Lee Sojung, Gabidullin Bulat, Richeson Darrin
Department of Chemistry and Biomolecular Sciences and Centre for Catalysis Research and Innovation, University of Ottawa, Ottawa, Ontario K1N6N5, Canada.
ACS Omega. 2018 Jun 19;3(6):6587-6594. doi: 10.1021/acsomega.8b00437. eCollection 2018 Jun 30.
The first synthesis, isolation, and characterization of permidin-2-ylidene complexes of Pd(II) is reported with entry resulting from either a direct reaction with isolable six-membered N-heterocyclic carbene or from the enetetramine, arising from dimerization of the carbene. Furthermore, a simplified method to prepare N,N'-disubstituted perimidinium bromide salts, precursors to 1,3-disubstituted perimidin-2-ylidene, was achieved using ammonium bromide as a source of weak acid. Through synthesis and nuclear magnetic resonance spectroscopic analysis of a carbene-phosphinidine adduct, an interrogation of the fundamental π-bonding ability of 1,3-diisopropylperimidin-2-ylidene revealed this interaction to be weak and of a similar order to unsaturated imidazol-2-ylidenes.
报道了钯(II)的二亚胺基配合物的首次合成、分离和表征,其产物是通过与可分离的六元氮杂环卡宾直接反应或由卡宾二聚产生的烯四胺反应得到的。此外,使用溴化铵作为弱酸源,实现了一种制备N,N'-二取代的二亚胺溴盐的简化方法,该盐是1,3-二取代的二亚胺基的前体。通过卡宾-磷亚胺加合物的合成和核磁共振光谱分析,对1,3-二异丙基二亚胺基的基本π键合能力进行了研究,结果表明这种相互作用较弱,与不饱和咪唑-2-亚基的相互作用相似。