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S = 2 Fe IV ═O centers generated in the active sites of nonheme iron oxygenases cleave substrate C-H bonds at rates significantly faster than most known synthetic Fe IV ═O complexes. Unlike the majority of the latter, which are S = 1 complexes, [Fe IV (O)(tris(2-quinolylmethyl)amine)(MeCN)] 2+ ( 3 ) is a rare example of a synthetic S = 2 Fe IV ═O complex that cleaves C-H bonds 1000-fold faster than the related [Fe IV (O)(tris(pyridyl-2-methyl)amine)(MeCN)] 2+ complex ( 0 ). To rationalize this significant difference, a systematic comparison of properties has been carried out on 0 and 3 as well as related complexes 1 and 2 with mixed pyridine (Py)/quinoline (Q) ligation. Interestingly, 2 with a 2-Q-1-Py donor combination cleaves C-H bonds at 233 K with rates approaching those of 3 , even though Mössbauer analysis reveals 2 to be S = 1 at 4 K. At 233 K however, 2 becomes S = 2, as shown by its 1 H NMR spectrum. These results demonstrate a unique temperature-dependent spin-state transition from triplet to quintet in oxoiron(IV) chemistry that gives rise to the high C-H bond cleaving reactivity observed for 2 .

Reaction of the complex [(Tp Ph,Me )Fe II (NCMe) 3 ]BF 4 , where Tp Ph,Me = hydrotris(3-phenyl,5-methyl-1-pyrazolyl)borate, with the iodonium heteroylide PhI═NTs (1.5 equiv) is proposed to result in the insertion of N-tosylnitrene into one C-H bond at the ortho ring position of a 3-pyrazole phenyl substituent; subsequent deprotonation of the nascent aniline and one-electron oxidation of iron forms TsNH 2 (0.5 equiv) as a coproduct. The covalent ligand modification and oxidation results in an intense purple-brown anilinato-iron(III) LMCT chromophore. This intramolecular reaction is utilized as a consistent clock to determine relative rates of competitive intermolecular nitrene transfer to added substrates, specifically to para-substituted styrenes and thioanisoles. Prior addition of substrate to the reaction of PhI═NTs with the iron(II) complex attenuates the CT absorbance of the equilibrium solution. Fitting of the concentration-dependent absorption data gives the ratio of intra- versus intermolecular nitrene transfer. Because the former is independent of substrate, ratios for various substrates are directly comparable, and this approach enables acquisition of data for a single substrate under nearly stoichiometric, as opposed to competitive catalytic, conditions. Hammett analyses of such data are consistent with an electrophilic intermediate consistent with known or suspected imidoiron(IV) complexes. Because this intermediate was not observed directly, plausible geometric and electronic structures were modeled and assessed using density functional theory.

Thiol-ene click chemistry has become a powerful paradigm in synthesis, materials science, and surface modification in the past decade. In the photoinitiated thiol-ene reaction, an induction period is often observed before the major change in its kinetic curve, for which a possible mechanism is proposed in this report. Briefly, light soaking generates radicals following the zeroth-order reaction kinetics. The radical is the reactant that initializes the chain reaction of thiol-ene coupling, which is a first-order reaction. Combining both and under the light-limited conditions, a surprising kinetics represented by a Gaussian-like model evolves that is different from the exponential model used to describe the first-order reaction of the final product. The experimental data are fitted well with the new model, and the reaction kinetic constants can be pulled out from the fitting., Competing Interests: The authors declare no competing financial interest.

Successive surface reactions on hydrophilic silica substrates were designed and performed to immobilize ethanolamine-modified magnetic ferrite-based nanoparticle (NP) for surface characterization. The various surfaces were monitored using sum-frequency generation (SFG) spectroscopy. The surface of the hydrophilic quartz substrate was first converted to a vinyl-terminated surface by utilizing a silanization reaction, and then, the surface functional groups were converted to carboxylic-terminated groups via a thiol-ene reaction. The appearance and disappearance of the vinyl (═CH 2 ) peak at ∼2990 cm -1 in the SFG spectra were examined to confirm the success of the silanization and thiol-ene reactions, respectively. Acyl chloride (-COCl) formation from carboxy (-COOH) functional group was then performed for further attachment of magnetic amine-functionalized magnesium ferrite nanoparticles (NPs) via amide bond formation. The scattered NPs attached on the modified silica substrate was then used to study the changes in the spectral profile of the ethanolamine modifier of the NPs for in situ lead(II) (Pb 2+ ) adsorption at the solid-liquid interface using SFG spectroscopy. However, due to the limited number of NPs attached and sensitivity of SFG spectroscopy toward expected change in the modifier spectroscopically, no significant change was observed in the SFG spectrum of the modified silica with magnetic NPs during exposure to Pb 2+ solution. Nevertheless, SFG spectroscopy as a surface technique successfully monitored the modifications from a clean fused substrate to -COCl formation that was used to immobilize the decorated magnetic nanoparticles. The method developed in this study can provide a reference for many surface or interfacial studies important for selective attachment of adsorbed organic or inorganic materials or particles.