意识形态特质和个人层面的激进化路径:解开当代极端主义的变异动态
1University of Liverpool, Liverpool, UK.
概括
隐秘极端主义融合了信仰,挑战了当前的政策. 研究必须扩展,以了解这些复杂的,个人的激进化路径和情绪因素.
科学领域:
- 社会科学 社会科学 社会科学
- 政治科学 政治科学是指政治学.
- 心理学 心理学 心理学
背景情况:
- "混合"极端主义的兴起,特别是神秘的变化,挑战了传统的意识形态界限.
- 非教义性的极端主义形式,以一种流动的态度和信仰的布里科拉奇为特征,超越现有的政策分类.
- 极端主义线索融合的更广泛的生态系统仍然未得到充分探索,尽管研究了诸如inceldom.com这样的现象.
研究的目的:
- 为了照亮激进化途径的不断变化的景观.
- 通过探索极端主义参与的特殊模式来扩大激进化研究.
- 培养对激进化的关系和情感层面的更深入的理解.
主要方法:
- 对极端主义的"混合"和神秘形式的分析.
- 检查非教义和流动的信仰体系.
- 批评现有的分类和政策反应,如预防战略.
主要成果:
- 隐秘极端主义由于其非教义性和流动性而带来了重大的概念和监管挑战.
- 个人的激进化路径是异质的,不可预测的,受到关系和情感因素的影响.
- 传统的意识形态分类过于简单,不足以理解当代极端主义.
结论:
- 现有的政策框架,如预防战略,努力解决当代极端主义的变异动态.
- 需要适应性框架来承认个性化的代理,不断变化的结构条件和不断演变的激进化生态系统.
- 扩大激进化研究以包括特殊的参与模式对于有效的反极端主义战略至关重要.
相关概念视频
Group Polarization
35.5K
Group polarization is the strengthening of an original group attitude following the discussion of views within a group (Teger & Pruitt, 1967). That is, if a group initially favors a viewpoint, after discussion the group consensus is likely a stronger endorsement of the viewpoint. Conversely, if the group was initially opposed to a viewpoint, group discussion would likely lead to stronger opposition.
35.5K
Radical Reactivity: Overview
2.2K
Radicals, the highly reactive species, gain stability by undergoing three different reactions. The first reaction involves a radical-radical coupling, in which a radical combines with another radical, forming a spin‐paired molecule. The second reaction is between a radical and a spin‐paired molecule, generating a new radical and a new spin‐paired molecule. The third reaction is radical decomposition in a unimolecular reaction, forming a new radical and a spin‐paired...
2.2K
Radical Reactivity: Steric Effects
2.0K
The presence of electron-donating, electron-withdrawing, or conjugating groups adjacent to a radical center, imparts electronic stabilization to the radicals. Examples of such electronically-stabilized radicals are triphenylmethyl, tetramethylpiperidine‐N‐oxide, and 2,2‐diphenyl‐1‐picrylhydrazyl. These radicals are remarkably stable and are known as persistent radicals. Some of the persistent radicals can even be isolated and purified.
Along with electronic...
Along with electronic...
2.0K
Radical Reactivity: Electrophilic Radicals
2.0K
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...
2.0K
Radicals: Electronic Structure and Geometry
4.3K
This lesson delves into the geometry of a radical, which is influenced by the electronic structure of the molecule. The principle is similar to that of a lone pair, where the unpaired electron influences the geometry at the radical center.
Accordingly, the structure of a trivalent radical lies between the geometries of carbocations and carbanions. An sp2-hybridized carbocation is trigonal planar, while an sp3-hybridized carbanion is trigonal pyramidal. Here, the difference in geometry is...
Accordingly, the structure of a trivalent radical lies between the geometries of carbocations and carbanions. An sp2-hybridized carbocation is trigonal planar, while an sp3-hybridized carbanion is trigonal pyramidal. Here, the difference in geometry is...
4.3K
Radical Reactivity: Nucleophilic Radicals
2.2K
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...
2.2K


