Iron Coordination Polymer Research Articles

Synthesis, Characterization and Photocatalytic Activity of Iron(II) and Iron(III) Coordination Polymers Derived from Terephthalic Acid

Synthesis, Characterization and Photocatalytic Activity of Iron(II) and Iron(III) Coordination Polymers Derived from Terephthalic Acid

Photoinduced morphological transformation of a self-assembled iron(ii) coordination polymer: high-performance, non-precious metal, and self-enhancing photocatalytic CO2 reduction

Herein, uncommon self-enhancing photocatalysis has been demonstrated through photoinduced morphology transformation of a self-assembled iron coordination polymer for CO2 photoreduction.

Single-Crystal Structure Analysis of Three Novel Iron(II) Coordination Polymers with Bridging 1,3,5-Tris((1H-1,2,4-triazol-1-yl)methyl)benzene

Three novel iron(II) coordination polymers, namely [Fe(H2O)2(ttmb)2](ClO4)2·4H2O (1), [Fe(H2O)2(ttmb)2](BF4)2·4H2O (2) and [Fe(NCS)2(ttmb)2] (3), were synthesized with the linker 1,3,5-tris((1H-1,2,4-triazol-1-yl)methyl)benzene (ttmb). The single-crystal structures show that all three compounds form a double-chain structure with the adjacent iron atoms being bridged by two ttmb linkers. The iron(II) ions are octahedrally surrounded by four N4 donor atoms from the 1,2,4-triazol-1-yl groups of four different ttmb linkers which form an equatorial plane and two trans-coordinated aqua ligands in 1 and 2 or isothiocyanato ligands in 3 in the axial positions. In view of the neutral bridging ttmb linker, there is a non-coordinated counter-anion in 1 and 2 (ClO4 and BF4, respectively), and a coordinated NCS anion in 3. Compounds 1 and 2 are isostructural. Interestingly, the ttmb linker only utilizes two of its three potentially coordinating triazole groups. All iron(II) coordination networks are colorless or have a light-yellow color, being indicative of the high-spin state.

Observation of Two-Step Spin Transition in Graphene Oxide-Based Hybrids with Iron(II) 4-amino-1,2,4-triazole Spin Crossover Nanoparticles.

A novel experimental protocol based on a reverse micellar method is presented for the synthesis of graphene oxide (GO)-based hybrids with spin crossover nanoparticles (SCO NPs) of the 1D iron(II) coordination polymer with the formula [Fe(NH2trz)3](Br2). By introducing different quantities of 0.5% and 1.0% of GO (according to iron(II)) into the aqueous phase, two hybrids, NP4 and NP5, were synthesized, respectively. The morphological homogeneity of the NPs on the surface of the GO flakes is greatly improved in comparison to the pristine [Fe(NH2trz)3](Br2) NPs. From the magnetic point of view and at a low magnetic sweep rate of 1 K/min, a two-step hysteretic behavior is observed for NP4 and NP5, where the onset of the low-temperature second step appeared at 40% and 30% of the HS fraction, respectively. For faster sweep rates of 5-10 K/min, the two steps from the cooling branch are progressively smeared out, and the critical temperatures observed are T1/2↑ = 343 K and T1/2↓ = 288 K, with a thermal width of 55 K for both NP4 and NP5. A Raman laser power-assisted protocol was used to monitor the thermal tolerance of the hybrids, while XPS analysis revealed electronic interactions between the SCO NPs and the GO flakes.

Nanocomposites Based on Spin-Crossover Nanoparticles and Silica-Coated Gold Nanorods: A Nonlinear Optical Study.

A nanocomposite based on silica-coated AuNRs with the aminated silica-covered spin-crossover nanoparticles (SCO NPs) of the 1D iron(II) coordination polymer with the formula [Fe(Htrz)2(trz)](BF4) is presented. For the synthesis of the SCO NPs, the reverse micelle method was used, while the gold nanorods (AuNRs) were prepared with the aspect ratio AR = 6.0 using the seeded-growth method and a binary surfactant mixture composed of cetyltrimethylammonium bromide (CTAB) and sodium oleate (NaOL). The final nanocomposite was prepared using the heteroaggregation method of combining different amounts of SCO NPs with the AuNRs. The nonlinear optical (NLO) properties of the hybrid AuNRs coated with different amounts of SCO NPs were studied in detail by means of the Z-scan technique, revealing that the third-order NLO properties of the AuNRs@SCO are dependent on the amount of SCO NPs grafted onto them. However, due to the resonant nature of the excitation, SCO-induced NLO switching was not observed.

