Phosphinic acid complexes

K. Inaba, S. Murahdharan, and H. Freiser, Simultane-ons characterization of extraction eqnilibria and back-extraction kinetics Use of arsenazo III to characterize lanthanide-bis(2,4,4-trimethylpentyl)phosphinic acid complexes in surfactant micelles. Anal. Chem. 65 1510 (1993). 

Complexes of diorganophosphinous acids, R2P(0)H, with tin(iv) chloride have been reported. Co-ordination of the dialkylphosphinic and dialkyl-phosphinothioic acids to tin in the complexes [R R P(0)YH]2,SnX4 (Y = O or S) is effected through the phosphoryl oxygen in both cases. The phosphinic acid complexes lose hydrogen chloride at 120—140 °C to form the compounds [R R P(0)0]2SnCl2, which appear to be chain polymers of the type (18.) ... 

Recently Li reported that air stable phosphine oxides 2a [RR P(0)H] in the presence of transition metals undergo tautomerization to the less stable phosphi-nous acids 2b [RR POH], which subsequently coordinate to Pd centers through phosphorus atoms to form Pd phosphinous acid complexes 2c, which behave as active catalysts for unactivated aryl chlorides [19]. Their Pd complexes XVIII-4 (POPd), -5 (POPdl) and -6 (POPd2) are commercially available (Table 1.18). 

Commercially available, air-stable Pd phosphinous acid complex is an active catalyst for the thioether formation by the reaction of 1-cyclopentenyl chloride (49) with thiophenol (50) and hexylmercaptan (52) to give the thioethers 51 and 53 [15]. 1-Cyclopentenyl phenyl thioether (55) was obtained by the reaction of 1-cyclopentenyl triflate (54) with lithium phenyl sulfide [16]. 

PaUadium-phosphinous acid complexes can be used for StUle couplings of aryl chlorides in water. In the case of 4,7-dichloroquinobne, a highly selective coupling at the 4-position is observed, with no products from coupling at the 7-position being detected (Equation 2.45) [81, 82). 

Other highly active palladium chloride-based catalysts include di-2-pyridylmethylamine-based paUadium, tr(WM-bidentate pyridine, and PdCl2/phosphinous acid complexes. Typical examples are shown in Scheme 2. This section is concerned with the coupling reactions of aryl chlorides using the above PdCh-based catalysts. Chloro arenes are cheap to manufacture and therefore play a vital role as intermediates in the chemical industry. The low reactivity of chlorides is usually attributed to the strength of the C-Cl bond. Remarkable progress has been achieved since 1998 in the development of palladium-based catalysts that can in fact accomplish cross-couplings and Heck reactions. ... 

Preparation and Properties of Organophosphines. AUphatic phosphines can be gases, volatile Hquids, or oils. Aromatic phosphines frequentiy are crystalline, although many are oils. Some physical properties are Hsted in Table 14. The most characteristic chemical properties of phosphines include their susceptabiUty to oxidation and their nucleophilicity. The most common derivatives of the phosphines include halophosphines, phosphine oxides, metal complexes of phosphines, and phosphonium salts. Phosphines are also raw materials in the preparation of derivatives, ie, derivatives of the isomers phosphinic acid, HP(OH)2, and phosphonous acid, H2P(=0)0H. 

The chlorination of phosphonic and phosphinic acids and esters are of considerable importance. PCI5 can also act as a Lewis acid to give 6-coordinate P complexes, e.g. pyPClf, and pyz-PCI5, where py = C5H5N (pyridine) and pyz = cyclo-1, 4-C4H4N2 (pyrazine). ... 

It has been found that certain 2 + 2 cycloadditions that do not occur thermally can be made to take place without photochemical initiation by the use of certain catalysts, usually transition metal compounds. Among the catalysts used are Lewis acids and phosphine-nickel complexes.Certain of the reverse cyclobutane ring openings can also be catalytically induced (18-38). The role of the catalyst is not certain and may be different in each case. One possibility is that the presence of the catalyst causes a forbidden reaction to become allowed, through coordination of the catalyst to the n or s bonds of the substrate. In such a case, the... 

