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Synthesis and Structures of Iron(II) Alkyl and Thiolate Compounds Containing Sterically Hindered N-Functionalized Alkyl Ligands

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journal contribution
posted on 02.04.1996, 00:00 by Wing-Por Leung, Hung Kay Lee, Lin-Hong Weng, Bao-Sheng Luo, Zhong-Yuan Zhou, Thomas C. W. Mak
Iron(II) dialkyl compounds [FeR2] (R = C(SiMe3)2C5H4N-2 (1), C(Ph)(SiMe3)C5H4N-2 (2), CH(SiMe3)C9H6N-8 (4)) and [{Fe(CHSitBuMe2C5H4N-2)2}2] (3) have been prepared from the reaction of FeCl2 with the appropriate N-functionalized alkyllithium reagent in a 1:2 molar ratio. The monoalkylated iron(II) complex [Fe{CPhSiMe3C5H4N-2}(Cl)(TMEDA)] (5) has been prepared by treating FeCl2 with a stoichiometric amount of the organolithium reagent. X-ray analysis revealed that the alkyl ligands are bonded to the metal centers in a chelating manner in the mononuclear compounds 1 and 5, whereas in 3 one of the alkyl ligands forms an interligand bridge betwen the two iron centers. Compounds 1, 2, 4, and 5 have magnetic moments in the range 4.24−4.96 μB that are characteristic of a high-spin d6 electronic configuration with four unpaired electrons. The magnetic moment of the binuclear compound 3 is 2.92 μB per iron atom, apparently a consequence of antiferromagnetic coupling between the two metal centers. Subsequent reaction of 1 with ArMeOH (ArMe = 2,6-tBu2-4-MeC6H2) and ArSH (Ar = 2,4,6-tBu3C6H2) gave the neutral monomeric iron(II) bis(aryloxide) [Fe(OArMe)2{CH(SiMe3)2C5H4N-2}] (6) and dithiolate [Fe(SAr)2{CH(SiMe3)2C5H4N-2}] (7), respectively. Both of the latter compounds have a rare coordination number of 3 at the iron(II) center. The magnetic moment of 5.11 μB for 7 indicates a high-spin configuration with four unpaired electrons on the iron(II) center. Electrochemical studies on the compoounds are also reported.