Abdijacobsen7422

The nitrogenase enzymes are responsible for all biological nitrogen reduction. How this is accomplished at the atomic level, however, has still not been established. The molybdenum-dependent nitrogenase has been extensively studied and is the most active catalyst for dinitrogen reduction of the nitrogenase enzymes. The vanadium-dependent form, on the other hand, displays different reactivity, being capable of CO and CO2 reduction to hydrocarbons. Only recently did a crystal structure of the VFe protein of vanadium nitrogenase become available, paving the way for detailed theoretical studies of the iron-vanadium cofactor (FeVco) within the protein matrix. The crystal structure revealed a bridging 4-atom ligand between two Fe atoms, proposed to be either a CO32- or NO3- ligand. Using a quantum mechanics/molecular mechanics model of the VFe protein, starting from the 1.35 Å crystal structure, we have systematically explored multiple computational models for FeVco, considering either a CO32- or NO3- ligand, threemilar cofactors suggest an explanation for distinct differences in reactivity.There is a large interest in developing oxidative transformations catalyzed by palladium complexes that employ environmentally friendly and economical oxidizing reagents such as dioxygen. Recently, we have reported the isolation and characterization of various mononuclear PdIII and PdIV complexes supported by the tetradentate ligands N,N'-dialkyl-2,11-diaza[3.3](2,6)pyridinophane (RN4, R = tBu, iPr, Me), and the aerobically induced C-C and C-heteroatom bond formation reactivity was investigated in detail. Given that the steric and electronic properties of the multidentate ligands were shown to tune the stability and reactivity of the corresponding high-valent Pd complexes, herein we report the use of an asymmetric N4 ligand, N-mehtyl-N'-tosyl-2,11-diaza[3.3](2,6)pyridinophane (TsMeN4), in which one amine N atom contains a tosyl group. The N-Ts donor atom exhibits a markedly reduced donating ability, which led to the formation of transiently stable PdIII and PdIV complexes, and consequently the corresponding O2 oxidation reactivity and the subsequent C-C bond formation were improved significantly.Alzheimer's disease is characterized by the presence of extracellular amyloid-β plaques. Positron emission tomography (PET) imaging with tracers radiolabeled with positron-emitting radionuclides that bind to amyloid-β plaques can assist in the diagnosis of Alzheimer's disease. With the goal of designing new imaging agents radiolabeled with positron-emitting copper-64 radionuclides that bind to amyloid-β plaques, a family of bis(thiosemicarbazone) ligands with appended substituted stilbenyl functional groups has been prepared. https://www.selleckchem.com/products/mg-101-alln.html The ligands form charge-neutral and stable complexes with copper(II). The new ligands can be radiolabeled with copper-64 at room temperature. Two lead complexes were demonstrated to bind to amyloid-β plaques present in post-mortem brain tissue from subjects with clinically diagnosed Alzheimer's disease and crossed the blood-brain barrier in mice. The work presented here provides strategies to prepare compounds with radionuclides of copper that can be used for targeted brain PET imaging.Ag-Ti nanocomposite materials have drawn increasing research attention because of their superior catalytic properties. However, the preparation of a crystalline Ag-Ti material is an important challenge in synthetic chemistry. Herein, we report a family of atomically precise Ag-doped polyoxotitanium nanoclusters (PTCs) (PTC-253-PTC-256) with a size of 19.56 × 19.02 Å. Each Ag-PTC is made up of a tiny Ag2 kernel and a double-decker Ti12 nanowheel as well as an organic protective shell. Hence, they can be regarded as Ag2@Ti12@(L)14(OMe) n unique triple core-shell structures. Notably, the peripheral organic shell can be modified with different benzoate derivatives. With precise atomic information, these compounds can be used as ideal molecular models of Ag-Ti nanocomposite materials for studying the growth or reaction mechanism via theoretical calculations. Meanwhile, a PTC-255-modified electrode presents efficient electrocatalytic CO2 reduction activity with a Faradaic efficiency (FE) of 29.4%. This work demonstrates that Ag-doped crystalline PTC materials are promising candidates for application to the electrocatalytic CO2 reduction reaction (CO2RR).Titanium is one of the most abundant elements on Earth but is commonly thought to have no role in biology because of its propensity to hydrolyze. Nature stabilizes hard Lewis acidic metals from hydrolysis using a variety of mechanisms, providing inspiration for how titanium can be stabilized using biological ligands. The well-characterized Due Ferri single-chain (DFsc) de novo designed protein was developed to bind and stabilize iron and provides a binding site with hard Lewis basic residues able to bind two metal ions. We demonstrate that the DFsc scaffold stably binds 2 equiv of titanium and protects them from unwanted hydrolysis. The Ti4+-DFsc protein complex was tested for its ability to hydrolytically cleave DNA, where it was seen to linearize plasmid DNA in an overnight reaction. Ti4+-DFsc is thus the first example of a functional, soluble titanium-protein complex.Herein we report a new high-denticity chelator based on the iron siderophore desferrioxamine (DFO). Our new chelator-DFO2-is acyclic and was designed and synthesized with the purpose of improving the coordination chemistry and radiolabeling performance with radioactive zirconium-89. link2 The radionuclide zirconium-89 ([89Zr]Zr4+) has found wide use for positron emission tomography (PET) imaging when it is