Macrocyclic Metal Complexes Bearing Rigid Polyaromatic Ligands: Synthesis and Catalytic Activity

被引:15
|
作者
Yamamoto, Koji [1 ,2 ]
Higuchi, Kazuki [1 ]
Ogawa, Masahiro [1 ]
Sogawa, Hiromitsu [1 ,3 ]
Kuwata, Shigeki [4 ]
Hayashi, Yoshihiro [4 ]
Kawauchi, Susumu [4 ]
Takata, Toshikazu [1 ]
机构
[1] Tokyo Inst Technol, Dept Chem Sci & Engn, Midori Ku, 4259 Nagatsuta Cho, Yokohama, Kanagawa 2268503, Japan
[2] Gunma Univ, Fac Sci & Technol, Div Mol Sci, 1-5-1 Tenjin Cho, Kiryu, Gunma 3768515, Japan
[3] RIKEN Ctr Sustainable Resource Sci, Biomacromol Res Team, 2-1 Hirosawa, Wako, Saitama 3510198, Japan
[4] Tokyo Inst Technol, Dept Chem Sci & Engn, Meguro Ku, 2-12-1 Ookayama, Tokyo 1528552, Japan
基金
日本科学技术振兴机构;
关键词
hydrosilylation; macrocyclic ligands; polyaromatic ligands; topology; transition metals; PLATINUM(II) COMPLEXES; PINCER COMPLEXES; 2ND-SPHERE COORDINATION; SIMULTANEOUS; 1ST-SPHERE; C BOND; BINDING; 1,3-BIS(2-PYRIDYL)BENZENE; METALLORECEPTORS; DERIVATIVES; EPOXIDATION;
D O I
10.1002/asia.201901561
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We synthesised palladium and platinum complexes possessing cyclic and acyclic pincer-type polyaromatic ligands and investigated their structural effect on the catalysis. The pincer-type bis(6-arylpyridin-2-yl)benzene skeleton was constructed via Krohnke pyridine synthesis under transition metal-free conditions on gram-scale quantity. Ligand structure significantly influenced catalytic activity toward the platinum-catalysed hydrosilylation of diphenyl acetylenes, despite the ligand-independence of the conformations and electronic properties of these complexes.
引用
收藏
页码:356 / 359
页数:4
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