Xue Ting, Ma Cheng, Liu Le, Xiao Chunhui, Ni Shao-Fei, Zeng Rong
School of Chemistry, Xi'an Jiaotong University, Xi'an, 710049, PR China.
Department of Chemistry and Key Laboratory for Preparation and Application of Ordered Structural Materials of Guangdong, Shantou University, Shantou, 515063, Guangdong, PR China.
Nat Commun. 2024 Feb 16;15(1):1455. doi: 10.1038/s41467-024-45686-1.
Photoexcitation of the electron-donor-acceptor complexes have been an effective approach to achieve radicals by triggering electron transfer. However, the catalytic version of electron-donor-acceptor complex photoactivation is quite underdeveloped comparing to the well-established utilization of electronically biased partners. In this work, we utilize 4-nitrophthalonitrile as an electron acceptor to facilitate the efficient π-stacking with electron-rich aromatics to form electron-donor-acceptor complex. The characterization and energy profiles on the cocrystal of 4-nitrophthalonitrile and 1,3,5-trimethoxybenzene disclose that the electron transfer is highly favorable under the light irradiation. This electron acceptor catalyst can be efficiently applied in the benzylic C-H bond photoactivation by developing the Giese reaction of alkylanisoles and the oxidation of the benzyl alcohols. A broad scope of electron-rich aromatics can be tolerated and a mechanism is also proposed. Moreover, the corresponding π-anion interaction of 4-nitrophthalonitrile with potassium formate can further facilitate the hydrocarboxylation of alkenes efficiently.
通过触发电子转移,对电子供体-受体复合物进行光激发一直是产生自由基的有效方法。然而,与已成熟的电子偏向型分子对的应用相比,电子供体-受体复合物光活化的催化形式仍相当不完善。在这项工作中,我们利用4-硝基邻苯二甲腈作为电子受体,促进其与富电子芳烃形成有效的π-堆积,从而形成电子供体-受体复合物。对4-硝基邻苯二甲腈与1,3,5-三甲氧基苯共晶体的表征和能量分布表明,在光照下电子转移非常有利。通过开发烷基苯甲醚的吉泽反应和苄醇的氧化反应,这种电子受体催化剂可有效地应用于苄基C-H键的光活化。该反应可以耐受多种富电子芳烃,并提出了相应的反应机理。此外,4-硝基邻苯二甲腈与甲酸钾的相应π-阴离子相互作用可以进一步有效地促进烯烃的氢羧化反应。