More Like this

1. Shift from Entropic Cu ²⁺ Binding to Enthalpic Cu ⁺ Binding Determines the Reduction Thermodynamics of Blue Copper Proteins

   https://doi.org/10.1021/jacs.9b06836  

   North, Molly L.; Wilcox, Dean E. (August 2019, Journal of the American Chemical Society)
2. ⁵⁹ Co Thermal Sensitivity in Co(III) Trisdithiocarbamate Complexes

   https://doi.org/10.1021/acs.inorgchem.4c05385  

   Üngör, Ökten; Termos, Sara; Schurko, Robert W; Zadrozny, Joseph M (April 2025, Inorganic Chemistry)
3. Forging Strong Co–C(sp ² ) Bonds in Co-Macrocycle: Mono- and Bis-Aryl Complexes of Co ^III (TIM)

   https://doi.org/10.1021/acs.organomet.5c00097  

   McGuire, Kyle J; Ebarb, Austin J; Gautam, Prakhar; Ren, Tong (July 2025, Organometallics)
4. Short DNA Oligonucleotide as a Ag ⁺ Binding Detector

   https://doi.org/10.1021/acsomega.0c03372  

   Shen, Fusheng; Mao, Song; Mathivanan, Johnsi; Wu, Ying; Chandrasekaran, Arun Richard; Liu, Hehua; Gan, Jianhua; Sheng, Jia (November 2020, ACS Omega)
5. Distinct Bimetallic Cooperativity Among Water Reduction Catalysts Containing [Co ^III Co ^III ], [Ni ^II Ni ^II ], and [Zn ^II Zn ^II ] Cores

   https://doi.org/10.1002/chem.202104426  

   Morgan, Fredricka; Schaugaard, Richard; Anderson, Dennis; Schlegel, H_Bernhard; Verani, Cláudio_N (March 2022, Chemistry – A European Journal)

   Abstract Three binuclear species [LCo^III₂(μ‐Pz)₂](ClO₄)₃(1), [LNi^II₂(CH₃OH)₂Cl₂]ClO₄(2), and [LZn^II₂Cl₂]PF₆(3) supported by the deprotonated form of the ligand 2,6‐bis[bis(2‐pyridylmethyl) amino‐methyl]‐4‐methylphenol were synthesized, structurally characterized as solids and in solution, and had their electrochemical and spectroscopic behavior established. Species1–3had their water reduction ability studied aiming to interrogate the possible cooperative catalytic activity between two neighboring metal centers. Species1and2reduced H₂O to H₂effectively at an applied potential of −1.6 V_Ag/AgCl, yielding turnover numbers of 2,820 and 2,290, respectively, after 30 minutes. Species3lacked activity and was used as a negative control to eliminate the possibility of ligand‐based catalysis. Pre‐ and post‐catalytic data gave evidence of the molecular nature of the process within the timeframe of the experiments. Species1showed structural, rather than electronic cooperativity, while species2displayed no obvious cooperativity. DFT methods complemented the experimental results determining plausible mechanisms. 

   more » « less