CuII Salts Research Articles

Room-Temperature Photochemical Copper-Mediated Fluorination of Aryl Iodides.

This report describes a method for the photochemical Cu-mediated fluorination of aryl iodides with AgF via putative aryl radical (Ar•) intermediates. It involves irradiating an aryl iodide with UVB light (λmax = 313 nm) in the presence of a mixture of CuI and CuII salts and AgF. Under these conditions, fluorination proceeds at room temperature for substrates containing diverse substituents, including alkoxy and alkyl groups, ketones, esters, sulfonate esters, sulfonamides, and protected amines. This method has been translated to radiofluorination using a combination of K18F, K3PO4, and AgOTf.

Structural Diversity and Rare η1 Cu-C Interactions in CuI Complexes of 1,2,3-Triazole-Functionalized Bisphosphines.

This manuscript describes the synthesis of copper complexes of 1,2,3-triazolyl-phosphines: o-Ph2P(C6H4){1,2,3-N3CC6H5)C(PPh2)} (L1), (C6H5){1,2,3-N3C(C6H4(o-PPh2))-C(PPh2)} (L2), 3-Ph2P(C5H3N){1,2,3-N3C(C6H5)C(PPh2)} (L3), o-Ph2P(C6H4){1,2,3-N3C(C5H5N)C(PPh2)} (L4), and {(3,5-Ph2PC6H4-o)21,2,3-N3CCH} (L5). The reactions of L1-L3 with CuI salts afforded dimeric complexes having the general formula [Cu2(μ -X)2L2] (L = L1, X = Cl, Br and I: 1 - 3; L= L2, X = Cl, Br and I: 4- 6; L = L3; X = Cl, Br, and I: 7-9). The reaction of L4 with CuI in a 1:2 molar ratio afforded 1D-coordination polymer [{(CuI)2{o-Ph2P(C6H4){1,2,3-N3C(C5H5N)C(PPh2)}-μ-((k1-N)(k2-P,P))}}]n (10). The reaction of L5 with cuprous halides (CuX) (X = Br, I) yielded mononuclear complexes [CuX{(3,5-Ph2PC6H4-o)21,2,3-N3CCH}-κ2P,P] (X = Br, 12; I, 13). Crystal structures of complexes 12 and 13 showed close interactions between CuI and the triazole C7 carbon. These relatively short Cu···C7 separations may be due to the η1-C interaction (dπ-pπ bond) between the triazolic carbon atom (via pz orbital) and CuI or three-centered two-electron interaction between CuI and the triazolic C-H bond. The existence of the Cu···C interaction was further evinced by the QTAIM analysis in compounds 12 and 13.

Supramolecular compounds assembled from the heteroleptic tetrahedral complex [{CpMo(CO)2}2(μ,η2-AsSb)] and metal salts.

The reaction of the tetrahedral complex [{CpMo(CO)2}2(μ,η2-AsSb)] with CuI and AgI salts is presented which gives unprecedented neutral and cationic supramolecular aggregates featuring mixed As/Sb-donor molecules as ligands/linkers between metal ions.

Ultrahigh density copper (Ⅰ) single atom enzymes for tumor self-cascade catalytic therapy

Cu (Ⅰ) single-atom enzymes (SAEs) have attracted considerable attention in tumor sequential catalysis therapy. However, their complex preparation process, lower atom loading capacity and uncontrollable valence state limit their clinical practices. Herein, we propose a convenient strategy for preparing Cu (Ⅰ) SAEs through the self-carbonization and reduction of organic solvents and CuⅡ salts. Formamide can easily be condensed into a linear macromolecular chain for chelating CuⅡ because of its high N content and vacant ligand sites. The resultant carbon nitride-based fragments reduce CuⅡ to CuⅠ. An unprecedented sequential catalytic performance for glutathione depletion and subsequent amplified hydroxyl radical generation is performed on the obtained C3N4 supported Cu (Ⅰ) SAEs (denoted as Cu-CN) with an ultrahigh density of 2.19 atoms/nm2 (23.36 wt%), in which the CuⅠ species serve as the active sites. The subversion of the homeostasis of the tumor microenvironment brought about by the Cu-CN produces efficient ferroptosis and apoptosis in cancer cells, resulting in a high tumor inhibition rate of 89.17 %. This study provides a novel strategy for fabricating valence controlled SAEs supported on C3N4 for catalytic applications.

Dimetal-Binding Scaffold 2-(Pyridin-2-yl)imidazo[1,5-b]pyridazine-7-ylidene: Synthesis of Trinuclear Heterobimetallic Complexes Involving Gold-Metal Interactions.

