Photoinduced stepwise charge hopping in π-stacked perylene bisimide donor–bridge–acceptor arrays
Nature Chemistry
by Leander Ernst, Hongwei Song, Dongho Kim, Frank Würthner
6h ago
Nature Chemistry, Published online: 14 March 2025; doi:10.1038/s41557-025-01770-7 Understanding the distance dependence and mechanistic behaviour of light-driven charge separation is crucial to advance artificial photosynthesis and solar energy conversion. It has now been shown that donor–bridge–acceptor null-coupled perylene bisimide arrays are good candidates for generating long-lived excitons and display ‘through-stack’ photoinduced electron transfer through pronounced π-orbital overlap ..read more
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Vinyl polymers with fully degradable carbon backbones enabled by aromatization-driven C–C bond cleavage
Nature Chemistry
by Zhen-Hua Zhang, Yangyang Sun, Thayalan Rajeshkumar, Yuesheng Li, Laurent Maron, Miao Hong
2d ago
Nature Chemistry, Published online: 13 March 2025; doi:10.1038/s41557-025-01751-w Degradation of carbon-backbone polymers, which make up most plastics, remains a formidable challenge owing to their strong and inert main-chain C–C bonds. Now it has been shown that aromatization-driven C–C bond cleavage is a viable strategy to endow full degradability into carbon backbones under mild conditions ..read more
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Publisher Correction: Amphoteric chalcogen-bonding and halogen-bonding rotaxanes for anion or cation recognition
Nature Chemistry
by Yuen Cheong Tse, Andrew Docker, Igor Marques, Vítor Félix, Paul D. Beer
2d ago
Nature Chemistry, Published online: 12 March 2025; doi:10.1038/s41557-025-01799-8 Publisher Correction: Amphoteric chalcogen-bonding and halogen-bonding rotaxanes for anion or cation recognition ..read more
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Designing single-polymer-chain nanoparticles to mimic biomolecular hydration frustration
Nature Chemistry
by Tianyi Jin, Connor W. Coley, Alfredo Alexander-Katz
3d ago
Nature Chemistry, Published online: 12 March 2025; doi:10.1038/s41557-025-01760-9 Native proteins use hydration frustration—regulating the dehydration of hydrophilic residues and the hydration of hydrophobic residues—to enhance their activity. Now it has been shown that single-polymer-chain nanoparticles made from random heteropolymers can exhibit similar hydration frustration, following design rules orthogonal to those of proteins ..read more
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Aging-dependent evolving electrochemical potentials of biomolecular condensates regulate their physicochemical activities
Nature Chemistry
by Wen Yu, Xiao Guo, Yu Xia, Yuefeng Ma, Zhongli Tong, Leshan Yang, Xiaowei Song, Richard N. Zare, Guosong Hong, Yifan Dai
3d ago
Nature Chemistry, Published online: 12 March 2025; doi:10.1038/s41557-025-01762-7 The mechanisms that regulate the electrochemical equilibrium of condensates are not well understood. Now it has been shown that the aging process of biomolecular condensates can dynamically modulate the electrochemical equilibrium between phases, thereby affecting the physicochemical functions of condensates. This process potentially provides an active mechanism modulating intracellular ion flux ..read more
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General strategy for the synthesis of N-monofluoromethyl amides
Nature Chemistry
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3d ago
Nature Chemistry, Published online: 11 March 2025; doi:10.1038/s41557-025-01769-0 N-monofluoromethyl amides (N-CH2F) have been challenging to prepare. Now, a general method for the synthesis of N-CH2F amides is developed. The strategy can be applied for the N-CH2F modification of peptides and drug derivatives. Moreover, the N-CH2F amides are relatively stable in various media, which could be beneficial for drug development ..read more
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Aryl halide cross-coupling via formate-mediated transfer hydrogenation
Nature Chemistry
by Yoon Cho, Yu-Hsiang Chang, Kevin P. Quirion, Zachary H. Strong, Zachary J. Dubey, Nam Nguyen, Seoyoung Lee, Natalie S. Taylor, Jessica M. Hoover, Nicholas A. White, Peng Liu, Michael J. Krische
4d ago
Nature Chemistry, Published online: 11 March 2025; doi:10.1038/s41557-024-01729-0 Transfer hydrogenation is challenging to apply to aryl halide reductive cross-couplings because of competing hydrogenolysis. Now aryl halide cross-couplings mediated by sodium formate have been developed. These processes display orthogonality to Suzuki and Buchwald–Hartwig couplings as pinacol boronates and anilines are tolerated and, owing to chelated intermediates, effective for challenging 2-pyridyl systems ..read more
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Biomimetic 1,2-amino migration via photoredox catalysis
Nature Chemistry
by Weitai Fan, Yuang Cui, Beibei Zhan, Yizhou Chen, Lei Bao, Yufan Liang, Xiaheng Zhang
1w ago
Nature Chemistry, Published online: 07 March 2025; doi:10.1038/s41557-025-01775-2 Enzyme-catalysed 1,2-amino migration represents a viable biochemical process that is currently underutilized within the synthetic organic chemistry community. Building upon this biocatalytic mechanism, a biomimetic photoredox-catalysed 1,2-amino migration method has been developed. By integrating photoredox-catalysed conditions, this approach enables the modular synthesis of a diverse library of γ-substituted β-amino acids ..read more
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Discovery of a fluorinated macrobicyclic antibiotic through chemical synthesis
Nature Chemistry
by Ben I. C. Tresco, Kelvin J. Y. Wu, Antonio Ramkissoon, Elena V. Aleksandrova, Michael Purdy, Dominic N. Y. See, Richard Y. Liu, Yury S. Polikanov, Andrew G. Myers
1w ago
Nature Chemistry, Published online: 07 March 2025; doi:10.1038/s41557-025-01738-7 Antibiotic resistance can be addressed by reinventing classes of antibiotics through chemical synthesis. Here BT-33—a fully synthetic antibiotic—affords broad-spectrum activity against the bacterial ribosome. X-ray crystallography, theoretical calculations and structure–activity relationship studies reveal the structural features that contribute to the enhanced antibacterial activity and metabolic stability of BT-33 ..read more
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Non-enzymatic methylcyclization of alkenes
Nature Chemistry
by Immanuel Plangger, Elias Schmidhammer, Sebastian Schaar, Klaus Wurst, Maren Podewitz, Thomas Magauer
1w ago
Nature Chemistry, Published online: 07 March 2025; doi:10.1038/s41557-025-01774-3 Bifunctional methyltransferase–cyclases both transfer a methyl group to alkenes and induce cyclization—a process called methylcyclization. Now a non-enzymatic silver(I)-mediated electrophilic methylcyclization has been reported. The reaction uses commercial reagents, is applicable to a wide range of substrates and affords structures that are difficult to access by conventional synthetic methods ..read more
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