Aqueous Electrochemical Direct Air Capture Using Alizarin Red S.

Direct Air Capture (DAC) is an emerging form of atmospheric carbon dioxide removal. Conventional DAC sorbents utilize swings in temperature and/or pressure, which are energy intensive and hinders large-scale deployment. In this work, we demonstrate a green, aqueous electrochemical DAC system that employs Alizarin Red S (ARS) as an electroactive capturing agent.

Passivation-Free, Liquid-Metal-Based Electrosynthesis of Aluminum Metal-Organic Frameworks Mediated by Light Metal Activation.

The production of aluminum (Al) metal-organic frameworks (MOFs) by electrosynthesis using solid-state Al electrodes always faces significant challenges due to the formation of a passivating aluminum oxide layer in the process. Here, we developed a liquid-metal-based method to electrosynthesize an aluminum Al-MOF (MIL-53). This method uses a liquid-state gallium (Ga) anode as a reservoir and activator for a light metal, Al, in the form of Al-Ga alloys that releases Al for the electrosynthesis of Al-MOFs.

3D Printing of Monoliths Using TIFSIX-Ni-Based Formulations for the Electric Swing Adsorption of CO.

The hybrid ultraporous material TIFSIX-Ni ([Ni(pyrazine)(TiF)]) was incorporated into a composite ink for the first time for the three-dimensional (3D) printing of monoliths. The large-scale synthesis of TIFSIX-Ni was completed using two different Ni(II) salts, with CO uptakes of 1.90 mmol g achieved using mechanochemically assisted thermal synthesis.

Chiral metal-organic frameworks for photonics.

Recently, there has been significant interest in the use of chiral metal-organic frameworks (MOFs) and coordination polymers (CPs) for photonics applications. The promise of these materials lies in the ability to tune their properties through judicious selection of the metal and ligand components. Additionally, the interaction of guest species with the host framework can be exploited to realise new functionalities.

Electronic Spin Qubit Candidates Arrayed within Layered Two-Dimensional Polymers.

Molecular electronic spin qubits are promising candidates for quantum information science applications because they can be reliably produced and engineered via chemical design. Embedding electronic spin qubits within two-dimensional polymers (2DPs) offers the possibility to systematically engineer inter-qubit interactions while maintaining long coherence times, both of which are prerequisites to their technological utility. Here, we introduce electronic spin qubits into a diamagnetic 2DP by -doping naphthalene diimide subunits with varying amounts of CoCp and analyze their spin densities by quantitative electronic paramagnetic resonance spectroscopy.

Two-step spin crossover by guest-disorder induced local symmetry breaking within a 3D Hofmann-like framework.

A 3D Hofmann-like metal-organic framework has been prepared which contains a 2,1,3-benzothiadiazole-based pillaring ligand. Encapsulation of a polycyclic aromatic hydrocarbon, chrysene, within the pore structure leads to a new pathway to multi-step spin crossover behaviour in which the observed two-step spin transition arises due to the presence of multiple site environments associated with local guest positional effects within the host lattice.

Multi-Redox Responsive Behavior in a Mixed-Valence Semiconducting Framework Based on Bis-[1,2,5]-thiadiazolo-tetracyanoquinodimethane.

The two-dimensional (2-D) framework, [Cu(BTDAT)(MeOH)] {BTDAT = bis-[1,2,5]-thiadiazolo-tetracyanoquinodimethane}, possesses remarkable multi-step redox properties, with electrochemical studies revealing six quasi-stable redox states in the solid state. In situ electron paramagnetic resonance and visible-near infrared spectroelectrochemistry elucidated the mechanism for these multi-step redox processes, as well as the optical and electrochromic behavior of the BTDAT ligand and framework. In studying the structural, spectroscopic, and electronic properties of [Cu(BTDAT)(MeOH)], the as-synthesized framework was found to exist in a mixed-valence state with thermally-activated semiconducting behavior.

How Reproducible are Surface Areas Calculated from the BET Equation?

Porosity and surface area analysis play a prominent role in modern materials science. At the heart of this sits the Brunauer-Emmett-Teller (BET) theory, which has been a remarkably successful contribution to the field of materials science. The BET method was developed in the 1930s for open surfaces but is now the most widely used metric for the estimation of surface areas of micro- and mesoporous materials.

The electrochemical reduction of a flexible Mn(II) salen-based metal-organic framework.

A new metal-organic framework (MOF) containing a Mn(II) salen complex (BET surface area = 967 ± 6 m g) undergoes a reversible crystalline-to-amorphous transformation. Experimental studies and computational calculations show that the MOF is stable to a one-electron reduction at more anodic potentials than the corresponding discrete complex.

