Decarbonylative ether dissection by iridium pincer complexes

被引:9
|
作者
Yoo, Changho [1 ]
Dodge, Henry M. [1 ]
Farquhar, Alexandra H. [1 ]
Gardner, Kristen E. [1 ]
Miller, Alexander J. M. [1 ]
机构
[1] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
基金
美国国家科学基金会;
关键词
H BOND ACTIVATION; METHANOL CARBONYLATION; ALKANE DEHYDROGENATION; OXIDATIVE ADDITION; WATER ELIMINATION; CLEAVAGE; CATALYST; LIGAND; GENERATION; REACTIVITY;
D O I
10.1039/d0sc03736b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A unique chain-rupturing transformation that converts an ether functionality into two hydrocarbyl units and carbon monoxide is reported, mediated by iridium(i) complexes supported by aminophenylphosphinite (NCOP) pincer ligands. The decarbonylation, which involves the cleavage of one C-C bond, one C-O bond, and two C-H bonds, along with formation of two new C-H bonds, was serendipitously discovered upon dehydrochlorination of an iridium(iii) complex containing an aza-18-crown-6 ether macrocycle. Intramolecular cleavage of macrocyclic and acyclic ethers was also found in analogous complexes featuring aza-15-crown-5 ether or bis(2-methoxyethyl)amino groups. Intermolecular decarbonylation of cyclic and linear ethers was observed when diethylaminophenylphosphinite iridium(i) dinitrogen or norbornene complexes were employed. Mechanistic studies reveal the nature of key intermediates along a pathway involving initial iridium(i)-mediated double C-H bond activation.
引用
收藏
页码:12130 / 12138
页数:9
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