A Scalable Approach for Dendrite-Free Alkali Metal Anodes via Room-Temperature Facile Surface Fluorination

2019 ◽  
Vol 11 (5) ◽  
pp. 4962-4968 ◽  
Author(s):  
Gang Wang ◽  
Xunhui Xiong ◽  
Dong Xie ◽  
Xiangxiang Fu ◽  
Zhihua Lin ◽  
...  

2021 ◽  
pp. 162815
Author(s):  
Xianyu Liu ◽  
Lei Zhang ◽  
Zheng Liu ◽  
Yanping Zheng ◽  
Yuan Zhao ◽  
...  


2018 ◽  
Vol 8 (18) ◽  
pp. 1800635 ◽  
Author(s):  
Ying Zhang ◽  
Chengwei Wang ◽  
Glenn Pastel ◽  
Yudi Kuang ◽  
Hua Xie ◽  
...  


2016 ◽  
Vol 4 (31) ◽  
pp. 12188-12196 ◽  
Author(s):  
Ihor Z. Hlova ◽  
Andra Castle ◽  
Jennifer F. Goldston ◽  
Shalabh Gupta ◽  
Timothy Prost ◽  
...  

A simple, highly efficient and environmentally benign mechanochemical process is described for potentially scalable synthesis of catalyst and additive-free alkali-metal hydrides at room-temperature.



2020 ◽  
Author(s):  
Lucas A. Freeman ◽  
Akachukwu D. Obi ◽  
Haleigh R. Machost ◽  
Andrew Molino ◽  
Asa W. Nichols ◽  
...  

The reduction of the relatively inert carbon–oxygen bonds of CO<sub>2</sub> to access useful CO<sub>2</sub>-derived organic products is one of the most important fundamental challenges in synthetic chemistry. Facilitating this bond-cleavage using earth-abundant, non-toxic main group elements (MGEs) is especially arduous because of the difficulty in achieving strong inner-sphere interactions between CO<sub>2</sub> and the MGE. Herein we report the first successful chemical reduction of CO<sub>2</sub> at room temperature by alkali metals, promoted by a cyclic(alkyl)(amino) carbene (CAAC). One-electron reduction of CAAC-CO<sub>2</sub> adduct (<b>1</b>) with lithium, sodium or potassium metal yields stable monoanionic radicals clusters [M(CAAC–CO<sub>2</sub>)]<sub>n</sub>(M = Li, Na, K, <b> 2</b>-<b>4</b>) and two-electron alkali metal reduction affords open-shell, dianionic clusters of the general formula [M<sub>2</sub>(CAAC–CO<sub>2</sub>)]<sub>n </sub>(<b>5</b>-<b>8</b>). It is notable that these crystalline clusters of reduced CO<sub>2</sub> may also be isolated via the “one-pot” reaction of free CO<sub>2</sub> with free CAAC followed by the addition of alkali metals – a reductive process which does not occur in the absence of carbene. Each of the products <b>2</b>-<b>8</b> were investigated using a combination of experimental and theoretical methods.<br>



2021 ◽  
pp. 2101745
Author(s):  
Ziyang Lu ◽  
Yong Guo ◽  
Siwei Zhang ◽  
Shichao Wu ◽  
Rongwei Meng ◽  
...  
Keyword(s):  


2021 ◽  
Author(s):  
Blake Stanley Norman Huchenski ◽  
Alexander William Harrison Speed

Upon treatment with sulfur hexafluoride, alkali metal diphenyl or dicyclohexyl phosphides are oxidized within seconds to tetraphenyl or tetracyclohexyl diphosphines. When bulky di-tert-butylphosphide is employed, fluorophosphine intermediates are detected. This...



Author(s):  
Robert E. Dinnebier ◽  
Hanne Nuss ◽  
Martin Jansen

AbstractThe crystal structures of solvent-free lithium, sodium, rubidium, and cesium squarates have been determined from high resolution synchrotron and X-ray laboratory powder patterns. Crystallographic data at room temperature of Li



2017 ◽  
Vol 96 ◽  
pp. 13-26 ◽  
Author(s):  
G. Plusquellec ◽  
M.R. Geiker ◽  
J. Lindgård ◽  
J. Duchesne ◽  
B. Fournier ◽  
...  


2014 ◽  
Vol 69 (7) ◽  
pp. 793-798
Author(s):  
Laurent Plasseraud ◽  
Hélène Cattey

The title compound was isolated from the treatment of Tp*Sn(Cl)2Bu (1) with a large excess of sodium hydroxide in a mixture of acetone-water at room temperature. [(Me2CO)3(NaTp*)2] (2) crystallizes at 4 °C as prismatic colorless crystals, in the monoclinic space group P21/c with Z = 4, a = 12.2837(6), b = 24.3197(12), c = 16.9547(8) Å, β = 110.017(1)°, and V = 4759.0(4) Å3. The X-ray crystallographic analysis revealed a dinuclear unit in which two Tp*Na moieties are held together by three bridging acetone molecules acting as oxygen-based donors.



ChemInform ◽  
2010 ◽  
Vol 28 (12) ◽  
pp. no-no
Author(s):  
K. XU ◽  
S. ZHANG ◽  
C. A. ANGELL


Sign in / Sign up

Export Citation Format

Share Document