Multifunctional Coordination Polymer Exhibiting Reversible Mechanical Motion Allowing Selective Uptake of Guests and Leading to Enhanced Electrical Conductivity.

A remarkably flexible, multifunctional, 2D coordination polymer exhibiting an unprecedented mode of reversible mechanical motion, enabling pores to open and close, is reported. Such multifunctional materials are highly sought after, owing to the potential to exploit coexisting electronic and mechanical functionalities that underpin useful technological applications such as actuators and ultrasensitive detectors. The coordination polymer, of composition Mn(FTCNQ)(py) (FTCNQ = 2,3,5,6-tetrafluoro-7,7,8,8-tetracycanoquinodimethane; py = pyridine), consists of Mn(II) centers bridged by FTCNQ dianions and coordinated by py molecules that extend above and below the 2D network.

Substituent effects on through-space intervalence charge transfer in cofacial metal-organic frameworks.

Electroactive metal-organic frameworks (MOFs) are an attractive class of materials owing to their multifunctional 3-dimensional structures, the properties of which can be modulated by changing the redox states of the components. In order to realise both fundamental and applied goals for these materials, a deeper understanding of the structure-function relationships that govern the charge transfer mechanisms is required. Chemical or electrochemical reduction of the framework [Zn(BPPFTzTz)(tdc)]·2DMF, hereafter denoted ZnFTzTz (where BPPFTzTz = 2,5-bis(3-fluoro-4-(pyridin-4-yl)phenyl)thiazolo[5,4-]thiazole), generates mixed-valence states with optical signatures indicative of through-space intervalence charge transfer (IVCT) between the cofacially stacked ligands.

A cofacial metal-organic framework based photocathode for carbon dioxide reduction.

Innovative and robust photosensitisation materials play a cardinal role in advancing the combined effort towards efficient solar energy harvesting. Here, we demonstrate the photocathode functionality of a Metal-Organic Framework (MOF) featuring cofacial pairs of photo- and electro-active 1,4,5,8-naphthalenediimide (NDI) ligands, which was successfully applied to markedly reduce the overpotential required for CO reduction to CO by a well-known rhenium molecular electrocatalyst. Reduction of [Cd(DPNDI)(TDC)] (DPNDI = ,'-di(4-pyridyl)-1,4,5,8-naphthalenediimide, HTDC = thiophene-2,5-dicarboxylic acid) to its mixed-valence state induces through-space Intervalence Charge Transfer (IVCT) within cofacial DPNDI units.

Visible Light Stimulated Bistable Photo-Switching in Defect Engineered Metal-Organic Frameworks.

The incorporation of photoactive donor-acceptor Stenhouse adduct (DASA) moieties into Metal-Organic Frameworks (MOFs) provides a new route to the development of visible light switching materials. Herein, a DUT-5 mixed-linker defect series was exploited to produce a derivative group of DASA-modified materials via postsynthetic modification (PSM). The photoactive MOFs exhibited conversion stimulated by visible wavelengths and were stable following multiple cycles.

Persistent Radical Tetrathiafulvalene-Based 2D Metal-Organic Frameworks and Their Application in Efficient Photothermal Conversion.

A series of stable radical 2D metal-organic frameworks has been assembled. (m-TTFTB) (m-Tetrathiafulvalene-tetrabenzoate) trimer building blocks are beneficial for the stability of the radicals due to delocalization of the unpaired electron. Hexanuclear rare-earth-cluster-based 1D chains further enhance the stability of the frameworks.

Rare-Earth Metal Tetrathiafulvalene Carboxylate Frameworks as Redox-Switchable Single-Molecule Magnets.

Using the redox-active tetrathiafulvalene tetrabenzoate (TTFTB ) as the linker, a series of stable and porous rare-earth metal-organic frameworks (RE-MOFs), [RE (μ -OH) (μ -O)(H O) (TTFTB) ] (1-RE, where RE=Y, Sm, Gd, Tb, Dy, Ho, and Er) were constructed. The RE (μ -OH) (μ -O) (H O) ](CO ) clusters within 1-RE act as segregated single-molecule magnets (SMMs) displaying slow relaxation. Interestingly, upon oxidation by I , the S=0 TTFTB linkers of 1-RE were converted into S= TTFTB radical linkers which introduced exchange-coupling between SMMs and modulated the relaxation.

A Metal-Organic Framework Based on a Nickel Bis(dithiolene) Connector: Synthesis, Crystal Structure, and Application as an Electrochemical Glucose Sensor.

