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Cu(Ⅱ) and Cu(Ⅰ) complexes based on derivatives of imidazo[1,5-a]pyridine:Synthesis,structures,in situ metal-ligand reactions,and catalytic activity
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作者 JIA Bofei LIU Zhihao +7 位作者 GAO Zongyuan ZHOU Shuai WU Mengxiang ZHANG Qian ZHANG Xiamei CHEN Shuzhong YANG Xiaohan LI Yahong 《无机化学学报》 北大核心 2025年第5期1020-1036,共17页
Three efficient methods for the synthesis of a series of Cu(Ⅱ) and Cu(Ⅰ) complexes based on imidazo[1,5-a]pyridine derivatives were developed.These methods include the following:(ⅰ)Cu(Ⅱ) salts were used as metal s... Three efficient methods for the synthesis of a series of Cu(Ⅱ) and Cu(Ⅰ) complexes based on imidazo[1,5-a]pyridine derivatives were developed.These methods include the following:(ⅰ)Cu(Ⅱ) salts were used as metal sources and N,N-dimethylformamide was employed as a solvent as well as a reductant to produce Cu(Ⅰ) complexes.(ⅱ) An iodide-containing compound was utilized as a ligand and iodide source to prepare complexes.An in situ metalligand reaction occurred and an iodide-bridged copper complex was generated.(ⅲ) A series of aldehydes were added to the reaction systems to induce in situ metal-ligand reactions between the aldehydes and the imidazo[1,5-a]pyridine derivatives,producing polydentate ligand scaffolds.Eight complexes were prepared and characterized.The catalytic activities of these complexes toward the ketalization of ketones by ethylene glycol were investigated.With the exception of complex4,the remaining seven complexes all showed high catalytic activity.The lower activity of 4 may be due to the larger radius of bridging iodide ions and the shorter Cu(Ⅰ)…Cu(Ⅰ) distance.CCDC:2357696,1·2CH_(2)Cl_(2);2357697,2;2018292,3;2092192,4;2092190,5;2155557,6;2406155,7;2406156,8·EtOH. 展开更多
关键词 copper complexes imidazo[1 5‑a]pyridine in situ metal-ligand reactions ketalization reactions
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钯催化的苯甲酸邻位碳氢键氟化反应研究 被引量:1
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作者 汪成 张志鹏 《华东理工大学学报(自然科学版)》 CAS CSCD 北大核心 2022年第6期776-783,共8页
含氟有机分子通常具有一些独特的物理、化学以及生物学性质,因而在材料科学和药物化学中有着重要的应用价值。利用惰性碳氢键的活化来实现有机分子的官能团化近年来受到了极其广泛的关注,因此通过碳氢键的氟化反应来合成含氟有机分子也... 含氟有机分子通常具有一些独特的物理、化学以及生物学性质,因而在材料科学和药物化学中有着重要的应用价值。利用惰性碳氢键的活化来实现有机分子的官能团化近年来受到了极其广泛的关注,因此通过碳氢键的氟化反应来合成含氟有机分子也是有机合成中重要且具有挑战性的研究方向。以苯甲酸作为反应底物、以羧基作为导向基,通过对反应的添加剂、溶剂、氟化试剂和配体等进行筛选,实现了苯甲酸邻位碳氢键的氟化反应,以最高13%的分离收率得到了相应的单氟化产物。 展开更多
关键词 碳氢键活化 羧基导向基 氟化 吡啶酮配体
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