The study, led by Professor Fabien Cougnon and published in Angewandte Chemie International Edition, introduces an approach the team calls hierarchical sequence control. At its heart lies a deceptively simple idea: rather than trying to force a molecule into a desired shape through brute-force conditions or external templates, the researchers embedded the selection logic directly into the molecule itself, distributing it across two distinct stages of information. The result was a synthetic assembly that reliably formed a triple helix — three molecular strands winding around one another in an anticlockwise direction — while competing structures that might otherwise have emerged were effectively shut down.

To appreciate why this matters, it helps to consider what typically happens when synthetic molecules are designed to self-assemble. Molecular strands with the right chemical complementarity can, in principle, wrap around each other to form helices, much as DNA’s two strands intertwine. But in practice, such systems rarely deliver a single product. A mixture of strands might form double helices or triple helices, helices that coil clockwise or anticlockwise, and aggregates of varying stoichiometry, all coexisting in solution. Each of these outcomes may differ only modestly in energy, so the final mixture reflects a compromise among many nearly equally plausible structures. For chemists hoping to use self-assembly to build functional materials, this promiscuity has been a persistent obstacle: a material whose molecular architecture is a statistical mixture cannot be relied upon to behave in a predictable way.

The Jyväskylä team’s two-stage strategy attacks this problem directly. In the first layer of hierarchical control, the molecular sequence performs an initial selection that restricts the space of possible outcomes. Instead of allowing the strands to explore every conceivable assembly, this first layer narrows the field to four types of helices. The assembly process is thus no longer a free-for-all; it has been channeled into a small, well-defined set of options before the second layer of information comes into play. That second layer then provides an additional level of selection, favoring one specific helix among the four — the anticlockwise, or left-handed, triple helix. The combination of the two layers means that the molecule carries enough information not merely to assemble, but to choose, decisively, among the structures available to it.

Professor Cougnon emphasized that the precision of this control depends on how carefully the molecular sequence is tuned. By fine-tuning the sequence, the researchers found, they could determine which three-dimensional structure ultimately formed. Careful sequence optimization proved crucial: small changes in the arrangement of building blocks along the strands shifted the balance among the competing helices, and only the right sequence delivered the high level of structural selectivity the team was seeking. In this sense, the work echoes a lesson that molecular biology has long taught — that sequence is destiny, but only when the sequence is exactly right.

The concept of encoding structural information in molecular sequences is, of course, nature’s own invention. Nucleic acids store their instructions in the order of their bases, and proteins in the order of their amino acids. In both cases, the sequence does far more than specify composition; it encodes the folding pathway, the final architecture, and often the function of the resulting molecule. Synthetic chemists have made impressive strides in mimicking fragments of this logic, from foldamers that adopt predictable helical shapes to DNA nanotechnology that exploits base pairing to build elaborate nanostructures. What has remained difficult is layering multiple levels of selection into a single synthetic molecule, so that one layer of information narrows the possibilities and a second refines them further — a hierarchical scheme that mirrors how biological systems achieve their remarkable specificity.

By demonstrating that such layering is possible in an artificial molecule, the Finnish team has shown that synthetic systems can, in principle, replicate the decision-making architecture that underlies biological molecular organization. The anticlockwise triple helix that emerged from their design is not merely a curiosity of handedness. Controlling chirality — the direction in which a helix winds — is a genuine challenge in supramolecular chemistry, because left-handed and right-handed helices are mirror images that differ subtly in their interactions with other chiral molecules, including many biological targets. A system that selects one handedness exclusively, rather than producing a racemic mixture of the two, offers a level of determinism that could matter for applications ranging from chiral materials to molecular recognition.

The implications extend beyond the helix itself. The researchers describe the work as a step toward programmable molecular self-assembly — the vision of designing molecules whose structures can be predicted and controlled with increasing precision, simply by writing the right information into their sequences. If synthetic molecules could be programmed as reliably as proteins are by evolution, the consequences for materials science could be profound. Smart materials that reconfigure in response to their environment, molecular devices that perform defined mechanical or electronic tasks, and advanced technologies built from the bottom up, one precisely specified molecule at a time, all belong to this long-term horizon. Cougnon points to exactly these possibilities, framing programmable self-assembly as a route to smart materials, molecular devices, and other advanced technologies.

