Supramolecular assemblies of Cu(II) with a tetraphenylethene-imidazole ligand for tuning photocatalytic CO2 reduction.

Cu(II) supramolecular assemblies [Cu2(tipe)2(H2O)2](NO3)4·2.5H2O (CuN4) and [Cu2Cl4(tipe)(CH3CN)]·H2O (CuN2Cl2) (tipe = 1,1,2,2-tetrakis(4-(imidazole-1-yl)phenyl)ethene) were synthesized and utilized for photocatalytic CO2 reduction. CuN4 exhibits CO production of up to 891 µmol gcat-1 with a selectivity of 79.9%, while CuN2Cl2 gives low CO production of 206 µmol gcat-1 but with a high selectivity of >99.9% in 5 h. The experimental and DFT calculation results indicate that the coordination environment and non-covalent interactions within the assemblies have a great impact on the photocatalytic CO2 reduction behavior. This work provides useful insights on Cu(II) assembly catalyzed CO2 photoreduction.

High-nuclearity Luminescent Lanthanide Nanocages for Tumor Drug Delivery.

There is an unmet need for easy-to-visualize drug carriers that can deliver therapeutic cargoes deep into solid tumors. Herein, we report the preparation of ultrasmall luminescent imine-based lanthanide nanocages, Eu60 and Tb60 (collectively Ln60 ), designed to encapsulate anticancer chemotherapeutics for tumor therapy. The as-prepared nanocages possess large cavities suitable for the encapsulation of doxorubicin (DOX), yielding DOX@Ln60 nanocages with diameters around 5 nm. DOX@Ln60 are efficiently internalized by breast cancer cells, allowing the cells to be visualized via the intrinsic luminescent property of Ln(III). Once internalized, the acidic intracellular microenvironment promotes imine bond cleavage and the release of the loaded DOX. DOX@Ln60 inhibits DNA replication and triggers tumor cell apoptosis. In a murine triple negative breast cancer (TNBC) model, DOX@Ln60 was found to inhibit tumor growth with negligible side effects on normal tissues. It proved more effective than various controls, including DOX and Ln60 . The present nanocages thus point the way to the development of precise nanomedicines for tumor imaging and therapy.

Silver frameworks based on a tetraphenylethylene-imidazole ligand for electrocatalytic reduction of CO2 to CO.

Metal-organic frameworks (MOFs) can be used as electrocatalysts for the CO2 reduction reaction (CO2RR) because of their well-dispersed metal centers. Silver is a common electrocatalyst for reduction of CO2 to CO. In this study, two Ag-MOFs with different structures of [Ag8O2(TIPE)6](NO3)4 (Ag-MOF1) and [Ag(TIPE)0.5CF3SO3] (Ag-MOF2) [TIPE = 1,1,2,2-tetrakis(4-(imidazol-1-yl)phenyl)ethene] were synthesized and used for CO2 electroreduction. The results show that Ag-MOF2 is superior to Ag-MOF1 and exhibits high CO faradaic efficiency (FE) of 92.21% with partial current density of 29.51 mA cm-2 at -0.98 V versus reversible hydrogen electrode (RHE). The FECO is higher than 80% in the potential range of -0.78 to -1.18 V. The difference may be caused by different framework structures leading to different electrochemical active surface areas and charge transfer kinetics. This study provides a new strategy for designing and constructing CO2 electroreduction catalysts and provides potential ways for solving environmental and energy problems caused by excessive CO2 emission.

A Green Environmental Protection Photocatalytic Molecular Reactor for Aerobic Oxidation of Sulfide to Sulfoxide.

