Coordination Motifs Research Articles

Uranium Chemistry: Identifying the Next Frontiers†.

While uranium is the most extensively studied actinide in terms of chemical properties, there remains much to be explored about its fundamental chemistry. Organometallic and organoactinide chemistry first emerged in the 1950s with research that found inspiration from transition-metal chemistry with the synthesis and characterization of uranocene, expanding new opportunities for organoactinide chemistry. Since then, a significant amount of research has pursued many avenues characterizing the fundamental nature of the f orbitals and their modes of bonding as well as their potential in catalysis. Uranium(III/IV) arene complexes dominate much of uranium organometallic chemistry, with bonding interactions stabilized by δ-back-bonding. Recent additions to this area of chemistry include the first UI and new additions of UII organouranium compounds. Uranium-transition metal complexes are still rare and maintain UIV oxidation states, with variable bond lengths determining the transition-metal oxidation state. Resultant reactivities are discussed as synthetic complexes, and unique bonding and coordination motifs are highlighted. This Viewpoint will focus on significant developments in uranium chemistry from the last 15 years while considering key areas for future research.

Polynuclear Cobalt Cluster-Based Coordination Polymers for Efficient Nitrate-to-Ammonia Electroreduction.

The electrocatalytic nitrate reduction reaction (NITRR) holds great promise for purifying wastewater and producing valuable ammonia (NH3). However, the lack of efficient electrocatalysts has impeded the achievement of highly selective NH3 synthesis from the NITRR. In this study, we report the design and synthesis of two polynuclear Co-cluster-based coordination polymers, {[Co2(TCPPDA)(H2O)5]·(H2O)9(DMF)} and {Co1.5(TCPPDA)[(CH3)2NH2]·(H2O)6(DMF)2} (namely, NJUZ-2 and NJUZ-3), which possess distinct coordination motifs with well-defined porosity, high-density catalytic sites, accessible mass transfer channels, and nanoconfined chemical environments. Benefitting from their intriguing multicore metal-organic coordination framework structures, NJUZ-2 and NJUZ-3 exhibit remarkable catalytic activities for the NITRR. At a potential of -0.8 V (vs. RHE) in an H-type cell, they achieve an optimal Faradaic efficiency of approximately 98.5% and high long-term durability for selective NH3 production. Furthermore, the electrocatalytic performance is well maintained even under strongly acidic conditions. When operated under an industrially relevant current density of 469.9 mA cm-2 in a flow cell, a high NH3 yield rate of up to 3370.6 mmol h-1 g-1cat. was observed at -0.5 V (vs. RHE), which is 20.1-fold higher than that obtained in H-type cells under the same conditions. Extensive experimental analyses, in combination with theoretical computations, reveal that the great enhancement of the NITRR activity is attributed to the preferential adsorption of NO3- and the reduction in energy input required for the hydrogenation of *NO3 and *NO2 intermediates.

Heteronuclear Complexes of Hg(II) and Zn(II) with Sodium Monensinate as a Ligand.

The commercial veterinary antibiotic sodium monensinate (MonNa) binds mercury(II) or zinc(II) cations as thiocyanate [Hg(MonNa)2(SCN)2] (1) or isothiocyanate [Zn(MonNa)2(NCS)2] (2) neutral coordination compounds. The structure and physicochemical properties of 1 and 2 were evaluated by the methods of single crystal and/or powder X-ray diffraction, infrared, nuclear magnetic resonance, X-ray photoelectron spectroscopies, and electrospray-mass spectrometry. The primary cores of the two complexes comprise HgS2O2 (1) and ZnN2O2 (2) coordination motifs, respectively, due to the ambidentate binding modes of the SCN-ligands. The directly bound oxygen atoms originate from the carboxylate function of the parent antibiotic. Sodium cations remain in the hydrophilic cavity of monensin and cannot be replaced by the competing divalent metal ions. Zinc(II) binding does not influence the monensin efficacy in the case of Bacillus cereus and Staphylococcus aureus whereas the antimicrobial assay reveals the potential of complex 2 as a therapeutic candidate for the treatment of infections caused by Bacillus subtilis, Kocuria rhizophila, and Staphylococcus saprophyticus.

