MII Ions Research Articles

Effect of transition metal ions on the dielectric properties of chromium potassium phosphates

Potassium ions are important for developing electrode materials because they have similar properties to lithium and sodium ions. Mixed chromium phosphates (KMIICr(PO4)2) with substituted MII sites using divalent elements (M = Ni, Co, Cu) were synthesized using a solid-state reaction method. The samples were analyzed using various techniques such as powder X-ray diffraction, Fourier transform infrared, Raman, and electron paramagnetic resonance spectroscopy. The proposed phosphates had a monoclinic phase structure with a P21/n space group, and they contained large tunnels occupied by K+ cations. The dielectric properties showed that the Ni-based phosphates had slower dielectric relaxation, while the Co and Cu-based phosphates had quicker polarization and depolarization processes. Additionally, the resistance of the grains decreased from Ni to Co to Cu-based phosphates, indicating easier charge movement in each material, consistent with the increase in conductive losses and a.c. conductivity when changing the MII ions.

Synthesis, structure and photoluminescence properties of heterometallic-based coordination polymers of trimesic acid.

Reacting trimesic acid (H3TMA, C9H6O6) with CaCl2 and MCl2 at 110 °C under hydrothermal conditions gave the isostructural heterobimetallic coordination polymers (CPs) catena-poly[[tetraaquazinc(II)]-μ-5-carboxybenzene-1,3-dicarboxylato-[tetraaquacalcium(II)]-μ-5-carboxybenzene-1,3-dicarboxylato], [CaZn(HTMA)2(H2O)8]n, 1, and catena-poly[[tetraaquacobalt(II)]-μ-5-carboxybenzene-1,3-dicarboxylato-[tetraaquacalcium(II)]-μ-5-carboxybenzene-1,3-dicarboxylato], [CaCo(HTMA)2(H2O)8]n, 2. Compounds 1 and 2 crystallize in the monoclinic space group C2/c. The solid-state structures consist of eight-coordinate CaII ions and six-coordinate MII ions. These ions are connected by a doubly deprotonated HTMA2- ligand to create a one-dimensional (1D) zigzag chain. Poly[[decaaquabis(μ3-benzene-1,3,5-tricarboxylato)calcium(II)dizinc(II)] dihydrate], {[CaZn2(TMA)2(H2O)10]·2H2O}n, 3, was found incidentally as a minor by-product during the synthesis of 1 at a temperature of 140 °C. It forms crystals in the orthorhombic space group Ccce. The structure of 3 consists of a two-dimensional (2D) layer composed of [Zn(TMA)] chains that are interconnected by CaII ions. The presence of aromatic carboxylic acid ligands and water molecules, which can form numerous hydrogen bonds and π-π interactions, increases the stability of the three-dimensional (3D) supramolecular architecture of these CPs. Compounds 1 and 2 exhibit thermal stability up to 420 °C, as indicated by the thermogravimetric analysis (TGA) curves. The powder X-ray diffraction (PXRD) data reveal the formation of unidentified phases in methanol and dimethyl sulfoxide, while 1 exhibits chemical stability in a wide range of solvents. The luminescence properties of 1 dispersed in various low molecular weight organic solvents was also examined. The results demonstrate excellent selectivity, sensitivity and recyclability for detecting acetone molecules in aqueous media. Additionally, a possible sensing mechanism is also outlined.

Chromium-Thiolate Complex Undergoing C-S Bond Cleavage.