coupled with proteins, antibodies, and nanoparticles. DFO2 has a potential coordination number of 12, which uniquely positions this chelator for binding large, high-valent, and oxophilic metal ions. Following synthesis of the DFO2 chelator and the [natZr]Zr-(DFO2) complex we performed density functional theory calculations to study its coordination sphere, followed by zirconium-89 radiolabeling experiments for comparisons with the "gold standard" chelator DFO. DFO (CN 6) can coordinate with zirconium in a hexadentate fashion, leaving two open coordination sites where water is thought to coordinate (total CN 8). Dsis, apo-transferrin, hydroxyapatite, and EDTA challenges. These results suggest that DFO2 is a promising next-generation scaffold for zirconium-89 chelators and holds promise for radiochemistry with even larger radionuclides, which we anticipate will expand the utility of DFO2 into theranostic applications.Photosubstitution reactions of ruthenium complexes with pyrazole ligands, cis-[Ru(bpy)2(pzH)2]2+ (1a), cis-[Ru(bpy)2(pz)(pzH)]+ (1b), and cis-[Ru(bpy)2(pz)2]0 (1c) (pzH = pyrazole, bpy = 2,2'-bipyridine), were investigated. Dicationic complex 1a was deprotonated to 1b using moderate base (pKa = 15.2, MeCN), while the second deprotonation to give 1c required more severe conditions (pKa = 26.9). Monocationic complex 1b possessed an N-H···N-type intramolecular hydrogen bond between the pyrazole and pyrazolate ligands, as corroborated by the solid-state crystal structure. The photosubstitution quantum yield of 1a (Φ = 0.26) was comparable to that of cis-[Ru(bpy)2(pyridine)2]2+ (Φ = 0.24) in acetonitrile solution. In contrast, the photodissociation of a pzH ligand was strongly suppressed by the deprotonation of a pyrazole ligand N-H group. link3 In the presence of 10 000 equiv of 4,4'-dimethylaminopyridine, the quantum yield dropped to ∼2 × 10-6 in acetonitrile. The photosubstitution quantum yield of 1b was even smaller than that of neutral complex 1c, although 1c had a smaller HOMO-LUMO energy gap than monocationic complex 1b. The small quantum yield of 1b was attributed to intramolecular hydrogen bonding between pyrazole and pyrazolate ligands. The apparent rate constants for the photosubstitution of 1b were highly solvent-dependent. The photosubstitution of 1b was suppressed in aprotic solvents, while the reaction was accelerated by 2 orders of magnitude in protic solvents with strong proton donor abilities.The stereodynamics of an ultrafast (picosecond) isomerization in a penta-coordinated ruthenium complex, Ru(S2C2(CF3)2)(CO)(PPh3)2, were characterized by density functional theory (DFT). The ruthenium complex crystallizes in two almost-square pyramidal (SP) forms. The violet form has an apical PPh3 ligand, the orange form has an apical CO ligand, and their solution displays three CO stretching frequencies. With 4 possible centers of chirality (1 ruthenium, 2 phosphines, and 1 dithiolate), there are 24 stereoisomers. DFT calculations of these stereoisomers show structures ranging from almost-perfect SP (τ5 ≈ 0) to structures significantly distorted toward trigonal bipyramidal (TBP) (τ5 ≈ 0.6). The stereoisomers fall neatly into three groups, with νCO ≈ 1960 cm-1, 1940 cm-1, and 1980 cm-1. These isomers were found to interconvert over relatively small barriers via Ru-S bond twisting, CF3 rotation, phenyl twisting, PPh3 rotation, and, in some cases, by coupled motions. The composite energy surface for each CO frequency group shows that interconversions among the low-energy structures are possible via both the direct and indirect pathways, while the indirect pathway via isomers in the νCO ≈ 1980 cm-1 group is more favorable, which is a result consistent with recent experimental work. This work provides the first complete mechanistic picture of the ultrafast isomerization of penta-coordinated, distorted SP, d6-transition-metal complexes.La15(FeC6)4H was synthesized from the reaction of iron and anthracene in La/Ni eutectic flux. Anthracene was the source of both the carbon and hydrogen in the product. The structure of this metal carbide hydride features hydride ions in tetrahedral interstitial sites surrounded by lanthanum ions, which was confirmed by single-crystal neutron diffraction studies. The trigonal planar FeC6 units in which the central iron atom is coordinated by three ethylenide groups are similar to those found in La3.67FeC6, a previously reported compound that is formed in the absence of a hydride source. Magnetic susceptibility data confirm that the iron sites do not have magnetic moments. Density of states calculations indicate that La15(FeC6)4H is metallic and is stabilized by the incorporation of hydride anions.In order to examine the possibility of Lewis acid-Lewis base (LA-LB) interactions between the boron atom of B(C6F5)2OH and the oxo groups ("yl" oxygen atoms) of uranyl β-diketonato complexes, we have measured the 1H, 11B, 17O, 19F NMR and IR spectra of toluene solutions containing β-diketonato complexes [UO2(acac)2DMSO or UO2(dfh)2DMSO, where acac = 2,4-pentanedionate, dfh = 1,1,1,2,2,6,6,7,7,7-decafluoroheptane-3,5-dionate, and DMSO = dimethyl sulfoxide] and B(C6F5)2OH. 11B and 17O NMR spectra of solutions containing UO2(dfh)2DMSO and B(C6F5)2OH showed no change in their chemical shifts regardless of the [B(C6F5)2OH]/[UO2(dfh)2DMSO] ratio. This indicates that there were no apparent interactions between B(C6F5)2OH and UO2(dfh)2DMSO. On the other hand, in the corresponding NMR spectra of solutions containing UO2(acac)2DMSO and B(C6F5)2OH, new signals were observed at a higher field than signals observed in the solutions containing only B(C6F5)2OH or UO2(acac)2DMSO, and their intensity changed with the [B(C6F5)2OH]/[UO2(acac)2DMSO] ratio.