As a dimetal-binding rigid scaffold, 2-(pyridin-2-yl)imidazo[1,5-b]pyridazine-7-ylidene was introduced. The scaffold was first converted into a meridional Au,N,N-tridentate ligand through binding of a Au(I)Cl moiety at the carbene center. The Au(I) center and the N,N-chelating moiety were expected to function as metallophilic and 4e-σ-donative interaction sites, respectively, in the binding of the second metal center. In this manner, various trinuclear heterobimetallic complexes were synthesized with different 3d-metal sources, such as cationic CuI, CuII, NiII, and CoII salts. SC-XRD analysis showed that the mono-3d-metal di-gold(I) trinuclear heterobimetallic complexes were constructed through gold(I)-metal interactions. Metallophilic interactions were also investigated by quantum chemical calculations including the AIM and IGMH methods.

A Diode-Like Dye-Cu Anisotropic Junction in a Coordination Polymer as a Logic State Ratchet for Intratumor Redox Photomodulation.

Redox logic materials offer new avenues to modulate intracellular pathologic redox environment area-specifically, but the unambiguity of redox logic states and their unidirectional and repetitive switchability are challenging to realize. By merging a bistable diisophthalic phenazine dye ligand with CuII salt, a multistable coordination polymer (CP) was constructed, of which the dye-Cu anisotropic junction achieved the diode-like unidirectional electron transfer and logic state ratchet for the first time. Radical cationic CP maintained OFF status with low toxicity in healthy tissues, but was reduced to the neutral SERVO state by the overexpressed glutathione (GSH) in hypoxic tumors. After photoirradiation, the stabilized charge-separated ON status promoted photo-Fenton reaction for reactive oxygen species (ROS) signal transduction, and simultaneously recovered the initial state for catalytic signal amplification of ROS, furnishing intratumor redox photomodulation for therapy.

A Diode‐Like Dye‐Cu Anisotropic Junction in a Coordination Polymer as a Logic State Ratchet for Intratumor Redox Photomodulation

AbstractRedox logic materials offer new avenues to modulate intracellular pathologic redox environment area‐specifically, but the unambiguity of redox logic states and their unidirectional and repetitive switchability are challenging to realize. By merging a bistable diisophthalic phenazine dye ligand with CuII salt, a multistable coordination polymer (CP) was constructed, of which the dye‐Cu anisotropic junction achieved the diode‐like unidirectional electron transfer and logic state ratchet for the first time. Radical cationic CP maintained OFF status with low toxicity in healthy tissues, but was reduced to the neutral SERVO state by the overexpressed glutathione (GSH) in hypoxic tumors. After photoirradiation, the stabilized charge‐separated ON status promoted photo‐Fenton reaction for reactive oxygen species (ROS) signal transduction, and simultaneously recovered the initial state for catalytic signal amplification of ROS, furnishing intratumor redox photomodulation for therapy.

Evaluating Coordinative Binding Mechanisms through Experimental and Computational Studies of Methoxy‐Substituted Arylazothioformamide Copper(I) Complexes

AbstractRedox‐active arylazothioformamide (ATF) ligands, when reacted with CuI salts, coordinate to form a variety of 1 : 1 dimers and 2 : 1 ligand‐metal complexes through a N=N−C=S chelation motif. In this study, monosubstituted (ortho/meta/para) methoxy regioisomers of ATF were synthesized and evaluated with CuI halide and BF4 salts. UV‐Vis binding association studies revealed a 2 : 1 binding association model against all species producing a para ≫ ortho > meta pattern across the methoxy substitution range. To understand why the 2 : 1 non‐linear binding model was preferred over a 1 : 1 model for CuI halide salt dimers (i. e., A2B2), a series of mechanisms were computed indicating that metal salt dimers (i. e., B+B→B2) or ligand‐metal salt‐metal salt‐ (i. e., AB+B→AB2) interactions provide favorable pathways. Combined, the data substantiate the 2 : 1 binding association mechanistically even as the substitution pattern, steric bulk, and electronics alter the coordination strength of the ligands to the CuI center.

Metallo‐Supramolecular Octahedral Cages with Three Types of Chirality towards Spontaneous Resolution

Chirality is one of the most important intrinsic properties of (supra)molecules. In this study, we obtained enantiomeric metallo-supramolecular octahedra without using any chiral sources. Such cages were self-assembled by prochiral trispyridine ligand L based on a C3h truxene core and CuII salts. Crystallization of the cages with BF4 - as counterions afforded racemate crystals; while crystallizations of cages with ClO4 - and OTf- as counterions resulted in conglomerates with spontaneous resolution. Three types of chirality were observed in each cage, including planar chirality of the truxene core, axial chirality from the pyridyl and truxene moieties, and propeller chirality of the pyridyl-CuII coordination sites. The cages reported here are among the largest discrete synthetic metallo-supramolecules ever reported with chiral self-sorting behavior. Remarkably, the chiral cages exhibited very slow racemization even at low concentrations, suggesting their high stability in solution.

