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Phosphorus complexes

NMR spectroscopy of these phosphorus complexes has been used for structure elucidation. Depending on the bulkiness of the thiourea substituents, a single isomer (bulky) or two isomers (small size, example in Scheme 11 with two possibihties for the relative position of the cyano group)... [Pg.240]

The tetrahedral phosphorus complex 2010 is, likewise, readily oxidized by BTSP 1949 to give the complex 2011, with two PO groups as complex ligands, and HMDSO 7 [181] (Scheme 12.52). A similar oxidation of tetraphosphocubane is described elsewhere [182]. [Pg.292]

Nazarov, A. A. Dyson, P. J. Metal phosphorus complexes as antitumor agents. In Phosphorus Chemistry Catalysis and Material Science Applications, Vol. 37 (eds. Gonsalvi, L. Peruzzini, M.) 445-461 (Springer 2011). [Pg.6]

One explanation for the adverse effects of excessive phosphorus intakes on bone health of rodents is that of secondary hyperthyroidism (4,j>,6). Under these circumstances, PTH activities and cAMP urinary excretions would be expected to increase and blood serum phosphorus would be expected to increase. This in turn would be expected to result in formation of calcium-phosphorus complexes, decrease in serum ionized calcium, parathyroid stimulation and bone resorption. [Pg.91]

Metalloporphyrins containing low valent main group elements show hyper-type UV-visible spectra and the corresponding higher valent complexes show normal spectra. Despite this, the phosphorus complexes [P(OEP)R2] show spectra with distinctly hyper character, with two extra Soret bands apparent. The extra Soret band in hyper complexes has been assigned to charge transfer from the low... [Pg.326]

There is a recent review of two-coordinate phosphorus complexes.306 Malisch et a/.307 observed the reversible reaction (86), in which a metal-arsenic(III) double bond is formed, i.e. the M—As a bond is augmented by the arsenic lone pair to form a n bond system (since the cyclopentadienyl coligand is not coplanar with the M=As, the arsenic double bond is isolated). Complex (58) undergoes reactions typical of double bond molecules (Scheme 14). Phosphorus analogues have also been prepared (Scheme 15) the crystal structure of product (c) in Scheme 15 has been solved (59a). The d(W—P) of 2.181 A is shorter than the predicted rf(W=P) of 2.26 A, and the trigonal planar coordination of phosphorus indicates sp2 hybridization.308... [Pg.1052]

One of the most common applications of VCD is the AC determinations of chiral compounds. Two recent studies on anthracycline analogs and on pentacoordinate phosphorus complexes from our group are included below as examples. [Pg.201]

Although electrophilic character is expected for cationic phosphenium complexes, only a few examples have been reported. Mer-10 readily reacts with Nu- (Me-, OEt-) to generate 29 [Eq. (20)].20 This shows that mer-10 is susceptible to nucleophilic attack at the phosphenium phosphorus. Complex 29 is not obtained in the reaction of the corresponding phosphite complex (30) with Me- or OEt-. [Pg.115]

Phosphorus complexes are rather rare. The 8-coordinate complex U[P(CH2CH2PMe2)2]433 is isostructural with its thorium analogue. [Pg.1149]

The title reagent, studied as an oxidizing agent for furans,104 converts tetraphenylpyrrole into a phosphorus complex, which is hydrolyzed by water to the hydrochloride of 2-hydroxypyrrolenine (32).63 The methyl ether (91) is obtained when the crude complex is treated with sodium methoxide. [Pg.93]

Some defect spectroscopy measurements in n-type a-Si H have been interpreted in terms of close P D pairs (Kocka 1987) and there is also evidence of boron-phosphorus complexes in compensated a-Si H (Boyce et al. 1987). The driving force for pairing is the Coulomb interaction between oppositely charged states. Such a paired state must be treated as a distinct species in the defect reaction, which takes the form,... [Pg.196]

G. L. Simon and Lawrence F. Dahl First naked phosphorus complex... [Pg.898]

These elements, with five valence electrons, form bonds which are almost exclusively covalent in character. For this reason, it is not generally profitable to invoke an ionic description, however formal, and the definition of an ionic radius is usually of Httle value. An exception might be made in certain phosphorus complexes where an empirical radius may be defined and used in the usual way. [Pg.317]