There is also a broader scientific lesson in the result. The study, an experimental investigation published on 13 October 2026, suggests that the gap between biological and synthetic molecular organization is not a fundamental barrier but an engineering challenge — one that can be addressed by thinking carefully about how information is distributed within a molecule. Rather than adding more chemical functionality or harsher assembly conditions, the Jyväskylä approach adds more information, structured in layers, so that each stage of the assembly process performs a distinct act of selection. It is a strategy that scales conceptually: additional layers of sequence information could, in future designs, impose further levels of control, potentially steering molecules toward structures of even greater complexity than a triple helix.

For now, the anticlockwise triple helix stands as a demonstration that synthetic chemistry can encode, within a single artificial molecule, enough hierarchical information to reproduce one of nature’s most characteristic feats: the reliable formation of a complex, chiral, three-dimensional structure from a simple sequence. As researchers refine the technique and apply it to new molecular systems, the boundary between what biology builds and what chemistry can program continues to shift — and with it, the prospects for a new generation of materials designed with the precision that living systems have perfected over billions of years.

Subject of Research: Hierarchical sequence control of artificial molecular self-assembly into a triple helix

Article Title: New method guides molecules into precisely defined structures

Article References: New method guides molecules into precisely defined structures. Original publication (Bibliographic details unavailable.)

Image Credits: AI Generated

DOI: Not provided

Keywords: molecular self-assembly, supramolecular chemistry, triple helix, hierarchical sequence control, chirality, programmable molecules, synthetic chemistry, University of Jyväskylä, Angewandte Chemie, smart materials, molecular devices, sequence information

Metal-organic frameworks, commonly abbreviated as MOFs, are built from metal atoms or clusters connected by organic molecules into highly ordered, repeating lattices. The geometry of these connections produces structures riddled with pores measured in fractions of a nanometre, giving MOFs an enormous internal surface area relative to their mass. That porosity is the key structural feature that creates the internal space necessary for MOFs to interact with target molecules, which is why the materials are under intense investigation for applications ranging from gas storage and separation to sensing, catalysis, bio-imaging, and magnetic materials. Because both the metal nodes and the organic linkers can be varied, MOFs have long been regarded as among the most customisable classes of solid materials in modern chemistry.

The new material, designated UoB-116, belongs to a subset of the MOF family built around rare-earth metals. In the first stage of the study, the researchers created and structurally characterised fifteen individual versions of the framework, each incorporating a different rare-earth metal. This step established that the underlying structure was robust enough to accommodate a wide range of metal ions without collapsing or losing its crystalline order. The team then moved to progressively more complex compositions, combining two, four, twelve, and finally fifteen different metals within the same framework, demonstrating at each stage that the crystal retained its ordered architecture.

The final and most striking step was the addition of indium, a metal drawn from outside the rare-earth family. The resulting MOF contained sixteen different metals simultaneously: yttrium, indium, and fourteen of the lanthanides. According to the researchers, UoB-116 is the first reported MOF to combine metals drawn from three different regions of the periodic table — the d-block, the p-block, and the f-block — within a single framework. That breadth of chemical compatibility is what gives the material its mix-and-match character, allowing elements with very different electronic structures to sit side by side in one ordered lattice.

To show that this compositional freedom translates into functional control, the team focused on two of the sixteen metals, dysprosium and lanthanum, and systematically varied the balance between them. The results were unambiguous. Increasing the dysprosium content increased the material’s magnetic response, while the characteristic near-infrared light absorption associated with dysprosium could be adjusted simply by altering its concentration. Porosity responded in the opposite direction: adding more lanthanum progressively reduced the material’s measured surface area. Most dramatically, the amount of carbon dioxide the material could take up under the conditions tested fell from 5.72 millimoles per gram for the all-dysprosium version to 1.23 millimoles per gram for the all-lanthanum version — a demonstration that gas-storage behaviour can be changed by adjusting the metals alone, with no change to the framework’s underlying architecture.

