对于 (逆-) cyclopropanation的潜在能量表面:与一个阴阳性黄金复合体的转化
Alexey Fedorov1, Laurent Batiste, Andreas Bach
1Laboratorium für Organische Chemie, ETH Zürich, Wolfgang-Pauli-Strasse 10, CH-8093 Zürich, Switzerland.
Journal of the American Chemical Society
|June 24, 2011
概括
量子化学计算解释了黄金-伊利丁与烯的反应. 一个深度潜在的最小值澄清了循环和转化,包括气相速率和溶液相反循环.
科学领域:
- 有机金属化学 有机金属化学
- 计算化学的计算化学
- 反应机制 反应机制
背景情况:
- 支持联的黄金亚里里丁与电子丰富的烯酸具有循环和转化反应活性.
- 了解这些反应途径对于催化剂设计和机械学阐明至关重要.
研究的目的:
- 通过量子化学计算阐明黄金阿里里丁的气相循环和转化机制.
- 将理论发现与实验观察相关联,包括电子效应和产品比率.
主要方法:
- 密度函数理论 (DFT) 的计算被用来绘制潜在能量表面.
- 对过渡状态和中间体的分析,以确定速率决定的步骤.
主要成果:
- 确定了一个金属结合的环烯添加物的深潜在最小值,与实验能量保持一致.
- 气相循环化受到易斯酸金属碎片解离的限制.
- 转化途径涉及产物解离附近的多个限制速率的过渡状态.
结论:
- 计算的潜在能量表面准确地解释了观察到的气相和溶液相反应.
- 阿里里丁和基联体的电子效应影响产品的分布.
- 该研究提供了一个全面的机理理解金催化循环和转化.
相关概念视频
Thermal and Photochemical Electrocyclic Reactions: Overview
Electrocyclic reactions are reversible reactions. They involve an intramolecular cyclization or ring-opening of a conjugated polyene. Shown below are two examples of electrocyclic reactions. In the first reaction, the formation of the cyclic product is favored. In contrast, in the second reaction, ring-opening is favored due to the high ring strain associated with cyclobutene formation.
Thermal Electrocyclic Reactions: Stereochemistry
The stereochemistry of electrocyclic reactions is strongly influenced by the orbital symmetry of the polyene HOMO. Under thermal conditions, the reaction proceeds via the ground-state HOMO.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Cycloaddition Reactions: Overview
Cycloadditions are one of the most valuable and effective synthesis routes to form cyclic compounds. These are concerted pericyclic reactions between two unsaturated compounds resulting in a cyclic product with two new σ bonds formed at the expense of π bonds. The [4 + 2] cycloaddition, known as the Diels–Alder reaction, is the most common. The other example is a [2 + 2] cycloaddition.
Cycloaddition Reactions: MO Requirements for Thermal Activation
Thermal cycloadditions are reactions where the source of activation energy needed to initiate the reaction is provided in the form of heat. A typical example of a thermally-allowed cycloaddition is the Diels–Alder reaction, which is a [4 + 2] cycloaddition. In contrast, a [2 + 2] cycloaddition is thermally forbidden.
Olefin Metathesis Polymerization: Overview
Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
Photochemical Electrocyclic Reactions: Stereochemistry
The absorption of UV–visible light by conjugated systems causes the promotion of an electron from the ground state to the excited state. Consequently, photochemical electrocyclic reactions proceed via the excited-state HOMO rather than the ground-state HOMO. Since the ground- and excited-state HOMOs have different symmetries, the stereochemical outcome of electrocyclic reactions depends on the mode of activation; i.e., thermal or photochemical.
Selection Rules: Photochemical Activation
Selection Rules: Photochemical Activation


