RESUMEN
In this article, we report sterically-controlled iron sites based on non-chelating bulky imidazole ligands. Adding 6 equiv. of 1,2-dimethylimidazole (1,2-Me2Im) to Fe(OTf)2â 2CH3CN affords the first example of a 5-coordinate imidazoleiron complex ([Fe(1,2-Me2Im)5](OTf)2, 1). The structure is distorted square pyramidal (τ5 = 0.41). When an iPr group is substituted for the methyl group at the 2-position on the imidazole (2-iPr-1-MeIm), the 14-electron complex ([Fe(2-iPr-1-MeIm)4](OTf)2, 2) is obtained. This complex exhibits slightly distorted tetrahedral geometry (τ'4 = 0.93) with four N-donors and serves as a 4-His iron structural model complex for carotenoid cleavage dioxygenases (CCD). The electronic structure of 1 and 2 were characterized by Mössbauer spectroscopy. Reactions of 1 and 2 with model olefin substrates (1-R-4-(1-methoxyprop-1-en-2-yl)benzene; R = Me or Br) in the presence of oxygen result in olefin cleavage yielding ketone and aldehyde products, although 2 yields more products than 1. Support for a proposed reaction mechanism for 2 is offered from Density Functional Theory (DFT) calculations.
RESUMEN
Bicyclic pyrazabole-bridged ferrocenes with BH groups at their bridgehead positions were prepared from [Li(thf)]2[1,1'-fc(BH3)2] and pyrazole or 3,5-dimethylpyrazole in the presence of Me3SiCl (1 or 1Me, respectively; 1,1'-fc = 1,1'-ferrocenylene); Me3SiH and H2 are released as byproducts. Treatment of 1 or 1Me with 1 eq. of the hydride scavenger [Ph3C][B(C6F5)4] afforded the borenium salts [2][B(C6F5)4] (72%) and [2Me][B(C6F5)4] (77%). According to X-ray crystallography, [2Me]+ contains one trigonal-planar borenium cation, the cyclopentadienyl (Cp) rings of the 1,1'-fc fragment remain parallel to each other, but the Cp-B bond vector is bent out of the Cp plane by an unprecedentedly large dip angle α* of 40.6°. The Feâ¯B(sp2) distance is very short (2.365(4) Å) and the 11B NMR signal of the cationic B(sp2) center is remarkably upfield shifted (23.4 ppm), suggesting a direct Fe(3d) â B(2p) donor-acceptor interaction. Although this interpretation is confirmed by quantum-chemical calculations, the coupling between the associated orbitals corresponds to an energy of only 12 kJ mol-1. Accordingly, both the experimental (e.g., Gutmann-Beckett acceptor number AN = 111) and theoretical assessment (e.g., Et3PO and F--ion affinities) of the Lewis acidity proves that [2]+ is among the strongest boron-based Lewis acids available to date.
RESUMEN
Phonon modes play a vital role in the cooperative phenomenon of light-induced spin transitions in spin crossover (SCO) molecular complexes. Although the cooperative vibrations, which occur over several hundreds of picoseconds to nanoseconds after photoexcitation, are understood to play a crucial role in this phase transition, they have not been precisely identified. Therefore, we have performed a novel optical laser pump-nuclear resonance probe experiment to identify the Fe-projected vibrational density of states (pDOS) during the first few nanoseconds after laser excitation of the mononuclear Fe(II) SCO complex [Fe(PM-BiA)2(NCS)2]. Evaluation of the so obtained nanosecond-resolved pDOS yields an excitation of â¼8% of the total volume of the complex from the low-spin to high-spin state. Density functional theory calculations allow simulation of the observed changes in the pDOS and thus identification of the transient inter- and intramolecular vibrational modes at nanosecond time scales.
RESUMEN
Iron oxide nano-crystals 0.1-1.1 µm in diameter were generated on sulfur-doped amorphous carbon surfaces by electron beam irradiation of the novel 13e- high-spin complex [Fe(4-methyl-1,2-benzenedithiolate)2][NHEt3] encapsulated in a triblock copolymer. Possible relevance to iron nano-mineralization from Fe-S ferredoxin proteins and iron dysregulation in neurological disorders is discussed.