Corresponding author Professor Neil Champness of the University of Birmingham framed the advance as a step toward materials that behave almost like software. “Our findings confirm a route towards ‘programmable’ porous materials, where scientists could choose a combination of metals to dial magnetic, optical, chemical, or gas-adsorption behaviour,” he said. “The ability to predict how strongly particular metals will be incorporated potentially offers much finer control over future multi-metal materials. Rather than having to invent a completely new material every time they want different properties, researchers can potentially change the metallic ‘recipe’ within the same underlying structure.”

That question of predictability is central to why the work matters beyond its record-setting composition. In many multicomponent materials, different metal ions compete for the same structural sites in ways that are difficult to anticipate, and the final distribution of metals can be chaotic. The Birmingham-led team reports that the incorporation of particular metals into UoB-116 follows a bias linked to the radius of the cations, meaning that how strongly each metal is taken up into the framework can be predicted from its ionic size. If that predictive relationship holds across other metal combinations, it would give chemists a design rule for dialling in specific property profiles rather than discovering them by trial and error.

The practical stakes are considerable, because MOFs already serve as custom molecular sponges across several major industries. In clean energy, they are studied for compact hydrogen storage in fuel-cell vehicles and for selective carbon capture from industrial emissions. In environmental safety, related frameworks are being explored for harvesting drinkable water from arid air and for the safe storage of toxic gases used in semiconductor manufacturing. In industrial chemistry, energy-saving adsorptive separations based on MOFs could replace cryogenic distillation, one of the most energy-intensive unit operations in the chemical industry. In biomedicine, high-capacity frameworks are being developed for targeted drug delivery and as imaging contrast agents. A single tunable platform that can be re-optimised for each of these tasks by swapping metals could dramatically shorten development cycles.

The study, titled “Rare-Earth Multivariate Metal–Organic Frameworks: Cationic Radius Biased Compositional Control and Property Tuning,” was led by Adnan Ishaq and Professor Neil R. Champness at Birmingham, with contributions from Joseph O. Ogar, Asif Raza, Danielle E. Schier, Stephen P. Argent, Musa M. Mahmud, Lucy Clark, Jacob L. Brownlee, and Soumya Mukherjee across the collaborating institutions. The work appeared in Angewandte Chemie on 26 September 2026, and its publication marks one of the most extensive demonstrations yet of compositional control in a multivariate framework.

For the broader field of materials chemistry, UoB-116 offers a proof of concept that the boundary between designing new materials and tuning existing ones can be blurred. If the same principle — a robust framework that tolerates many metals in predictable proportions — can be extended to other linker chemistries and other metal families, the result could be a generation of porous materials whose properties are specified on demand: more magnetic here, more porous there, tuned for carbon capture or near-infrared optics by nothing more than a change in the recipe. For now, the sixteen-metal framework stands as evidence that the periodic table itself can be treated as a palette, and that the next breakthrough material may not need to be built from scratch at all.

Subject of Research: Multivariate rare-earth metal-organic frameworks with tunable properties through compositional control of incorporated metals

Article Title: ‘Mix-and-match’ material’s properties can be tuned by changing its metallic ‘recipe’

Article References: ‘Mix-and-match’ material’s properties can be tuned by changing its metallic ‘recipe’. (n.d.). Original publication

Image Credits: AI Generated

DOI: Not provided

Keywords: metal-organic frameworks, MOFs, rare-earth metals, lanthanides, porous materials, gas storage, carbon capture, magnetism, light absorption, materials chemistry, University of Birmingham, Angewandte Chemie

The challenge comes down to a distinction that sounds minor but matters enormously. In the syn form of a β-amino alcohol, the amino and hydroxyl groups sit on the same side of the carbon chain; in the anti form, they point to opposite sides. Both forms are chemically valid, but enzymes and drug targets can distinguish between them with ruthless precision, so a synthesis that delivers an uncontrolled mixture of the two is of limited use. The workhorse transformation for building these frameworks is the Henry reaction, a well-studied carbon–carbon bond-forming process that couples an aldehyde with a nitroalkane to produce a β-nitro alcohol. Because the nitro group can later be reduced to an amino group using well-established chemistry, the Henry reaction is a natural gateway to β-amino alcohols. The problem is that most catalytic versions of the reaction favor the syn product, leaving the anti form frustratingly out of reach.

