Metal Phosphide Nitrides

Metal phosphide nitrides include LiioP4N,o, Li7PN4, MgjPN2 (Chapter 4.5). 

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Phosphides. Compounds of phosphoms containing the more electropositive elements are generally called phosphides. A large number of binary phosphides as well as many ternary mixed-metal phosphides, metal phosphide nitrides, etc, are known. Some binary phosphides, such as those of nickel, exhibit a variety of stoichiometries (Ni P, Ni P2, Nq2P5, Ni2P, Ni P, NiP, NiP2, NiP ), whereas others, such as aluminum, form only one (AlP). Metalloids such as B and Si also form phosphides. 

Tetraamminelithium dihydrogenphosphide, 4590 Thorium dicarbide, 1023 Titanium carbide, 0558 Trimercury tetraphosphide, 4611 Tungsten carbide, 0560 Uranium carbide, 0559 Uranium dicarbide, 1024 Zinc phosphide, 4870 Zirconium dicarbide, 1025 METAL ACETYLIDES N-METAL DERIVATIVES METAL HYDRIDES METAL OXIDES METAL SULFIDES NITRIDES... 

Multiatom metal, metal oxide, metal sulfide, metal carbide, metal nitride, or metal phosphide nanoclusters that are so small that they have properties different from those of the corresponding bulk materials... 

Ignition or explosive reaction with metals (e.g., aluminum, antimony powder, bismuth powder, brass, calcium powder, copper, germanium, iron, manganese, potassium, tin, vanadium powder). Reaction with some metals requires moist CI2 or heat. Ignites with diethyl zinc (on contact), polyisobutylene (at 130°), metal acetylides, metal carbides, metal hydrides (e.g., potassium hydride, sodium hydride, copper hydride), metal phosphides (e.g., copper(II) phosphide), methane + oxygen, hydrazine, hydroxylamine, calcium nitride, nonmetals (e.g., boron, active carbon, silicon, phosphoms), nonmetal hydrides (e.g., arsine, phosphine, silane), steel (above 200° or as low as 50° when impurities are present), sulfides (e.g., arsenic disulfide, boron trisulfide, mercuric sulfide), trialkyl boranes. 

In the fifteen years since publication of the first edition of Comprehensive Coordination Chemistry (CCC, 1987), group 5 chemistry has been part of the intensive development of ceramic, optical, and magnetic materials based upon metal borides, nitrides, phosphides, oxides, and sulfides. A major impetus came from the discovery of the high-temperature superconducting oxides. In addition, the search for new routes to these materials via sol-gel or chemical vapor deposition techniques has spurred growth in metal amido, oxo, alkoxo, thio, and carboxylato chemistry. 

Nanostructured materials, obtainable as fine powders, thin films or in bulk forms, often exhibit properties dramatically different from those of the same materials in larger more ordinary forms. The latter are often unknown in the case of cavity structures which are characteristic of the material itself. Nanostructures of other kinds, for example, nanotubes, nanowires or nanocrystals can be formed with metal phosphides (Chapter 8) and phosphorus nitrides (Chapter 4.5). 

The majority of metal phosphides have a metal arsenide analogue which they usually resanble in properties and structure (Table 8.2). Metal phosphides, arsenides and nitrides not infrequently exhibit properties similar to those of metal carbides, silicides and germanides. Some metal phosphides are very useful semiconductors, while others shew superconduction or a variety of magnetic properties. Light-emitting diodes (LEDs) and nanostructured materials are other modem applications (Chapter 12.19). 

The metal-rich transition metal phosphides (<60% P) are dark coloured and insoluble in water, they have high chemical and thermal stability, they are dense, hard and brittle and have high thermal and electrical conductivities. These properties they have in common with the transition metal borides and silicides (and in some cases carbides and nitrides) to which they are often structurally related. With few exceptions, the transition metal phosphides, borides and silicides are not attacked by dilute acids and bases and may remain unaffected by hot concentrated mineral acids. 

