双稳定型二博 ((4) 和酸物种及其与基基因的化学反应
Asif Ahmad1, Sourav Gayen1, Shivankan Mishra1
1Department of Chemistry, Indian Institute of Technology Madras, Chennai 600036, India.
Inorganic chemistry
|February 8, 2024
概括
研究人员开发了一种未催化方法,使用四二复合物 ([BH3·THF]) 和二二.合成diborane(4) 衍生物. 这项研究详细介绍了新型双稳定型diborane(4) 物种及其与素的反应.
科学领域:
- 有机化学 有机化学
- 无机合成 无机合成
- 主群 化学 化学
背景情况:
- 由于其反应性,二 ((4)) 化合物难以分离.
- 稳定策略对于研究二博 ((4) 衍生物至关重要.
- 默卡波皮里丁配体具有稳定化合物的潜力.
研究的目的:
- 开发一种高效的非催化方法,用于合成二博 ((4) 衍生物.
- 为了表征新型双基稳定型diborane(4) 物种.
- 为了探索diborane的反应性(4) B-B与原子的键.
主要方法:
- 在四二复合物 ([BH3·THF]) 的存在下,二甲皮里丁的热解.
- 用于结构阐明的光谱分析 (NMR,X射线晶体学).
- 使用元素硫 (S) 和 (Se) 的氧化插入反应.
主要成果:
- 成功合成了一种双基稳定型diborane(4) 物种 ([HB(μ-C5H4NS) ]2).
- 一种异构性酸物种的分离和特征.
- 通过氧化插入到B-B键中,形成基-二博物种.
结论:
- 已经建立了一个高效的,未催化途径到diborane(4) 衍生物.
- 新的稳定型diborane(4) 和borato-boronium物种被合成和特征化.
- 稳定型二博中的B-B键(4) 经历了氧化插入与石墨素.
相关概念视频
Hydroboration-Oxidation of Alkenes
8.2K
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.
8.2K
Regioselectivity and Stereochemistry of Hydroboration
8.1K
A significant aspect of hydroboration–oxidation is the regio- and stereochemical outcome of the reaction.
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn...
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn...
8.1K
Valence Bond Theory
8.6K
Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...
8.6K
Hybridization of Atomic Orbitals I
47.1K
The mathematical expression known as the wave function, ψ, contains information about each orbital and the wavelike properties of electrons in an isolated atom. When atoms are bound together in a molecule, the wave functions combine to produce new mathematical descriptions that have different shapes. This process of combining the wave functions for atomic orbitals is called hybridization and is mathematically accomplished by the linear combination of atomic orbitals. The new orbitals that...
47.1K
Exceptions to the Octet Rule
28.2K
Many covalent molecules have central atoms that do not have eight electrons in their Lewis structures. These molecules fall into three categories:
28.2K
Halogenation of Alkenes
15.6K
Halogenation is the addition of chlorine or bromine across the double bond in an alkene to yield a vicinal dihalide. The reaction occurs in the presence of inert and non-nucleophilic solvents, such as methylene chloride, chloroform, or carbon tetrachloride.
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
15.6K