Chemoselective Post-Synthesis Modification of Pyridyl-Substituted, Aromatic Phosphorus Heterocycles: Cationic Ligands for Coordination Chemistry.

Triazaphospholes are potential polydentate ligands due to the presence of both phosphorus and nitrogen donor atoms within the aromatic 5-membered heterocycle. The incorporation of an additional pyridyl-substituent opens up the possibility of a post-synthesis modification via chemoselective and also stepwise alkylation exclusively of the nitrogen atoms. This can be controlled by the choice and by the stoichiometry of the electrophile and allows the targeted synthesis of a variety of novel mono- and dicationic ligands. Reaction with Cu(I)-halides causes the formation of cuprates of the type [CuXn](n-1)-, which enables coordination of the π-acidic phosphorus donor to the negatively charged metal core, which is favored over the coordination by a strongly σ-donating nitrogen atom. The use of cationic triazaphosphole derivatives can be used as a strategy to enforce the coordination of the ligand to an electron rich metal solely via the phosphorus atom. However, there is a subtle balance between the formation of either coordination polymers or dimeric structures, as the substitution pattern on the heterocycle and the nature of the halide have a large influence on the coordination motifs formed.

Probing the Interfacial Molecular Structure of a Co‐Prussian Blue In Situ

AbstractMolecular‐level insight into the interfacial composition of electrodes at the solid‐electrolyte and the solid‐electrode interface is essential to understanding the charge transfer processes, which are vital for electrochemical (EC) and photoelectrochemical (PEC) applications. However, spectroscopic access to both interfaces, particularly upon application of an external bias, remains a challenge. Here, in situ surface sensitive vibrational sum‐frequency generation (VSFG) spectroscopy is used for the first time to directly access the interfacial structure of a cobalt‐containing Prussian blue analog (Co‐PBA) in contact with the electrolyte and TiO2/Au surface. Structural and compositional changes of the Prussian blue layer during electrochemical oxidation are studied by monitoring the stretching vibration of the CN group. At open circuit potential, VSFG reveals a non‐homogeneous distribution of oxidation states of metal sites: FeIII–CN–CoII and FeII–CN–CoIII coordination motifs are dominantly observed at the Co‐PBA|TiO2 interface, while it is only the FeII–CN–CoII unit at the electrolyte interface. Upon increasing the potential applied to the electrode, the partial oxidation of FeII–CN–CoII to FeIII–CN–CoII is observed followed by its transformation to FeII–CN–CoIII via charge transfer and, finally, the formation of FeIII–CN–CoIII species at the interface with TiO2 and the electrolyte.

Precisely constructing orbital coupling-modulated iron dinuclear site for enhanced catalytic ozonation performance

The advancement of atomically precise dinuclear heterogeneous catalysts holds great potential in achieving efficient catalytic ozonation performance and contributes to the understanding of synergy mechanisms during reaction conditions. Herein, we demonstrate a "ship-in-a-bottle and pyrolysis" strategy that utilizes Fe2(CO)9 dinuclear-cluster to precisely construct Fe2 site, consisting of two Fe1-N3 units connected by Fe-Fe bonds and firmly bonded to N-doped carbon. Systematic characterizations and theoretical modeling reveal that the Fe-Fe coordination motif markedly reduced the devotion of the antibonding state in the Fe-O bond because of the strong orbital coupling interaction of dual Fe d-d orbitals. This facilitates O-O covalent bond cleavage of O3 and enhances binding strength with reaction intermediates (atomic oxygen species; *O and *OO), thus boosting catalytic ozonation performance. As a result, Fe dinuclear site catalyst exhibits 100% ozonation efficiency for CH3SH elimination, outperforming commercial MnO2 catalysts by 1,200-fold. This research provides insights into the atomic-level structure-activity relationship of ozonation catalysts and extends the use of dinuclear catalysts in catalytic ozonation and beyond.

