Catálogo de publicaciones - revistas

Compartir en
redes sociales


Science

Resumen/Descripción – provisto por la editorial

No disponible.

Palabras clave – provistas por la editorial

No disponibles.

Disponibilidad
Institución detectada Período Navegá Descargá Solicitá
No detectada desde mar. 1997 / hasta dic. 2023 Science Journals

Información

Tipo de recurso:

revistas

ISSN impreso

0036-8075

ISSN electrónico

1095-9203

Editor responsable

American Association for the Advancement of Science (AAAS)

País de edición

Estados Unidos

Fecha de publicación

Cobertura temática

Tabla de contenidos

Editorial Expression of Concern

H. Holden Thorp (eds.)

Palabras clave: Multidisciplinary.

Pp. 729-729

Arctic change reduces risk of cold extremes

Russell Blackport; John C. Fyfe; James A. Screen

Palabras clave: Multidisciplinary.

Pp. 729-729

Arctic change reduces risk of cold extremes—Response

Judah Cohen; Laurie Agel; Mathew Barlow; Chaim I. Garfinkel; Ian White

Palabras clave: Multidisciplinary.

Pp. 729-730

Empowering Afro-Indigenous girls

Carolina Orozco Donneys; Jose Dario Perea

Palabras clave: Multidisciplinary.

Pp. 730-730

In Science Journals

Michael Funk (eds.)

<jats:p> Highlights from the <jats:italic>Science</jats:italic> family of journals </jats:p>

Palabras clave: Multidisciplinary.

Pp. 731-733

In Other Journals

Caroline Ash; Jesse Smith (eds.)

<jats:p>Editors’ selections from the current scientific literature</jats:p>

Palabras clave: Multidisciplinary.

Pp. 732-733

Self-assembled monolayers direct a LiF-rich interphase toward long-life lithium metal batteries

Yujing LiuORCID; Xinyong TaoORCID; Yao WangORCID; Chi Jiang; Cong MaORCID; Ouwei ShengORCID; Gongxun Lu; Xiong Wen (David) LouORCID

<jats:p> High–energy density lithium (Li) metal batteries (LMBs) are promising for energy storage applications but suffer from uncontrollable electrolyte degradation and the consequently formed unstable solid-electrolyte interphase (SEI). In this study, we designed self-assembled monolayers (SAMs) with high-density and long-range–ordered polar carboxyl groups linked to an aluminum oxide–coated separator to provide strong dipole moments, thus offering excess electrons to accelerate the degradation dynamics of carbon-fluorine bond cleavage in Li bis(trifluoromethanesulfonyl)imide. Hence, an SEI with enriched lithium fluoride (LiF) nanocrystals is generated, facilitating rapid Li <jats:sup>+</jats:sup> transfer and suppressing dendritic Li growth. In particular, the SAMs endow the full cells with substantially enhanced cyclability under high cathode loading, limited Li excess, and lean electrolyte conditions. As such, our work extends the long-established SAMs technology into a platform to control electrolyte degradation and SEI formation toward LMBs with ultralong life spans. </jats:p>

Palabras clave: Multidisciplinary.

Pp. 739-745

Modular terpene synthesis enabled by mild electrochemical couplings

Stephen J. HarwoodORCID; Maximilian D. PalkowitzORCID; Cara N. GannettORCID; Paulo PerezORCID; Zhen YaoORCID; Lijie SunORCID; Héctor D. AbruñaORCID; Scott L. AndersonORCID; Phil S. BaranORCID

<jats:p> The synthesis of terpenes is a large field of research that is woven deeply into the history of chemistry. Terpene biosynthesis is a case study of how the logic of a modular design can lead to diverse structures with unparalleled efficiency. This work leverages modern nickel-catalyzed electrochemical sp <jats:sup>2</jats:sup> –sp <jats:sup>3</jats:sup> decarboxylative coupling reactions, enabled by silver nanoparticle–modified electrodes, to intuitively assemble terpene natural products and complex polyenes by using simple modular building blocks. The step change in efficiency of this approach is exemplified through the scalable preparation of 13 complex terpenes, which minimized protecting group manipulations, functional group interconversions, and redox fluctuations. The mechanistic aspects of the essential functionalized electrodes are studied in depth through a variety of spectroscopic and analytical techniques. </jats:p>

Palabras clave: Multidisciplinary.

