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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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