Optimization of Carbon-Defect Engineering to Boost Catalytic Ozonation Efficiency of Single Fe─N4 Coordination Motif.

Carbon-defect engineering in single-atom metal-nitrogen-carbon (M─N─C) catalysts by straightforward and robust strategy, enhancing their catalytic activity for volatile organic compounds, and uncovering the carbon vacancy-catalytic activity relationship are meaningful but challenging. In this study, an iron-nitrogen-carbon (Fe─N─C) catalyst is intentionally designed through a carbon-thermal-diffusion strategy, exposing extensively the carbon-defective Fe─N4 sites within a micro-mesoporous carbon matrix. The optimization of Fe─N4 sites results in exceptional catalytic ozonation efficiency, surpassing that of intact Fe─N4 sites and commercial MnO2 by 10 and 312 times, respectively. Theoretical calculations and experimental data demonstrated that carbon-defect engineering induces selective cleavage of C─N bond neighboring the Fe─N4 motif. This induces an increase in non-uniform charges and Fermi density, leading to elevated energy levels at the center of Fe d-band. Compared to the intact atomic configuration, carbon-defective Fe─N4 site is more activated to strengthen the interaction with O3 and weaken the O─O bond, thereby reducing the barriers for highly active surface atomic oxygen (*O/*OO), ultimately achieving efficient oxidation of CH3SH and its intermediates. This research not only offers a viable approach to enhance the catalytic ozonation activity of M─N─C but also advances the fundamental comprehension of how periphery carbon environment influences the characteristics and efficacy of M─N4 sites.

Enabling a bioinspired N,N,N-copper coordination motif through spatial control in UiO-67: synthesis and reactivity.

Metal-organic frameworks (MOFs) featuring zirconium-based clusters are widely used for the development of functionalized materials due to their exceptional stability. In this study, we report the synthesis of a novel N,N,N-ligand compatible with a biphenyl dicarboxylic acid-based MOF. However, the resulting copper(I) complex exhibited unexpected coordination behaviour, lacking the intended trifold coordination motif. Herein, we demonstrate the successful immobilization of a bioinspired ligand within the MOF, which preserved its crystalline and porous nature while generating a well-defined copper site. Comprehensive spectroscopic analyses, including X-ray absorption, UV/Vis, and infrared spectroscopy, were conducted to investigate the copper site and its thermal behaviour. The immobilized ligand exhibited the desired tridentate coordination to copper, providing access to a coordination motif otherwise unattainable. Notably, water molecules were also found to coordinate to copper. Upon heating, the copper centre within the MOF exhibited reversible dehydration, suggesting facile creation of open coordination sites. Furthermore, the copper site displayed reduction at elevated temperatures and subsequent susceptibility to oxidation by molecular oxygen. Lastly, both the molecular complexes and the MOF were evaluated as catalysts for the oxidation of cyclohexane using hydrogen peroxide. This work highlights the successful immobilization of a bioinspired ligand in a zirconium-based MOF, shedding light on the structural features, thermal behaviour, and catalytic potential of the resulting copper sites.

Role of ancillary ligands in S-nitrosothiol and NO generation from nitrite-thiol interactions at mononuclear zinc(ii) sites.