57Fe Mössbauer spectroscopy and high-pressure structural analysis for the mechanism of pressure-induced unique magnetic behaviour in (cation)[FeIIFeIII(dto)3] (cation = Ph4P and nPrPh3P; dto = 1,2-dithiooxalato).

A mixed-valence iron(II,III) coordination polymer, (Ph4P)[FeIIFeIII(dto)3] (2; Ph4P = tetraphenylphosphonium, dto = 1,2-dithiooxalato), exhibits a thermal hysteresis loop and a low temperature shift of the ferromagnetic phase transition temperature, with increasing pressure. The latter magnetic behaviour can also be observed in a novel compound (nPrPh3P)[FeIIFeIII(dto)3] (3; nPrPh3P = n-propyltriphenylphosphonium). To understand the structural information under pressure, we performed high-pressure powder X-ray diffraction, and the result suggests that there was no structural phase transition for either compound. Considering the 57Fe Mössbauer spectroscopy studies, both 2 and 3 may have a high transition entropy, and this finding is caused by pressure-induced unique magnetic behaviours.

Synergetic Spin-Crossover and Luminescent Properties in a Multifunctional 2D Iron(II) Coordination Polymer.

We designed and synthesized a strong fluorescent tetradentate pyridine ligand, 3,6,11,12-tetra(pyridin-4-yl)dibenzo[a,c]phenazine (TPDP), by covalently grafting pyridyl to fluorescent dye dbpz, which can react with the Fe(NCX)2 (X = S and Se) unit, obtaining two new 2D [4 × 4] square-grid compounds, namely, {FeII(TPDP)2(SCN)2·CHCl3·4CH3OH}n (1) and {[FeII(TPDP)2(SeCN)2]·CH2Cl2·4CH3OH}n (2). Both of them show expected one-step spin-crossover (SCO) properties, and complex 2vacuum exhibits a combination of the SCO phenomenon and fluorescence in a synergetic way. The energy transfer mechanism of 2vacuum is verified by the theoretical calculations and experimental results. This study provides an effective strategy to synthesize large conjugated fluorescent ligands using dyes to further form SCO-luminescent bifunctional materials.

A reactive oxygen species-replenishing coordination polymer nanomedicine disrupts redox homeostasis and induces concurrent apoptosis-ferroptosis for combinational cancer therapy

Reactive oxygen species (ROS) are important signal molecules and imbalanced ROS level could lead to cell death. Elevated ROS levels in tumor tissues offer an opportunity to design ROS-responsive drug delivery systems (DDSs) or ROS-based cancer therapies such as chemodynamic therapy. However, their anticancer efficacies are hampered by the ROS-consuming nature of these DDSs as well as the high concentration of reductive agents like glutathione (GSH). Here we developed a doxorubicin (DOX)-incorporated iron coordination polymer nanoparticle (PCFD) for efficient chemo-chemodynamic cancer therapy by using a cinnamaldehyde (CA)-based ROS-replenishing organic ligand (TCA). TCA can ROS-responsively release CA to supplement intracellular ROS and deplete GSH by a thiol-Michael addition reaction, which together with DOX-triggered ROS upregulation and Fe3+-enabled GSH depletion facilitated efficient DOX release and enhanced Fenton reaction, thereby inducing redox dyshomeostasis and cancer cell death in a concurrent apoptosis-ferroptosis way. Both in vitro and in vivo studies revealed that ROS-replenishing PCFD exhibited much better anticancer effect than ROS-consuming control nanoparticle PAFD. The ingenious ROS-replenishing strategy could be expanded to construct versatile ROS-responsive DDSs and ROS-based nanomedicines with potentiated anticancer activity. Statement of significanceWe develop a doxorubicin (DOX)-incorporated iron coordination polymer nanoparticle (PCFD) for efficient chemo-chemodynamic cancer therapy by using a cinnamaldehyde-based reactive oxygen species (ROS)-replenishing organic ligand. This functional ligand can ROS-responsively release cinnamaldehyde to supplement intracellular H2O2 and deplete glutathione (GSH) by a thiol-Michael addition reaction, which together with DOX-triggered ROS upregulation and Fe3+-enabled GSH depletion facilitates efficient DOX release and enhanced Fenton reaction, thereby inducing redox dyshomeostasis and cancer cell death in a concurrent apoptosis-ferroptosis way. Both in vitro and in vivo studies reveal that ROS-replenishing PCFD exhibit much better anticancer effect than ROS consuming counterpart. This study provides a facile and straightforward strategy to design ROS amplifying nanoplatforms for cancer treatment.

