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1. Interplay of Isomorphs and Polymorphs of Amidino-Copper(II) Complexes with Different Halides

   https://doi.org/10.3390/cryst14040319  

   Yamba, Zaina; Peoble, Anna; Novikov, Egor; Castañeda, Raúl; Timofeeva, Tatiana (April 2024, Crystals)

   To increase the number of potential materials for application as MRI contrast agents, several Cu(II) complexes were synthesized. Cu(II) complexes were chosen because they are less expensive in comparison with the presently used Gd(III), Mn(II) and other agents. Pyridine-2-carboximidamide (1), pyrimidine-2-carboximidamide (2) and pyrazole-2-carboximidamide (3) in the form of different salts along with CuCl2 and NaCl or CuBr2 and NaBr were used to obtain four Cu(II) complexes: dichloro-pyrimidine-2-carboximidamide copper(II) (4), dibromo-pyrimidine-2-carboximidamide copper(II) (5), dichloro-pirazole-2-carboximidamide copper(II) (6), and dibromo-pirazole-2-carboximidamide copper(II) (7). X-ray diffraction analysis revealed that molecular complexes 4–7 contain square planar coordinated Cu(II) atoms and their structures are very similar, as well as their packing in crystals, which allows us to consider them isomorphs. The same synthetic approach to complex preparation where NaCl or NaBr was not used brought us to the formation of dimeric complexes μ-chloro{chloro(pyridine-2-carboximidamide)copper(II)} (8) and μ-chloro{chloro(pyrimidine-2-carboximidamide)copper(II)} (9). In the dimeric complexes, two fragments which were the same as in monomeric complexes 4–7 are held together by bridging Cu-Cl bonds making the coordination of Cu equal to 5 (square pyramid). In dimeric complexes, axial Cu-Cl bonds are 2.7360 and 2.854 Å. These values are Cu-Cl bonds on the edge of existence according to statistical data from CSD. Synthesized complexes were characterized by IR spectroscopy, TGA, PXRD, EPR, and quantum chemical calculations. The higher thermal stability of monomer pyrimidine-based complexes with Cl and Br substituents makes them more prospective for further studies. 

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2. Experimental and theoretical investigations of infrared multiple photon dissociation spectra of arginine complexes with Zn ²⁺ and Cd ²⁺

   https://doi.org/10.1039/c8cp03484b  

   Chalifoux, Aaron M.; Boles, Georgia C.; Berden, Giel; Oomens, Jos; Armentrout, P. B. (January 2018, Physical Chemistry Chemical Physics)

   Arginine (Arg) complexes with Zn 2+ and Cd 2+ were examined by infrared multiple photon dissociation (IRMPD) action spectroscopy using light from a free electron laser. Electrospray ionization generated complexes of deprotonated Arg with Zn 2+ , [Zn(Arg–H)] + , and Arg with CdCl + , CdCl + (Arg). Possible low-energy conformers of these species were found using quantum chemical calculations, and their calculated IR spectra were compared to experimentally measured IRMPD spectra. Calculations were performed at the B3LYP/6-311+G(d,p) level for Zn 2+ complexes and B3LYP/def2-TZVP with an SDD effective core potential on cadmium for CdCl + complexes. [Zn(Arg–H)] + was found to adopt a charge-solvated, tridentate [N,CO − ,N ω ′] structure where Zn 2+ binds to the backbone amine, carbonyl oxygen, and side-chain terminal guanidine nitrogen (N ω ′). The CdCl + (Arg) species was suggested to be a mixture of a dominant (∼85%) charge-solvated, tridentate [N,CO,N ω ′] structure where the CdCl + binds to the backbone amine, carbonyl, and side-chain imine (N ω ′) and a minor (∼15%) bidentate [N,CO − ](N ω ′H 2 + ) zwitterionic structure where the metal center binds to the backbone amine and carbonyl oxygen with intramolecular proton migration from the hydroxyl to the N ω ′ guanidine nitrogen (as designated in parenthesis). 

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3. Synthesis of diphenyl-(2-thienyl)phosphine, its chalcogenide derivatives and a series of novel complexes of lanthanide nitrates and triflates

   https://doi.org/10.1039/d2dt01570f  

   Luster, Troy; Van de Roovaart, Hannah J.; Korman, Kyle J.; Sands, Georgia G.; Dunn, Kylie M.; Spyker, Anthony; Staples, Richard J.; Biros, Shannon M.; Bender, John E. (June 2022, Dalton Transactions)