Generation of S-nitrosothiol (RSNO) and nitric oxide (NO) mediated by zinc(ii) coordination motifs is of prime importance for understanding the role of zinc(ii)-based cofactors in redox-signalling pathways. This study uniquely employs a set of mononuclear [L2ZnII]2+ cores (where L = Me4PzPz/Me2PzPy/Me2PzQu) for introducing subtle alterations of the primary coordination sphere and investigates the role of ligand tuning in the transformation of NO2 - in the presence of thiols. Single crystal X-ray diffraction (SCXRD) analyses on [L2ZnII-X](X) (where X = perchlorate/triflate) illustrate consistent changes in the bond distances, thereby showing variations of the metal-ligand interactions depending on the nature of the heterocyclic donor arms (pyrazole/pyridine/quinoline). Moreover, such tuning of the ligands affects the Lewis-acidity of the [L2ZnII]2+ cores as evaluated by 31P NMR and SCXRD studies on the 1 : 1 acid-base adducts [L2ZnII(OPEt3)]2+. Crystallographic and 15N NMR spectroscopic analyses on the nitrite complexes [L2ZnII(κ2-nitrite)](ClO4) reveal that the chemical environments of the nitrite anions in these complexes are nearly identical, despite the dissimilarity in the Lewis-acidity of the [L2ZnII]2+ cores. Interestingly, RSNO and NO generation from the reactions of [L2ZnII(κ2-nitrite)](ClO4) with 4-tert-butylbenzylthiol ( t BuBnSH) exhibits that the [(Me2PzQu)2ZnII]2+ core is the most efficient in promoting nitrite-thiol interactions due to the ease of available hemilabile coordination sites at the Lewis acidic [ZnII]. Detailed UV-vis studies in tandem with computational investigation, for the first time, provide an unambiguous demonstration of the nitrous acid (HNO2) intermediate generated through an intramolecular proton-transfer from thiol to nitrite at zinc(ii).

A triradical-containing trinuclear Pd(II) complex: spin-polarized electronic transmission, analog resistive switching and neuromorphic advancements.

Neuromorphic computation has emerged as a potential alternative to subvert the von Neumann bottleneck issue in conventional computing. In this context, the development of resistive switching-based memristor devices mimicking various synaptic functionalities has engendered paramount attention. Here, we report a triradical-containing trinuclear Pd(II) cluster with a cyclohexane-like framework constituted by the Pd-Se coordination motif displaying facile memristor property with neuromorphic functionality as a thin-film device. The metal-ligand complex (complex 1) possessed an St = 1/2 ground state by experiencing a spin-frustrated-type magnetic coupling phenomenon amongst the three ligand-based organic radicals (SR = 1/2), coordinated to the Pd(II) ions. Three reversible one-electron reduction waves countered with a one-electron and one two-electron reversible oxidation waves were noticed in the cyclic voltammogram of the complex, confirming electrons accepting and releasing capacity of the complex at low potentials, i.e., within +0.2 V to -1.1 V. Employing the radical-containing complex 1 as the active thin-film sandwiched between two orthogonal electrodes, resistive switching based memristor property with biological synaptic actions were successfully emulated. Intriguingly, the artificial neural network (ANN) simulated efficient pattern recognition demonstrated using the recorded potentiation and depression curves from the device, which is a step ahead for the hardware realization of neuromorphic computing. The performance of the ANN on MNIST data with reduced image resolution has further been evaluated. Density functional theory (DFT)-based theoretical calculation predicted that the spin-polarized electronic transmission substantiated the memristive property in the neutral complex 1.

New ALD ZnO Precursors and Processes for Protective Coatings on Lithium-Ion Battery Cathodes