That long-standing gap is now the target of a new study from Chiba University in Japan. A research team led by Professor Takayoshi Arai of the Graduate School of Science, working with co-authors Dr. Soushi Tsurusaki and Dr. Hidesato Iwama, has designed a chiral nickel catalyst that steers the Henry reaction decisively toward the anti product. The study, published online in the journal Angewandte Chemie International Edition on September 24, 2026, describes a catalyst architecture that does something conceptually elegant: it recruits several different types of molecular interactions at once, marshaling them in a single coordinated system to control how two reacting molecules find each other.

The catalyst, designated o-X-F4-PyBidine-Ni(OTf)2, where X is either bromine or iodine, is built around a nickel complex containing a molecular scaffold called PyBidine. The key innovation lies in a deliberate chemical modification: the researchers installed a bromine or iodine atom at a specific position on the ligand, creating a site capable of forming a halogen bond. Halogen bonding is a non-covalent interaction that arises when a region of positive electrostatic potential, known as a σ-hole, forms on the outer surface of a halogen atom. That positively charged patch can attract electron-rich functional groups on a nearby molecule, effectively gripping the aldehyde substrate and locking it into a defined orientation before the reaction takes place.

But halogen bonding is only one player in what is essentially a molecular choreography. Alongside the halogen bond, conventional hydrogen bonding, the familiar attractive force between a hydrogen atom and an electronegative atom, helps hold the aldehyde in place and simultaneously activates it toward reaction. Meanwhile, the nickel center, working in concert with a base called triethylamine, activates the nitroalkane, priming it to form the new carbon–carbon bond. The result of this multi-pronged arrangement is that the two reacting partners are held in a stretched-out, precisely aligned geometry that channels the reaction toward the anti product rather than the syn product that conventional catalysts tend to deliver.

The performance numbers are striking. Using alcohol as the solvent, the catalyst achieved up to 96:4 selectivity for the anti form over the syn form across many combinations of reactants, meaning that for every hundred product molecules, as many as ninety-six carried the desired anti geometry. Equally impressive is the enantioselectivity: the reaction delivered up to 99 percent enantiomeric excess, which means nearly every product molecule was the same one of the two possible mirror-image versions of the anti form. For a field where controlling both relative and absolute stereochemistry simultaneously is the central difficulty, those figures represent the kind of result that can change how chemists approach an entire class of targets.

The substrate scope adds to the practical appeal. The method proved compatible with a wide range of aromatic aldehydes, including examples bearing heterocyclic rings, which are common features in pharmaceutical compounds and often complicate catalytic reactions. Several kinds of nitroalkanes also worked as coupling partners. That breadth matters because a synthetic method that only functions with a narrow set of substrates rarely escapes the laboratory; one that tolerates diverse aromatic and heteroaromatic aldehydes has a realistic path toward applications in medicinal chemistry, where β-amino alcohol motifs recur constantly. As Professor Arai put it, the coordinated functioning of diverse interactions on a single catalyst represents an advance in state-of-the-art catalytic chemistry.

Curious about why the system works so well, the team turned to computer simulations to dissect the mechanism at a finer level of detail. These calculations revealed that the most favorable reaction pathway involves a halogen bond between the catalyst’s bromine atom and the aromatic ring of the aldehyde, working in tandem with hydrogen bonding and interactions between the nickel center and the nitro group of the nitroalkane. In other words, the selectivity is not the product of any single interaction but of several weak forces acting simultaneously, each contributing to the precise positioning of the reacting molecules. Interestingly, the bromine version of the catalyst was often more active than the iodine variant, possibly because bromine’s smaller size leaves more room for the substrate molecules to approach the reactive site.

