Franco Dario, Marchenko Anatoliy, Koidan Georgyi, Hurieva Anastasiia N, Kostyuk Aleksandr, Biffis Andrea
Dipartimento di Scienze Chimiche, Università di Padova, via Marzolo 1, Padova 35131, Italy.
Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Murmanska 5, Kyiv-94 02660, Ukraine.
ACS Omega. 2018 Dec 20;3(12):17888-17894. doi: 10.1021/acsomega.8b02619. eCollection 2018 Dec 31.
The catalytic potential of palladium(II) complexes with chelating -phosphanyl--heterocyclic carbenes featuring a saturated imidazolin-2-ylidene or tetrahydropyrimid-2-ylidene ring has been investigated in intermolecular alkyne hydroamination reactions. The complexes were found to be among the most active Pd-based catalysts for these processes and to enable the use of low reaction temperatures (40 °C) and of solventless conditions. The Pd complexes require activation by 2 equiv of a silver salt to remove chlorido ligands from the metal coordination sphere; they can however also be presynthesized in active form, which allows their use under silver-free conditions. The hydroamination reaction was found to efficiently proceed with terminal alkynes and different ring-substituted, primary arylamine substrates.
研究了钯(II)与具有饱和咪唑啉-2-亚基或四氢嘧啶-2-亚基环的螯合膦基杂环卡宾配合物在分子间炔烃氢胺化反应中的催化潜力。发现这些配合物是这些反应中活性最高的钯基催化剂之一,能够在低温(40°C)和无溶剂条件下使用。钯配合物需要2当量的银盐活化以从金属配位球中除去氯配体;然而,它们也可以以活性形式预合成,这使得它们可以在无银条件下使用。发现氢胺化反应能有效地与末端炔烃和不同的环取代的伯芳胺底物进行。