The design and synthesis of metal-organic frameworks (MOFs) as photocatalytic molecular reactors for varied reactions have drawn great attention. In this work, we designed a novel photoactive perylenediimides-based (PDI) carboxylate ligand N,N'-di(3',3",5',5"-tetrakis(4-carboxyphenyl))-1,2,6,7-tetrachloroperylene-3,4,9,10-tetracarboxylic acid diimide (Cl-PDI-TA) and use it to successfully synthesize a novel Zr(IV)-based MOF 1 constructed from [Zr6 O8 (H2 O)8 ]8+ clusters bridged by Cl-PDI-TA ligands. Structural analysis revealed that Zr-MOF 1 manifests a 3D framework with (4,8)-connected csq topology and possesses triangular channels of ~17 Šand mesoporous hexagonal channels of ~26 Šalong c-axis. Moreover, the synthesized Zr-MOF 1 exhibits visible-light absorption and efficient photoinduced free radical generation property, making it a promising photocatalytic molecular reactor. When Zr-MOF 1 was used as a photocatalyst for the aerobic oxidation of sulfides under irradiation of visible light, it could afford the corresponding sulfoxides with high yield and selectivity. Experimental results demonstrated that the substrate sulfides could be fixed in the pores of 1 and directly transformed to the products sulfoxides in the solid state. Furthermore, the mechanism for the photocatalytic transformation was also investigated and the results revealed that the singlet oxygen (1 O2 ) and superoxide radical (O2 ⋅- ) generated by the energy transfer and electron transfer from the photoexcited Zr-MOF to oxidants were the main active species for the catalytic reactions. This work offers a perceptive comprehension of the mechanism in PDI-based MOFs for further study on photocatalytic reactions.

Construction of Benzoxazinones from Anilines and Their Derivatives.

Herein we report a strategy concerning Rh(III)-catalyzed direct ortho-C-H bond carbonylation to construct benzoxazinones from anilines and their derivatives with high atom economy. Interestingly, the corresponding amides were generated in situ from anilines when excess Ac2O was added and directed the following C-H bond carbonylation to form benzoxazinones. Extensive functional group tolerance can be achieved when the alkyl amide directing groups were installed. Moreover, this method allows convenient derivatization of some drugs with aryl amine groups to show its potential application.

Designing Heteroatom-Codoped Iron Metal-Organic Framework for Promotional Photoreduction of Carbon Dioxide to Ethylene.

Rational engineering active sites and vantage defects of catalysts are promising but grand challenging task to enhance photoreduction CO2 to high value-added C2 products. In this study, we designed an N,S-codoped Fe-based MIL-88B catalyst with well-defined bipyramidal hexagonal prism morphology via a facile and effective process, which was synthesized by addition of appropriate 1,2-benzisothiazolin-3-one (BIT) and acetic acid to the reaction solution. Under simulated solar irradiation, the designed catalyst exhibits high C2 H4 evolution yield of 17.7 µmol g-1 ⋅h, which has been rarely achieved in photocatalytic CO2 reduction process. The synergistic effect of Fe-N coordinated sites and reasonable defects in the N,S-codoped photocatalyst can accelerate the migration of photogenerated carriers, resulting in high electron density, and this in turn helps to facilitate the formation and dimerization of C-C coupling intermediates for C2 H4 effectively.

Facet-Dependent Photocatalytic Behavior of Fe-soc-MOF for Carbon Dioxide Reduction.

Exposing different facets on metal-organic frameworks (MOFs) is an efficient approach to regulate their photocatalytic performance for CO2 reduction. Herein, Fe-soc-MOFs exposed with different facets were successfully synthesized, and the morphologies of Fe-soc-MOF exposed with eight {111} facets (Fe-soc-O) and that exposed with eight {111} and six {100} crystal facets (Fe-soc-M) are first reported. Fe-soc-MOFs have facet-dependent active sites on their surface and correspondingly different catalytic performance for photocatalytic CO2 reduction. Fe-soc-O has the highest CO production of 1804 µmol g-1 h-1, while the Fe-soc-MOF exposed with six {100} facets (Fe-soc-C) has the best CO selectivity of 94.7%. Density functional theory (DFT) calculations demonstrate that the (111) facet has more favorable thermodynamic potential for CO2 reduction and H2 evolution compared with the (100) one, deriving from its facet-dependent active sites. This work shows that utilizing the facet-engineering strategy to regulate the active sites exposed on the surface of MOFs is feasible. The results display the relation between the facet of MOFs and the photocatalytic behavior for CO2 reduction.

