Boron and Boronate Compounds

Jul 1, 2021 | RESEARCH

Boronate Acid Compounds

Boronates are esters and salts of boronic acid. Boronic acid is a compound related to boric acid in which one of the three hydroxyl groups has been replaced by either an alkyl or an aryl group. The boronic acids are derived from boron, an element that is found in the earth’s crust as boric oxide (B(OH)O). Boronic acids can be produced by reacting a borate salt with either acetic or propionic acid to form the corresponding borinic acid.

boron - boronate compound


Different compounds known as boronates are borinic esters and boric acid. The compounds can be obtained from borate esters[18] by condensation with alcohols and diols. Phenylboronic acid can be selfcondensed to the cyclic trimer called triphenyl anhydride or triphenylboroxin. Boric acids are boronates that have a borate anion as their conjugate base. Boronic esters contain boric acid with the carboxylic acid replaced by another organic group, such as alkyl or phenyl groups. The boronic esters can be hydrolyzed to boronic acids. Different boronates are used in the production of polymers, detergents, pesticides, and more. They also have many other uses as well such as use as a catalyst for organic reactions. A borate salt can be hydrolyzed to form boric acid or acylated with an acid to form boronic acid. Boric oxide is boronate salt that has a borate anion as its conjugate base. Boronic esters contain boric acid with the carboxylic acid replaced by another organic group, such as alkyl or phenyl groups. The boronic esters can be hydrolyzed to boronic acids. The use of boronate compounds has grown over the period of time and advancement in boronic acid-related chemistry. In the global world today, boronates are used in a wide variety of products like toothpaste, cosmetics, detergents, plastics, and insecticides. 


Boronate esters are used as catalysts for organic reactions, such as hydroboration-oxidation, borylation, and pinacol coupling reactions to name just a few examples. These are explained as: The hydroboration-oxidation reaction is the reaction in which boron-containing substrates are brominated, then oxidized to borate esters. The borylation reaction is the process of adding boron trihalides (for example BCl) or boric acid derivatives such as orthoboric acid and metaboric acid to alkenes, alkynes, or other unsaturated compounds. boron-containing substrates are brominated, then oxidized to borate esters The pinacol coupling reaction is the process of adding a boronic acid or its related compound with pinacols and catalysts in sequence to form long chains. Diethanolamine complexed heterocyclic boronic acids (DABO boronates) are air-stable reagents that can be used directly in Suzuki-Miyaura reactions, which are the reactions in which boronic acids are used to form boron-carbon bonds and it is an organic reaction, classified as a cross-coupling reaction, where the coupling partners are a boronic acid and an organohalide and the catalyst is a palladium(0) complex. In simple words, it is the reaction where boronic acid esters are in the presence of water or a protic co-solvent. Boronates, which are also classified as organoborate compounds, have been used in chemical catalysis for many years because they can easily form electron deficiency with boron-oxygen bonds with an atom in a broad range of organic substrates. Boronic esters have proved to act as protective groups in carbohydrate chemistry: processes for acylation, silylation and alkylation of glycoside-derived boronates Acylation is the process in which boronates are converted to a boronic acid ester with an acyl group and then the boronic acid is treated with the base. Silylation is the process in which the  boronate ester reacts with a silyl halide, in which boronic acid is an electron-deficient boron atom. Alkylation is the process of adding an alkyl group to boric acids (B(OH)) and borate salts are formed through the reaction of alcohols or amines.


Recrystallization in benzene, dichloroethane, and EtOAc can be good to moderate yielding. Derivatization follows treating the impure product with the base, separating the resultant salt (obtained from base) by solvent extraction, and treating the salt with acid to afford the pure boronic acids. Recrystallization in benzene is the process in which boronic acid is dissolved in benzene and the solution is heated to evaporate. The resultant crystals are filtered, washed with anhydrous ether, and dried under a vacuum. Derivatization is defined as the process in which boronic acid is treated with a base to produce an alkali borate and the salt is extracted as such from the mixture of boronate esters. The resultant salts are subsequently hydrolyzed or acylated, yielding pure boronic acids.
Boron in Coffee

Boron in Coffee

Coffee is one of the most susceptible crops to boron shortage. Boron in coffee is needed for coffee cultivation to improve yield and support healthy growth via cell divisions and cell wall formation in association with calcium, water uptake, roots growth, growth of internodes, setting, calcium uptake, lower aluminum toxicity, and drought resistance.

ABR Production 3x

ABR Boron Production 3x

According to a press release from ABR on November 16th, 2021, the company has announced 'ABR production triples' with a near tripling of production capability for the critical mineral boron at its Fort Cady operations in Southern California. Boron is becoming recognized as an essential mineral for use in multiple applications in decarbonization, advanced energy - batteries- and food security- as a micronutrient.


Boron Protects your Body and the Environment

Micronutrients are substances that are needed in small amounts to aid the body's functions and maintain health. These micronutrients not only help protect our bodies from disease but also play an important role in environmental protection. mainly, the role of micronutrients in plant growth and productivity influences its intensity to protect the environment.