The cleavage of C-S bonds represents a crucial step in fossil fuel refinement to remove organosulfur impurities. Efforts are required to identify alternatives that can replace the energy-intensive hydrodesulfurization process currently in use. In this context, we have developed a series of bis-thiolato-ligated CrIII complexes supported by the L2- ligand (L2- = 2,2'-bipyridine-6,6'-diyl(bis(1,1-diphenylethanethiolate), one of them displaying desulfurization of one thiolate of the ligand under reducing and acidic conditions at ambient temperature and atmospheric pressure. While only 5-coordinated complexes were previously isolated by reaction of L2- with 3d metal MIII ions, both 5- and 6-coordinated mononuclear complexes have been obtained in the case of CrIII, viz., [CrIIILCl], [CrIIILCl2]-, and [CrIIILCl(CH3CN)]. The investigation of the reactivity of [CrIIILCl(CH3CN)] under reducing conditions led to a dinuclear [CrIII2L2(μ-Cl)(μ-OH)] compound and, in the presence of protons, to the mononuclear CrIII complex [CrIII(LN2S)2]+, where LN2S- is the partially desulfurized form of L2-. A desulfurization mechanism has been proposed involving the release of H2S, as evidenced experimentally.

Theoretical exploration of single-molecule magnetic and single-molecule toroic behaviors in peroxide-bridged double-triangular {MII3LnIII3} (M = Ni, Cu and Zn; Ln = Gd, Tb and Dy) complexes.

Detailed state-of-the-art ab initio and density functional theory (DFT) calculations have been undertaken to understand both Single-Molecule Magnetic (SMM) and Single-Molecule Toroic (SMT) behaviors of fascinating 3d-4f {M3Ln3} triangular complexes having the molecular formula [MII3LnIII3(O2)L3(PyCO2)3](OH)2(ClO4)2·8H2O (with M = Zn; Ln = Dy (1), Tb (2) & Gd (3) and M = Cu; Ln = Dy (4), Tb (5) & Gd (6)) and [Ni3Ln3(H2O)3(mpko)9(O2)(NO3)3](ClO4)·3CH3OH·3CH3CN (Ln = Dy (7), Tb (8), and Gd (9)) [mpkoH = 1-(pyrazin-2-yl)ethanone oxime]. All these complexes possess a peroxide ligand that bridges the {LnIII3} triangle in a μ3-η3:η3 fashion and the oxygen atoms/oxime of co-ligands that connect each MII ion to the {LnIII3} triangle. Through our computational studies, we tried to find the key role of the peroxide bridge and how it affects the SMM and SMT behavior of these complexes. Primarily, ab initio Complete Active Space Self-Consistent Field (CASSCF) SINGLE_ANISO + RASSI-SO + POLY_ANISO calculations were performed on 1, 2, 4, 5, 7, and 8 to study the anisotropic behavior of each Ln(III) ion, to derive the magnetic relaxation mechanism and to calculate the LnIII-LnIII and CuII/NiII-LnIII magnetic coupling constants. DFT calculations were also performed to validate these exchange interactions (J) by computing the GdIII-GdIII and CuII/NiII-GdIII interactions in 3, 6, and 9. Our calculations explained the experimental magnetic relaxation processes and the magnetic exchange interactions for all the complexes, which also strongly imply that the peroxide bridge plays a role in the SMM behavior observed in these systems. On the other hand, this peroxide bridge does not support the SMT behavior. To investigate the effect of bridging ions in {M3Ln3} systems, we modeled a {ZnII3DyIII3} complex (1a) with a hydroxide ion replacing the bridged peroxide ion in complex 1 and considered a hydroxide-bridged {CoIII3DyIII3} complex (10) having the formula [Co3Dy3(OH)4(OOCCMe3)6(teaH)3(H2O)3](NO3)2·H2O. We discovered that as compared to the LoProp charges of the peroxide ion, the greater negative charges on the bridging hydroxide ion reduce quantum tunneling of magnetization (QTM) effects, enabling more desirable SMM characteristics and also leading to good SMT behavior.

Electronic Transition and Magnetic Coupling Regulation in Trimetallic Complexes Featuring a New Bridging Ligand Obtained by Oxidative Addition.