A palladium catalyst with a less electron-rich ligand, 2,2-dipyridyl-methylamine-based palladium complexes (4.2), is effective for coupling of aryl iodides or bromides with terminal alkynes in the presence of pyrrolidine and tetrabutylammonium acetate (TBAB) at 100°C in water.37 However, the reactions were shown to be faster in NMP solvent than in water under the reaction conditions. Palladium-phosphinous acid (POPd) was also reported as an effective catalyst for the Sonogashira cross-coupling reaction of aryl alkynes with aryl iodides, bromides, or chlorides in water (Eq. 4.18).38... 

The reaction of alcohols with CO was catalyzed by Pd compounds, iodides and/or bromides, and amides (or thioamides). Thus, MeOH was carbonylated in the presence of Pd acetate, NiCl2, tV-methylpyrrolidone, Mel, and Lil to give HOAc. AcOH is prepared by the reaction of MeOH with CO in the presence of a catalyst system comprising a Pd compound, an ionic Br or I compound other than HBr or HI, a sulfone or sulfoxide, and, in some cases, a Ni compound and a phosphine oxide or a phosphinic acid.60 Palladium(II) salts catalyze the carbonylation of methyl iodide in methanol to methyl acetate in the presence of an excess of iodide, even without amine or phosphine co-ligands platinum(II) salts are less effective.61 A novel Pd11 complex (13) is a highly efficient catalyst for the carbonylation of organic alcohols and alkenes to carboxylic acids/esters.62... 

Similar to the addition of secondary phosphine-borane complexes to alkynes described in Scheme 6.137, the same hydrophosphination agents can also be added to alkenes under broadly similar reaction conditions, leading to alkylarylphosphines (Scheme 6.138) [274], Again, the expected anti-Markovnikov addition products were obtained exclusively. In some cases, the additions also proceeded at room temperature, but required much longer reaction times (2 days). Treatment of the phosphine-borane complexes with a chiral alkene such as (-)-/ -pinene led to chiral cyclohexene derivatives through a radical-initiated ring-opening mechanism. In related work, Ackerman and coworkers described microwave-assisted Lewis acid-mediated inter-molecular hydroamination reactions of norbornene [275]. 

Standard cyclisation methodology was used to access the cyclic monophosphinic acid derivative 78 by reaction of ammonium phosphonate and ethyldiisopropylamine, followed by the addition of chlorotrimethylsilane, with 2,2 -bis (bromomethyl)-l,l -biphenyl. Silane reduction of 78 gave the secondary phosphine. The secondary phosphine borane complex 79 could be used in alkylation or Michael addition reactions. For example the Michael adduct 80 was produced in high yield by treatment of 78 with a NaH suspension in THF followed by the addition of diethylvinylphosphonate . 

Chiral bis-phosphine acylplatinum complex 210 with a strong acid such as TfOH serves as an effective enantio-selective catalyst for aldol-type reactions of aldehydes with ketene silyl acetals (Equation (127)).486 The presence of water and oxygen in the catalyst preparation step is required to obtain the highly enantioselective catalyst. The intermediacy of a C-bound platinum enolate was suggested by IR and 31P NMR spectroscopies. 

Phosphine complexes, osmium, 19 642 Phosphine coordination complexes, of uranium, 25 436 Phosphine derivatives, 19 28 Phosphine oxide(s), 11 495-496 19 66 predicted deviations from Raoult s law based on hydrogen-bonding interactions, 8 814t in salicylic acid manufacture, 22 8 Phosphine oxide diols/triols, 11 501 Phosphine selenides, 22 90 Phosphinic acid, 19 20, 54-55 Phosphinic anhydride, 11 499 Phosphinothricin acetyltransferase (PAT) proteins, 13 360 Phosphite esters, 19 20 Phosphites, in VDC polymer stabilization, 25 720... 

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