N−H Bond Formation at a Diiron Bridging Nitride

Despite their connection to ammonia synthesis, little is known about the ability of iron-bound, bridging nitrides to form N−H bonds. Herein we report a linear diiron bridging nitride complex supported by a redox-active macrocycle. The unique ability of the ligand scaffold to adapt to the geometric preference of the bridging species was found to facilitate the formation of N−H bonds via proton-coupled electron transfer to generate a μ-amide product. The structurally analogous μ-silyl- and μ-borylamide complexes were shown to form from the net insertion of the nitride into the E−H bonds (E=B, Si). Protonation of the parent bridging amide produced ammonia in high yield, and treatment of the nitride with PhSH was found to liberate NH₃ in high yield through a reaction that engages the redox-activity of the ligand during PCET.     

Measurement of gas flow parameters in the vicinity of bodies with the front stalling zone

Problems associated with the development of a new method for the diagnostics of gas flows, which is suitable for ballistic experiments, are considered. The method is based of shock wave sensing of the flow under investigation. Various methods are proposed for introducing sensing perturbations into the flow. These methods are used for measuring the parameters of a gas streamlining flying vehicles with the front stalling zone.     

Z-selective, catalytic internal alkyne semihydrogenation under H2/CO mixtures by a niobium(III) imido complex

The discovery of a Nb(III)-mediated catalytic hydrogenation of internal alkynes to (Z)-alkenes that proceeds through an unprecedented mechanism is reported. The mechanistic proposal involves initial reduction of the alkyne by the Nb(III) complex (BDI)Nb(N(t)Bu)(CO)(2) to provide a Nb(V) metallacyclopropene, itself capable of σ-bond metathesis reactivity with H(2). The resulting alkenyl hydride species then undergoes reductive elimination to provide the (Z)-alkene product and regenerate a metal complex in the Nb(III) oxidation state. Support for the proposed mechanism is derived from (i) the dependence of the product selectivity on the relative concentrations of CO and H(2), (ii) the isolation of complexes closely related to those proposed to be part of the catalytic cycle, (iii) H/D crossover experiments, and (iv) DFT studies of multiple possible reaction pathways.     

Extension of linear free energy relationships to multiple ionizations

The linear additivity of free energies of ionization of substituted acids relative to the unsubstituted parent acid is described in terms of the Hammett relationship and as the weighted sums of microscopic free energies for benzenetricarboxylic acids.     

A new ternary Cu (II) complex with 4,7-dimethyl-1,10-phenanthroline and NOO-type tridentate Schiff base ligand: Synthesis,crystal structure,biomacromolecular interactions,and radical scavenging activities

NOO-type tridentate Schiff base, N-salicylidene-2-aminobenzoic acid, (H₂L), and its ternary Cu (II) complex containing H₂L Schiff base and 4,7-dimethyl-1,10-phenanthroline (4,7-dmphen), [Cu(4,7-dmphen)(H₂L)]₂7H₂O, have been synthesized and characterized by CHN analysis, ESI-MS, FTIR, and single-crystal X-ray diffraction techniques. The interaction of alone H₂L Schiff base ligand and ternary Cu (II) complex with biomacramolecules {calf thymus DNA (CT-DNA) and bovine serum albumin (BSA)} has been investigated by electronic absorption and fluorescence spectroscopy. The experimental results indicate that H₂L Schiff base ligand and ternary Cu (II) complex bind to CT-DNA by means of a moderate intercalation mode. Furthermore, the fluorescence quenching mechanism between H₂L Schiff base ligand and ternary Cu (II) complex with BSA possesses a static quenching process. Radical scavenging activity of H₂L Schiff base ligand and ternary Cu (II) complex was measured in terms of EC₅₀, using the DPPH and H₂O₂ methods. Biomacromolecule interactions and scavenging activity studies revealed that ternary Cu (II) complex yielded better results than H₂L Schiff base ligand alone.     

An unusally diverse array of products formed upon carbonylation of a dialkylniobium complex

The reaction of carbon monoxide with a beta-diketiminato dimethyl niobium complex (BDI)Me2Nb(NtBu) is shown to lead to a variety of products whose distribution displays a remarkable dependence on the reaction conditions. Among these, the products of metal reduction, enediolate formation, and intramolecular C-H activation have been fully characterized. An investigation into the individual steps leading to these products points to a transient initial monoacyl complex, whose fate may be perturbed via reaction conditions to allow for control over the product distribution. Furthermore, the reaction of (BDI)Me2Nb(NCMe3) with XylNC (Xyl = 2,6-Me2C6H3) yields the eta2-ketimine complex (BDI)(Me2C=NXyl)Nb(NCMe3), whose characterization and reactivity enhance our understanding of the sequences involving CO.     

Using internal electrostatic fields to manipulate the valence manifolds of copper complexes

A series of tetradentate tris(phosphinimine) ligands (^R3P₃tren) was developed and bound to Cu^I to form the trigonal pyramidal, C_3v-symmetric cuprous complexes [^R3P₃tren-Cu][BAr^F₄] (1PR3) (PR₃ = PMe₃, PMe₂Ph, PMePh₂, PPh₃, PMe₂(NEt₂), BAr^F₄ = B(C₆F₅)₄). Electrochemical studies on the Cu^I complexes were undertaken, and the permethylated analog, 1PMe3, was found to display an unprecedentedly cathodic Cu^I/Cu^II redox potential (−780 mV vs. Fc/Fc⁺ in isobutyronitrile). Elucidation of the electronic structures of 1PR3via density functional theory (DFT) studies revealed atypical valence manifold configurations, resulting from strongly σ-donating phosphinimine moieties in the xy-plane that destabilize 2e (d_xy/d_x²−y²) orbital sets and uniquely stabilized a₁ (d_z²) orbitals. Support is provided that the a₁ stabilizations result from intramolecular electrostatic fields (ESFs) generated from cationic character on the phosphinimine moieties in ^R3P₃tren. This view is corroborated via 1-dimensional electrostatic potential maps along the z-axes of 1PR3 and their isostructural analogues. Experimental validation of this computational model is provided upon oxidation of 1PMe3 to the cupric complex [^Me3P₃tren-Cu][OTf]₂ (2PMe3), which displays a characteristic Jahn–Teller distortion in the form of a see-saw, pseudo-C_s-symmetric geometry. A systematic anodic shift in the potential of the Cu^I/Cu^II redox couple as the steric bulk in the secondary coordination sphere increases is explained through the complexes'' diminishing ability to access the ideal C_s-symmetric geometry upon oxidation. The observations and calculations discussed in this work support the presence of internal electrostatic fields within the copper complexes, which subsequently influence the complexes'' properties via a method orthogonal to classic ligand field tuning.

Secondary coordination sphere electrostatic effects tune the valence manifolds of copper centers, impacting molecular geometries, photophysical properties, and redox potentials.