (dimethylamido) bromo zirconium(iv) (4), have been prepared via a modification of the solvent and stoichiometry from the previously reported methodology. The reactivity of 3 and 4 in hydroamination/cyclisation is reported. Both diamido complexes have been found to improve catalytic activity as compared with the previously reported mono-amido analogues. Complexes 3 and 4 were observed to be selective for primary amines over secondary amines in hydroamination/cyclisation. The lack of reactivity with secondary amines is consistent with a mechanism involving requisite formation of a Zr-imido intermediate.
Answers are grounded in this paper and cite their sources.
No takes yet. Share an insight, caveat, or question.
Valle et al. (2016) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: