Communications Chemistry <p><em>Communications Chemistry</em>&nbsp;is an open access journal from Nature Portfolio publishing high-quality research, reviews and commentary in all areas of the chemical sciences. Research papers published by the journal represent significant advances bringing new chemical insight to a specialized area of research. We also aim to provide a community forum for issues of importance to all chemists, regardless of sub-discipline.</p> <p>Scope includes, but is not limited to, the core subject areas of analytical, inorganic, organic, physical and materials chemistry, and covers the broad spectrum of chemical research including chemical biology, catalysis, computational chemistry, energy materials, green chemistry, environmental chemistry, medicinal chemistry, polymer chemistry, supramolecular chemistry, chemical nanoscience and surface chemistry. &nbsp;We also consider submissions from adjacent research fields where the central advance of the study is of interest to chemists, for example biochemistry, chemical engineering, materials science and nanoscience.</p> <p>The submission and review processes are managed by our in-house professional editors supported by our Editorial Board Members, who provide technical expertise across the breadth of the chemical&nbsp;sciences. We are committed to rapid dissemination of important research results. Articles are published on a continuous basis with minimal time from acceptance to publication.</p> http://feeds.nature.com/commschem/rss/current Nature Publishing Group en © 2025 Macmillan Publishers Limited, part of Springer Nature. All rights reserved. Communications Chemistry © 2025 Macmillan Publishers Limited, part of Springer Nature. All rights reserved. [email protected]
  • Communications Chemistry https://www.nature.com/uploads/product/commschem/rss.gif http://feeds.nature.com/commschem/rss/current <![CDATA[Reaction-conditioned generative model for catalyst design and optimization with CatDRX]]> https://www.nature.com/articles/s42004-025-01732-7 <![CDATA[

    Communications Chemistry, Published online: 23 October 2025; doi:10.1038/s42004-025-01732-7

    Designing effective catalysts is a key process for optimizing catalytic reactions, however, existing generative approaches are often limited to specific reaction classes and predefined fragment categories. Here, the authors present CatDRX, a catalyst discovery framework powered by a reaction-conditioned variational autoencoder to generate potential catalysts and predict their activities, integrating optimization and validation based on reaction mechanisms and chemical knowledge.]]> <![CDATA[Reaction-conditioned generative model for catalyst design and optimization with CatDRX]]> Apakorn KengkannaYuta KikuchiTakashi NiwaMasahito Ohue doi:10.1038/s42004-025-01732-7 Communications Chemistry, Published online: 2025-10-23; | doi:10.1038/s42004-025-01732-7 2025-10-23 Communications Chemistry 10.1038/s42004-025-01732-7 https://www.nature.com/articles/s42004-025-01732-7 <![CDATA[Evaluating sodium-ion pouch cell battery for renewable energy storage under extreme conditions]]> https://www.nature.com/articles/s42004-025-01709-6 <![CDATA[

    Communications Chemistry, Published online: 22 October 2025; doi:10.1038/s42004-025-01709-6

    Sodium-ion batteries are a commercially viable option for sustainable energy storage, but their performance at low temperatures remains underexplored. Here, the authors present a sodium-ion battery pouch cell designed for ultra-low temperatures, demonstrating its performance in laboratory conditions at -25 °C and -50 °C, in the presence of wind and snow, and in combination with a solar cell at -100 °C.]]>
    <![CDATA[Evaluating sodium-ion pouch cell battery for renewable energy storage under extreme conditions]]> Mehul ShelkeJamee M. BoyerVinay MirzapureVilas G. Pol doi:10.1038/s42004-025-01709-6 Communications Chemistry, Published online: 2025-10-22; | doi:10.1038/s42004-025-01709-6 2025-10-22 Communications Chemistry 10.1038/s42004-025-01709-6 https://www.nature.com/articles/s42004-025-01709-6
    <![CDATA[Tailoring aggregation-induced emission in luminescent solar concentrators through controlled polymerization]]> https://www.nature.com/articles/s42004-025-01700-1 <![CDATA[

    Communications Chemistry, Published online: 17 October 2025; doi:10.1038/s42004-025-01700-1

    Aggregation-induced emission (AIE) luminogens can enhance the photonic response of luminescent solar concentrators (LSCs), but their controlled polymerization to produce macromolecular networks for LSC structures remains underexplored. Here, the authors develop a series of copolymers based on methyl methacrylate and an AIE-active monomer (tetraphenyl ethylene methacrylate) through free radical and reversible addition-fragmentation chain transfer (RAFT) polymerization, showing that RAFT-based LSCs exhibit more consistent device performance.]]>
    <![CDATA[Tailoring aggregation-induced emission in luminescent solar concentrators through controlled polymerization]]> Elisavet TatsiGaia Roberta RagnoAndrea NittiChiara BottaStefano TurriDario PasiniGianmarco Griffini doi:10.1038/s42004-025-01700-1 Communications Chemistry, Published online: 2025-10-17; | doi:10.1038/s42004-025-01700-1 2025-10-17 Communications Chemistry 10.1038/s42004-025-01700-1 https://www.nature.com/articles/s42004-025-01700-1
    <![CDATA[Spotlighting the criticality of lipid quality control through a mechanistic investigation of mRNA activity loss in lipid nanoparticles]]> https://www.nature.com/articles/s42004-025-01699-5 <![CDATA[

    Communications Chemistry, Published online: 17 October 2025; doi:10.1038/s42004-025-01699-5

    Lipid nanoparticles (LNPs) are essential carriers for mRNA delivery, but lipid peroxide impurities in ionizable lipids can degrade into reactive aldehyde species, leading to loss of mRNA’s translation efficiency in vitro. Here, the authors underscore the importance of rigorous lipid stability and purity analysis to ensure the quality and stability of mRNA encapsulated in the LNPs.]]>
    <![CDATA[Spotlighting the criticality of lipid quality control through a mechanistic investigation of mRNA activity loss in lipid nanoparticles]]> Richard S. KangZhichun WangHima SapaZhijun CaoYing ZhangJiang Qian doi:10.1038/s42004-025-01699-5 Communications Chemistry, Published online: 2025-10-17; | doi:10.1038/s42004-025-01699-5 2025-10-17 Communications Chemistry 10.1038/s42004-025-01699-5 https://www.nature.com/articles/s42004-025-01699-5
    <![CDATA[Development of a <sup>1</sup>H qNMR method for the identification and quantification of monosaccharides in dietary fibre fractions]]> https://www.nature.com/articles/s42004-025-01696-8 <![CDATA[

    Communications Chemistry, Published online: 16 October 2025; doi:10.1038/s42004-025-01696-8

    Dietary fibre (DF) analysis is crucial for understanding its health benefits, yet traditional methods lack molecular detail. Here, the authors develop a 1H NMR spectroscopy method to directly analyze hydrolysed DF fractions with high recovery and fast preparation while revealing detailed structural information including monosaccharide composition, carbohydrate modifications and the degradation products.]]>
    <![CDATA[Development of a <sup>1</sup>H qNMR method for the identification and quantification of monosaccharides in dietary fibre fractions]]> Clara PedrazzaniAndrea FusoPio ViscusiVeronica LolliAugusta Caligiani doi:10.1038/s42004-025-01696-8 Communications Chemistry, Published online: 2025-10-16; | doi:10.1038/s42004-025-01696-8 2025-10-16 Communications Chemistry 10.1038/s42004-025-01696-8 https://www.nature.com/articles/s42004-025-01696-8
    <![CDATA[Remote difunctionalization of alkenes through a photocatalytically triggered radical clock and α-carbonyl carbocation generation]]> https://www.nature.com/articles/s42004-025-01695-9 <![CDATA[

    Communications Chemistry, Published online: 15 October 2025; doi:10.1038/s42004-025-01695-9

    Cα-tetrasubstituted amides and esters are biologically important but are typically constructed through several-step transformations. Here, the authors report the synthesis of α,ε-difunctionalized γ,δ-unsaturated amides and esters via a photocatalyzed three-component remote 1,5-difunctionalization of alkenes using a tandem CF3 radical addition/radical clock cleavage approach with Umemoto reagents.]]>
    <![CDATA[Remote difunctionalization of alkenes through a photocatalytically triggered radical clock and α-carbonyl carbocation generation]]> Xiaoxiao LiuDi ChaoNana MaQingfeng LiuZhiguo ZhangTongxin LiuXingjie ZhangGuisheng Zhang doi:10.1038/s42004-025-01695-9 Communications Chemistry, Published online: 2025-10-15; | doi:10.1038/s42004-025-01695-9 2025-10-15 Communications Chemistry 10.1038/s42004-025-01695-9 https://www.nature.com/articles/s42004-025-01695-9
    <![CDATA[Palladium single-atom/cluster cocatalyst supported on non-enzymatic browning glucose breaks the activity-selectivity trade-off in C(sp<sup>3</sup>)-H arylation]]> https://www.nature.com/articles/s42004-025-01693-x <![CDATA[

    Communications Chemistry, Published online: 14 October 2025; doi:10.1038/s42004-025-01693-x

    Using Pd homogeneous catalysts for direct C–H arylation is an attractive approach for synthesizing natural products and organic functional materials, but limitations in terms of cost and catalyst recovery could be alleviated by alternative heterogeneous catalytic processes. Here, the authors report a Pd single-atom/cluster cocatalyst supported on non-enzymatic browning glucose for the direct coupling of inert C-H bonds with aryl iodides that breaks the activity-stability trade-off via a PdII/PdIV catalytic cycle, and demonstrate C(sp3)-H or C(sp2)-H bond activation tunability by tailoring the structure of the catalyst support.]]>
    <![CDATA[Palladium single-atom/cluster cocatalyst supported on non-enzymatic browning glucose breaks the activity-selectivity trade-off in C(sp<sup>3</sup>)-H arylation]]> Xiaojie HeWunengerile ZhangChaolumen BaiDan LiuAgula BaoTegshi MuschinYong-Sheng Bao doi:10.1038/s42004-025-01693-x Communications Chemistry, Published online: 2025-10-14; | doi:10.1038/s42004-025-01693-x 2025-10-14 Communications Chemistry 10.1038/s42004-025-01693-x https://www.nature.com/articles/s42004-025-01693-x
    <![CDATA[Terminal sialic acids in the nanoparticle corona modulate cellular uptake]]> https://www.nature.com/articles/s42004-025-01677-x <![CDATA[

    Communications Chemistry, Published online: 14 October 2025; doi:10.1038/s42004-025-01677-x

    Nanoparticles (NPs) hold promise for therapeutic applications, but their interactions with biological environments remain poorly understood. Here, the authors reveal that the glycosylation of the biomolecular corona, particularly sialic acid content, significantly influences NP interactions with cellular uptake processes, offering new insights into predicting NPs’ biological fate.]]>
    <![CDATA[Terminal sialic acids in the nanoparticle corona modulate cellular uptake]]> Marko DobricicAlberto Martinez-SerraClaudia DurallAnna NakonechnaJack CheesemanRoger PrestonJames S. O’DonnellDaniel I. R. SpencerTeodor AastrupMarco P. Monopoli doi:10.1038/s42004-025-01677-x Communications Chemistry, Published online: 2025-10-14; | doi:10.1038/s42004-025-01677-x 2025-10-14 Communications Chemistry 10.1038/s42004-025-01677-x https://www.nature.com/articles/s42004-025-01677-x