Органофосфорлық қосылыстар: құрамы, қасиеттері және қолданылуы

Organic compound with at least one covalent carbon–phosphorus bond
Organophosphorus chemistry is the scientific study of the synthesis and properties of organophosphorus compounds, which are organic compounds containing phosphorus. They are used primarily in pest control as an alternative to chlorinated hydrocarbons that persist in the environment. Some organophosphorus compounds are highly effective insecticides, although some are extremely toxic to humans, including sarin and VX nerve agents. Phosphorus, like nitrogen, is in group 15 of the periodic table, and thus phosphorus compounds and nitrogen compounds have many similar properties. The definition of organophosphorus compounds is variable, which can lead to confusion. In industrial and environmental chemistry, an organophosphorus compound need contain only an organic substituent, but need not have a direct phosphorus carbon (P C) bond. Thus a large proportion of pesticides (e. g., malathion), are often included in this class of compounds. Phosphorus can adopt a variety of oxidation states, and it is general to classify organophosphorus compounds based on their being derivatives of phosphorus(V) vs phosphorus(III), which are the predominant classes of compounds. In a descriptive but only intermittently used nomenclature, phosphorus compounds are identified by their coordination number σ and their valency λ. In this system, a phosphine is a σ3λ3 compound.

Phosphate esters have the general structure P(=O)(OR)3 feature P(V). Such species are of technological importance as flame retardant agents, and plasticizers. Lacking a P−C bond, these compounds are in the technical sense not organophosphorus compounds but esters of phosphoric acid. Many derivatives are found in nature, such as phosphatidylcholine. Phosphate ester are synthesized by alcoholysis of phosphorus oxychloride. A variety of mixed amido alkoxo derivatives are known, one medically significant example being the anti cancer drug cyclophosphamide. Also derivatives containing the thiophosphoryl group (P=S) include the pesticide malathion. The organophosphates prepared on the largest scale are the zinc dithiophosphates, as additives for motor oil. Several million kilograms of this coordination complex are produced annually by the reaction of phosphorus pentasulfide with alcohols. In the environment, these compounds break down via hydrolysis to eventually afford phosphate and the organic alcohol or amine from which they are derived.

Phosphonates are esters of phosphonic acid and have the general formula RP(=O)(OR')2. Phosphonates have many technical applications, a well known member being glyphosate, better known as Roundup. With the formula (HO)2P(O)CH2NHCH2CO2H, this derivative of glycine is one of the most widely used herbicides. Bisphosphonates are a class of drugs to treat osteoporosis. The nerve gas agent sarin, containing both C–P and F–P bonds, is a phosphonate. Phosphinates feature two P–C bonds, with the general formula R2P(=O)(OR'). A commercially significant member is the herbicide glufosinate. Similar to glyphosate mentioned above, it has the structure CH3P(O)(OH)CH2CH2CH(NH2)CO2H. The Michaelis–Arbuzov reaction is the main method for the synthesis of these compounds. For example, dimethylmethylphosphonate (see figure above) arises from the rearrangement of trimethylphosphite, which is catalyzed by methyl iodide. In the Horner–Wadsworth–Emmons reaction and the Seyferth–Gilbert homologation, phosphonates are used in reactions with carbonyl compounds. The Kabachnik–Fields reaction is a method for the preparation of aminophosphonates. These compounds contain a very inert bond between phosphorus and carbon. Consequently, they hydrolyze to give phosphonic and phosphinic acid derivatives, but not phosphate.

Phosphine oxides (designation σ4λ5) have the general structure R3P=O with formal oxidation state V. Phosphine oxides form hydrogen bonds and some are therefore soluble in water. The P=O bond is very polar with a dipole moment of 4.51 D for triphenylphosphine oxide. Compounds related to phosphine oxides include phosphine imides (R3PNR') and related chalcogenides (R3PE, where E = S, Se, Te). These compounds are some of the most thermally stable organophosphorus compounds.

Compounds with the formula [PR4+]X− comprise the phosphonium salts. These species are tetrahedral phosphorus(V) compounds. From the commercial perspective, the most important member is tetrakis(hydroxymethyl)phosphonium chloride, [P(CH2OH)4]Cl, which is used as a fire retardant in textiles. Approximately 2M kg are produced annually of the chloride and the related sulfate.

The parent compound of the phosphines is PH3, called phosphine in the US and British Commonwealth, but phosphane elsewhere. Replacement of one or more hydrogen centers by an organic substituents (alkyl, aryl), gives PH3−xRx, an organophosphine, generally referred to as phosphines. From the commercial perspective, the most important phosphine is triphenylphosphine, several million kilograms being produced annually. It is prepared from the reaction of chlorobenzene, PCl3, and sodium. Phosphorus halides undergo nucleophilic displacement by organometallic reagents such as Grignard reagents. Organophosphines are nucleophiles and ligands. Two major applications are as reagents in the Wittig reaction and as supporting phosphine ligands in homogeneous catalysis. Their nucleophilicity is evidenced by their reactions with alkyl halides to give phosphonium salts. Phosphines are nucleophilic catalysts in organic synthesis, e. g. the Rauhut–Currier reaction and Baylis Hillman reaction. Phosphines are reducing agents, as illustrated in the Staudinger reduction for the conversion of organic azides to amines and in the Mitsunobu reaction for converting alcohols into esters. In these processes, the phosphine is oxidized to phosphorus(V). Phosphines have also been found to reduce activated carbonyl groups, for instance the reduction of an α keto ester to an α hydroxy ester.

Compounds with carbon phosphorus(III) multiple bonds are called phosphaalkenes (R2C=PR) and phosphaalkynes (RC≡P). They are similar in structure, but not in reactivity, to imines (R2C=NR) and nitriles (RC≡N), respectively. In the compound phosphorine, one carbon atom in benzene is replaced by phosphorus. Species of this type are relatively rare but for that reason are of interest to researchers. A general method for the synthesis of phosphaalkenes is by 1,2 elimination of suitable precursors, initiated thermally or by base such as DBU, DABCO, or triethylamine:

Thermolysis of Me2PH generates CH2=PMe, an unstable species in the condensed phase.