The ever-increasing demand for Li-ion batteries commands their performance to increase while at the same time size and mass to decrease. One promising cathode material to achieve this is the Ni-rich LiNi0.8Mn0.1Co0.1, (NMC811), a high-capacity layered oxide cathode material. However, NMC811 suffers from capacity fading during electrochemical cycling of the cells. This phenomenon is connected to the dissolution of the active transition metal ions in the cathodes, phase changes and to side reactions happening at the interface of the cathode and the electrolyte or with formed HF but remains poorly understood.[1] To mitigate these problems, many different coating processes have been employed. In the realm of atomic layer deposition (ALD), the predominant coating material is the very stable insulating Al2O3 prepared from trimethyl aluminum and H2O. However, ZnO is an alternative transition metal oxide coating that shows promise since it is an amphoteric conductor. Recently, amorphous ZnO coatings prepared by sol-gel methods were shown to significantly boost the capacity retention of NMC cathodes.[2] Taking inspiration from a recent study that compared different ALD Al2O3 precursors and their ability to precisely tune the protective coating, we set out to investigate the suitability of ZnO ALD films as protective coatings and the influence of different precursors used for that purpose.[3] We selected four Zn precursors for cathode surface treatments in this study with different coordination motifs, metal-to-ligand bonds and reactivities, (Fig. 1). The ZnO ALD processes for these precursors were established by in-situ spectroscopic ellipsometry, and the resulting films were subjected to compositional analysis by XPS and RBS/NRA proving high purity ZnO. Further, UV-VIS measurements were conducted to investigate the band gaps of the materials which showed interesting precursor dependent differences. To analyze the growth behavior of the different precursors, in-situ FTIR studies were conducted hinting at distinct decomposition/deposition behavior of each precursor, as shown by the FTIR difference spectra for ZnEt(HMDS) in Fig. 2. The in-situFTIR studies also revealed different nucleation behaviors for the ALD ZnO precursors on the NMC811 cathode surface. Next, we coated NMC811 powder with 1 and 5 ZnO ALD cycles and performed XPS to verify successful ZnO ALD, analyze the surface species, and probe for potential oxidation state changes caused by the applied precursors. Whereas the observed changes in the oxidation states were small, a reproducible reduction was seen for the Ni, Co, and Mn transition metals in the cathode material, see exemplarily the ratio of Co 2+ and 3+ species in Fig. 3. Coin cell cycling tests of cathodes fabricated from the ALD ZnO-coated NMC811 powders prepared using the different Zn precursors are ongoing. These results will be especially noteworthy and showcase how the choice of ALD precursor influences the properties of a battery protective coating and allows fine tuning of the cathode surface properties.[1] Z. Ruff, C. Xu, C. P. Grey, J. Electrochem. Soc. 2021, 168, 060518.[2] Y. Li, X. Li, J. Hu, W. Liu, H. Maleki Kheimeh Sari, D. Li, Q. Sun, L. Kou, Z. Tian, L. Shao, C. Zhang, J. Zhang, X. Sun, Energy Environ. Mater. 2020, 3, 522–528.[3] D. Kang, R. E. Warburton, A. U. Mane, J. Greeley, J. W. Elam, Applied Surface Science 2022, 599, 153329. Figure 1

Iminopyrrole‐Based Self‐Assembly: A Route to Intrinsically Flexible Molecular Links and Knots

AbstractThe use of 2,5‐diformylpyrrole in self‐assembly reactions with diamines and Zn(II)/Cd(II) salts allowed the preparation of [2]catenane, trefoil knot, and Borromean rings. The intrinsically dynamic nature of the diiminopyrrole motif rendered all of the formed assemblies intramolecularly flexible. The presence of diiminopyrrole revealed new coordination motifs and influenced the host–guest chemistry of the systems, as illustrated by hexafluorophosphate encapsulation by Borromean rings.

Iminopyrrole-Based Self-Assembly: A Route to Intrinsically Flexible Molecular Links and Knots.

The use of 2,5-diformylpyrrole in self-assembly reactions with diamines and Zn(II)/Cd(II) salts allowed the preparation of [2]catenane, trefoil knot, and Borromean rings. The intrinsically dynamic nature of the diiminopyrrole motif rendered all of the formed assemblies intramolecularly flexible. The presence of diiminopyrrole revealed new coordination motifs and influenced the host-guest chemistry of the systems, as illustrated by hexafluorophosphate encapsulation by Borromean rings.

Modeling Reactivity of Nitrite and Nitrous Acid at a Phenolate Bridged Dizinc(II) Site: Insights into NO Signaling at Zinc.

