| 词条 | TPPTS |
| 释义 |
| Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 423355784 | ImageFile = TPPTS.png | IUPACName= Trisodium 3,3',3-phosphinetriyltribenzenesulfonate | OtherNames = {{ubl|Trisodium 3-bis(3-sulfonatophenyl)phosphanylbenzenesulfonate|3,3′,3″-Phosphanetriyltris(benzenesulfonic acid) trisodium salt| Tris(3-sulfophenyl)phosphine trisodium salt}} | Section1 = {{Chembox Identifiers | CASNo_Ref = {{cascite|correct|??}} | CASNo = 63995-70-0 | PubChem = 4348292 | ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} | ChemSpiderID = 3552062 | SMILES = c1cc(cc(c1)S(=O)(=O)[O-])P(c2cccc(c2)S(=O)(=O)[O-])c3cccc(c3)S(=O)(=O)[O-].[Na+].[Na+].[Na+] | StdInChI_Ref = {{stdinchicite|changed|chemspider}} | StdInChI = 1S/C18H15O9PS3.3Na/c19-29(20,21)16-7-1-4-13(10-16)28(14-5-2-8-17(11-14)30(22,23)24)15-6-3-9-18(12-15)31(25,26)27;;;/h1-12H,(H,19,20,21)(H,22,23,24)(H,25,26,27);;;/q;3*+1/p-3 | StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} | StdInChIKey = MYAJTCUQMQREFZ-UHFFFAOYSA-K | Section2 = {{Chembox Properties | C=18 | H=12 | O=9 | P=1 | S=3 | Na=3 | Appearance = White microcrystalline solid | Solubility = Soluble | Section3 = {{Chembox Hazards | RPhrases = {{R36/37/38}} | SPhrases = {{S26}} }}3,3′,3″-Phosphanetriyltris(benzenesulfonic acid) trisodium salt (abbreviated TPPTS when isolated and tppts as a ligand), is an organic compound that is also known as sodium triphenylphosphine trisulfonate. The compound has the formula P(C6H4SO3Na)3. This white microcrystalline solid is an unusual example of a water-soluble phosphine. Its complex with rhodium is used in the industrial production of butyraldehyde.[1] SynthesisTppts is synthesized by sulfonation of triphenylphosphine. The sulfonation occurs at one meta-position of each of the three phenyl rings. The sulfonation agent is oleum, a solution of sulfur trioxide in sulfuric acid. The resulting trisulfonic acid is then treated with triisooctylamine and sodium hydroxide. Immediately upon dissolving in the reaction medium, the phosphine is protonated. It is the phosphonium salt that undergoes the sulfonation: HP(C6H5)3+ + 3 SO3 → [HP(C6H4SO3H)3]+ [HP(C6H4SO3H)3]+ + 4 N(C8H17)3 → [HN(C8H17)3]3[P(C6H4SO3)3] + [HN(C8H17)3]+ [HN(C8H17)3]3[P(C6H4SO3)3] + 3 NaOH → P(C6H4SO3Na)3 + 3 N(C8H17)3 + 3 H2O As a Lewis base, tppts is stronger than triphenylphosphine. Uses in hydroformylationComplexes of tppts are very soluble in water, which is the basis of its industrial application. Tppts-based rhodium catalysts were introduced in 1984 for a two-phase hydroformylation of propene by Ruhrchemie. Hydroformylation, also known as oxo synthesis, is the reaction of an alkene with carbon monoxide and hydrogen. Traditionally, hydroformylation is catalyzed by rhodium and cobalt complexes in nonaqueous solution.[2] References1. ^{{cite journal |author1=Herrmann, W.A. |author2=Kohlpaintner, C.W. | year = 1998 | title = Synthesis of Water-Soluble Phosphines and Their Transition Metal Complexes | journal = Inorganic Syntheses | volume = 32 | pages = 8–25 | isbn = 0-471-24921-1 | publisher = John Wiley & Sons | location = New York | oclc = 219831361 | doi = 10.1002/9780470132630.ch2|series=Inorganic Syntheses }} 2. ^Boy Cornils, Richard W. Fischer, Christian Kohlpaintner "Butanals" in Ullmann's Encyclopedia of Industrial Chemistry, 2000, Wiley-VCH, Weinheim. {{DOI|10.1002/14356007.a04_447}} 2 : Tertiary phosphines|Sulfonates |
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