Shared posts

26 Jul 14:43

Shade is an essential solution for hotter cities

by V. Kelly Turner

Nature, Published online: 26 July 2023; doi:10.1038/d41586-023-02311-3

One of the most effective ways to keep people cool is often neglected in urban planning. Cities must work to provide cover and reverse the ‘shade deserts’ common in low-income communities.
26 Jul 07:09

[ASAP] Pyridine N-Oxide-Promoted Cobalt-Catalyzed Dioxygen-Mediated Methane Oxidation

by Bingyin Meng, Luyao Liu, Xiaotong Shen, Wu Fan, and Suhua Li

TOC Graphic

The Journal of Organic Chemistry
DOI: 10.1021/acs.joc.3c00770
26 Jul 06:56

[ASAP] An Atomically Dispersed Mn-Photocatalyst for Generating Hydrogen Peroxide from Seawater via the Water Oxidation Reaction (WOR)

by Peng Ren, Tong Zhang, Noopur Jain, H. Y. Vincent Ching, Aleksander Jaworski, Giovanni Barcaro, Susanna Monti, Joaquin Silvestre-Albero, Veronica Celorrio, Lata Chouhan, Anna Rokicińska, Elke Debroye, Piotr Kuśtrowski, Sabine Van Doorslaer, Sandra Van Aert, Sara Bals, and Shoubhik Das

TOC Graphic

Journal of the American Chemical Society
DOI: 10.1021/jacs.3c03785
24 Jul 07:04

[ASAP] Methane Pyrolysis Using a Multiphase Molten Metal Reactor

by Saurav Sorcar and Brian A. Rosen

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ACS Catalysis
DOI: 10.1021/acscatal.3c02955
24 Jul 07:04

[ASAP] Suzuki–Miyaura Cross-Coupling of Amides by N–C Cleavage Mediated by Air-Stable, Well-Defined [Pd(NHC)(sulfide)Cl2] Catalysts: Reaction Development, Scope, and Mechanism

by Shiyi Yang, Xiang Yu, Yaxu Liu, Michele Tomasini, Lucia Caporaso, Albert Poater, Luigi Cavallo, Catherine S. J. Cazin, Steven P. Nolan, and Michal Szostak

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The Journal of Organic Chemistry
DOI: 10.1021/acs.joc.3c00912
24 Jul 07:01

How to create a lab-group logo that stands out from the crowd

by Andy Tay

Nature, Published online: 20 July 2023; doi:10.1038/d41586-023-02358-2

An eye-catching logo says a lot about your lab’s research, workplace culture and collaborative potential. Take time to get it right.
24 Jul 07:01

Cobalt-catalysed allylic fluoroalkylation of terpenes

by Shengchun Wang

Nature Synthesis, Published online: 20 July 2023; doi:10.1038/s44160-023-00365-9

C(sp3)–H fluoroalkylation of bioactive molecules is a challenge. Now, a scalable and site-selective allylic fluoroalkylation of terpenes and olefins has been developed using a cobaloxime catalyst. Mechanistic studies reveal the process probably proceeds through halogen-atom transfer and hydrogen-atom transfer steps.
24 Jul 07:01

Activation of light alkanes at room temperature and ambient pressure

24 Jul 06:57

Daily briefing: Why your department should throw a party

by Flora Graham

Nature, Published online: 19 July 2023; doi:10.1038/d41586-023-02364-4

How to throw a simple celebratory gathering to help students and staff to reflect on their accomplishments. Plus, the true cost of science’s language barrier for non-native English speakers, and a mammal wrestles a dinosaur in an extraordinary fossil.
24 Jul 06:49

[ASAP] Silver(I)-Catalyzed Synthesis of Cuneanes from Cubanes and their Investigation as Isosteres

by Elliot Smith, Kieran D. Jones, Luke O’Brien, Stephen P. Argent, Christophe Salome, Quentin Lefebvre, Alain Valery, Mina Böcü, Graham N. Newton, and Hon Wai Lam

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Journal of the American Chemical Society
DOI: 10.1021/jacs.3c03207
20 Jul 14:14

[ASAP] Gold-Catalyzed Oxidative Transformation of Free Sugars into Biobased Platform Molecules

by Lucie Quéhon, Frédéric Sauvage, Hania Ahouari, Sema Golonu, Hervé Vezin, Anne Wadouachi, and Gwladys Pourceau