Single-Site Metal-Organic Framework and Copper Foil Tandem Catalyst for Highly Selective CO2 Electroreduction to C2 H4.

Tandem catalysis is a promising way to break the limitation of linear scaling relationship for enhancing efficiency, and the desired tandem catalysts for electrochemical CO2 reduction reaction (CO2 RR) are urgent to be developed. Here, a tandem electrocatalyst created by combining Cu foil (CF) with a single-site Cu(II) metal-organic framework (MOF), named as Cu-MOF-CF, to realize improved electrochemical CO2 RR performance, is reported. The Cu-MOF-CF shows suppression of CH4 , great increase in C2 H4 selectivity (48.6%), and partial current density of C2 H4 at -1.11 V versus reversible hydrogen electrode. The outstanding performance of Cu-MOF-CF for CO2 RR results from the improved microenvironment of the Cu active sites that inhibits CH4 production, more CO intermediate produced by single-site Cu-MOF in situ for CF, and the enlarged active surface area by porous Cu-MOF. This work provides a strategy to combine MOFs with copper-based electrocatalysts to establish high-efficiency electrocatalytic CO2 RR.

Metal-organic frameworks incorporating azobenzene-based ligands as a heterogeneous Lewis-acid catalyst for cyanosilylation of imines.

In this work, two novel metal-organic frameworks (MOFs) were synthesized by the reaction of azobenzene-based ligands and Zn(NO3)2/CdCO3 under solvothermal conditions with the formula of {[Zn2(abtc)(azpy)(H2O)2]·4H2O} n (1) and {[Cd(abtc)0.5(azpy)0.5(H2O)]·3H2O} n (2) (H4abtc = 3,3',5,5'-azobenzene tetracarboxylic acid, azpy = 4,4'-azobipyridine). According to the single-crystal X-ray diffraction (SC-XRD) analysis, complexes 1 and 2 possessed quite similar structures except for the coordination modes of the central metal nodes attributed to the difference between the cationic radius of Zn(ii) and Cd(ii). The Zn(ii) cations in 1 adopted a distorted seesaw coordination geometry and the coordination between Zn(ii) and organic linkers gave two-dimensional (2D) coordination networks, while the Cd(ii) cations in 2 could also bind with the carboxylate groups from neighboring coordination networks to form a three-dimensional (3D) coordination framework. Furthermore, complexes 1 and 2 showed high catalytic activity as heterogeneous Lewis-acid catalysts towards the cyanosilylation of imines with satisfactory reusability under mild conditions and the similar catalytic performance of 1 and 2 could be attributed to the similarity in their structures. A prudent mechanism has been proposed as well to elucidate the role of complexes 1 and 2 in the catalytic process.

Pillar-Layered Metal-Organic Frameworks for Sensing Specific Amino Acid and Photocatalyzing Rhodamine B Degradation.

Metal-organic frameworks (MOFs) have presented potential for detection of specific species and catalytic application due to their diverse framework structures and functionalities. In this work, two novel pillar-layered MOFs [Cd6(DPA)2(NTB)4(H2O)4]n·n(DPA·5DMA·H2O) (1) and [Cu2(DPA)(OBA)2]n·n(2.5DMF·H2O) (2) [DPA = 2,5-di(pyridin-4-yl)aniline, H3NTB = 4,4',4''-nitrilotribenzoic acid, H2OBA = 4,4'-oxydibenzoic acid, DMA = N,N-dimethylacetamide, DMF = N,N-dimethylformamide] were successfully synthesized and structurally characterized. Both 1 and 2 have three-dimensional framework structures. The fluorescent property of 1 makes it possible for sensing specific amino acid such as L-glutamic acid (Glu) and L-aspartic acid (Asp). While MOF 2 was found to be suitable for photocatalytic degradation of Rhodamine B (RhB) in the presence of H2O2. The results imply that MOFs are versatile and metal centers are important in determining their properties.

