The study of asymmetric phosphine compounds and their applications and the appearance of various novel compounds have greatly enriched organophosphorus chemistry. Phosphorus-containing antioxidants, stabilizers, and extractants and complexing agents used as rare elements have been widely used in the chemical industry. The organic phosphine compound in the organism is an important energy source and an important component in the formation of biopolymer DNA and RNA backbone. Organophosphorus compounds in nucleic acids, coenzymes, organophosphorus toxic gases, organophosphate insecticides, organophosphorus bactericides, organophosphorus herbicides, chemotherapeutic agents, plasticizers, antioxidants, surfactants, complexing agents, organophosphorus It is widely used in extractants, flotation agents and flame retardants. The chemical structure of organic phosphine compounds can be roughly classified into the following categories: 1. Phosphonates. Phosphoric acid is a tribasic acid, that is, three hydrogen atoms which can be replaced. These hydrogen atoms are replaced by organic groups, called phosphonates. When these three groups are not identical, they are called mixed esters. Many of the pesticides are mixed esters of phosphoric acid, such as dichlorvos, which is a mixed ester of phosphoric acid. 2. Thio, dithio and trithiophosphonates. The oxygen atom in the phosphate molecule is replaced by a sulfur atom, which is called a thiophosphonate, such as parathion, dimethoate, and rice blast. 3. Phosphoramide and thiophosphoramide. The hydroxyl group in the phosphoric acid molecule is replaced by an amino group, which is called phosphoramide. The remaining oxygen atom in the phosphoramide molecule may be replaced by a sulfur atom to become a thiophosphoramide such as methamidophos or fertile phosphorus. 4. Pyrophosphonates, thiopyrophosphonates and pyrophosphamides. The two phosphoric acid molecules remove one molecule of water to form pyrophosphoric acid, and the hydrogen, oxygen and hydroxyl groups in the pyrophosphate can also be replaced by an organic group, a sulfur atom and an amino group, respectively, such as a phosphorus. 5. Phosphonates and thiophosphonates. One of the hydroxyl groups in the phosphoric acid is replaced by an organic group, that is, a PC bond is formed in the molecule called a phosphonic acid, and some phosphonic acids and sulfur-substituted compounds thereof have been promoted as pesticides, such as phoxim. 6. Derivatives of phosphorous acid. Some pesticides are derivatives of phosphorous acid. In the molecule of phosphorous acid, phosphorus is trivalent, such as defoliation. 7. Phosphine. When the hydrogen in the phosphine molecule is replaced by an organic group, it is called a phosphine. The structures of these compounds are similar to those of the nitrogen compounds ammonia, amine and ammonium salts, and are called phosphines and ortho-phosphines. 8. The hydroxyl group in the phosphoric acid or phosphonic acid molecule is replaced by a halogen.
-
Amino compound
>
-
Oxy-containing amino compound
Cycloalkylamines, aromatic monoamines, aromatic polyamines and derivatives and salts thereof
Acyclic monoamines, polyamines and their derivatives and salts
Amide compound
Sulfonic acid amino compound
-
Alcohols, phenols, phenolic compounds and derivatives
>
-
2-cycloalcohol
Halogenated, sulfonated, nitrated or nitrosated derivatives of alcohols
Extremely halogenated, sulfonated, nitrated or nitrosated derivatives of phenols
Phenol and its halogenated, sulfonated, nitrated or nitrosated derivatives
Acyclic alcohol
-
Nitrogen-containing compound
-
-
Nitrile compound
-
-
Organic derivative of hydrazine or hydrazine
-
-
Terpenoid
-
-
Ether compounds and their derivatives
>
-
Ether, ether alcohol
Halogenation, sulfonation, nitration or nitrosation of ethers, ether alcohols, ether phenols
-
Aldehyde
-
-
Carboxylic compounds and derivatives
>
-
Cyclic carboxylic acid
Halogenation, sulfonation, nitration or nitrosation of carboxylic acids
Halogenation, sulfonation, nitration or nitration of carboxylic anhydrides
Carboxylic acid halide
Carboxylic esters and their derivatives
Salt of carboxylic acid ester and its derivatives
Acyclic carboxylic acid
-
Hydrocarbon compounds and their derivatives
>
-
Aromatic hydrocarbon
Cyclic hydrocarbon
Hydrocarbon sulfonate
Hydrocarbon halide
Hydrocarbon nitrite
Acyclic hydrocarbon
-
Ketone compound
-
-
Alkyl ureas and their derivatives and salts
-
-
Inorganic acid ester
-
-
Heterocyclic compound
-
-
Diazo, azo or azo compound
-
-
Organosilicon compound
-
-
Organometallic compound
>
-
Organic palladium
Organic germanium, cobalt, strontium, barium, gallium, germanium, germanium, germanium, germanium, etc.
Organic calcium
Zirconium
Organic potassium
Organic
Organic lithium
Organic
Organic aluminum
Organotin
Organic manganese
Organic sodium
Organic nickel
Organic titanium
Organic iron
Organic copper
Organotin
Organic zinc
Organic
Organic
Organic germanium, mercury, silver, platinum, etc.
Organic germanium, antimony, bismuth, tungsten, antimony, bismuth, lead, vanadium, molybdenum, chromium, antimony, etc.
-
Organic sulfur compound
-
-
Organic phosphine compound
-
-
Organometallic salt
-
-
Organic fluorine compound
>
-
Fluorobenzoic acid series
Fluorobenzonitrile series
Fluorobenzaldehyde series
Fluorobenzyl alcohol series
Fluoroanisole series
Fluoroaniline series
Fluorophenylacetic acid series
Fluorophenol series
Fluorobenzoic acid series
Fluoronitrobenzene series
Fluoropyridine series
Potassium fluoroborate series
Fluorobenzyl alcohol series
Fluorotoluene series
Fluorine red series
Fluoroethane series
Fluoropropane series