Pressure-Induced Structural and Charge-Transfer Phase Transitions for a Two-Dimensional Mixed-Valence Iron(II,III) Coordination Polymer

A two-dimensional (2D) mixed-valence iron(II,III) coordination polymer, (Ph4P)[FeIIFeIII(dto)3] (1; Ph4P = tetraphenylphosphonium, dto = 1,2-dithiooxalato), was prepared, and its crystal structure was revealed. Compound 1 exhibited a 2D honeycomb structure and a rigid layered framework, due to a hydrogen bond between the cation and anion layers. The temperature dependence of the magnetic susceptibilities for 1 under high pressure showed a thermal hysteresis loop corresponding to a charge-transfer phase transition, although there was no charge-transfer phase transition under ambient pressure.

Manganese-doped iron coordination polymer nanoparticles with enhanced peroxidase-like activity for colorimetric detection of antioxidants.

A convenient and sensitive antioxidant assay with high performance is essential for assessing food quality and monitoring the oxidative stress level of biological matrices. Although coordination polymer nanoparticles (CPNs)-based nanozymes have emerged as candidates in the analytical field, strategies to improve the catalytic activity of CPNs have been scarcely revealed and studied. Herein, we demonstrate a manganese (Mn) doping strategy to enhance the peroxidase-mimetic activity of Fe-based CPNs. By tuning the Mn doping amounts and selecting 2,5-dihydroxyterephthalic acid (H4DHTP) as ligands, the produced nanozymes in amorphous state followed the catalytic activity order of Fe5Mn-DHTP > Fe8Mn-DHTP > Fe2Mn-DHTP > Fe-DHTP > Mn-DHTP. Ulteriorly, benefitting from the best catalytic performance and definite catalytic mechanism of Fe5Mn-DHTP, versatile colorimetric assays for ultrasensitive detection of one exogenous antioxidant (ascorbic acid, AA) and two endogenous antioxidants (glutathione, GSH; cysteine, Cys) have been deftly devised based on the inhibition of the 3,3',5,5'-tetramethylbenzidine chromogenic reaction in presence of H2O2. It was found that mercaptan (GSH and Cys) and AA exhibited different inhibition mechanisms. Practically, such a colorimetric assay was viable to determine the total antioxidant capacity of drugs and foods with desirable results. This work proposes a feasible strategy for embellishing CPN nanozymes used for designing sensitive and convenient assays for various antioxidants based on an explicit detection mechanism.

Approach toward Iron(II) Coordination Polymers Based on Chain Motifs with Thiolate or Mixed Thiolate/Carboxylate Bridges: Structures and Magnetic Properties.

The search for iron-sulfur-based coordination polymers (CPs) has become an attractive field in recent years. Here we demonstrate how it is possible to synthesize new iron-sulfur-based CPs by solvothermal reactions of [CpFe(CO)2]2 (Cp = cyclopentadienyl) with two positional isomeric ligands 6-mercaptonicotinic acid (6-H2mna) and 2-mercaptoisonicotinic acid (2-H2mina) in different mixed-solvent systems. The reactions afforded, in moderate yields, a variety of desired CPs, namely, [Fe(6-Hmna)2] (1), [Fe3(6-Hmna)2(6-mna)2] (2), [Fe2(6-mna)2]·H2O (3), and [Fe(2 mina)(H2O)] (4 and 5). The structures of these compounds have been characterized by single-crystal X-ray diffraction, which reveals that they all contain 1D chain motifs of iron held together in different ways by thiolate or mixed thiolate/carboxylate bridges. These chains are further connected through the ligand backbones to form 3D networks of 1-3 and 5 and a 2D sheet of 4. Moreover, magnetic investigations indicate that both 1 and 4 display canted antiferromagnetic behavior with weak ferromagnetism, while 2 and 5 possess short-range antiferromagnetic order at ∼20 K. CP 3 exhibits paramagnetic behavior down to 2 K with strong spin frustration.

Sterically Encumbered Coordination Sites. Iron(II) Complexes of Jäger‐type ligands with a Terphenyl Backbone

AbstractA Schiff base‐like ligand H2LTerPh featuring a para‐terphenyl backbone was synthesized and converted in two steps to an octahedral iron(II) coordination polymer with 1,2‐bis‐(4‐pyridyl)‐ethylene as bridging ligand. Single crystal X‐ray structure analysis was possible for the free ligand and the two octahedral iron(II) complexes. The Schiff base‐like ligand features a [N2O2]2− coordination sphere for the metal center and the para‐terphenyl backbone introduces intrinsic steric constraint. Characterization of the coordination polymer with an N4O2 coordination sphere around the iron center via magnetic measurements (SQUID) and room temperature Mössbauer spectroscopy revealed HS character in the entire temperature range investigated. Structure modelling with DFT calculations supports the findings, but support also the possibility of spin crossover in solution.