A series of trimetallic complexes [FeIII(μ-L)(py)]2MII(py)n (n = 2, MII = MnII, 1; FeII, 2; CoII, 3; ZnII, 4; n = 3, MII = CdII, 5) with a new bridging ligand L4- (deprotonated 1,2-N1,N2-bis(2-mercaptoanil) oxalimidic acid) were synthesized and fully characterized by elemental analysis, single-crystal X-ray crystallography, IR, and Mössbauer spectra. Interestingly, the bridging ligand was obtained by oxidative addition of the (gma•)3- ligand from the mononuclear precursor Fe(gma)py (gma = glyoxal-bis(2-mercaptoanil)). In the obtained complexes, the bridging ligand L4- coordinates to the terminal FeIII ions (intermediate-spin with SFe = 3/2) by the N, S atoms, and coordinate to the central metal MII ion by the four O atoms. The resonance structure of the bridging ligand can be described as the two 4π-electron delocalized systems connected by one single-bond (C1-C2), which is different from the electronic structure of the precursor Fe(gma)py. Remarkably, the magnetic coupling interaction can be regulated through the central metal. The ferromagnetic coupling constant J gradually decreases as MII changes from FeII to CoII and MnII, while the paramagnetic behaviors are presented when MII = ZnII and CdII, confirmed by the magnetic susceptibility measurements and further supported by using the PHI program. Furthermore, the bridging ligand to the terminal FeIII charge transfer (LMCT) transitions emerged in all complexes but the central FeII to terminal FeIII charge transfer (MMCT) only presented in complex 2, strongly supported by the UV/vis-NIR electronic spectra and TDDFT calculations.

Ferromagnetically coupled single-chain magnets exhibiting a magnetic hysteresis of 0.42 Tesla in cyano-bridged FeIII2MII (M = Ni, Fe) coordination polymers.

The synthesis, single-crystal structures and magnetic properties of two new double-zigzag-chain cyano-bridged heterobimetallic {[MII(Py-NOH)2][FeIII(Tp*)(CN)3]2}·H2O ([FeIII2MII]) (Py-NOH = 4-pyridinealdoxime, Tp* = tris(3,5-dimethylpyrazol-1-yl)borohydride, M = Ni (1), Fe (2)) compounds are reported. The crystal structures of both compounds were determined by single-crystal X-ray diffraction. Complexes 1 and 2 are isostructural, with the crystal structure comprising neutral double-zigzag (4,2-ribbon-like) bimetallic chains. The FeIII ion is coordinated by three cyanide carbon atoms and three nitrogen atoms of Tp* anions. However, the MII ion is surrounded by four cyanide nitrogen atoms and two nitrogen atoms from two Py-NOH ligands. The crystal structures and magnetic studies demonstrate that both complexes behave as single-chain magnetics (SCMs) with intrachain ferromagnetic coupling. Furthermore, [FeIII2NiII] exhibits an excellent coercive field of 0.42 T at 1.8 K, among cyano-bridged 3d transition-metal-based SCMs reported thus far. Preliminary theoretical calculations provide a deep understanding of the magnetic properties of [FeIII2NiII].

Keeping dysprosium in line: Trinuclear heterometallic MII2DyIII complexes with M=Cd, Co and Cu

AbstractFour new heterometallic trinuclear essentially linear (“in‐line”) MII2DyIII complexes (M=CdII (1), CoII (2), CuII (3, 4) were synthesised using the ligand 3,5‐di‐tert‐butylbenzoic acid (dtbbaH) in a MeCN : iPrOH (1–3) or in a MeOH : iPrOH : DMF (4) mixture. Single crystal structure analyses revealed the formation of [Cd2Dy(dtbba)6(iPrOH)2(H2O)2NO3] ⋅ iPrOH (1), [Co2Dy(dtbba)6(iPrOH)2(H2O)2NO3] ⋅ iPrOH (2), [Cu2Dy(dtbba)6(MeCN)4NO3] ⋅ MeCN (3) and [Cu2Dy(dtbba)6(iPrOH)1.68(DMF)1.32(H2O)NO3] ⋅ 3iPrOH ⋅ H2O (4). The M−Dy−M angles become more acute from (1) to (3) leading to decreased M⋅⋅M distances. The DyIII ions are 8‐coordinate with a distorted triangular dodecahedron geometry and a D2d symmetry whereas the geometry of the 5‐coordinate terminal MII ions can best be described as either distorted vacant octahedra or as spherical square pyramids with a C4v symmetry. Magnetic susceptibility measurements were performed on (1), (2) and (3) which allows a comparison of the effect of replacing highly anisotropic CoII with the quantum spin of CuII. Both (2) and (3) show effects of ferromagnetic interactions at low temperatures.

