Phosphorus molecular weight

Phosphorus(III) oxide dissolves in several organic solvents, for example benzene, carbon disulphide the molecular weight in these solvents corresponds to the formula P40(, as does the density of the vapour, and the structure is ... 

The melting and boiling points of a series of similar covalent halides of a given element are found to increase from the fluoride to the iodide, i.e. as the molecular weight of the halide increases. Thus, the trihalides of phosphorus have melting points PF3 = 121.5 K. PCI3 = 161.2 K, PBrj = 233 K, PI3 = 334 K. 

The melting points of these esters are usually much lower than those of the corresponding 3 5 dinitrobenzoates their preparation, therefore, offers no advantages over the latter except for alcohols of high molecular weight and for polyhydroxy compounds. The reagent is, however, cheaper than 3 5 dinitrobenzoyl chloride it hydrolyses in the air so that it should either be stored under light petroleum or be prepared from the acid, when required, by the thionyl chloride or phosphorus pentachloride method. 

Attempted polymerization of ds-7,9 dioxabicyclo[4.3.0]nonane 43 with phosphorus pentafluoride as initiator at temperatures ranging from -25 to 0 °C provided only a cyclic dimer 44 in high yield35. Under similar conditions trans-7,9-dioxabicyclo-[4.3.0]nonane 45 polymerized almost instantly to polymer 46 with number average molecular weight of several thousands, along with a small amount of a cyclic dimer 47. 

A common theme in the speculated polymerization reactions discussed in this section is that the polymers were generally uncharacterized or were composed of small cyclic oligomers. No evidence for high molecular weight polymers from low-coordinate phosphorus compounds was obtained. Of course, multiple bond formation, not polymerization, was the focus of these studies. 

The monomer 19 can also be polymerized using analogous methods of initiation to those employed in organic polymer science. Radical initiators afford regioirregular polymers, whereas anionic initiators add selectively to the phosphorus atom of the P=C bond and thus yield a regioregular polymer [85]. The product of the initial addition of MeLi across the P=C bond, Mes(Me)P-CPh2Li, was identified spectroscopically. The polymers obtained from anionic initiation are spectroscopically identical to those obtained from the thermolysis. Reasonable molecular weights (ca. 5000-10,000 g mol 0 are obtained when methyllithium is used as an initiator. 

Although of limited success, this Ni-catalysed coupling strategy builds on a previous report of the successful, direct synthesis of poly(4,4 -diphenylphenyl-phosphine oxide) (70c) from bis(p-chlorophenyl)-phenylphosphine oxide (71) (Scheme 21) [66]. The white soluble material (70c) (Aj ax 280 nm) was found to have a single phosphorus environment by NMR spectroscopy, a comparatively high molecular weight (Mn= 15,300) together with a low molecular... 

F. S. Zhang, J. Ma, and Y. P, Cao, Phosphorus deficiency enhances root exudation of low-molecular weight organic acids and utilization of sparingly soluble inorganic phosphates by radish (Raphanus. sativus L.) and rape Bra.ssica napus L.) plants. 

An overview of the synthesis and characterization of a unique class of polymers with a phosphorus-nitrogen backbone Is presented, with a focus on poly(dichloro-phosphazene) as a common Intermediate for a wide variety of poly(organophosphazenes). Melt and solution polymerization techniques are Illustrated, Including the role of catalysts. The elucidation of chain structure and molecular weight by various dilute solution techniques Is considered. Factors which determine the properties of polymers derived from poly(dichlorophos-phazene) are discussed, with an emphasis on the role that the organic substituent can play In determining the final properties. 

When used purely as an insulator, foam densities can be as low as 0.02 to 0.08 g/cm3. In structural applications the foam s density can rise to 0.4 to 0.7 g/cm3. The use of fluorocarbons as blowing agents has largely given way to more environmentally friendly agents, such as low molecular weight hydrocarbons. We can impart flame retardancy by incorporating chlorine-or phosphorus-based compounds. 

Most of the methods of synthesis reported above present some limitations and constraints lack of solubility for polycationic phosphorus-containing dendrimers from generation 3 [2], dendrimers of weak molecular weight [4], difficulties to overcome cross Unking reactions [6], possibility only to incorporate phosphorus groups on the surface of dendrimers [3], etc. 

Phosphorus dendrimers are among the largest dendrimers reported till now (generation 12, molecular weight higher than 3 000000). 

MATHEY Phosphorus-Carbon Heterocyclic Chemistry The Rise of a New Domain McKILLOP Advanced Problems in Organic Reaction Mechanisms OBRECHT Solid Supported Combinatorial and Parallel Synthesis of Small-Molecular-Weight Compound Libraries... 

NR is c/ s -1,4-polyisoprcnc, of molecular weight 200,000-500,000, but it also contains a small level of highly important non-rubber constituents. Of these, the most important are the proteins, sugars and fatty acids which are antioxidants and activators of cure. Trace elements present include potassium, manganese, phosphorus, copper and iron which can act as catalysts for oxidation. 

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