See other pages where Phosphorus complexes is mentioned: [Pg.47]    [Pg.141]    [Pg.195]    [Pg.142]    [Pg.189]    [Pg.314]    [Pg.324]    [Pg.331]    [Pg.87]    [Pg.244]    [Pg.551]    [Pg.551]    [Pg.1092]    [Pg.61]    [Pg.273]    [Pg.294]    [Pg.378]    [Pg.148]    [Pg.151]    [Pg.325]    [Pg.52]    [Pg.160]    [Pg.50]    [Pg.222]    [Pg.224]    [Pg.226]    [Pg.228]    [Pg.230]    [Pg.232]    [Pg.234]    [Pg.236]    [Pg.238]    [Pg.240]    [Pg.242]    [Pg.244]   
See also in sourсe #XX -- [ Pg.5 ]




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2- aminopyridines, phosphorus complexes

Actinide complexes phosphorus oxides

Aluminum chloride-phosphorus oxychloride complex

Aluminum complexes phosphorus oxychloride

Arsenic complexes phosphorus ligands

Arsenic ligands phosphorus-palladium complexes

Borane complexes phosphorus-metal

Borane complexes phosphorus-nitrogen

Borane complexes phosphorus-transition metal

Boron-phosphorus complexes

Carbene complexes phosphorus-stabilized

Chiral phosphines phosphorus-palladium complexes

Chloride compounds phosphorus-palladium complexes

Cobalt complexes phosphorus ligands

Complex hydrides phosphorus halides

Complex phosphorus halides

Complexes of Phosphorus, Arsenic, and Antimony

Coordination complexes of phosphorus-carbon compounds

Cross-coupling reactions phosphorus-palladium complexes

Enzyme complexes phosphorus-containing compounds

Gold complexes phosphorus donor ligands

Gold complexes phosphorus-donors

Gold complexes with coordinated phosphorus atoms

Hafnium complexes phosphorus ligands

Iridium complexes phosphorus donors

Iridium complexes phosphorus ligands

Iron complexes phosphorus ligands

Ligand synthesis phosphorus-palladium complexes

Manganese complexes phosphorus ligands

Mercury complexes phosphorus ligands

Metal-phosphorus triple bond complexes

Molybdenum complexes phosphorus donor ligands

Nickel complexes phosphorus sulfide

Organometallic complexes of boron, silicon and phosphorus analogues

Osmium complexes phosphorus donors

Osmium complexes phosphorus trihalide

Osmium complexes phosphorus trihalides

Palladium complexes phosphorus donor atoms

Palladium complexes phosphorus donors

Palladium complexes phosphorus ligands

Palladium complexes sulfur-phosphorus ligands

Phosphine ligands phosphorus-palladium complexes

Phosphites, phosphorus-palladium complexes

Phosphorus chloride complexes

Phosphorus chlorides complex compounds

Phosphorus complexes amides

Phosphorus complexes porphyrins

Phosphorus complexes synthesis

Phosphorus compounds and complexes

Phosphorus heterocycles transition metal complexes

Phosphorus in (/-block metal complexes

Phosphorus ligands trigonal bipyramidal complexes

Phosphorus oxychloride metal complexes

Phosphorus reaction with carbene complexes

Phosphorus transition metal complex

Phosphorus trichloride complexes

Phosphorus trichloride metal complexes

Phosphorus trifluoride complexes

Phosphorus ylide complexes, carbonyl

Phosphorus ylide complexes, carbonyl stabilized

Phosphorus ylides carbene complexes

Phosphorus ylides transition metal complexes

Phosphorus, dithiocarbamate complexes

Phosphorus-containing compounds complexes with

Phosphorus-donor ligand complexes

Phosphorus-palladium complexes, nitrogen ligands

Phosphorus/metal interconversion complex

Platinum complexes chelating phosphorus ligands

Platinum complexes phosphorus donors

Rhodium complexes phosphorus donors

Ruthenium complexes phosphorus donors

Ruthenium complexes, reactions phosphorus ligand, addition

Silver complexes phosphorus-donors

Tetrahedral phosphorus complexes

Titanium complexes phosphorus

Uranium phosphorus complexes

Vanadium complexes phosphorus ligands

Ylides, phosphorus ylide complexes

Zirconium complexes phosphorus ligands

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