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Lanthanum(III) Iodide
Lanthanum(III) iodide is an inorganic compound containing lanthanum and iodine with the chemical formula . Synthesis Lanthanum(III) iodide can be synthesised by the reaction of lanthanum metal with mercury(II) iodide: :2 La + 3 HgI2 → 2 LaI3 + 3 Hg It can also be prepared from the elements, that is by the reaction of metallic lanthanum with iodine: :2 La + 3 I2 → 2 LaI3 While lanthanum(III) iodide solutions can be generated by dissolving lanthanum oxide in hydroiodic acid, the product will hydrolyse and form polymeric hydroxy species: :La2O3 + 6 HI → 2 LaI3 + 3 H2O ''→ further reactions'' Structure Lanthanum(III) iodide adopts the same crystal structure as plutonium(III) bromide, with 8-coordinate metal centres arranged in layers. This orthorhombic structure is typical of the triiodides of the lighter lanthanides (La–Nd), whereas heavier lanthanides tend to adopt the hexagonal bismuth(III) iodide structure. Reactivity and applications Lanthanum(III) iodide is very ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Inorganic Compound
In chemistry, an inorganic compound is typically a chemical compound that lacks carbon–hydrogen bonds, that is, a compound that is not an organic compound. The study of inorganic compounds is a subfield of chemistry known as '' inorganic chemistry''. Inorganic compounds comprise most of the Earth's crust, although the compositions of the deep mantle remain active areas of investigation. Some simple carbon compounds are often considered inorganic. Examples include the allotropes of carbon (graphite, diamond, buckminsterfullerene, etc.), carbon monoxide, carbon dioxide, carbides, and the following salts of inorganic anions: carbonates, cyanides, cyanates, and thiocyanates. Many of these are normal parts of mostly organic systems, including organisms; describing a chemical as inorganic does not necessarily mean that it does not occur within living things. History Friedrich Wöhler's conversion of ammonium cyanate into urea in 1828 is often cited as the starting point of modern ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Deliquescent
Hygroscopy is the phenomenon of attracting and holding water molecules via either absorption or adsorption from the surrounding environment, which is usually at normal or room temperature. If water molecules become suspended among the substance's molecules, adsorbing substances can become physically changed, e.g., changing in volume, boiling point, viscosity or some other physical characteristic or property of the substance. For example, a finely dispersed hygroscopic powder, such as a salt, may become clumpy over time due to collection of moisture from the surrounding environment. ''Deliquescent'' materials are sufficiently hygroscopic that they absorb so much water that they become liquid and form an aqueous solution. Etymology and pronunciation The word ''hygroscopy'' () uses combining forms of '' hygro-'' and '' -scopy''. Unlike any other ''-scopy'' word, it no longer refers to a viewing or imaging mode. It did begin that way, with the word ''hygroscope'' referring in th ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Iodides
An iodide ion is the ion I−. Compounds with iodine in formal oxidation state −1 are called iodides. In everyday life, iodide is most commonly encountered as a component of iodized salt, which many governments mandate. Worldwide, iodine deficiency affects two billion people and is the leading preventable cause of intellectual disability. Structure and characteristics of inorganic iodides Iodide is one of the largest monatomic anions. It is assigned a radius of around 206 picometers. For comparison, the lighter halides are considerably smaller: bromide (196 pm), chloride (181 pm), and fluoride (133 pm). In part because of its size, iodide forms relatively weak bonds with most elements. Most iodide salts are soluble in water, but often less so than the related chlorides and bromides. Iodide, being large, is less hydrophilic compared to the smaller anions. One consequence of this is that sodium iodide is highly soluble in acetone, whereas sodium chloride is not. T ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Lanthanum Compounds
Lanthanum is a chemical element with the symbol La and atomic number 57. It is a soft, ductile, silvery-white metal that tarnishes slowly when exposed to air. It is the eponym of the lanthanide series, a group of 15 similar elements between lanthanum and lutetium in the periodic table, of which lanthanum is the first and the prototype. Lanthanum is traditionally counted among the rare earth elements. Like most other rare earth elements, the usual oxidation state is +3. Lanthanum has no biological role in humans but is essential to some bacteria. It is not particularly toxic to humans but does show some antimicrobial activity. Lanthanum usually occurs together with cerium and the other rare earth elements. Lanthanum was first found by the Swedish chemist Carl Gustaf Mosander in 1839 as an impurity in cerium nitrate – hence the name ''lanthanum'', from the Ancient Greek (), meaning 'to lie hidden'. Although it is classified as a rare earth element, lanthanum is the 28th most abund ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Solid State Physics
Solid-state physics is the study of rigid matter, or solids, through methods such as quantum mechanics, crystallography, electromagnetism, and metallurgy. It is the largest branch of condensed matter physics. Solid-state physics studies how the large-scale properties of solid materials result from their atomic-scale properties. Thus, solid-state physics forms a theoretical basis of materials science. It also has direct applications, for example in the technology of transistors and semiconductors. Background Solid materials are formed from densely packed atoms, which interact intensely. These interactions produce the mechanical (e.g. hardness and elasticity), thermal, electrical, magnetic and optical properties of solids. Depending on the material involved and the conditions in which it was formed, the atoms may be arranged in a regular, geometric pattern (crystalline solids, which include metals and ordinary water ice) or irregularly (an amorphous solid such as common wi ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Tetragonal Crystal System
