Activation of robust bonds by carbonyl complexes of Mn, Fe and Co
Historic discoveries and recent advances in activation of strong C–H, C–F, and C–O bonds using carbonyl complexes of Mn, Fe, and Co are reviewed.
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Historic discoveries and recent advances in activation of strong C–H, C–F, and C–O bonds using carbonyl complexes of Mn, Fe, and Co are reviewed.
The activity of a cobalt phosphino–thiolate complex towards the electrochemical reduction of CO 2 in the presence of H 2 O is observed to produce formate with a selectivity as high as 94%, displaying negligible current degradation over long-term electrolyses.
A trapped-valent Ce III/IV –TCNQ complex is assembled through Lewis acid-promoted donor–acceptor potential shifts providing a magnetic and luminescent compound.
A novel Ta/Os complex [Ta(CH 2 t Bu) 3 (μ-H) 3 OsCp*], and its iridium analogue [Ta(CH 2 t Bu) 3 (μ-H) 2 IrCp*], efficiently cleave CO 2 under mild conditions, forming tantalum oxo species and CpIr(CO)H 2 or CpOs(CO)H 3 .
Here we report the synthesis and characterization of diiron complexes containing triaryl N 4 and N 2 S 2 ligands derived from o -phenylenediamine.
This study explores the versatile binding properties of a tetrapodal ligand framework with nickel, demonstrating ligand fluxionality through the interconversions of several complexes.
Synthesis of cerium yldiide complexes and their reactivity with CO is demonstrated.
Correction for ‘Impacts of trace level chromium on formation of superoxide within uranyl triperoxide complexes’ by Sarah K. Scherrer et al. , Chem. Commun. , 2024, 60 , 10584–10587, https://doi.org/10.1039/D4CC03194F.
Examining the importance of tunneling in the oxo-insertion and radical recombination mechanisms of CH hydroxylation with dicopper-dioxo complexes.
Stability constants of simple reactions involving addition of the NO 3 − ion to hydrated metal complexes, [M(H 2 O) x ] n + are calculated with a computational workflow developed using cloud computing resources.
Correction for ‘Impact of lanthanide ion complexation and temperature on the chemical reactivity of N , N , N ′, N ′-tetraoctyl diglycolamide (TODGA) with the dodecane radical cation’ by Gregory P. Horne et al. , Phys. Chem. Chem. Phys. , 2023, 25 , 16404–16413, https://doi.org/10.1039/D3CP01119D.
A structural and functional biomimetic Ni( ii )N 3 O complex, capable of O 2 mediated dioxygenase like C–C bond cleavage, via a putative high-valent Ni intermediate.
Macrocyclic uranyl complexes have been prepared that incorporate a range of secondary metal cations. Structural and spectroscopic studies have been used to study how the cations and macrocyclic structure influence the [UO 2 ] core moiety.
Side chain engineering of non-planar zinc( ii ) complexes of azadipyrromethene enables either very high hole mobility, high electron mobility or both as estimated by the space-charge limited current (SCLC) method in diodes.
This study examines the intricate area of refractory-based high entropy alloys (RHEAs), focusing on a series of complex compositions involving nine diverse refractory elements: Ti, V, Cr, Zr, Nb, Mo, Hf, Ta, and W.
We report a comprehensive study on the synthesis, reactivity, mechanism, and computation for the β-alkynyl eliminations of secondary and tertiary propargylic alkoxides of Cu( i ) complexes supported by N-heterocyclic carbenes and diphosphines.
Enabling coherent spin-control in integer spin complexes with molecular color center design.
This study examines nitrate and nitrite reduction by a tetrapodal iron complex, identifying key intermediates in the reaction via a bimetallic mechanism.