Most of the studies on catalytic activity of the 1st, 2nd and 3rd TMS supported on carbon have been using various model compounds, although to a lesser extent real feeds have also been included in the studies. In this case, the Fe supported on AC have attracted some attention. In recent years, the carbon-supported metal carbides, nitrides and phosphides were also tested as catalysts for hydroprocessing reactions. 

Noble metals (NM) supported on carbons have been tested as catalysts for various model reactions, as well as for real feeds. In this regard, HDS, HDN, HCR and HDO activities were determined. In similar reactions, metal carbides, metal nitrides and metal phosphides supported on various forms of carbon have also been receiving attention. 

In most cases, the energy of a nonmetal atom is lowered by the addition of an electron. However, energy is always required to add more than one electron. The necessary energy is often supplied by other processes that occur simultaneously (such as an attraction between positive and negative ions). Nonmetal ions with a charge of —3 are rare. However, some metal nitrides containing the nitride ion, and some metal phosphides containing the phosphide ion, P , are known. 

Phosphides resemble in many ways the metal borides (p. 145), earbides (p. 297), and nitrides (p. 417), and there are the same diffieulties in elassifieation and deseription of bonding. Perhaps the least-eontentious proeedure is to elassify aeeording to stoiehiometry, i.e. (a) metal-rieh phosphides (M/P >1), (b) monophosphides (M/P =1), and (e) phosphorus-rieh phosphides (M/P < 1) ... 

Such reactions are discussed at appropriate points throughout the book as each individual compound is being considered. A particularly important set of reactions in this category is the synthesis of element hydrides by hydrolysis of certain sulfides (to give H2S), nitrides (to give NH3), phosphides (PH3), carbides (C Hm), borides (B Hm), etc. Useful reviews are available on hydrometallurgy (the recovery of metals by use of aqueous solutions at relatively low temperatures), hydrothermal syntheses and the use of supercritical water as a reaction medium for chemistry. 

Soft, silver white metal that melts in the hand (29.8 °C) and remains liquid up to 2204 °C (difference 2174 °C, suitable for special thermometers). Gallium is quite widespread, but always in small amounts in admixtures. Its "career" took off with the advent of semiconductors. Ga arsenide and Ga phosphide, which are preferential to silicon in some applications, have extensive uses in microchips, diodes, lasers, and microwaves. The element is found in every mobile phone and computer. Ga nitride (GaN) is used in UV LEDs (ultraviolet light-emitting diodes). In this manner, a curiosity was transformed into a high-tech speciality. 

The extension of this approach to artificial leaves based on titanates, niobates, tantalates, metal nitrides and phosphides, metal sulfides, and other transition metal oxides appears possible and useful in order to enhance the photocatalytic efficiency. In addition, the construction of multicomponent systems such as Ti02-CdS or MoS2-CdSe for overall water splitting could also lead to further improvements. This... 

Most nonmetallic elements will react with the group IA and IIA metals to give binary compounds. Heating the metals with nitrogen or phosphorus gives nitrides and phosphides of the metals. 

No, the editor didn t know what this name meant either.) It means salts of the triva-lent anions of Group V, restricted in [1] to arsenides, antimonides and bismuthides and prepared by reaction of sodium pnictides with anhydrous halides of transition and lanthanide metals. This violently exothermic reaction may initiate as low as 25°C. Avoidance of hydrated halides is cautioned since these are likely to react uncontrollably on mixing. Another paper includes a similar reaction of phosphides, initiated by grinding [2], Nitrides are reported made from the thermally initiated reaction of sodium azide with metal halides, a very large sealed ampoule is counselled to contain the nitrogen [3],... 

These are usually reactions of anhydrous transition and B metal halides with dry alkali metal salts such as the sulphides, nitrides, phosphides, arsenides etc. to give exchange of anions. They tend to be very exothermic with higher valence halides and are frequently initiated by mild warming or grinding. Metathesis is... 

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