Theoretical study of heptadentate bispidine ligands for radiopharmaceutic applications

The complexes of radiopharmaceutically relevant trivalent metals (MIII = InIII, BiIII, LaIII, LuIII, AcIII) with two heptadentate bispidine-based ligands (L) have been investigated by DFT calculations. The main questions included the encapsulation efficiency of the ligands for the different-size metals, the differences in bonding, the possibility and characteristics of octa- and nonacoordination achieved by attachment of H2O ligands to the ML complexes as well as the thermodynamic stabilities under isolated and aqueous solution conditions. The results supported high efficiencies of the ligands resulting in very good stabilities of the complexes. The bonding analysis revealed small differences based on a gentle interplay of the sizes and electronic structures of the MIII ions as well as on the difference in two donor groups of the ligands. The present heptadentate ligands form tighter interactions with the metals as compared to the octadentate derivative, and leave less space for coordination of additional ligands.

Metal-ligand bonding in bispidine chelate complexes for radiopharmaceutical applications

The complexes of selected radionuclides relevant for nuclear medicine (InIII, BiIII, LuIII, AcIII and in addition LaIII for comparative purposes) with the octadentate (6,6′-((9-hydroxy-1,5-bis(methoxycarbonyl)-2,4-di(pyridin-2-yl)-3,7-diazabicyclo[3.3.1]nonane-3,7-diyl)bis(methylene))dipicolinic acid) ligand, H2bispa2, have been studied by density functional theory calculations modelling both isolated and aqueous solution conditions. The properties in focus are the encapsulation efficiency of the ligand for the different-size metals (M), the differences in bonding with the various MIII ions analysed using Bader’s atoms in molecules theory and the possibility and characteristics of nona- and decacoordination by H2O ligands. The computed results confirmed strong steric effects in the case of the In complex excluding higher than octacoordination. The studied properties depend strongly on the interplay of the sizes and electronic structures of the MIII ions. The computations support high stability of the complexes in aqueous solution, where also the solvation energies of the MIII ions (as dissociation products) play a significant role.

Ba4Cl] Cations Directed Perovskite-like Polar Metal Formate Frameworks {[Ba4Cl][M3(HCO2)13]}n (M = Mn, Co, and Mg): Microwave-Assisted Synthesis, Structures, and Properties.

Novel 3D metal formate frameworks {[Ba4Cl][M3(HCO2)13]}n (M = Mn for 1, Co for 2, and Mg for 3) were successfully assembled via microwave-assisted synthesis. The complexes are rare coordination polymers crystallized at space group P4cc with the polar point group C4v. In the structure, the MII ions are bridged by two types of anti-anti formate in forming a 3D pcu framework, and additional formates coordinate to the unsaturated sites of the MII ions in the framework, giving an anionic M-formate net. Ba4Cl clusters take the cavities of the net as charge balance, in which the chloride ion deviates from the center of the barium ions. The asymmetric Ba4Cl structure is transmitted throughout the crystal resulting in polar structure, which is further confirmed by nonlinear optical and piezoelectric test. Nonlinear optical activity tests of 1 and 3 show SHG signals 0.32 and 0.28 times that of KDP, while 2 has a piezoelectric coefficient d33 of 6.8 pC/N along polar axis. Magnetic studies reveal antiferromagnetic coupling between MII ions in 1 and 2. Spin canting was found only in 2 with anisotropic CoII ions, and 2 is a canted antiferromagnetically with TN = 5 K. Further field-induced spin flop was also found in 2 with a critical field 0.9 T.