In crystallography, the tetragonal crystal system is one of the 7 crystal systems. Tetragonal crystal lattices result from stretching a cubic lattice along one of its lattice vectors, so that the cube becomes a rectangular prism with a square base (''a'' by ''a'') and height (''c'', which is different from ''a''). Bravais lattices There are two tetragonal Bravais lattices: the primitive tetragonal and the body-centered tetragonal. The base-centered tetragonal lattice is equivalent to the primitive tetragonal lattice with a smaller unit cell, while the face-centered tetragonal lattice is equivalent to the body-centered tetragonal lattice with a smaller unit cell. Crystal classes The point groups that fall under this crystal system are listed below, followed by their representations in international notation, Schoenflies notation, orbifold notation, Coxeter notation and mineral examples.Hurlbut, Cornelius S.; Klein, Cornelis, 1985, ''Manual of Mineralogy'', 20th ed., pp. ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Praseodymium Diiodide
Praseodymium diiodide is a chemical compound with the empirical formula of PrI2, consisting of praseodymium and iodine. It is an electride, with the ionic formula of Pr3+(I−)2e−, and therefore not a true praseodymium(II) compound. Preparation Praseodymium diiodide can be obtained by reacting praseodymium(III) iodide with metallic praseodymium at 800 °C to 900 °C in an inert atmosphere: :Pr + 2 PrI3 → 3 PrI2 It can also be obtained by reacting praseodymium with mercury(II) iodide where praseodymium displaces mercury: :Pr + HgI2 → PrI2 + Hg Praseodymium diiodide was first obtained by John D. Corbett in 1961. Properties Praseodymium diiodide is an opaque, bronze-coloured solid with a metallic lustre that is soluble in water. The lustre and very high conductivity can be explained by the formulation , with one electron per metal centre delocalised in a conduction band. The compound is extremely hygroscopic, and can only be stored and handled under carefull ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Electride
An electride is an ionic compound in which an electron is the anion. Solutions of alkali metals in ammonia are electride salts. In the case of sodium, these blue solutions consist of a(NH3)6sup>+ and solvated electrons: :Na + 6 NH3 → a(NH3)6sup>+ + e− The cation a(NH3)6sup>+ is an octahedral coordination complex. Solid salts Addition of a complexant like crown ether or -cryptand.html" ;"title="''2.2.2/nowiki>-cryptand">''2.2.2/nowiki>-cryptand to a solution of a(NH3)6sup>+e− affords a (crown ether)sup>+e− or a(2,2,2-crypt)sup>+e−. Evaporation of these solutions yields a blue-black paramagnetic solid with the formula a(2,2,2-crypt)sup>+e−. Most solid electride salts decompose above 240 K, although a24Al28O64sup>4+(e−)4 is stable at room temperature. In these salts, the electron is delocalized between the cations. Electrides are paramagnetic Paramagnetism is a form of magnetism whereby some materials are weakly attracted by an externally applied ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Lanthanum Diiodide
Lanthanum diiodide is an iodide of lanthanum, with the chemical formula of LaI2. It is an electride, actually having a chemical formula of La3+ I−)2e− Preparation Lanthanum diiodide can be obtained from the reduction of lanthanum(III) iodide with lanthanum metal under a vacuum at 800 to 900 °C: : It can also be obtained by reacting lanthanum and mercury(II) iodide: : It was first created by John D. Corbett in 1961. Properties Lanthanum diiodide is a blue-black solid with metallic lustre, which is easily hydrolyzed Hydrolysis (; ) is any chemical reaction in which a molecule of water breaks one or more chemical bonds. The term is used broadly for substitution, elimination, and solvation reactions in which water is the nucleophile. Biological hydrolysis ... into the iodide oxide. It has a MoSi2-type structure, with the space group ''I''4/''mmm'' (No. 139). References {{Lanthanide halides Lanthanum compounds Iodides Electrides Substances discovere ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Cyclopentadienyl Complex
A cyclopentadienyl complex is a coordination complex of a metal and cyclopentadienyl groups (, abbreviated as Cp−). Cyclopentadienyl ligands almost invariably bind to metals as a pentahapto (''η''5-) bonding mode. The metal–cyclopentadienyl interaction is typically drawn as a single line from the metal center to the center of the Cp ring.Elschenbroich, C. "Organometallics" (2006) Wiley-VCH: Weinheim. Examples ''Bis''cyclopentadienyl complexes are called metallocenes. A famous example of this type of complex is ferrocene (FeCp2), which has many analogues for other metals, such as chromocene (CrCp2), cobaltocene (CoCp2), and nickelocene (NiCp2). When the Cp rings are mutually parallel the compound is known as a sandwich complex. This area of organometallic chemistry was first developed in the 1950s. Bent metallocenes are represented by compounds of the type Cp2Lx Some are catalysts for ethylene polymerization. Metallocenes are often thermally stable, and find use as cata ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Metal Amides
Metal amides (systematic name metal azanides) are a class of coordination compounds composed of a metal center with amide ligands of the form NR2−. Amide ligands have two electron pairs available for bonding. In principle, they can be terminal or bridging. In these two examples, the dimethylamido ligands are both bridging and terminal: File:Tris(dimethylamino)aluminium dimer.png, Tris(dimethylamino)aluminium dimer File:Tris(dimethylamino)gallium dimer.png, Tris(dimethylamino)gallium dimer File:Ti(NMe2)4.png, Tetrakis(dimethylamino)titanium File:Ta(NMe2)5.png, Pentakis(dimethylamido)tantalum In practice, bulky amide ligands have a lesser tendency to bridge. Amide ligands may participate in metal-ligand π-bonding giving a complex with the metal center being co-planar with the nitrogen and substituents. Metal bis(trimethylsilyl)amides form a significant subcategory of metal amide compounds. These compounds tend to be discrete and soluble in organic solvents. Alkali metal amid ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