Functionalizing the redox-active tetrathiafulvalene (TTF) core with groups capable of coordination to metals provides new perspectives on the modulation of architectures and electronic properties of organic-inorganic hybrid materials. With a view to extending this concept, we have now synthesized nickel bis(dithiolene-dibenzoic acid), [Ni(CS(CHCOOH))], which can be considered as the inorganic analogue of the organic tetrathiafulvalene-tetrabenzoic acid (HTTFTB). Likewise, [Ni(CS(CHCOOH))] is a redox-active linker for new functional metal-organic frameworks, as demonstrated here with the synthesis of [Mn{Ni(CS(CHCOO))}(HO)]·2DMF, (, DMF = -dimethylformamide).

Enhanced dielectricity coupled to spin-crossover in a one-dimensional polymer iron(ii) incorporating tetrathiafulvalene.

In designing multifunctional materials for potential switches that can be used as memory devices, the high-spin (HS) to low-spin (LS) crossover (SCO) one-dimensional polymer, [Fe(L)(4,4'-bpy)] , was constructed from a designed redox-active tetrathiafulvalene (TTF) functionalized Schiff-base and the ditopic linker 4,4'-bipyridine (bpy). It exhibits an 8 K hysteretic SCO centred at = 325 K which is coupled to changes in its dielectric constant. The crystal structures above and below the transition temperature reveal similar parallel linear ···Fe-bpy-Fe-bpy··· chains displaying expansion of the Fe octahedron in the HS state.

Spin crossover modulation in a coordination polymer with the redox-active bis-pyridyltetrathiafulvalene (pyTTF) ligand.

A one-dimensional Fe coordination polymer (CP) has been formed which includes the redox-active ligand bis-pyridyltetrathiafulvalene (pyTTF) and a Schiff base-like NO ligand. This CP is both spin crossover (SCO) and redox-active in the solid-state, and chemical oxidation results in SCO modification.

Reversible single crystal-to-single crystal double [2+2] cycloaddition induces multifunctional photo-mechano-electrochemical properties in framework materials.

Reversible structural transformations of porous coordination frameworks in response to external stimuli such as light, electrical potential, guest inclusion or pressure, amongst others, have been the subject of intense interest for applications in sensing, switching and molecular separations. Here we report a coordination framework based on an electroactive tetrathiafulvalene exhibiting a reversible single crystal-to-single crystal double [2 + 2] photocyclisation, leading to profound differences in the electrochemical, optical and mechanical properties of the material upon light irradiation. Electrochemical and in situ spectroelectrochemical measurements, in combination with in situ light-irradiated Raman spectroscopy and atomic force microscopy, revealed the variable mechanical properties of the framework that were supported using Density Functional Theory calculations.

Quantification of the mixed-valence and intervalence charge transfer properties of a cofacial metal-organic framework single crystal electronic absorption spectroscopy.

Gaining a fundamental understanding of charge transfer mechanisms in three-dimensional Metal-Organic Frameworks (MOFs) is crucial to the development of electroactive and conductive porous materials. These materials have potential in applications in porous conductors, electrocatalysts and energy storage devices; however the structure-property relationships pertaining to charge transfer and its quantification are relatively poorly understood. Here, the cofacial Cd(ii)-based MOF [Cd(BPPTzTz)(tdc)]·2DMF (where BPPTzTz = 2,5-bis(4-(pyridin-4-yl)phenyl)thiazolo[5,4-]thiazole, tdc = 2,5-thiophene dicarboxylate) exhibits Intervalence Charge Transfer (IVCT) within its three-dimensional structure by virtue of the close, cofacial stacking of its redox-active BPPTzTz ligands.

Effects of Mixed Valency in an Fe-Based Framework: Coexistence of Slow Magnetic Relaxation, Semiconductivity, and Redox Activity.

A 2-D coordination framework, (NEt)[Fe(fan)] (; Hfan = 3,6-difluoro-2,5-dihydroxy-1,4-benzoquinone), was synthesized and structurally characterized. The compound is structurally analogous to a formerly elucidated framework, (NEt)[Fe(can)] (Hcan = 3,6-dichloro-2,5-dihydroxy-1,4-benzoquinone), and adopts a 2-D (6,3) topology with the symmetrical stacking of [Fe(fan)] sheets that are held in position by the NEt cations between the sheets. The investigation of the dc and ac magnetic properties of revealed ferromagnetic ordering behavior and slow magnetization relaxation, as evinced from ac susceptibility measurements.