Beyond the immediate synthetic payoff, the study carries a broader conceptual message for chemists who design catalysts. Halogen bonding, though increasingly recognized in recent years, has rarely been deployed alongside hydrogen bonding and metal coordination within a single catalytic system, particularly in protic solvents like alcohols, where such delicate interactions are easily disrupted. Demonstrating that these forces can cooperate on a metal catalyst under practical conditions opens a design space that catalyst developers have barely explored. Professor Arai noted that the higher-ordered cooperation of halogen bonds and hydrogen bonds on a metal catalyst in protic solvents is fascinating for the development of artificial metalloenzymes and halogen-bond-driven medicines, pointing toward catalytic systems that mimic the sophisticated multi-interaction control that enzymes achieve naturally.

The longer-term implications extend in several directions at once. For synthetic chemists, the work provides a dependable route to anti-β-amino alcohols, since the nitro group in the products can be readily converted into an amino group by well-established reduction chemistry, completing the gateway from the Henry reaction to the desired building blocks. For catalyst designers, it offers a template for engineering selectivity not through brute-force steric bulk but through the cooperative action of multiple weak, directional interactions. And for the emerging field of artificial metalloenzymes, synthetic catalysts that aspire to enzyme-like precision, it demonstrates that nature’s strategy of combining many subtle molecular forces can be reproduced in a small, human-made framework. The research was supported by the IAAR Research Support Program at Chiba University and by JSPS KAKENHI grant number 26K01496, and the authors declare no conflicts of interest. What began as an attempt to solve a stubborn stereochemical problem may end up reshaping how chemists think about controlling reactions altogether, one weak interaction at a time.

Subject of Research: Halogen-bond-assisted anti-selective Henry reaction using a chiral nickel catalyst for β-amino alcohol synthesis

Article Title: Innovative nickel catalyst unlocks hard-to-make β-amino alcohols

Article References: Innovative nickel catalyst unlocks hard-to-make β-amino alcohols. (n.d.). Original publication

Image Credits: AI Generated

DOI: Not provided

Keywords: nickel catalyst, β-amino alcohols, Henry reaction, halogen bonding, hydrogen bonding, enantioselective synthesis, organocatalysis, stereochemistry, Angewandte Chemie, Chiba University, artificial metalloenzymes, pharmaceutical building blocks

The materials at the centre of the study are covalent organic frameworks, or COFs, a class of substances that has captivated chemists for the better part of two decades. COFs are constructed from organic molecules stitched together by strong covalent bonds into extended, ordered lattices riddled with pores measured in nanometres. This marriage of crystalline precision and internal void space makes them tantalising candidates for everything from electronic devices and chemical sensors to energy storage systems. Yet there has always been a catch. In their pristine form, most COFs are electrical insulators, and the standard remedy has been post-synthetic doping, in which external substances are introduced to supply the electrons or holes needed for conduction. That remedy comes at a price, because dopants can disrupt the framework’s structure, diminishing its crystallinity, its porosity and its long-term stability.

The CiQUS researchers, working across three groups led by Manuel Souto, Diego Peña and Francisco Rivadulla, proposed a fundamentally different route. Rather than injecting charge carriers after the framework has been assembled, they designed the building blocks to carry them from the outset. The key ingredients are neutral trioxotriangulene radicals, often abbreviated TOT, a family of organic molecules distinguished by a highly delocalised spin and a remarkable resistance to degradation. Because these radicals are stable in their neutral state, they can be woven into the framework as genuine structural components rather than added later as guests, and their unpaired electrons stand ready to serve as charge carriers without the need for counterions or any other external chemical species.

The results reported in the journal Angewandte Chemie International Edition are striking on several fronts. The radical-embedded framework crystallised into an ordered lattice and exhibited genuine semiconducting behaviour, with room-temperature electrical conductivity ranking among the highest values ever recorded for a neutral, non-doped COF. Crucially, the material did not sacrifice the property that makes COFs so attractive in the first place. The framework retained a specific surface area exceeding 1,200 square metres per gram, a figure that speaks to an internal landscape of pores preserved intact despite the electronic functionality now built into its walls.

