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Environmental assessments in green chemistry often rely on simplified metrics that enable comparisons between alternative routes but fail to shed light on whether they are truly sustainable in absolute terms, viz. relative to the Earth's ecological capacity. To expand our currently limited knowledge of the extent to which chemicals are environmentally sustainable, here we analyse 492 chemical products through the lens of seven planetary boundaries representing critical biophysical limits that should never be exceeded. We found that most of them transgress these environmental guardrails, mainly the ones strongly connected to greenhouse gas emissions (i.e., climate change, ocean acidification and biosphere integrity). However, their levels of transgression fail to correlate with their carbon footprints, currently the focus of most studies, implying that chemicals entailing higher greenhouse gas emissions are not necessarily less environmentally sustainable in absolute terms. Our work points towards the need to embrace absolute sustainability criteria in current environmental assessments, which will require agreeing on how to allocate shares of the planet's ecological capacity among anthropogenic activities, including chemicals' production. This work's absolute environmental sustainability assessment (AESA) method, which could complement standard life cycle assessment approaches, might help experimental researchers working in green chemistry develop truly 'green' products. The AESA method should be taken as a starting point to devise holistic approaches for quantifying the absolute environmental impact of chemicals to guide research and policymaking more sensibly. [ABSTRACT FROM AUTHOR]

Chemistry, a vital tool for sustainable development, faces a challenge due to the lack of clear guidance on actionable steps, hindering the optimal adoption of sustainability practices across its diverse facets from discovery to implementation. This Scientific Perspective explores established frameworks and principles, proposing a conciliated set of triple E priorities anchored on Environmental, Economic, and Equity pillars for research and decision making. We outline associated metrics, crucial for quantifying impacts, classifying them according to their focus areas and scales tackled. Emphasizing catalysis as a key driver of sustainable synthesis of chemicals and materials, we exemplify how triple E priorities can practically guide the development and implementation of processes from renewables conversions to complex customized products. We summarize by proposing a roadmap for the community aimed at raising awareness, fostering academia–industry collaboration, and stimulating further advances in sustainable chemical technologies across their broad scope. [ABSTRACT FROM AUTHOR]

Chemistry, a vital tool for sustainable development, faces a challenge due to the lack of clear guidance on actionable steps, hindering the optimal adoption of sustainability practices across its diverse facets from discovery to implementation. This Scientific Perspective explores established frameworks and principles, proposing a conciliated set of triple E priorities anchored on Environmental, Economic, and Equity pillars for research and decision making. We outline associated metrics, crucial for quantifying impacts, classifying them according to their focus areas and scales tackled. Emphasizing catalysis as a key driver of sustainable synthesis of chemicals and materials, we exemplify how triple E priorities can practically guide the development and implementation of processes from renewables conversions to complex customized products. We summarize by proposing a roadmap for the community aimed at raising awareness, fostering academia–industry collaboration, and stimulating further advances in sustainable chemical technologies across their broad scope. [ABSTRACT FROM AUTHOR]

C1 coupling reactions over zeolite catalysts are central to sustainable chemical production strategies. However, questions persist regarding the involvement of CO in ketene formation, and the impact of this elusive oxygenate intermediate on reactivity patterns. Using operando photoelectron photoion coincidence spectroscopy (PEPICO), we investigate the role of CO in methyl chloride conversion to hydrocarbons (MCTH), a prospective process for methane valorization with a reaction network akin to methanol to hydrocarbons (MTH) but without oxygenate intermediates. Our findings reveal the transformative role of CO in MCTH at the low pressures, inducing ketene formation in MCTH and boosting olefin production, confirming the Koch carbonylation step in the initial stages of C1 coupling. We uncover pressure‐dependent product distributions driven by CO‐induced ketene formation, and its subsequent desorption from the zeolite surface, which is enhanced at low pressure. Inspired by the above results, extension of the co‐feeding approach to CH3OH as another simple oxygenate showcases the additional potential for improved catalyst stability in MCTH at ambient pressure. [ABSTRACT FROM AUTHOR]

C1 coupling reactions over zeolite catalysts are central to sustainable chemical production strategies. However, questions persist regarding the involvement of CO in ketene formation, and the impact of this elusive oxygenate intermediate on reactivity patterns. Using operando photoelectron photoion coincidence spectroscopy (PEPICO), we investigate the role of CO in methyl chloride conversion to hydrocarbons (MCTH), a prospective process for methane valorization with a reaction network akin to methanol to hydrocarbons (MTH) but without oxygenate intermediates. Our findings reveal the transformative role of CO in MCTH at the low pressures, inducing ketene formation in MCTH and boosting olefin production, confirming the Koch carbonylation step in the initial stages of C1 coupling. We uncover pressure‐dependent product distributions driven by CO‐induced ketene formation, and its subsequent desorption from the zeolite surface, which is enhanced at low pressure. Inspired by the above results, extension of the co‐feeding approach to CH3OH as another simple oxygenate showcases the additional potential for improved catalyst stability in MCTH at ambient pressure. [ABSTRACT FROM AUTHOR]

Ammonia and methanol are essential to modern societies, but their production has been heavily reliant on natural gas, which contributes to supply disruptions and significant CO2 emissions. While low-carbon or green production routes have been extensively researched, their adoption has been hindered by higher costs, making them unsustainable. However, a recent energy crisis in Europe has created a unique opportunity to shift towards greener production technologies. Here we show that, green ammonia, produced through wind-powered water electrolysis, had the potential to outperform its fossil counterpart for six months as of December 2021, while methanol produced through CO2 capture and wind-based water electrolysis became an economically appealing alternative. With a coordinated effort from academia, industry, and policymakers, Europe can lead the grand transition towards more sustainable practices in the chemical industry. [ABSTRACT FROM AUTHOR]

Chemistry is vital for society , but its practices must align with sustainable development. While attention often focuses on individual pillars—environment, economy, or equity—true sustainability requires alignment across all three. The cover image depicts a sustainability compass, symbolizing the integration of diverse principles into a unified set of triple E priorities proposed by Javier Pérez‐Ramírez et al. in their Scientific Perspective (e202318676) to guide efforts in the chemical sciences...By Sharon Mitchell; Antonio J. Martín; Gonzalo Guillén‐Gosálbez and Javier Pérez‐RamírezReported by Author; Author; Author; Author [Extracted from the article]