Although nitrite-to-NO transformation at various transition metals including Fe and Cu are relatively well explored, examples of such a reaction at the redox-inactive zinc(II) site are limited. The present report aims to gain insights into the reactivity of nitrite anions, nitrous acid (HONO), and organonitrite (RONO) at a dizinc(II) site. A phenolate-bridged dizinc(II)-aqua complex [LH ZnII (OH2 )]2 (ClO4 )2 (1H -Aq, where LH =tridentate N,N,O-donor monoanionic ligand) is illustrated to react with t BuONO to provide a metastable arene-nitrosonium charge-transfer complex 2H . UV-vis, FTIR, multinuclear NMR, and elemental analyses suggests the presence of a 2 : 1 arene-nitrosonium moiety. Furthermore, the reactivity of a structurally characterized zinc(II)-nitrite complex [LH ZnII (ONO)]2 (1H -ONO) with a proton-source demonstrates HONO reactivity at the dizinc(II) site. Reactivity of both RONO (R=alkyl/H) at the phenolate-bridged dizinc(II) site provides NO+ charge-transfer complex 2H . Subsequently, the reactions of 2H with exogenous reductants (such as ferrocene, thiol, phenol, and catechol) have been illustrated to generate NO. In addition, NO yielding reactivity of [LH ZnII (ONO)]2 (1H -ONO) in the presence of the above-mentioned reductants have been compared with the reactions of complex 2H . Thus, this report sheds light on the transformations of NO2 - /RONO (R=alkyl/H) to NO/NO+ at the redox-inactive zinc(II) coordination motif.

Diverse Coordination Geometries Derived from Trisaminocyclohexane Ligands with Appended Outer‐Sphere Hydrogen Bond Donors

AbstractWith the aim of constructing hydrogen‐bonding networks in synthetic complexes, two new ligands derived from cis,cis‐1,3,5‐triaminocyclohexane (TACH) have been prepared that feature pendant pyrrole or indole rings as outer‐sphere H‐bond donors. The TACH framework offers a facial arrangement of three N‐donors, thereby mimicking common coordination motifs in the active sites of nonheme Fe and Cu enzymes. X‐ray structural characterization of a series of CuI‐X complexes (X=F, Cl, Br, NCS) revealed that these neutral ligands (H3LR, R=pyrrole or indole) coordinate in the intended facial N3 manner, yielding four‐coordinate complexes with idealized C3 symmetry. The N−H units of the outer‐sphere heterocycles form a hydrogen‐bonding cavity around the axial (pseudo)halide ligand, as verified by crystallographic, spectroscopic, and computational analyses. Treatment of H3Lpyrrole and H3Lindole with divalent transition metal chlorides (MIICl2, M=Fe, Cu, Zn) causes one heterocycle to deprotonate and coordinate to the M(II) center, giving rise to tetradentate ligands with two remaining outer‐sphere H‐bond donors. Further ligand deprotonation is observed upon reaction with Ni(II) and Cu(II) salts with weakly coordinating counteranions. The reported complexes highlight the versatility of TACH‐based ligands with pendant H‐bond donors, as the resulting scaffolds can support multiple protonation states, coordination geometries, and H‐bonding interactions.

Influences of Both N,N,N- and N,N,C-Coordination Modes of Tolyl-terpyridine on the Photophysical Properties of Cyclometalated Ru(II) Complexes: Combined Experimental and Theoretical Investigations on Acid/Base-Dependent Reversible Cyclometalation.