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ACS Sustainable Chemistry & Engineering
DOI: 10.1021/acssuschemeng.3c00975
19 Jul 07:29

[ASAP] Stereoselective Reductive Coupling Reactions Utilizing [1,2]-Phospha-Brook Rearrangement: A Powerful Umpolung Approach

by Ravneet Kaur and Ravi P. Singh

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The Journal of Organic Chemistry
DOI: 10.1021/acs.joc.3c01055
18 Jul 07:41

Chemoselective chromium-catalysed cross-coupling enables three-component tertiary alkane synthesis

by Fei Fan

Nature Synthesis, Published online: 13 July 2023; doi:10.1038/s44160-023-00364-w

Multiple-component cross-coupling reactions can often be unselective and inefficient, making them difficult to develop. Now a chemoselective chromium-catalysed process is reported, forming tertiary alkane centres from benzylic ethers, a Grignard reagent and a silyl chloride, alkyl tosylate or trifluoromethyl-substituted alkene.
18 Jul 07:37

[ASAP] Visible-Light-Mediated TiO2-Catalyzed Aerobic Dehydrogenation of N-Heterocycles in Batch and Flow

by Junghoon Noh, Jun-Young Cho, Mincheol Park, and Boyoung Y. Park

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The Journal of Organic Chemistry
DOI: 10.1021/acs.joc.3c00743
18 Jul 07:36

Aspartame is a possible carcinogen: the science behind the decision

by Miryam Naddaf

Nature, Published online: 14 July 2023; doi:10.1038/d41586-023-02306-0

More research is needed to investigate a potential link between the common sweetener and cancer.
18 Jul 07:33

[ASAP] Passive Daytime Cooling Foils for Everyone: A Scalable Lamination Process Based on Upcycling Aluminum-Coated Chips Bags

by Qimeng Song and Markus Retsch

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ACS Sustainable Chemistry & Engineering
DOI: 10.1021/acssuschemeng.3c00683
18 Jul 07:31

[ASAP] Heterogeneous Photocatalytic Oxidative Cleavage of Polystyrene to Aromatics at Room Temperature

by Zhikun Peng, Rongkui Chen, and Hongji Li

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ACS Sustainable Chemistry & Engineering
DOI: 10.1021/acssuschemeng.3c01282
13 Jul 13:49

[ASAP] Biocatalytic Furfuryl Alcohol Production with Ethanol as the Terminal Reductant Using a Single Enzyme

by Victor K. Sharma, Kylee J. Cosse, Thomas P. Binder, Jeffrey S. McFarlane, and Alan M. Allgeier

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ACS Sustainable Chemistry & Engineering
DOI: 10.1021/acssuschemeng.3c01588
05 Jul 11:34

Anti-ageing protein injection boosts monkeys’ memories

by Lilly Tozer

Nature, Published online: 04 July 2023; doi:10.1038/d41586-023-02214-3

First primate studies to show cognitive benefits of the protein klotho could be a step towards clinical applications.
29 Jun 12:43

Photocatalytic phosphine-mediated water activation for radical hydrogenation

29 Jun 12:37

Start-ups are adding antacids to the ocean to slow global warming. Will it work?

by Jeff Tollefson

Nature, Published online: 28 June 2023; doi:10.1038/d41586-023-02032-7

A New York experiment is part of a commercial race to develop ocean-based technologies to extract carbon dioxide from the atmosphere.
29 Jun 12:30

Trivalent Phosphine‐Catalyzed Reactions Using Fluorinated Building Blocks

by Yi-chao Li, Yuhao Wang, Subarna Jyoti Kalita, Yiyong Huang
Trivalent Phosphine-Catalyzed Reactions Using Fluorinated Building Blocks


Abstract

The development of novel synthetic methodologies to incorporate fluorine/s or fluoroalkyl group/s into the frameworks of organic molecules has become a highly prioritized research area because such modifications can tune their physiochemical and biological properties. In recent years, nucleophilic phosphine catalysis has been extensively explored to achieve this goal, and significant progress has been made. This review summarizes the methodological advancements of cycloaddition, addition and coupling reactions employing fluorinated building blocks as electrophilic and/or nucleophilic reaction partners under phosphine catalysis to construct structurally and synthetically valuable organofluorine compounds, with special emphasis on the synthetic strategies, proposed reaction mechanisms and synthetic utilities.

