Results 231 to 240 of about 22,231 (296)

Safety of Sodium‐Ion Batteries: Evaluation and Perspective from Component Materials to Cells, Modules, and Packs

Advanced Energy Materials, EarlyView.
This review provides a bottom‐up evaluation of sodium‐ion battery safety, linking material degradation mechanisms, cell engineering parameters, and module/pack assembly. It emphasizes that understanding intrinsic material stability and establishing coordinated engineering control across hierarchical levels are vital for preventing degradation coupling ...
Won‐Gwang Lim, Seoa Kim, Erik A. Wu, Darren H. S. Tan, Shawn Peng, Xiaolin Li   +5 more
wiley   +1 more source

Disorder-Induced Extremely Low Thermal Conductivity of Graphite Fluoride. [PDF]

Adv Sci (Weinh)
Lee W, Moon D, Qian Z, Kim J, Kim C, Lee Y, Yoo H, Wilson RB, Zheng Q, Lee GH, Jang H.   +10 more
europepmc   +1 more source

High-energy anode-free Li metal batteries with in-built surface-fluorinated Li-rich Mn-based cathodes. [PDF]

Sci Adv
Hu W, Yang Y, Liu Y, Ye Y, An Y, Meng F, Han X, Li A, Wang Y, Li B, Huang D, Pang Q, Zhao X, Zheng J, Zou R.   +14 more
europepmc   +1 more source

Synergistic Transition Metal and Hydrogen Bonding Phase-Transfer Catalysis Enables Enantioconvergent Allylic Fluorination with KF. [PDF]

J Am Chem Soc
Wang Z, Dooley C, Chen Z, Poškaitė G, Paton RS, Lloyd-Jones GC, Gouverneur V.   +6 more
europepmc   +1 more source

Overcoming cathode coating inhomogeneity: the role of LiF interlayer in enabling conformal LiNbO₃ protection on LiNi_0.8Co_0.1Mn_0.1O₂ for all solid-state batteries.

J Mater Chem A Mater
Ramasamy HV, Wullich RN, Lelotte B, Siller V, A F Vaz C, Müller E, El Kazzi M.   +6 more
europepmc   +1 more source

Microwave-assisted nucleophilic fluorination: a facile approach to the synthesis of 6',6'-<i>gem</i>-difluorinated carbocyclic nucleosides. [PDF]

Front Chem
Huang G, Li X, Cui D, Zhi W, Qi P, Hao X, Liu P.   +6 more
europepmc   +1 more source

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Fluorine biocatalysis

Current Opinion in Chemical Biology, 2020
The introduction of fluorine atoms into organic molecules has received considerable attention as these organofluorines have often found widespread applications in bioorganic chemistry, medicinal chemistry and biomaterial science. Despite innovation of synthetic C-F forming methodologies, selective fluorination is still extremely challenging. Therefore,
Linrui, Wu, Fleurdeliz, Maglangit, Hai, Deng   +2 more
openaire   +2 more sources

Biosynthesis with Fluorine

ChemBioChem, 2014
No longer in-F-able: fluorine building blocks can be used in polyketide biosynthesis. This represents a more flexible approach to organofluorines than the traditional use of fluorinated starter units in multistep organic syntheses, and will hopefully increase the number of compounds available for drug development.
Klopries, Stephan, Koopmans, Kyra R. M., Sánchez-García, Elsa, Schulz, Frank   +3 more
openaire   +4 more sources

Electrophilic Aromatic Fluorination with Fluorine: meta‐Directed Fluorination of Anilines.

ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
J.P. Alric, B. Marquet, T. Billard, B.R. Langlois   +3 more
openaire   +1 more source

α-Fluorination of carbonyls with nucleophilic fluorine

Nature Chemistry, 2019
Given the unique properties of fluorine, and the ability of fluorination to change the properties of organic molecules, there is significant interest from medicinal chemists in innovative methodologies that enable the synthesis of new fluorinated motifs.
Pauline Adler, Christopher J. Teskey, Daniel Kaiser, Marion Holy, Harald H. Sitte, Nuno Maulide   +5 more
openaire   +3 more sources