An iron diphosphineborane platform that was previously reported to facilitate a high degree of N2 functionalization is herein shown to effect reductive CO coupling. Disilylation of an iron dicarbonyl precursor furnishes a structurally unprecedented iron dicarbyne complex. Several complexes related to this process are also characterized which allows for a comparative analysis of their respective Fe-B and Fe-C bonding. Facile hydrogenation of the iron dicarbyne at ambient temperature and 1 atm H2 results in release of a CO-derived olefin.
A CO-derived iron dicarbyne that releases olefin upon hydrogenation.
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作者:Suess Daniel L M, Peters Jonas C
| 期刊: | Journal of the American Chemical Society | 影响因子: | 15.600 |
| 时间: | 2013 | 起止号: | 2013 Aug 28; 135(34):12580-3 |
| doi: | 10.1021/ja406874k | ||
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