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Activation of CO 2 , CS 2 , and Dehydrogenation of Formic Acid Catalyzed by Iron(II) Hydride Complexes
Author(s) -
Wang Lin,
Sun Hongjian,
Zuo Zhenyu,
Li Xiaoyan,
Xu Weiqin,
Langer Robert,
Fuhr Olaf,
Fenske Dieter
Publication year - 2016
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.201600642
Subject(s) - chemistry , dehydrogenation , formic acid , formate , hydride , catalysis , inorganic chemistry , reaction mechanism , ligand (biochemistry) , medicinal chemistry , photochemistry , metal , organic chemistry , biochemistry , receptor
Fluoroarylimine‐stabilized iron(II) hydrides were used for the activation of CO 2 . The resulting iron(II) formate complex 6 , which was obtained by formal CO 2 insertion into the Fe–H bond, turned out to be unstable in solution. CO was suitable for the formation of stable analogues of complex 6 . From the three‐component reaction of CO, CO 2 , and iron hydride, a series of stable carbonyl formate iron(II) complexes 7 – 9 were generated. Iron(II) formate complex 6 could also be obtained from the reaction of the iron(II) hydride complex with formic acid. On the basis of this result, the dehydrogenation of formic acid catalyzed by iron(II) hydrides was explored. The reaction was monitored by in situ 1 H NMR spectroscopy, and a possible mechanism was proposed. In addition, iron(II) hydrides also reacted with CS 2 to generate thiocarboxy iron(II) complexes 12 , 13 , 14 , and 16 . Unexpected complex 17 was produced from the three‐component reaction of CS 2 , complex 4 , and compound 15 . The possible mechanism of the three‐component reaction was also studied by operando IR spectroscopy.