With the goal of developing a new strategy for the synthesis of luminescent Ru(II) complexes, we have prepared herein a new set of bis-tridentate complexes of the type [(py-bpy-Ph-X)Ru(tpy-PhCH3)]ClO4 (X = -CH3, -CH2Br, and -CHO) incorporating both non-cyclometalated and cyclometalated coordination motifs of two isomeric forms of methylphenyl-terpyridine (tpy-PhCH3). Thorough characterization of the synthesized complexes is carried out using standard analytical tools and single crystal X-ray diffraction. Detailed investigations on their photophysical and electrochemical behaviors are carried out in MeCN. The presence of a carbanionic center in the cyclometalating unit increases the absorption spectral window of the complexes into a longer-wavelength region. The complexes also exhibit room-temperature luminescence in the NIR domain with enhanced excited-state lifetimes (up to 20.1 ns) compared to their non-cyclometalated counterpart, [Ru(tpy-PhCH3)2]2+. In the presence of acid, the non-coordinated nitrogen atom in the secondary coordination sphere of the complexes allows fine-tuning of the absorption and emission spectral properties. Excess acid induces de-coordination of the Ru-C bond, which is signaled by a remarkable alteration of their spectral profiles. Cleavage of the Ru-C bond is also possible upon treating the acidified solution of the complexes with visible light. Restoration of the Ru-C bond is again feasible upon treating the solution with base at an elevated temperature (∼70 °C). In essence, "on-off" and "off-on" switching of emission is facilitated upon alternating treatment of the Ru(II) complexes with acid, base, and temperature. DFT and TD-DFT calculations are also performed for assignments of the spectral bands as well as to understand structural changes associated with the switching behaviors of the complexes.

Recyclable, tough, bioinspired metal-coordination epoxy thermoset capable of intelligent temperature detection

Traditional epoxy thermosets are of technological significance for composite materials and smart device. But unsatisfactory degradability and extensibility limit its further development. For the thermosetting polymer, most properties can be achieved by engineering the cross-linked points and molecular chain structure. Inspired by the mussel, the epoxy network containing abundant imidazole-metal coordination bonds was constructed via designing a hardener similar to histidine. Those sacrificial coordination crosslinks provided high-efficiency access to energy dissipation, improving material’s stiffness and extensibility simultaneously. Optimal tensile toughness and impact strength were up to 15.92 MJ/m3 and 15.17 KJ/m2, which were about 4.7 and 1.8 folds of Neat EP. Notedly, such epoxy thermosets with reversible coordination motifs and flexible molecular chain were capable of thermal-driven shape memorizing and programming repeatedly. Based on this special feature, the intelligent temperature warning sensor was designed successfully, which embodied good sensitivity and demonstrated rapid detection response time within ∼1s. Meanwhile, the pH-susceptive motifs (imine bonds and coordination bonds) allowed the epoxy networks to be decomposed quickly, so as to realize the efficiently recycling of high-value Au particles. This work provided a flexible and practical platform for the exploration of multifunction and intellectualization of conventional thermosetting materials.

Atomically Dispersed FeN2P2 Motif with High Activity and Stability for Oxygen Reduction Reaction Over the Entire pH Range

AbstractThe past decade has witnessed the great potential of Fe‐based single‐atom electrocatalysis in catalyzing oxygen reduction reaction (ORR). However, it remains a grand challenge to substantially improve their intrinsic activity and long‐term stability in acidic electrolytes. Herein, we report a facile chemical vapor deposition strategy, by which high‐density Fe atoms (3.97 wt%) are coordinated with square‐planar para‐positioned nitrogen and phosphorus atoms in a hierarchical carbon framework. The as‐crafted atomically dispersed Fe catalyst (denoted Fe‐SA/PNC) manifests an outstanding activity towards ORR over the entire pH range. Specifically, the half‐wave potential of 0.92 V, 0.83 V, and 0.86 V vs. reversible hydrogen electrode (RHE) are attained in alkaline, neutral, and acidic electrolytes, respectively, representing the high performance among reported catalysts to date. Furthermore, after 30,000 durability cycles, the Fe‐SA/PNC remains to be stable with no visible performance decay when tested in 0.1 M KOH and 0.5 M H2SO4, and only a minor negative shift of 40 mV detected in 0.1 M HClO4, significantly outperforming commercial Pt/C counterpart. The coordination motif of Fe‐SA/PNC is validated by density functional theory (DFT) calculations. This work provides atomic‐level insight into improving the activity and stability of non‐noble metal ORR catalysts, opening up an avenue to craft the desired single‐atom electrocatalysts.

Atomically Dispersed FeN2 P2 Motif with High Activity and Stability for Oxygen Reduction Reaction Over the Entire pH Range.