Divalent metal release and antimicrobial effects of layered double hydroxides

Resistance to antimicrobial agents is responsible for major social and economic losses. The World Health Organization estimated 700,000 global deaths a year due to antimicrobial resistance. The use of layered double hydroxides (LDHs) as antibacterial materials could present a way to reduce the risk of bacterial infections and antibacterial resistance, by partial release of metallic ions in aqueous dispersion. The partial dissolution of different synthetic LDHs MII-AlIII (M = Zn, Cu, Ni, Co, Mg) was studied in Lysogeny Broth (LB) and Tryptic Soy Broth (TSB), growth media of Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) bacteria, respectively. The influence of several parameters (crystallinity, MII:AlIII ratio, type of intercalated anion {CO32−, Cl−, NO3−, ClO4−} and nature of MII cations) was investigated. In the absence of any post-synthetic hydrothermal treatment, ZnII-AlIII LDH showed a release of ZnII ions 6 times enhanced. Upon increasing ZnII:AlIII molar ratio to 3: 1 and exchanging carbonate anions with other anions having lower intercalating affinities, a similar effect was observed. The dissolution properties of MII-AlIII LDHs were correlated with the thermodynamic stability of their MII(OH)2 hydroxide counterparts with the exception of CuII-based LDH, which showed an amplified release of CuII due to its irregular structure presenting defects. Finally, the antibacterial activity was only noted for ZnII and CuII-based LDHs. The antimicrobial effect of the studied LDHs was linked in the first place to the nature of divalent metal itself, and to the amount of released MII ions into the culture media in the second place. This effect was more easily identified in ZnII-AlIII LDHs whose minimum inhibitory concentration was decreased significantly from 12 to 0.375 mg.mL−1 when higher amounts of ZnII ions were released.

Metal-Cocatalyst Interaction Governs the Catalytic Activity of MII-Porphyrazines for Chemical Fixation of CO2.

Chemical fixation of CO2 to produce cyclic carbonates can be a green and atomic efficient process. In this work, a series of porphyrazines (Pzs) containing electron-withdrawing groups and central MII ions (where M = Mg, Zn, Cu, and Co) were synthesized and investigated as catalysts for the cycloaddition of CO2 to epoxides. Then, the efficiency of the Pzs was tested by varying cocatalyst type and concentration, epoxide, temperature, and pressure. MgIIPz bearing trifluoromethyl groups (1) showed the best conversion, producing, selectively, 78% of propylene cyclic carbonate (PCC), indicating that a harder and stronger Lewis acid is more effective for epoxide activation. Moreover, cocatalyst variation showed a notable effect on the reaction yields. Spectrophotometric titrations, MALDI-TOF mass spectra, and theoretical calculations suggest poisoning of the catalyst when tetrabutylammonium chloride (TBAC) and large amounts of tetrabutylammonium bromide (TBAB) were used in the system. The same was not observed for tetrabutylammonium iodide (TBAI), indicating that the metal-cocatalyst interaction may govern the reaction rate. In addition, two rare examples of crystalline structures were obtained, proving the distorted square pyramidal geometry with water molecule as axial ligand. This is one of the first studies reporting Pzs as catalysts for the chemical fixation of CO2, and we believe that the intricate balance between cocatalyst concentration and conversion efficiency shown here may aid future studies in the area.

Synthesis, Crystal Structure and Magnetic Properties of 1D Chain Complexes Based on Azo Carboxylate Oxime Ligand

Two carboxylate-bridged one-dimensional chain complexes, {[MnII(MeOH)2][FeIII(L)2]2}n (1) and {[MnII(DMF)2][MnIII(L)2]2·DMF}n (2) [H2L = ((2-carboxyphenyl)azo)-benzaldoxime], containing a low-spin [FeIII(L)2]− or [MnIII(L)2]− unit were synthesized. Magnetic measurements show that the adjacent high-spin MnII and low-spin MIII ions display weak antiferromagnetic coupling via the syn–anti carboxyl bridges, with J = −0.066(2) cm−1 for complex 1 and J = −0.274(2) cm−1 for complex 2.

