Nitrogen-Carbon Bond Formation by Reactions of a Titanium-Potassium Dinitrogen Complex with Carbon Dioxide, tert-Butyl Isocyanate, and Phenylallene

被引:51
|
作者
Nakanishi, Yusuke [1 ]
Ishida, Yutaka [1 ]
Kawaguchi, Hiroyuki [1 ]
机构
[1] Tokyo Inst Technol, Dept Chem, Meguro Ku, Tokyo 1528551, Japan
关键词
nitrogen fixation; O ligands; potassium; titanium; tripodal ligands; INDUCED N-2 CLEAVAGE; SIDE-ON; MOLECULAR NITROGEN; END-ON; TANTALUM COMPLEXES; ZIRCONIUM; REACTIVITY; REDUCTION; LIGANDS; CO;
D O I
10.1002/anie.201704286
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nitrogen-carbon bond-forming reactions at coordinated dinitrogen in a bifunctional titanium-potassium system are reported. A titanium atrane complex with a tris(aryloxide)methyl ligand (1) was treated with two equivalents of potassium naphthalenide under N-2 atmosphere to generate a bifunctional complex (2) in which N-2 binds end-on to two titanium centers and side-on to three potassium cations. Dinitrogen complex 2 reacted with carbon dioxide, tert-butyl isocyanate, and phenylallene, forming nitrogen-carbon bonds and affording diverse N-functionalized products. The reaction of 2 with CO2 followed by addition of Me3SiCl resulted in the formation of the starting complex 1 with concomitant release of silylated carboxyl hydrazines while the reaction with two equivalents of tert-butyl isocyanate proceeded by insertion into the Ti-N bonds. Treatment of 2 with phenylallene afforded vinyl-substituted hydrazido complexes.
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页码:9193 / 9197
页数:5
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