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Communication—Semi-Rigid Ru(II)Porphyrinate-Based Macrocyclic Receptor as Endotopic Catalyst for Carbene Transfer Reactions
ECS Journal of Solid State Science and Technology ( IF 2.2 ) Pub Date : 2020-07-30 , DOI: 10.1149/2162-8777/aba912
Liniquer A. Fontana 1 , Arthur F. P. Alcntara 1, 2 , Vitor H. Rigolin 1 , Jackson D. Megiatto Jr. 1
Affiliation  

A 5,15- bis (1,1'-biphenyl)porphyrin-based macrocyclic receptor with a well-defined cavity is suitable for coordination of Ru(II) ions with carbonyl axial ligands. Axial ligand substitution reaction using diphenyldiazomethane as reactant affords a macrocyclic Ru(II)porphyrinate with a diphenylcarbene moiety that functions as an excellent endotopic catalysts for the dimerization reaction of ethyldiazoacetate. The extraordinary stability of the diphenylcarbene axial ligand in conjunction with the high reactivity of the Ru(II)porphyrinate moiety towards diazoderivatives render the macrocyclic complex a promising candidate for the active metal template synthesis of interlocked molecules.

中文翻译:

交流—基于卟啉的半刚性Ru(II)大环受体作为碳转移反应的内位催化剂

具有明确界定的腔的基于5,15-双(1,1'-联苯)卟啉的大环受体适用于Ru(II)离子与羰基轴向配体的配位。使用二苯基重氮甲烷作为反应物的轴向配体取代反应提供了带有二苯基碳烯部分的大环卟啉钌(II),它是乙基重氮乙酸乙酯二聚反应的出色内位催化剂。二苯卡宾轴向配体的非凡稳定性与Ru(II)卟啉酸酯部分对重氮衍生物的高反应性相结合,使大环配合物成为连锁分子活性金属模板合成的有希望的候选者。
更新日期:2020-07-31
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