One-dimensional manganese(III) and iron(III) coordination polymers assembled by N2O2-donor Schiff bases and 4,4′-bipyridine: syntheses, structures and properties

One-dimensional manganese(III) and iron(III) coordination polymers assembled by N2O2-donor Schiff bases and 4,4′-bipyridine: syntheses, structures and properties

Iron Coordination Polymer, Fe(oxalate)(H2O)2 Nanorods Grown on Nickel Foam via One-Step Electrodeposition as an Efficient Electrocatalyst for Oxygen Evolution Reaction.

Iron coordination polymer, Fe(ox)(H2O)2 (H2ox = oxalic acid) nanorods were grown on a nickel foam (NF) collector via a one-step electrodeposition method, which can be directly used as a freestanding and binder-free electrode for efficient oxygen evolution reaction (OER) electrocatalysis. The optimum sample, Fe(ox)(H2O)2/NF-(-1.4)-15, was obtained at an electrodeposition potential of -1.4 V vs Ag/AgCl for 15 min, which can deliver OER current densities of 40 and 100 mA cm-2 at overpotentials of 270 and 340 mV, respectively. The sample also exhibits good long-term OER activity during 80 h electrolysis at 20 mA cm-2, which is superior to those of previously reported metal-organic framework (MOF) catalysts. Furthermore, the formation mechanism of the Fe(ox)(H2O)2 nanorods is primarily investigated and the effect of the species of metal ions in MOF on the morphology and OER behavior is also explored. In addition, density functional theory (DFT) calculations reveal that the rate-limiting steps on Fe(ox)(H2O)2 and Ni(ox)(H2O)2 are the formation of Fe*-OOH and Ni*-OH intermediates with maximum ΔG values of 1.628 and 1.710 eV, respectively, which is attributed to the different electronic configurations of Ni and Fe, thus giving rise to different d-band centers and different affinities for adsorbates.

Spin States of 1D Iron(II) Coordination Polymers with Redox Active TTF(py)2 as Bridging Ligand

In this manuscript, we report the solvent‐dependent synthesis of 1D coordination polymers derived from two planar N2O2‐coordinate iron(II) complexes FeL1 and FeL2, which incorporate TTF(py)2 as a bridging bis‐monodentate ligand. The obtained 1D polymers were characterized through elemental analysis, Mössbauer spectroscopy, single crystal structure analysis for 2a·2 DMF, magnetic susceptibility measurements, X‐ray powder diffraction, cyclic voltammetry and diffuse reflectance spectroscopy, supplemented by DFT computation. The results revealed additive electronic properties of the sub‐units FeL and TTF(py)2 with only minor mutual influence. Intriguingly however, the solvent‐of‐synthesis is found to be a steering factor of the magnetic spin crossover properties of the resulting materials, yielding divergent behavior if obtained from DMF, MeCN or EtOH. This becomes strikingly evident for the magnetic properties of the DMF‐derived polymer which is found trapped in the low‐spin state in the single crystal 2a· 2 DMF, but shows a gradual spin crossover if all solvent is removed.

ON/OFF Photoswitching and Thermoinduced Spin Crossover with Cooperative Luminescence in a 2D Iron(II) Coordination Polymer.

A 2D coordination polymer, {[Fe(L)2(NCSe)2]·6MeOH·14H2O}n (1; L = 2,5-dipyridylethynylene-3,4-ethylenedioxythiophene), has been synthesized based on a redox active luminescence ligand. 1 possesses a 2D [4 × 4] square-grid network where the iron(II) center is in a FeN6 octahedral coordination environment. 1 displays reversible thermoinduced high-spin (HS; S = 2) to diamagnetic low-spin (LS; S = 0) ON/OFF spin-state switching with a T1/2 value of 150 K. Interestingly, optical reflectivity and photomagnetic studies at 10 K under light irradiation revealed an efficient conversion to a photoinduced metastable HS excited state from a LS ground state. Remarkably, the photoexcited HS state can be reversibly switched ON and OFF by using 625 and 850 nm light-emitting-diode lights. Intriguingly, the thermal dependence of the luminescence intensity of the maximum emission at 524 nm for 1 shows a minimum at around the spin-crossover (SCO) temperature, indicating a cooperative nature between the SCO and luminescence properties. Theoretical calculations confirmed the above findings.

Variable Cooperative Interactions in the Pressure and Thermally Induced Multistep Spin Transition in a Two-Dimensional Iron(II) Coordination Polymer.