   A novel synthesis of diphenyl(2-thienyl)phosphine, along with its’ oxide, sulfide and selenide derivatives, is reported here. These phosphines have been characterized by NMR, IR, MS and X-Ray crystallography. The phosphine oxide derivative was reacted with a selection of lanthanide( iii ) nitrates and triflates, LnX 3 , to give the resultant metal–ligand complexes. These complexes have also been characterized by NMR, IR, MS and X-Ray crystallography. Single crystal X-Ray diffraction data shows a difference in metal–ligand complex stoichiometry and stereochemistry depending on the counteranion (nitrate vs. triflate). The [Ln(Ar 3 PO) 3 (NO 3 ) 3 ] ligand–nitrate complexes are nine-coordinate to the metal in the solid state (bidentate nitrate), featuring a 1 : 3 lanthanide–ligand ratio and bear an overall octahedral arrangement of the six, coordinated ligands. Our [Ln(Ar 3 PO) 3 (NO 3 ) 3 ] ligand–nitrate complexes gave three examples of fac -stereochemistry, where mer -stereochemistry is almost universally observed in the literature of highly related [Ln(Ar 3 PO) 3 (NO 3 ) 3 ] complexes. For the Tb complexes, two different arrangements of the ligands around the metal were observed in the solid state for [Tb(Ar 3 PO) 3 (NO 3 ) 3 ] and [Tb(Ar 3 PO) 4 (OTf) 2 ] [OTf]. [Tb(Ar 3 PO) 3 (NO 3 ) 3 ] is strictly nine-coordinate, ligand mer -stereochemistry in the solid state, and [Tb(Ar 3 PO) 4 (OTf) 2 ] [OTf] is strictly octahedral, six-coordinate, with a square-planar stereochemical arrangement of the phosphine oxide ligands around the metal. 

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4. Synthesis and characterization of a series of CpW(CO)2PR3H, [CpW(CO)2PR3]−, [CpW(CO)2PR3(CH3CN)]+, and [CpW(CO)2PR3]2 complexes

   https://doi.org/10.1016/j.ica.2024.122238  

   Isaacs, Diane P; Dempsey, Jillian L (October 2024, Inorganica Chimica Acta)

   A series of tungsten cyclopentadienyl carbonyl complexes were prepared and characterized to quantify their thermochemical properties and explore their reactivity. The PR3 ligand was systematically varied across a series of CpW(CO)2PR3H metal hydride complexes, where PR3 = P(OEt)3, P(Bu)3, and P(Cy)3. These complexes are known to undergo multiple proton, electron, and proton-coupled electron transfer reactions to access a variety of species including [CpW(CO)2PR3]–, [CpW(CO)2PR3(CH3CN)]+, and [CpW(CO)2PR3]2. Cyclic voltammograms of the CpW(CO)2PR3H•+/0 and [CpW(CO)2PR3]•0/– couples are chemically irreversible, indicating chemical reactivity upon oxidation; the anodic peak potential shifts to lower potentials as the donating ability of phosphine is increased, agreeing with previous literature on similar complexes. Additionally, voltammograms of [CpW(CO)2P(Cy)3]– become chemically reversible at scan rates above 500 mV/s, indicating that the dimerization of the [CpW(CO)2PR3]• product, formed by the oxidation of [CpW(CO)2PR3]–, is slower with the sterically bulky phosphine P(Cy)3, and at high scan rates the species can be reduced before dimerization occurs. Further, as the donating ability of the phosphine increases, the pKa of the CpW(CO)2PR3H complexes increases. This work shows how ligand sterics and electronics can tune the thermochemical properties that underpin proton, electron, and proton-coupled electron transfer reactivity of these complexes. 

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5. Improved Synthesis of Chiral 1,4,7‐Triazacyclononane Derivatives and Their Application in Ni‐Catalyzed Csp ³ −Csp ³ Kumada Cross‐Coupling

   https://doi.org/10.1002/hlca.202300170  

   Hu, Chi‐Herng; Byeong Chae, Ju; Mirica, Liviu M. (December 2023, Helvetica Chimica Acta)

   Abstract Herein, we report four new chiral 1,4,7‐triazacyclononane (TACN) derivatives and their corresponding nickel(II) chloride complexes. All TACN ligands are bearing one chiral N‐substituent and two alkyl (methyl ortert‐butyl) N‐substituents, and we have developed a new synthetic method for the dimethyl‐substituted TACN derivative, in order to prevent the rotational isomers that hinder the cyclization reaction. The nickel complexes change their coordination geometry significantly depending on the steric bulk of the N‐alkyl substituents, from a dinuclear tris(μ‐chloro)dinickel complex to mononuclear Ni‐dichloride and Ni‐chloride complexes. These complexes were then employed in the alkyl‐alkyl Kumada cross‐coupling reaction and revealed that the more sterically hindered ligands produced more homocoupled product rather than the cross‐coupled product, while the mononuclear Ni‐dichloride complex exhibited significantly lower catalytic activity. These chiral complexes were also employed in enantioconvergent cross‐coupling reactions as well, to afford significant enantioenrichment. Overall, the least sterically hindered Ni complex yields the best yields in the alkyl‐alkyl Kumada cross‐coupling reaction among the four complexes investigated, as well as the highest enantioselectivity. 

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