28 Jun 10:00

Mars mission snaps striking ultraviolet view — image of the week

Nature, Published online: 27 June 2023; doi:10.1038/d41586-023-02156-w

The spacecraft is boosting understanding of the Martian surface and atmosphere.
28 Jun 08:48

What happens when you microwave that plastic bowl?

Nature, Published online: 27 June 2023; doi:10.1038/d41586-023-02091-w

Tests show that certain types of plasticware give off high levels of microscopic plastic particles when heated in an microwave oven.
27 Jun 07:39

A miniaturized toolkit for medicinal chemists

Nature Synthesis, Published online: 22 June 2023; doi:10.1038/s44160-023-00352-0

The most popular reactions used by medicinal chemists are often incompatible with nanoscale ultrahigh-throughput experimentation (ultraHTE). Now, a set of ultraHTE-amenable reaction conditions is reported for four of the most important transformations in drug discovery, and their generality and scalability tested on a range of complex natural products and drug candidates.
27 Jun 07:38

Methyl formate as a hydrogen energy carrier

27 Jun 07:17

Efficient solvent- and hydrogen-free upcycling of high-density polyethylene into separable cyclic hydrocarbons

21 Jun 14:29

Catalytic transfer hydrogenolysis of switchgrass lignin with ethanol using spinel-type mixed-metal oxide catalysts affords control of the oxidation state of isolated aromatic products

by Stephen, Chmely
Chemical reductions of lignin are useful to remove oxygen and create product slates that can function as renewable platform molecules for new fuels and chemicals. Catalytic transfer hydrogenolysis (CTH) is an underexplored method to conduct reductions of lignin that obviates the use of dangerous and non-renewable hydrogen gas. While noble metals are used extensively as catalysts for transfer hydrogenation, one major challenge for their deployment is related to their sustainability. In this work, we synthesized mixed-metal oxides of earth-abundant Co and Ni. We characterized these catalysts using powder x-ray diffraction (XRD) and tested their reactivity for CTH of acetophenone. Among the catalysts we tested, we noted that the spinel NiCo2O4 demonstrated the highest conversion of acetophenone (75%) and highest selectivity for ethylbenzene (90%), so we applied it to valorization of switchgrass lignin extracted under mild operating conditions by cosolvent enhanced lignocellulosic fractionation (CELF). The catalytically depolymerized lignin showed an increase in selectively deoxygenated monomeric compounds. Using 2D-NMR spectroscopy, we demonstrated the lignin displayed highly reduced aliphatic carbons resulting from the reduction reaction at the Cα sites mediated by our catalyst material. These results are critical to the further development of the lignin-first biorefinery as they demonstrate the use of sustainable catalyst materials and mild transformation conditions to generate and refine a suite of new bioproducts.
19 Jun 08:46

Rampant groundwater pumping has changed the tilt of Earth’s axis

by Davide Castelvecchi

Nature, Published online: 16 June 2023; doi:10.1038/d41586-023-01993-z

Human depletion of underground reservoirs has shifted the global distribution of water so much that the North Pole has drifted by more than 4 centimetres per year.
16 Jun 07:32

Direct valorization of biomass waste to gamma-valerolactone

by Martin, Nielsen
Biomass is the only renewable hydrocarbon resource on Earth and therefore plays an essential role in a future sustainable society. Nevertheless, biomass is underutilized for production of chemicals, and is instead burned for energy or left for compost. Derived from biogenic carbohydrates, gamma-valerolactone (GVL) holds pivotal potential as a green fuel, solvent, and platform compound. Converting carbohydrate-rich biomass waste directly to GVL is therefore highly attractive but also very challenging owing to the inert nature and high complexity of biomass, necessitating a versatile and selective catalytic system. Developing benign and complexity-preserving biomass valorization processes would not only allow for sustainable methods to synthesize valuable commodity chemicals, but also provide access to highly attractive carbon-negative procedures. Therefore, producing GVL, that preserves five out of six C–C bonds in hexoses and all the C–C bonds in pentoses, has a high potential. We describe the first direct conversion of raw lignocellulose, starch, and chitin biomass to GVL. Using 1.8 wt% of the homogeneous catalyst Ru-MACHO-BH in 10.9 M H3PO4(aq) with 30 bar of H2 at 140 °C for 24-120 hours provides GVL in excellent yields (10-26 wt%) from twelve different biogenic or industrially processed biowaste sources, either as individual substrates or a combined pool. This corresponds to 26-48mol% yields, or an average of approximately 80-90 mol% yield in each reaction step.