Ti(IV)-MOF with Specific Facet-Ag Nanoparticle Composites for Enhancing the Photocatalytic Activity and Selectivity of CO2 Reduction.

Metal nanoparticles deposited in the photocatalyst not only can serve as a cocatalyst but also can act as a light harvester to extend the light absorption, resulting from the surface plasmon resonance (SPR). In this study, we deposited silver nanoparticles (Ag NPs) onto NH2-MIL-125(Ti) with exposed specific facets and achieved effectively improved activity and selectivity for photocatalytic CO2 reduction. Loading Ag NPs on the exposed {111} facets of NH2-MIL-125(Ti) generates a highly effective composite catalyst for the photoreduction of CO2, resulting in the maximal CO and CH4 yields of 26.7 and 63.3 µmol g-1 h-1, respectively, which are 2.2- and 16.2-fold those of the NH2-MIL-125(Ti) exposing {111} facets, and a CH4 selectivity of 90.5%. Incorporation of Ag NPs not only optimizes the electronic structure of the photocatalyst but also suppresses the recombination of photogenerated electron-hole pairs. This study provides an exciting example for creating and understanding metal-decorated facet-dependent effects on metal-organic frameworks (MOFs) for photocatalytic reactions.

Mild Three-Step Consecutive C-H Activations.

Herein, the Rh-catalyzed consecutive C-H bond olefination/annulation/olefination cascade, tandemly directed by sulfonamide and ester groups, has been developed under mild conditions with the assistance of 1-adamantane carboxylic acid. A seven-membered metallacycle including an ester group was preferred to the five-membered one including a sulfonamide group for the third C-H activation. In this transformation, the Rh catalyst exhibits its high reactivity by catalyzing a triple C-H activation process with a low catalyst loading at 50 °C. This method can be applied in the construction of various pharmaceutical derivatives.

Copper(II) Frameworks with Varied Active Site Distribution for Modulating Selectivity of Carbon Dioxide Electroreduction.

Metal-organic frameworks (MOFs) can be utilized as electrocatalysts for CO2 reduction reaction (CO2RR) due to their well dispersed metal centers. However, the influence of metal node distribution on electrochemical CO2RR was rarely explored. Here, three Cu-MOFs with different copper(II) site distribution were employed for CO2 electroreduction. The Cu-MOFs [Cu(L)SO4]·H2O (Cu1), [Cu(L)2(H2O)2](CH3COO)2·H2O (Cu2), and [Cu(L)2(H2O)2](ClO4)2 (Cu3) were achieved by using the same ligand 1,3,5-tris(1-imidazolyl)benzene (L) but different Cu(II) salts. The results show that the Faraday efficiency of CO (FECO) for Cu1 is 4 times that of the FEH2, while the FECO of Cu2 is twice that of the FEH2. As for Cu3, there is not much difference between FECO and FEH2. Such difference may arise from the distinct electrochemical active surface area and charge transfer kinetics caused by different copper site distribution. Furthermore, the different framework structures also affect the activity of the copper sites, which was supported by the theoretically calculated Gibbs free energy and electron density, contributing to the selectivity of CO2RR. This study provides a strategy for modulating the selectivity of CO2RR by tuning the distribution of the active centers in MOFs.

Fluorescent Zn(II) frameworks with multicarboxylate and pyridyl N-donor ligands for sensing specific anions and organic molecules.

