收缩:与液体Na-K相结合的激进共价有机框架,朝着无树突的性金属阳极转向
概括
这项关于先进科学的研究因未经授权使用研究数据和作者不适当的资格而被撤回. 因此,这些发现是无效的,不应该引用.
科学领域:
- 材料科学 材料科学 材料科学
- 化学 化学 化学
背景情况:
- 这项研究旨在介绍新的研究发现.
- 在科学出版物中,作者身份和数据完整性至关重要.
研究的目的:
- 报告[特定领域的重大进展,如果已知].
- 在[特定应用,如果已知]中建立新的基准.
主要方法:
- 使用 [特定技术,如果已知] 获取数据.
- 使用 [分析方法,如果已知] 来解释结果.
主要成果:
- 提出的数据后来被发现是基于未经授权的研究.
- 包括不符合贡献资格的共同作者.
结论:
- 这篇文章已被作者,编辑和出版商收回.
- 由于数据和作者问题,所提出的研究的完整性受到损害.
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Alkali Metals
19.5K
Group 1 elements are soft and shiny metallic solids. They are malleable, ductile, and good conductors of heat and electricity. The melting points of the alkali metals are unusually low for metals and decrease going down the group, while the density increases going down the group with the exception of potassium (Table 1).
Table 1: Properties of the alkali metals
Table 1: Properties of the alkali metals
19.5K
Reduction of Alkynes to trans-Alkenes: Sodium in Liquid Ammonia
9.3K
Alkynes can be reduced to trans-alkenes using sodium or lithium in liquid ammonia. The reaction, known as dissolving metal reduction, proceeds with an anti addition of hydrogen across the carbon–carbon triple bond to form the trans product. Since ammonia exists as a gas (bp = −33°C) at room temperature, the reaction is carried out at low temperatures using a mixture of dry ice (sublimes at −78°C) and acetone.
When dissolved in liquid ammonia, an alkali metal,...
When dissolved in liquid ammonia, an alkali metal,...
9.3K
Electrolysis
26.9K
In a galvanic cell, the electrical work is done by a redox system on its surroundings as electrons produced by the spontaneous redox reactions are transferred through an external circuit. Alternatively, an external circuit does work on a redox system by imposing a voltage sufficient to drive an otherwise nonspontaneous reaction in a process known as electrolysis. For instance, recharging a battery involves the use of an external power source to drive the spontaneous (discharge) cell reaction in...
26.9K
Radical Reactivity: Electrophilic Radicals
1.9K
Radicals adjacent to electron‐withdrawing groups are called electrophilic radicals. These radicals readily react with nucleophilic alkenes. For example, the malonate radical, in which the radical center is flanked by two electron‐withdrawing groups, reacts readily with butyl vinyl ether, which consists of an electron‐donating oxygen substituent. The reaction between electrophilic malonate radical and nucleophilic vinyl ether is favored because the radical has a...
1.9K
Radical Reactivity: Nucleophilic Radicals
2.1K
Radicals adjacent to electron-donating groups are called nucleophilic radicals. These radicals readily react with electrophilic alkenes. The SOMO–LUMO interactions are the driving force for the reaction, where the high-energy SOMO of the electron-rich, nucleophilic radicals interacts with the low-energy LUMO of the electron-deficient, electrophilic alkenes. Such SOMO–LUMO interactions are the basis of reactive radical traps, affecting the selectivity in radical reactions. For...
2.1K
Radical Formation: Overview
2.1K
A bond can be broken either by heterolytic bond cleavage to form ions or homolytic bond cleavage to yield radicals. A fishhook arrow is used to represent the motion of a single electron in homolytic bond cleavage. There are two main sources from which radicals can be formed:
Radicals from spin-paired molecules:
Radicals can be obtained from spin-paired molecules either by homolysis or electron transfer. While two radicals are formed in the former, an electron is added in the...
Radicals from spin-paired molecules:
Radicals can be obtained from spin-paired molecules either by homolysis or electron transfer. While two radicals are formed in the former, an electron is added in the...
2.1K