The past decade has witnessed the great potential of Fe-based single-atom electrocatalysis in catalyzing oxygen reduction reaction (ORR). However, it remains a grand challenge to substantially improve their intrinsic activity and long-term stability in acidic electrolytes. Herein, we report a facile chemical vapor deposition strategy, by which high-density Fe atoms (3.97 wt%) are coordinated with square-planar para-positioned nitrogen and phosphorus atoms in a hierarchical carbon framework. The as-crafted atomically dispersed Fe catalyst (denoted Fe-SA/PNC) manifests an outstanding activity towards ORR over the entire pH range. Specifically, the half-wave potential of 0.92 V, 0.83 V, and 0.86 V vs. reversible hydrogen electrode (RHE) are attained in alkaline, neutral, and acidic electrolytes, respectively, representing the high performance among reported catalysts to date. Furthermore, after 30,000 durability cycles, the Fe-SA/PNC remains to be stable with no visible performance decay when tested in 0.1 M KOH and 0.5 M H2 SO4 , and only a minor negative shift of 40 mV detected in 0.1 M HClO4 , significantly outperforming commercial Pt/C counterpart. The coordination motif of Fe-SA/PNC is validated by density functional theory (DFT) calculations. This work provides atomic-level insight into improving the activity and stability of non-noble metal ORR catalysts, opening up an avenue to craft the desired single-atom electrocatalysts.

NO Generation from Nitrite at Zinc(II): Role of Thiol Persulfidation in the Presence of Sulfane Sulfur.

Nitrite-to-NO transformation is of prime importance due to its relevance in mammalian physiology. Although such a one-electron reductive transformation at various redox-active metal sites (e.g., Cu and Fe) has been illustrated previously, the reaction at the [ZnII] site in the presence of a sacrificial reductant like thiol has been reported to be sluggish and poorly understood. Reactivity of [(Bn3Tren)ZnII-ONO](ClO4) (1), a nitrite-bound model of the tripodal active site of carbonic anhydrase (CA), toward various organic probes, such as 4-tert-butylbenzylthiol (tBuBnSH), 2,4-di-tert-butylphenol (2,4-DTBP), and 1-fluoro-2,4-dinitrobenzene (F-DNB), reveals that the ONO-moiety in the [ZnII]-nitrite coordination motif of complex 1 acts as a mild electrophile. tBuBnSH reacts mildly with nitrite at a [ZnII] site to provide S-nitrosothiol tBuBnSNO prior to the release of NO in 10% yield, whereas the phenolic substrate 2,4-DTBP does not yield the analogous O-nitrite compound (ArONO). The presence of sulfane sulfur (S0) species such as elemental sulfur (S8) and organic polysulfides (tBuBnSnBntBu) during the reaction of tBuBnSH and [ZnII]-nitrite (1) assists the nitrite-to-NO conversion to provide NO yields of 65% (for S8) and 76% (for tBuBnSnBntBu). High-resolution mass spectrometry (HRMS) analyses on the reaction of [ZnII]-nitrite (1), tBuBnSH, and S8 depict the formation of zinc(II)-persulfide species [(Bn3Tren)ZnII-Sn-BntBu]+ (where n = 2, 3, 4, 5, and 6). Trapping of the persulfide species (tBuBnSS-) with 1-fluoro-2,4-dinitrobenzene (F-DNB) confirms its intermediacy. The significantly higher nucleophilicity of persulfide species (relative to thiol/thiolate) is proposed to facilitate the reaction with the mildly electrophilic [ZnII]-nitrite (1) complex. Complementary analyses, including multinuclear NMR, electrospray ionization-MS, UV-vis, and trapping of reactive S-species, provide mechanistic insights into the sulfane sulfur-assisted reactions between thiol and nitrite at the tripodal [ZnII]-site. These findings suggest the critical influential roles of various reactive sulfur species, such as sulfane sulfur and persulfides, in the nitrite-to-NO conversion.