What distinguishes this approach from earlier attempts to electrify COFs is the intimate integration of function and structure. The TOT radicals are not additives suspended within the pores or molecules grafted onto the surface as an afterthought. They are part of the molecular backbone itself, positioned by design so that their unpaired electrons can participate in charge transport. The ordered arrangement of these radical units throughout the framework creates pathways along which charges can move, turning the entire crystalline edifice into a conduit for electricity. In conventional doped systems, by contrast, the charge carriers and the framework often coexist uneasily, with the dopant acting as an intruder whose presence is tolerated rather than celebrated.

The significance of the achievement lies in the simultaneous preservation of three properties that chemists have historically struggled to reconcile: electrical conductivity, crystallinity and porosity. Materials that conduct well tend to be dense and disordered; materials that are porous and crystalline tend to be insulating. By embedding stable radicals into the framework’s architecture, the Spanish team has demonstrated that these attributes need not be mutually exclusive. The study further shows that the framework can be modified by selecting different molecular components and linkages, offering chemists a tunable dial for adjusting the electronic properties of the resulting materials. That modularity is one of the great promises of COF chemistry, and the new work suggests it can now be extended into the semiconducting regime without compromise.

The practical implications stretch across a remarkably broad technological canvas. Conductive, porous and crystalline organic frameworks could serve in electronics, where their processability and structural diversity offer advantages over rigid inorganic semiconductors. They could underpin spintronics, a field that exploits electron spin rather than charge alone, since the embedded radicals carry intrinsic spin character. Their porosity makes them natural candidates for sensors, where target molecules can diffuse into the material and modulate its electrical response, and for electrochemical devices where ion and electron transport must be coordinated. Energy storage looms particularly large on the horizon, because the TOT units can reversibly accept electrons, a property that points toward their use as active materials in batteries. The researchers are careful to note that these applications remain prospects for future investigation rather than demonstrated realities, but the foundational chemistry is now in place.

Behind the paper lies a story of interdisciplinary synergy within a single research centre. Synthesising a COF is a synthetic chemist’s challenge, demanding the precise design of molecular building blocks and the control of polymerisation conditions; characterising its electronic behaviour is a physicist’s task, requiring careful measurement of conductivity and charge transport; and understanding how structure governs function demands expertise spanning both. The groups of Souto, Peña and Rivadulla contributed complementary perspectives on the design, synthesis, characterisation and property studies of the new materials. The collaboration also extended beyond Spain’s borders, drawing in scientists at the CICECO-Aveiro Institute of Materials at the University of Aveiro in Portugal, whose contributions helped complete the picture of the framework’s structure and behaviour.

The work has already attracted attention beyond the specialist literature. Chemical & Engineering News, the news magazine of the American Chemical Society, recently highlighted the study as a new route to producing semiconducting COFs without dopants, a signal that the broader chemistry community regards the strategy as more than an incremental advance. Published under the title Semiconducting Covalent Organic Frameworks Based on Spin-Delocalized Trioxotriangulene Neutral Radicals, the paper arrives at a moment when demand is surging for organic electronic materials that can be manufactured cheaply, tuned molecularly and deployed in applications where silicon cannot follow. CiQUS, which holds María de Maeztu Unit of Excellence accreditation and CIGUS recognition from the Xunta de Galicia, and receives support from the European Union through the Galicia FEDER 2021–2027 Programme, has positioned itself at the forefront of that effort. If the radical-embedded framework approach proves general, the era of doping organic semiconductors may be drawing to a close, replaced by materials that carry their own charge, pore by pore, bond by bond.

Subject of Research: Dopant-free semiconducting covalent organic frameworks based on spin-delocalized trioxotriangulene neutral radicals

Article Title: New strategy to produce porous organic semiconductors without doping

Article References: New strategy to produce porous organic semiconductors without doping. (n.d.). Original publication

Image Credits: AI Generated

DOI: Not provided

Keywords: covalent organic frameworks, COFs, organic semiconductors, trioxotriangulene radicals, dopant-free conductivity, charge transport, porosity, crystallinity, energy storage, spintronics, CiQUS, Angewandte Chemie