Bifunctional activation of methane by bioinspired transition metal complexes. A simple methane protease model

Metal-based bifunctional methane activators are modeled utilizing density functional theory. The impact upon activation barriers of the metal among the late 3d metal MII ions (Co – Zn) is quite pronounced, ca. 7 kcal/mol. Alteration of the metal’s coordination environment without changing the supporting ligand types (e.g., comparing cis and trans coordination isomers) has a computed impact on methane activation barriers of ± 1 kcal/mol. One significant result involves the varying impact of fluorination of the imidazole, which serves as a simple mimic of a histidine side chain. Sequentially fluorinating the 3C–H bonds of imidazole produces a range in the calculated ΔH‡ of 4½ kcal/mol, an effect greater than any other modeled herein apart from the impact of changing the central metal ion of the active site. As such, the present research yields insight into possible avenues for bio-inspired methane activators.

Supramolecular complexes of Ni (II) and Co (II) 4‐aminobenzoate with 3‐cyanopyridine: Synthesis, spectroscopic characterization, crystal structure, and enzyme inhibitory properties

Two new complexes, [M (AB)2(CP)2(H2O)2] (where M = Ni and Co AB = 4‐aminobenzoate and CP = cyanopyridine), were synthesized and characterized using different techniques (elemental analysis, FT‐IR spectrophotometer, LC/MS, single‐crystal X‐ray diffraction, and TGA/DTA analysis). As a result of X‐ray structural analysis, it was determined that complexes are isostructural. In the crystalline structures, MII ions are bridged with their carboxylate oxygen and aminopyridine nitrogen atoms and their symmetry‐related counterparts to form a two‐dimensional polymeric structure. The MII ion is octa‐coordinated with two nitrogen atoms and two oxygen atoms of the AB and two atoms of the CP anions. In this study, the effect of these molecules, containing a biologically active group, was investigated on important metabolic enzymes (carbonic anhydrase isoenzymes I and II (hCA I and II), achethylcholinesterase (AChE), and α‐glycosidase (α‐Gly) enzymes).

Complexes with Furyl-Substituted 3-Hydroxychromone: Synthesis, Characterization and Fluorescence Studies

2-(2-Furyl)-3-hydroxychromone (HL) reacts with MII ions in the formation of quadratic [Cu(L)2] (3), octahedral [M(L)2(OH2)2] (M = Co (1), Ni (2), Zn (4), Mn (5)) and seesaw [M(L)2] (M = Sn (6), Pb (7)) complexes. Recrystallization of complexes 1-3 in presence of pyridine lead to [M(L)2(py)2] (1a-3a) adducts. All compounds were characterized by Fourier transform infrared spectroscopy (FTIR). Complexes 1-7 were analyzed by UV-Vis and diffuse reflectance spectroscopies. The estimated band gap energies range from 2.90-3.15 eV. The crystal structure of complexes 6 and 7 revealed the influence of the stereochemically active lone pair due to their electronic configuration ns2. An intense fluorescence emission band centered at approximately 600 nm (λexc centered at 340 nm) has been observed for complex 6 in the solid state. In N,N‑dimethylformamide (DMF) solution, complex 6 showed two emission bands (468 and 538 nm) when excited from 300 to 380 nm, and only one emission band (468 nm) when excited from 385 to 420 nm.

Boronate Ester-Capped Helicates.

Triple-stranded helicates were obtained by metal-templated multicomponent reactions of bispyridyloxime ligands with arylboronic acids. The helicates feature two hexa-coordinated MII ions (M=Fe, Zn, or Mn), which are embedded in a macrobicyclic ligand framework, and two arylboronate ester capping groups. The latter can be used to introduce functional groups such as pyridines, aldehydes, nitriles, and carboxylic acids in apical position. The functionalized helicates have the potential to be used as nanoscale building blocks for more complex assemblies, as evidenced by the synthesis of a 3 nm-sized trianglimine.

Novel Metal-Organic Framework-Based Photocrosslinked Hydrogel System for Efficient Antibacterial Applications.

