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1. Ethylene-Bridged Hexadentate Bis(amidines) and Bis(amidinates) with Variable Binding Sites

   https://doi.org/10.1021/acs.joc.9b01908  

   O’Dea, Connor; Ugarte Trejo, Omar; Arras, Janet; Ehnbom, Andreas; Bhuvanesh, Nattamai; Stollenz, Michael (October 2019, The Journal of Organic Chemistry)
2. Template-Free Synthesis of a Macrocyclic Bis(pyridine-dienamine) Proligand and Metal Complexes of Its Bis(pyridine-diimine) and Bis(pyridine-dienamido) Forms

   https://doi.org/10.1021/acs.inorgchem.9b02539  

   Reinhart, Erik D.; Jordan, Richard F. (November 2019, Inorganic Chemistry)
3. 2,6-Bis[bis(1,1-dimethylethyl)phosphinito-κP]phenyl-κC]-trans-chlorohydro(phenylphosphine)iridium(III)

   https://doi.org/10.3390/M1388  

   Mucha, Neil T.; Waterman, Rory (June 2022, Molbank)

   The molecular structure of an iridium complex featuring a phenylphosphine ligand is described. The reaction of (POCOP)IrHCl (1, POCOP = 2,6-(tBu2PO)2C6H3–) with phenylphosphine gives (POCOP)IrHCl(PH2Ph) (2) under mild conditions. The structural features are consistent with a classic pseudo-octahedral iridium compound with three neutral phosphine donors. Compound 1 is unreactive at elevated temperatures and is unreactive toward excess phenylphosphine under the sampled conditions. 

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4. Nickel-Templated Replacement of Phosphine Substituents in a Tetradentate Bis(amido)bis(phosphine) Ligand

   https://doi.org/10.1021/acs.inorgchem.1c02750  

   Lee, Kyounghoon; Thomas, Christine M. (November 2021, Inorganic Chemistry)
5. Cationic Bis(Gold) Indenyl Complexes

   https://doi.org/10.1002/cplu.202300691  

   Slinger, Brady_L; Zhu, Jiaqi; Widenhoefer, Ross_A (February 2024, ChemPlusChem)

   Abstract Reaction of (P)AuOTf [P=P(t‐Bu)₂o‐biphenyl] with indenyl‐ or 3‐methylindenyl lithium led to isolation of gold η¹‐indenyl complexes (P)Au(η¹‐inden‐1‐yl) (1 a) and (P)Au(η¹‐3‐methylinden‐1‐yl) (1 b), respectively, in >65 % yield. Whereas complex1 bis static, complex1 aundergoes facile, degenerate 1,3‐migration of gold about the indenyl ligand (ΔG^≠_153K=9.1±1.1 kcal/mol). Treatment of complexes1 aand1 bwith (P)AuNTf₂led to formation of the corresponding cationic bis(gold) indenyl complexestrans‐[(P)Au]₂(η¹,η¹‐inden‐1,3‐yl) (2 a) andtrans‐[(P)Au]₂(η¹,η²‐3‐methylinden‐1‐yl) (2 b), respectively, which were characterized spectroscopically and modeled computationally. Despite the absence of aurophilic stabilization in complexes2 aand2 b, the binding affinity of mono(gold) complex1 atoward exogenous (P)Au⁺exceed that of free indene by ~350‐fold and similarly the binding affinity of1 btoward exogenous (P)Au⁺exceed that of 3‐methylindene by ~50‐fold. The energy barrier for protodeauration of bis(gold) indenyl complex2 awith HOAc was ≥8 kcal/mol higher than for protodeauration of mono(gold) complex1 a. 

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