Metallo‐Supramolecular Octahedral Cages with Three Types of Chirality towards Spontaneous Resolution

AbstractChirality is one of the most important intrinsic properties of (supra)molecules. In this study, we obtained enantiomeric metallo‐supramolecular octahedra without using any chiral sources. Such cages were self‐assembled by prochiral trispyridine ligand L based on a C3h truxene core and CuII salts. Crystallization of the cages with BF4− as counterions afforded racemate crystals; while crystallizations of cages with ClO4− and OTf− as counterions resulted in conglomerates with spontaneous resolution. Three types of chirality were observed in each cage, including planar chirality of the truxene core, axial chirality from the pyridyl and truxene moieties, and propeller chirality of the pyridyl‐CuII coordination sites. The cages reported here are among the largest discrete synthetic metallo‐supramolecules ever reported with chiral self‐sorting behavior. Remarkably, the chiral cages exhibited very slow racemization even at low concentrations, suggesting their high stability in solution.

Copper-Catalyzed Monooxygenation of Phenols: Evidence for a Mononuclear Reaction Mechanism.

The CuI salts [Cu(CH3CN)4]PF and [Cu(oDFB)2]PF with the very weakly coordinating anion Al(OC(CF3)3)4 − (PF) as well as [Cu(NEt3)2]PF comprising the unique, linear bis‐triethylamine complex [Cu(NEt3)2]+ were synthesized and examined as catalysts for the conversion of monophenols to o‐quinones. The activities of these CuI salts towards monooxygenation of 2,4‐di‐tert‐butylphenol (DTBP‐H) were compared to those of [Cu(CH3CN)4]X salts with “classic” anions (BF4 −, OTf−, PF6 −), revealing an anion effect on the activity of the catalyst and a ligand effect on the reaction rate. The reaction is drastically accelerated by employing CuII‐semiquinone complexes as catalysts, indicating that formation of a CuII complex precedes the actual catalytic cycle. This result and other experimental observations show that with these systems the oxygenation of monophenols does not follow a dinuclear, but a mononuclear pathway analogous to that of topaquinone cofactor biosynthesis in amine oxidase.

Influence of the Reaction Sequence on the Complexation of an NS4-Macrocycle with CdII and CuI Salts Leading to the Formation of Supramolecular Isomers and an Endo/Exocyclic CuI Complex.

In the construction of metallosupramolecules, the reaction sequence in a three-reactant system (one ligand plus two metal ions) could be one of the controlling factors influencing the outcome of the reaction. In this work, the formation of supramolecular isomers (1 and 2) and an endo/exocyclic Cu+ complex (4) of the NS4-macrocycle (L) via different sequential metal addition protocols (routes I-III) is reported. In one-pot reactions of L with Cu(CH3CN)4PF6 in the absence (route I) and presence (route II) of CdI2, a cyclic dimer CuI complex, [Cu2(L)2](PF6)2 (1), and a one-dimensional coordination polymer, [Cu2(L)2]n·n[CdI4] (2), were obtained, respectively. Interestingly, the complex cations in 1 and 2 are supramolecular isomers formed via cyclization and polymerization upon complexation, respectively, probably due to different geometric and electronic complementarities, via the C-H···X- hydrogen bonds, between L and the counterion. In the two-step reaction (route III), an endocyclic Cd2+ complex, [Cd(L)I2] (3), obtained in the first step was utilized in the following reaction with Cu(CH3CN)4PF6, giving rise to an endo/exocyclic tetranuclear Cu+ complex, [Cu4(L)2(CH3CN)6](PF6)4 (4), via Cd2+ → 2Cu+ substitution, which is not accessible by conventional procedures. Solution studies by comparative NMR and electrospray ionization mass spectroscopy also support metal substitution by showing the stronger binding affinity of Cu+ over Cd2+. These results demonstrate that the metal substitution protocol could be useful for reaching novel metallosupramolecules difficult to obtain by other methods.

Versatile Coordination of AgI and CuI Ions towards cyclo-As5 Ligands.