Metal-organic frameworks (MOFs) can be applied in biology and medicine as drug delivery systems by carrying drugs on their surfaces or releasing bioactive ligands. To investigate the therapeutic potential of hydrogels that contain MOFs, three MOFs containing glutarate and 1,2-bis(4-pyridyl)ethylene ligands were synthesized by the previously reported hydrothermal or solvothermal reactions: Cu-MOF 1, Co-MOF 2, and Zn-MOF 3. Bioactive MOF-embedded hydrogels (hydrogel@Cu-MOF 1, hydrogel@Co-MOF 2, and hydrogel@Zn-MOF 3) were prepared by UV light-mediated thiol-ene photopolymerization using diacrylated polyethylene glycol (PEG), 4-arm-thiolated PEG, and MOFs. The activities of the MOF-embedded hydrogels were tested against the Gram-negative bacterium Escherichia coli and the Gram-positive bacterium Staphylococcus aureus. These MOF-embedded hydrogels were observed to be very stable, based on the release test of MII ions, and both hydrogel@Cu-MOF 1 and hydrogel@Co-MOF 2 showed excellent antibacterial activity. Although, in human dermal fibroblasts, hydrogel@Cu-MOF 1 showed no cytotoxic effects, it exhibited 99.9% antibacterial effects at the minimum bactericidal concentration. Physical properties such as the surface area and dimension of MOFs with different central metals appeared to be more important than the chemical properties of the ligands in determining the effects on bacteria. These MOF-embedded hydrogels may be useful in antibacterial applications such as cosmetics, treatment of skin diseases, and drug delivery owing to their low cytotoxicity and high bactericidal activity.

Evaluation of Octaethyl-7,17-dioxobacteriochlorin as a Ligand for Transition Metals

The propensity of octaethyl-7,17-dioxobacteriochlorin toward the formation of transition metal complexes was evaluated. A variety of MII ions (M = Co, Ni, Cu, Zn, Pd, Ag, and Cd) and Fe(III) could be inserted using standard methodologies or, more often, using more forcing conditions. The stable products were spectroscopically characterized. The solid-state structures of the Ni(II), Cu(II), Pd(II), and Ag(II) complexes could also be determined by single crystal X-ray diffractometry, whereby the [7,17-dioxobacteriochlorinato] chromophore was found to be largely planar in all cases. The rate of Zn(II) insertion into octaethyl-7,17-dioxobacteriochlorin was less than half that into the corresponding 7-oxochlorin, which itself was about half the rate into the parent octaethylporphyrin. These rate differences reflect the relative decreased basicity of the β-oxo-substituted chromophores and possibly also their decreased conformational flexibility. We compare the basicity of the dioxobacteriochlorin to that of a range of related products of varying reduction state (porphyrin, chlorin, bacteriochlorin), an isomer, and the absence or presence of oxo-functionality, like oxochlorin, chlorin, oxobacteriochlorins, and bacteriochlorin, quantifying the effects of these macrocycle modifications. The work rationalizes earlier reports of the inability of tolyporphin A, a natural product possessing a 7,17-dioxobacteriochlorin chromophore, to form metal complexes and provide a more quantitative understanding of the degree of modulation that β-oxo groups have on the coordination properties of porphyrinoids.

Effect of 3d heterometallic ions on the magnetic properties of azido-Cu(II) with isonicotinic acid coligands: A theoretical perspective

Based on density functional theory and the broken-symmetry approach, the magnetic properties of an azido-Cu(II) complex with isonicotinic acid coligands were studied at the B1LYP/def2-TZVP level. According to the molecular magnetic orbitals and Mulliken spin population analysis, there are strong orbital interactions between the paramagnetic CuII/NiII ions and the bridging azide ligands and isonicotinic ions. The supposedly empty 4s/4p/4d orbitals of the MII ions are found to play an important role in the mechanism of magnetic coupling and are probed using NBO analysis. As the number of unpaired electrons on the MII ions increases, the number of electrons that occupy the empty 4d orbitals with the highest energy and overlap integrals of the magnetic orbitals in the CuIIMII (M = Cu, Ni, Co, Fe, Mn) model complexes increases accordingly, and the magnetic coupling constant gradually decreases.