Pp. 745-752

Reducing adverse impacts of Amazon hydropower expansion

Alexander S. FleckerORCID; Qinru ShiORCID; Rafael M. AlmeidaORCID; Héctor AngaritaORCID; Jonathan M. Gomes-SelmanORCID; Roosevelt García-VillacortaORCID; Suresh A. SethiORCID; Steven A. ThomasORCID; N. LeRoy PoffORCID; Bruce R. ForsbergORCID; Sebastian A. HeilpernORCID; Stephen K. HamiltonORCID; Jorge D. AbadORCID; Elizabeth P. AndersonORCID; Nathan BarrosORCID; Isabel Carolina Bernal; Richard BernsteinORCID; Carlos M. CañasORCID; Olivier DanglesORCID; Andrea C. EncaladaORCID; Ayan S. FleischmannORCID; Michael GouldingORCID; Jonathan HigginsORCID; Céline JézéquelORCID; Erin I. LarsonORCID; Peter B. McIntyreORCID; John M. MelackORCID; Mariana MontoyaORCID; Thierry OberdorffORCID; Rodrigo PaivaORCID; Guillaume PerezORCID; Brendan H. Rappazzo; Scott Steinschneider; Sandra TorresORCID; Mariana VareseORCID; M. Todd WalterORCID; Xiaojian Wu; Yexiang Xue; Xavier E. Zapata-RíosORCID; Carla P. GomesORCID

<jats:p>Proposed hydropower dams at more than 350 sites throughout the Amazon require strategic evaluation of trade-offs between the numerous ecosystem services provided by Earth’s largest and most biodiverse river basin. These services are spatially variable, hence collective impacts of newly built dams depend strongly on their configuration. We use multiobjective optimization to identify portfolios of sites that simultaneously minimize impacts on river flow, river connectivity, sediment transport, fish diversity, and greenhouse gas emissions while achieving energy production goals. We find that uncoordinated, dam-by-dam hydropower expansion has resulted in forgone ecosystem service benefits. Minimizing further damage from hydropower development requires considering diverse environmental impacts across the entire basin, as well as cooperation among Amazonian nations. Our findings offer a transferable model for the evaluation of hydropower expansion in transboundary basins.</jats:p>

Palabras clave: Multidisciplinary.

Pp. 753-760

SARS-CoV-2 Omicron variant: Antibody evasion and cryo-EM structure of spike protein–ACE2 complex

Dhiraj MannarORCID; James W. SavilleORCID; Xing ZhuORCID; Shanti S. SrivastavaORCID; Alison M. BerezukORCID; Katharine S. TuttleORCID; Ana Citlali Marquez; Inna Sekirov; Sriram SubramaniamORCID

<jats:p>The newly reported Omicron variant is poised to replace Delta as the most prevalent severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variant across the world. Cryo–electron microscopy (cryo-EM) structural analysis of the Omicron variant spike protein in complex with human angiotensin-converting enzyme 2 (ACE2) reveals new salt bridges and hydrogen bonds formed by mutated residues arginine-493, serine-496, and arginine-498 in the receptor binding domain with ACE2. These interactions appear to compensate for other Omicron mutations such as the substitution of asparagine for lysine at position 417 (K417N) that are known to reduce ACE2 binding affinity, resulting in similar biochemical ACE2 binding affinities for the Delta and Omicron variants. Neutralization assays show that pseudoviruses that display the Omicron spike protein exhibit increased antibody evasion. The increase in antibody evasion and the retention of strong interactions at the ACE2 interface thus represent important molecular features that likely contribute to the rapid spread of the Omicron variant.</jats:p>

Palabras clave: Multidisciplinary.

Pp. 760-764