Related Experiment Video
Updated: Oct 13, 2026

Synthesis of High Purity Nonsymmetric Dialkylphosphinic Acid Extractants
Published on: October 19, 2017
Broadly Accessible and Highly Active Hydrophosphination Catalysis With Simple Calcium Compounds in DMSO Solution
Moniruzzaman Moniruzzaman1, Rory Waterman1,2
1Department of Chemistry, University of Vermont, Burlington, Vermont, USA.
Abstract:
Highly earth-abundant and simple calcium precatalysts are reported that address the long-standing challenge of broad scope in hydrophosphination catalysis. With more than 120 examples of hydrophosphination reactions, calcium catalysts are the broadest in scope, including traditional styrene substrates and activated alkenes (Michael acceptors), conjugated dienes, heterocumulenes, alkynes, unactivated alkenes, and even naturally occurring alkenes. Reactions are optimized to maximum conversion, and few examples have less than 90% conversion, making these the most active catalysts to date. Two features contribute to this exceptional scope and activity. The first feature is solvent. Reactions run in DMSO experience a step up in relative rate compared to those in lower-dielectric solvents. Second, more challenging substrates are readily accessed under photocatalytic conditions, a feature already established for calcium precatalysts. The simple precatalyst, Ca(HMDS)2(THF)2 (HMDS = -N(SiMe3)2, 1), works for all reactions described, and mechanistic evidence points to a nucleophilic attack for amenable substrates. This work highlights critical advances in hydrophosphination (solvent effects, s-block catalysts, and photocatalysis) to yield an abundant metal (calcium) in green solvent with low energy input to achieve hydrophosphination of the widest scope of substrates under operationally simple conditions.
Related Concept Videos
Acid Halides to Carboxylic Acids: Hydrolysis
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...
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction
Factors Affecting Solubility
Hydrolysis
Hydrolysis of ATP
If one phosphate group is removed, a molecule of ADP—adenosine diphosphate—remains, along with inorganic phosphate. ADP can be further hydrolyzed to AMP—adenosine monophosphate—by the removal of a second...
