Hydrophosphination of Unactivated Alkenes and Alkynes Using Iron(II): Catalysis and Mechanistic Insight

被引:56
作者
Espinal-Viguri, Maialen [1 ]
King, Andrew K. [1 ]
Lowe, John P. [1 ]
Mahon, Mary F. [1 ]
Webster, Ruth L. [1 ]
机构
[1] Univ Bath, Sch Chem, Claverton Down, Bath BA2 7AY, Avon, England
基金
英国工程与自然科学研究理事会;
关键词
alkenes; alkynes; phosphines; homogeneous catalysis; heterofunctionalization; P-C bond formation; iron; radicals; hydrofunctionalization; phospholanes; phosphinanes; C-P BOND; INTRAMOLECULAR HYDROPHOSPHINATION/CYCLIZATION; COMPLEXES; PHOSPHINES; LIGANDS; PHOSPHINOALKENES; CHEMISTRY; ACTIVATION; ELEMENTS; FACILE;
D O I
10.1021/acscatal.6b02290
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The catalytic addition of phosphines to alkenes and alkynes is a very attractive process that offers access to phosphines in a 100% atom-economic reaction using readily available and inexpensive materials. The products are potentially useful ligands and organocatalysts. Herein, we report the first example of intramolecular hydrophosphination of a series of nonactivated phosphinoalkenes and phosphinoalkynes with a simple iron beta-diketiminate complex. Kinetic studies suggest that this transformation is first-order with respect to both the phosphine and the catalyst. A mechanistic interpretation of the iron-catalyzed hydrophosphination is presented, supported by the experimental evidence collected.
引用
收藏
页码:7892 / 7897
页数:6
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