Cervantes-Reyes Alejandro, Rominger Frank, Rudolph Matthias, Hashmi A Stephen K
Organisch-Chemisches Institut, Heidelberg University, Im Neuenheimer Feld 270, 69120, Heidelberg, Germany.
Chemistry Department, Faculty of Science, King Abdulaziz University, Jeddah, 21589, Saudi Arabia.
Chemistry. 2019 Sep 6;25(50):11745-11757. doi: 10.1002/chem.201902458. Epub 2019 Aug 8.
Nine- and ten-membered N-heterocyclic carbene (NHC) ligands have been developed and for the first time their gold(I) complexes were synthesized. The protonated NHC pro-ligands 2 a-h were prepared by the reaction of readily available N,N'-diarylformamidines with bis-electrophilic building blocks, followed by anion exchange. In situ deprotonation of the tetrafluoroborates 2 a-h with tBuOK in the presence of AuCl(SMe ) provided fast access to NHC-gold(I) complexes 3-10. These new NHC-gold(I) complexes show very good catalytic activity in a cycloisomerization reaction (0.1 mol % catalyst loading, up to 100 % conversion) and their solid-state structures reveal high steric hindrance around the metal atom (%V up to 53.0) which is caused by their expanded-ring architecture.
已开发出九元和十元氮杂环卡宾(NHC)配体,并首次合成了它们的金(I)配合物。质子化的NHC前体配体2 a-h是通过易得的N,N'-二芳基甲脒与双亲电砌块反应,然后进行阴离子交换制备的。在AuCl(SMe )存在下,用tBuOK对四氟硼酸盐2 a-h进行原位脱质子化,可快速得到NHC-金(I)配合物3-10。这些新型NHC-金(I)配合物在环异构化反应中表现出非常好的催化活性(催化剂负载量为0.1 mol %,转化率高达100 %),并且它们的固态结构显示出金属原子周围存在高空间位阻(%V高达53.0),这是由其扩环结构引起的。