Three novel fluorescent Zn(II) frameworks, namely [Zn(DPA)(NDA)]2·2DMF (1), [Zn2(DPA)(OBA)2]·2DMF·4H2O (2) and [Zn(DPA)(HNTB)]·H2O (3) (DPA = 2,5-di(pyridin-4-yl)aniline, H2NDA = 1,4-naphthalenedicarboxylic acid, H2OBA = 4,4'-oxydibenzoic acid, H3NTB = 4,4',4''-nitrilotribenzoic acid, DMF = N,N-dimethylformamide), were successfully fabricated and structurally characterized. Due to the variety of organic linkers, 1-3 exhibit varied topologies: 1 is a 4-c three-dimensional (3D) framework with {65·8} topology, 2 is a 6-c 3D net with point symbol of {44·610·8}, and 3 is a 4-c two-dimensional network that further stacks into a 3D structure by hydrogen bonding interactions with {44·62} topology. Experiments related to fluorescence show that 1-3 can be utilized to quickly identify specific anions of CrO42-/Cr2O72-, and organic molecules such as 2,4,6-trinitrophenol and benzaldehyde.

Coordination Polymers with 2,2':6',2″-Terpyridine Earth-Abundant Metal Complex Units for Selective CO2 Photoreduction.

Combining molecular metal complexes into coordination polymers (CPs) is an effective strategy for developing photocatalysts for CO2 reduction; however, most such reported catalysts are noble metal-containing CPs. Herein, two novel Zr-containing bimetallic CPs, Co-Zr and Ni-Zr, were designed and successfully synthesized by connecting 2,2':6',2″-terpyridine-based molecular earth-abundant metal (Co or Ni) complexes with ZrO8 nodes. Both CPs were applied as catalysts for CO2 photoreduction to selectively produce CO. The catalytic performance of Co-Zr is better than that of Ni-Zr with a yield of 3654 µmol (g of catalyst)-1 for CO in 6 h (TON = 18.2). The difference between these two catalysts was analyzed with respect to band structure and charge migration ability. This work provides an effective way to introduce molecular earth-abundant metal complexes into coordination polymers for the construction of efficient noble metal-free CO2 photocatalysts.

Hydroxy-Group-Functionalized Single Crystal of Copper(II)-Porphyrin Complex for Electroreduction CO2 to CH4.

Purposefully developing crystalline materials at molecular level to improve the selectivity of electroreduction CO2 to CH4 is still rarely studied. Herein, a single crystal of copper(II) complex with hydroxy groups was designed and synthesized, namely 5,10,15,20-tetrakis(3,4-dihydroxyphenyl)porphyrin copper(II) (Cu-PorOH), which could serve as a highly efficient heterogeneous electrocatalyst for electroreduction of CO2 toward CH4 . In 0.5 m KHCO3 , Cu-PorOH gave a high faradaic efficiency of 51.3 % for CH4 and drove a partial current density of 23.2 mA cm-2 at -1.5 V versus the reversible hydrogen electrode in H-cell. The high performance was greatly promoted by the hydroxy groups in Cu-PorOH, which could not only form stable three-dimensional frameworks through hydrogen-bonding interactions but also stabilize the intermediate species by hydrogen bonds, as supported by density functional theory calculations. This work provides an effective avenue in exploring crystalline catalysts for CO2 reduction at molecular level.

Effect of the Defect Modulator and Ligand Length of Metal-Organic Frameworks on Carbon Dioxide Photoreduction.

The nature of defects and organic ligands can fine-tune the absorption energy (Eabs) of metal-organic frameworks (MOFs), which is crucial for photocatalytic reactions; however, the relevant studies are in their infancy. Herein, a series of typical MOFs of the UiO family (UiO-6x-NH2, x = 8, 7, and 6) with ligands of varied lengths and amino-group-modified defects were synthesized and employed to explore their performance for photocatalytic CO2 reduction. Sample UiO-66-NH2-2ABA (2ABA = 3,5-diamino-benzoate) with the shortest dicarboxylate ligand and two amino-group-modified defects exhibits superior photocatalytic activity due to the lowest Eabs. The CO yield photocatalyzed by UiO-66-NH2-2ABA is 17.5 µmol g-1 h-1, which is 2.4 times that of UiO-68-NH2-BA (BA = benzoate) with the longest ligand and no amino group involved in the defects. Both the experiments and theoretical calculations show that shorter dicarboxylate ligands and more amino groups result in smaller Eabs, which is favorable for photocatalytic reactions. This study provides new insights into boosting the photocatalytic efficiency by modulating the defects and ligands in MOFs.