Two types of experiments conducted to investigate the effect of pressure on the spin crossover (SCO) properties of the 2D Fe(II) coordination polymer formulated {Fe[bipy(ttr)2]}n are reported, namely, (1) magnetic measurements performed at variable temperature and at fixed pressure and (2) visible spectroscopy at variable pressure and fixed temperature. The magnetic experiments carried out under a hydrostatic pressure constraint of 0.04, 0.08, and 0.8 GPa reveal a two-step spin transition behavior. The characteristic critical temperatures of the spin transition are shifted upward in temperature as pressure increases. The slope of the straight-line of the Tc vs P plot, dTc/dP, is 775 K/GPa and 300 K/GPa, for the high temperature and the low temperature steps, respectively. These values are remarkably large and denote the extreme sensitivity of the material to the application of pressure. Indeed, the visible spectroscopic measurements performed at 293 K show that a complete spin transition is induced at pressures as low as 0.4 GPa. Moreover, the pressure-induced spin transition is reversible and shows an asymmetric hysteresis. An analysis of the cooperative interactions of the thermal- and pressure-induced spin transition in the framework of the model of elastic interactions reveals that the elastic energy of the lattice as well as the interaction parameter between the SCO centers change during the course of the spin transition. Consequently, the character of the spin transition varies from abrupt for the high temperature step to continuous for the low temperature step.

Spin Crossover in Bipyridine Derivative Bridged One-Dimensional Iron(III) Coordination Polymer

Herein, the syntheses, solid-state molecular structures, and characterization of two types of one-dimensional FeIII coordination polymers showing thermally induced spin crossover are reported. The reaction of [Fe(acen)Cl] (acen2− = N,N′-ethylenebis(acetylacetonylideneaminate) with 3,3′-bpy or 4,4′-bpy (bpy = bipyridine) produced zigzag and linear one-dimensional chain complexes, [Fe(acen)(3,3′-bpy)][BPh4] (1) or [NEt3H][Fe(acen)(4,4′-bpy)][BPh4]2·0.5(4,4′-bpy) (2), respectively, as confirmed by single crystal X-ray diffraction analysis. Variable-temperature single crystal X-ray diffraction measurements, continuous-wave X-band electron paramagnetic resonance (EPR) spectra, 57Fe Mössßauer spectra, and DC magnetic susceptibility data revealed that complex 1 exhibited a gradual and complete spin crossover at a transition temperature of 212 K, while complex 2 undergoes an incomplete spin crossover even at 400 K.

Influence of CF3 Substituents on the Spin Crossover Behavior of Iron(II) Coordination Polymers with Schiff Base‐like Ligands

A Schiff base‐like ligand bearing CF3 substituents was synthesized and converted to iron(II) coordination polymers [{FeL(Lax)}n] using five different bridging ligands Lax. The structure of the coordination polymers was investigated using powder X‐ray diffraction and single‐crystal X‐ray diffraction in the case of [{FeL(bipy)}n]. The later revealed an untypical ABAB pattern of alternating equatorial ligands rotated by 180° with regard to each other along the chain. The temperature‐dependent magnetic behavior was investigated with a SQUID magnetometer and the spin states at room temperature were confirmed by 57Fe‐Mössbauer spectroscopy. Three out of five coordination polymers show spin crossover behavior in the temperature range between 50 and 400 K with different kind of curve progressions (abrupt, gradual, step‐wise). The other two coordination polymers are either fully highspin or fully low spin.

Linear organic/inorganic iron(II) coordination polymer based on Nitrilo-tris(Methylenephosphonic acid): Spin crossover induced by Cd doping

Linear structure organic-inorganic coordination polymers [Fe(H2O)3μ-{NH(CH2PO3H)3}]n (Fe NTP H4) and [Fe7/8Cd1/8(H2O)3μ-{NH(CH2PO3H)3}]n (Fe7/8Cd1/8 NTP H4) have been synthesized. These polymers are used in anti-corrosive protective coatings for corrosion inhibition of carbon steels. The synthesized compounds have been studied by single-crystal XRD, XPS and Mössbauer spectroscopies. Doping Fe NTP H4 with cadmium (12.5 ​at. %) followed by the formation of Fe7/8Cd1/8 NTP H4 induces the spin-state transition of iron ions from their high-spin state 5D to their low-spin state 1S, with the covalency of the Fe–O(P) dipolar bond increasing in the backbone polymer chain. This probably provides better protective properties of coatings inhibited by the cadmium complexes of nitrilo-tris(methylenephosphonic acid) as compared to the free acid inhibition.