The reactions of the cyclo‐As5 complex [Cp*Fe(η5‐As5)] (B) with the AgI and CuI salts of the weakly coordinating anion (WCA) [FAl{OC6F10(C6F5)}3]− ([FAl]−) are studied. These reactions allow the synthesis of the mononuclear complexes [M(η5 : η2‐B)2][FAl] (M=Ag (1), Cu (2)) when a ratio of B/M(FAl) 2 : 1 is used. Compound 1 shows an unusual disorder of the central AgI cation between two π‐coordinating cyclo‐As5 ligands, which is absent in 2 pointing to a weak interaction of the Ag center towards the cyclo‐As5 ligands in B. When the ratio of B/Ag(FAl) is changed to 3 : 1 or 1 : 1, the respective coordination compounds [Ag(η2‐B)3][FAl] (3) and [Ag2(η2 : η2‐B)2][FAl]2 (4) are accessible. The coordination modes of the cyclo‐As5 units in 1, 3 and 4 are all different, reflecting the adaptive coordination behavior of B towards AgI ions. The optimized geometries in the gas phase of 1–4 are determined by DFT calculations to support the bonding situation observed in their solid‐state structures.

Crystal structure of di-aqua-(3,14-diethyl-2,6,13,17-tetra-aza-tri-cyclo-[16.4.0.07,12]docosa-ne)copper(II) dichloride tetra-hydrate.

The crystal structure of the novel hydrated CuII salt, [Cu(L)(H2O)2]Cl2·4H2O (L = 3,14-diethyl-2,6,13,17-tetra-aza-tri-cyclo-[16.4.0.07,12]docosane, C22H44N4) has been determined using synchrotron radiation. The asymmetric unit contains one half of the [Cu(L)(H2O)2]2+ cation (completed by crystallographic inversion symmetry), one chloride anion and two lattice water mol-ecules. The copper(II) atom exists in a tetra-gonally distorted octa-hedral environment with the four N atoms of the macrocyclic ligand in equatorial and two O atoms from water mol-ecules in axial positions. The latter exhibit a long axial Cu-O bond length of 2.7866 (16) Å due to the Jahn-Teller distortion. The macrocyclic ring adopts a stable trans-III conformation with typical Cu-N bond lengths of 2.0240 (11) and 2.0441 (3) Å. The complex is stabilized by hydrogen bonds formed between the O atoms of coordinated water mol-ecules and the NH groups as donors, and chloride anions as acceptors. The chloride anions are further connected to the lattice water solvent molecules through O-H⋯Cl hydrogen bonds, giving rise to a three-dimensional network structure.

Iron oxide (Fe3O4) magnetic nanoparticles supported on wrinkled fibrous nanosilica (WFNS) functionalized by biimidazole ionic liquid as an effective and reusable heterogeneous magnetic nanocatalyst for the efficient synthesis of N-sulfonylamidines

Wrinkled fibrous nanosilica (WFNS) which functionalized by ionic liquid modified Fe3O4 NPs and CuI salts has been synthesized and characterized with FE-SEM, TEM, FT-IR, FAAS, EDX, and, XRD, VSM, and BET-BJH analysis. This new and effective magnetic ceramic nanocatalyst has been applied towards rapid synthesis of N-sulfonylamidines using reaction of phenyl acetylene, substituted sulfonyl azide and various amines under solvent-free conditions in very short reaction time. Higher catalytic activity CuI/Fe3O4NPs@IL-DFNS in the reaction is because of special structure of DFNS and existence of ionic liquids on its pores which act as a robust anchors to the loaded various nano-particles. So, this lead to no leaching of them from the pore of the composite. Shorter reaction time, higher yield, recovery of the catalyst using an external magnet and its reusability for 8 series without noteworthy reduction in its activity are the advantages of newly synthetic catalyst toward efficient synthesis of N-sulfonylamidines.

CuII Complexes and Coordination Polymers with Pyridine or Pyrazine Amides and Amino Benzamides—Structures and EPR Patterns

Isonicotine amide, picoline amide, pyrazine 2-amide, 2- and 4-amino benzamides and various CuII salts were used to target CuII complexes of these ligands alongside with 1D and 2D coordination polymers. Under the criterion of obtaining crystalline and single phased materials a number of new compounds were reliably reproduced. Remarkably, for some of these compounds the ideal Cu:ligand ratio of the starting materials turned out to be very different from Cu:ligand ratio in the products. Crystal and molecular structures from single-crystal XRD were obtained for all new compounds; phase purity was checked using powder XRD. We observed exclusively the Oamide and not the NH2amide function binding to CuII. In most of the cases; this occurred in chelates with the second pyridine, pyrazine or aminophenyl N function. µ-O,N ditopic bridging was frequently observed for the N = pyridine, pyrazine or aminophenyl functions, but not exclusively. The geometry around CuII in these compounds was very often axially elongated octahedral or square pyramidal. X-band EPR spectra of powder samples revealed various spectral symmetry patterns ranging from axial over rhombic to inverse axial. Although the EPR spectra cannot be unequivocally correlated to the observed geometry of CuII in the solid state structures, the EPR patterns can help to support assumed structures as shown for the compound [Cu(Ina)2Br2] (Ina = isonicotine amide). As UV-vis absorption spectroscopy and magnetic measurement in the solid can also be roughly correlated to the surrounding of CuII, we suggest the combination of EPR, UV-vis spectroscopy and magnetic measurements to elucidate possible structures of CuII compounds with such ligands.