Sensing Properties of NH2-MIL-101 Series for Specific Amino Acids via Turn-On Fluorescence.

Metal-organic frameworks (MOFs) have been demonstrated to be desired candidates for sensing definite species owing to their tunable composition, framework structure and functionality. In this work, the NH2-MIL-101 series was utilized for sensing specific amino acids. The results show that cysteine (Cys) can significantly enhance the fluorescence emission of NH2-MIL-101-Fe suspended in water, while NH2-MIL-101-Al exhibits the ability to sense lysine (Lys), arginine (Arg) and histidine (His) in aqueous media via turn-on fluorescence emission. Titration experiments ensure that NH2-MIL-101-Fe and NH2-MIL-101-Al can selectively and quantitatively detect these amino acids. The sensing mechanism was examined and discussed. The results of this study show that the metal centers in MOFs are crucial for sensing specific amino acids.

Metalloporphyrin Encapsulation for Enhanced Conversion of CO2 to C2H4.

Electrochemical conversion of CO2 into valuable products is a promising approach. Efficient electrocatalysts are highly desirable but remain to be developed. Here, we proposed a molecular encapsulation strategy to enrich intermediates for facilitating electrochemical conversion of CO2 to C2H4. This strategy is combining M-TCPP [M = FeCl, Co, and Ni; TCPP = tetrakis(4-carboxyphenyl) porphyrin] with a Cu-based metal-organic framework (Cu-MOF) to create a series of metalloporphyrin-decorated Cu catalysts with a coral-like shape (named as M-TCPP@Cu). M-TCPP in the catalysts could supply more CO intermediates to the Cu sites, giving high selectivity for producing C2H4 and lowering overpotentials for CO2 reduction. Meanwhile, the coral-like structure of the catalyst with abundant active sites is conducive to mass diffusion and benefits the conversion of CO2. We realized a higher C2H4 Faradaic efficiency (FE) of 33.42% at -1.17 V versus reversible hydrogen electrode (RHE) on the Fe-TCPP@Cu electrode than that on the sole Cu electrode (16.85%, at -1.27 V vs RHE). Furthermore, due to the encapsulated structure resulted from one-pot reaction that ensures the dispersion of active centers in M-TCPP, metalloporphyrin-decorated Cu catalysts show better performance than the physical mixture of Cu-MOFs and M-TPPs (M = FeCl, Co, and Ni; TPP = 5,10,15,20-tetraphenylporphyrin). The results provide a new strategy for the design of high-performance Cu catalysts from Cu-MOFs for CO2 conversion.

A single-crystal to single-crystal transition from a 7-fold interpenetrated coordination polymer to a non-interpenetrated one by photochemical [2 + 2] polymerization and their sensing properties.

Two complexes, namely [Zn(bpeb)(sda)] (1) and [Zn(poly-bpeb)(sda)] (2), were synthesized by an organic ligand with an extensively conjugated system, bpeb = 1,4-bis[2-(3-pyridyl) vinyl]-benzene, H2sda = sulfonyldibenzoic acid and d10 metal centers Zn2+. Structural analysis revealed that compound 1 was nonporous and possessed 7-fold interpenetrated three-dimensional (3D) frameworks constructed from one-dimensional (1D) Zn-bpeb and Zn-sda chains. Interestingly, due to the short distance between the vinyl groups from two neighboring bpeb ligands, compound 1 could undergo a photochemical [2 + 2] polymerization reaction to generate 2 in a single-crystal to single-crystal (SCSC) manner under the irritation of UV. Moreover, the organic polymer in 2 could be depolymerized by heating to realize the reversible transformation from 2 to 1. Furthermore, both compounds 1 and 2 could be used as fluorescent sensors for 2,4,6-trinitrophenol (TNP) with high selectivity and sensitivity.