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Updated: Jun 30, 2025

Protocol of Electrochemical Test and Characterization of Aprotic Li-O2 Battery
08:18

Protocol of Electrochemical Test and Characterization of Aprotic Li-O2 Battery

Published on: July 12, 2016

11.5K

简单的合成类似花生的MoCoFe-HO@CoMo-LDH,用于高效的氧演化反应

Enwei Guo1, Lin Hao2, Youhua Huo1

  • 1State Key Laboratory of New Pharmaceutical Preparations and Excipients, Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of the Ministry of Education, Key Laboratory of Analytical Science and Technology of Hebei Province, College of Chemistry and Materials Science, Hebei University, 071002 Baoding, PR China.

Journal of colloid and interface science
|March 16, 2024
PubMed
概括

开发高效,经济的非贵金属电催化剂对于氧化演化反应 (OER) 至关重要. 这项研究介绍了一种新的核心外材料MoCoFe-HO@CoMo-LDH,其表现出色的OER性能和稳定性.

关键词:
有 CoMo 层的双氧化物.核心-外结构 核心-外结构氧的演化反应反应的反应.

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Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate02:21

Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate

Alkenes can be dihydroxylated using potassium permanganate.  The method encompasses the reaction of an alkene with a cold, dilute solution of potassium permanganate under basic conditions to form a cis-diol along with a brown precipitate of manganese dioxide.
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In ozonolysis, ozone is used to cleave a carbon–carbon double bond to form aldehydes and ketones, or carboxylic acids, depending on the work-up.
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
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Alkenes are converted to 1,2-diols or glycols through a process called dihydroxylation. It involves the addition of two hydroxyl groups across the double bond with two different stereochemical approaches, namely anti and syn. Dihydroxylation using osmium tetroxide progresses with syn stereochemistry.
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Oxymercuration–reduction of alkenes is one of the major reactions converting alkenes to alcohols. It involves the hydration of alkenes with mercuric acetate in a mixture of tetrahydrofuran and water, forming an organomercury adduct. This is followed by a demercuration step in which the adduct is reduced to an alcohol using sodium borohydride.
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In addition to the oxymercuration–demercuration method, which converts the alkenes to alcohols with Markovnikov orientation, a complementary hydroboration-oxidation method yields the anti-Markovnikov product. The hydroboration reaction, discovered in 1959 by H.C. Brown, involves the addition of a B–H bond of borane to an alkene giving an organoborane intermediate. The oxidation of this intermediate with basic hydrogen peroxide forms an alcohol.
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