CuI/Fe3O4 NPs@Biimidazole IL‐KCC‐1 as a leach proof nanocatalyst for the synthesis of imidazo[1,2‐a]pyridines in aqueous medium

In the present work, an innovative leach proof nanocatalyst based on dendritic fibrous nanosilica (DFNS) modified with ionic liquid loaded Fe3O4 NPs and CuI salts was designed and applied for the rapid synthesis of imidazo[1,2‐a]pyridines from the reaction of phenyl acetylene, 2‐aminopyridine, and aldehydes in aqueous medium. The structure of the synthesized nanocatalyst was studied by field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), Fourier transform infrared (FT‐IR), flame atomic absorption spectroscopy (FAAS), energy‐dispersive X‐ray (EDX), and X‐ray diffraction (XRD), vapor–liquid–solid (VLS), and adsorption/desorption analysis (Brunauer–Emmett–Teller [BET] equation) instrumental techniques. CuI/Fe3O4NPs@IL‐KCC‐1 with high surface area (225 m2 g−1) and porous structure not only exhibited excellent catalytic activity in aqueous media but also, with its good stability, simply recovered by an external magnet and recycled for eight cycles without significant loss in its intrinsic activity. Higher catalytic activity of CuI/Fe3O4NPs@IL‐KCC‐1 is due to exceptional dendritic fibrous structure of KCC‐1 and the ionic liquid groups that perform as strong anchors to the loaded magnetic nanoparticles (MNPs) and avoid leaching them from the pore of the nanocatalyst. Green reaction media, shorter reaction times, higher yields (71–97%), easy workup, and no need to use the chromatographic column are the advantages of the reported synthetic method.

Linking of CuI Units by Tetrahedral Mo2 E2 Complexes (E=P, As).

The reaction of [Cp2Mo2(CO)4(μ,η2:2‐E2)] (A: E=P, B: E=As, Cp=C5H5) with the WCA‐containing CuI salts ([Cu(CH3CN)4][Al{OC(CF3)3}4] (CuTEF, C), [Cu(CH3CN)4][BF4] (D) and [Cu(CH3CN)3.5][FAl{OC6F10(C6F5)}3] (CuFAl, E)) affords seven unprecedented coordination compounds. Depending on the E2 ligand complex, the counter anion of the copper salt and the stoichiometry, four dinuclear copper dimers and three trinuclear copper compounds are accessible. The latter complexes reveal first linear Cu3 arrays linked by E2 units (E=P, As) coordinated in an η2:1:1 coordination mode. All compounds were characterized by X‐ray crystallography, NMR and IR spectroscopy, mass spectrometry and elemental analysis. To define the nature of the Cu⋅⋅⋅Cu⋅⋅⋅Cu interactions, DFT calculations were performed.

Synthesis and structures of tris(2-hydroxypropyl)amine complexes with NiII, ZnII, CuII, and CoII salts of biologically active carboxylic acids

New trimethylhydrometallatranes, tris(2-hydroxypropyl)amine complexes with NiII, ZnII, CuII, and CoII salts of biologically active carboxylic acids (benzoic, cinnamic, salicylic, succinic), were synthesized. The structure of the tris(2-hydroxypropyl)amine complex with nickel(II) cinnamate was determined by single-crystal X-ray diff raction. Thermal stability of the synthesized tris(2-hydroxypropyl)amine complexes was compared with that of tris(2-hydroxyethyl)- amine complexes.

Straightforward Preparation of a Solid‐state Luminescent Cu11 Polymetallic Assembly via Adaptive Coordination‐driven Supramolecular Chemistry

The tridentate dpmp ligand was reacted with CuI salt and cyano ligand affording selectively and unexpectedly the polymetallic Cu11 complex 2 along one‐step reaction. The formation of this derivative 2 can be explained by self‐assembling processes controlled by adaptive coordination‐driven supramolecular chemistry. The solid‐state photophysical behavior of 2 was studied suggesting TADF properties.