相关实验视频
Updated: Jul 13, 2026

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Synthesis of High Purity Nonsymmetric Dialkylphosphinic Acid Extractants
Published on: October 19, 2017
设计,合成和化学的硬质无要求的初级双氨酸
Nagavarakishore Pillarsetty1, Kannan Raghuraman, Charles L Barnes
1Department of Chemistry, University of Missouri-Columbia, Columbia, Missouri 65211, USA.
Journal of the American Chemical Society
|January 6, 2005
概括
研究人员合成了新型化双素,其固体阻碍最小,显示出高热和氧化稳定性. 这些氨酸与和等过渡金属具有强烈的协调.
科学领域:
- 有机金属化学 有机金属化学
- 协调化学 协调化学
- 合成化学 合成化学
背景情况:
- 化双素是有机金属化学中的关键配体.
- 开发稳定且高度核友的素配体仍然是一个关键的挑战.
- 绝缘散体通常被认为是稳定低坐标中心的必要条件.
研究的目的:
- 设计和合成新型化双素,在P(III) 中心具有最小的硬质量,具有功能性.
- 为了研究这些素的热和氧化稳定性.
- 探索它们与过渡金属的协调化学.
主要方法:
- 初级双素的合成 ((PH(2) CH(2)) (((2) CHCH(2) NHPh和 (PH(2) CH(2)) ((2) CHCONHPh).
- 一种空气稳定的双素的X射线结构特征.
- 双素与六碳烯 (W(CO) 6和五碳烯化物 (Re(CO) 5Br) 的反应.
主要成果:
- 成功合成了具有P-H键的稳定在空气中的初级双素.
- 证明P(III) 中心的热/氧化稳定性不需要大量的替代剂.
- 高核性和双素与W(0) 和Re(I) 的强有力的协调.
- 形成稳定的和碳复合物.
结论:
- 最小的硬质障碍不会阻碍合双素的稳定性或协调能力.
- 这些新型氨酸为过渡金属化学提供了一种新型的配体.
- 这些发现挑战了在氨酸连接体设计中对硬质要求的传统理解.
相关概念视频
Acid Strength and Molecular Structure
Binary Acids and Bases
In the absence of any leveling effect, the acid strength of binary compounds of hydrogen with nonmetals (A) increases as the H-A bond strength decreases down a group in the periodic table. For group 17, the order of increasing acidity is HF < HCl < HBr < HI. Likewise, for group 16, the order of increasing acid strength is H2O < H2S < H2Se < H2Te. Across a row in the periodic table, the acid strength of binary hydrogen compounds increases with increasing...
In the absence of any leveling effect, the acid strength of binary compounds of hydrogen with nonmetals (A) increases as the H-A bond strength decreases down a group in the periodic table. For group 17, the order of increasing acidity is HF < HCl < HBr < HI. Likewise, for group 16, the order of increasing acid strength is H2O < H2S < H2Se < H2Te. Across a row in the periodic table, the acid strength of binary hydrogen compounds increases with increasing...
Leveling Effect and Non-Aqueous Acid-Base Solutions
This lesson defines the leveling effect in acidic and basic solutions and its role in aqueous and non-aqueous solutions. It is essential to understand the competing nature of various species in a chemical system.
The Leveling Effect of a Solvent
A generic acid (HA) reacts with the generic base (B-) to yield the corresponding conjugate base (A-) and conjugate acid (HB):
The Leveling Effect of a Solvent
A generic acid (HA) reacts with the generic base (B-) to yield the corresponding conjugate base (A-) and conjugate acid (HB):
Acid Halides to Carboxylic Acids: Hydrolysis
Hydrolysis of acid halides is a nucleophilic acyl substitution reaction in which acid halides react with water to give carboxylic acids. The reaction occurs readily and does not require acid or a base catalyst.
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic acid...
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic acid...
Preparation of Acid Anhydrides
One of the methods for preparing symmetrical or unsymmetrical acid anhydrides involves the treatment of acid chlorides with the sodium salt of carboxylic acids. The reaction proceeds via a nucleophilic acyl substitution.
The carboxylate ion acts as a nucleophile that attacks the carbonyl carbon of the acid chloride to form a tetrahedral intermediate. Subsequently, the re-formation of the carbonyl group with the loss of the chloride ion as a leaving group leads to the formation of an acid...
The carboxylate ion acts as a nucleophile that attacks the carbonyl carbon of the acid chloride to form a tetrahedral intermediate. Subsequently, the re-formation of the carbonyl group with the loss of the chloride ion as a leaving group leads to the formation of an acid...
Acid-Catalyzed Aldol Addition Reaction
The aldol reaction of a ketone under acidic conditions successfully forms an unsaturated carbonyl as the final product instead of an aldol. The acid-catalyzed aldol reaction is depicted in Figure 1.
Production of Organic Acids
Lactic acid, an important organic acid extensively applied in food, pharmaceutical, and biodegradable polymer industries, is primarily produced via microbial fermentation. This method is favored over chemical synthesis due to its environmental sustainability and capacity for enantiomerically pure product formation. Among various microbial processes, the fermentation of starch-based substrates stands out due to the abundance and renewability of raw materials like corn and potatoes.Hydrolysis of...

