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Tetracyanonickelate
The cyanonickelates are a class of chemical compound containing anions consisting of nickel atoms, and cyanide groups. The most important of these are the tetracyanonickelates containing four cyanide groups per nickel. The tetracyanonickelates contain the [Ni(CN)4]2− anion. This can exist in solution or in solid salts. The ion has cyanide groups arranged in a square around the central nickel ion. The symmetry of the ion is Dihedral symmetry in three dimensions, D4''h''. The distance from the nickel atom to the carbon is 1.87 Å, and the carbon-nitrogen distance is 1.16 Å. Tetracyanonickelate(II) can be oxidised electrochemically in solution to yield tetracyanonickelate(III) [Ni(CN)4]−. [Ni(CN)4]− is unstable and Ni(III) oxidises the cyanide to cyanate OCN−. Tetracyanonickelate(III) can add two more cyanide groups to form hexacyanonickelate(III). In combination with alkyldiamines, and other metal ions, tetracyanonickelate ions can form cage structure that can ac ...
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Tetracyanonickelate(II)-3D-balls
The cyanonickelates are a class of chemical compound containing anions consisting of nickel atoms, and cyanide groups. The most important of these are the tetracyanonickelates containing four cyanide groups per nickel. The tetracyanonickelates contain the [Ni(CN)4]2− anion. This can exist in solution or in solid salts. The ion has cyanide groups arranged in a square around the central nickel ion. The symmetry of the ion is Dihedral symmetry in three dimensions, D4''h''. The distance from the nickel atom to the carbon is 1.87 Å, and the carbon-nitrogen distance is 1.16 Å. Tetracyanonickelate(II) can be oxidised electrochemically in solution to yield tetracyanonickelate(III) [Ni(CN)4]−. [Ni(CN)4]− is unstable and Ni(III) oxidises the cyanide to cyanate OCN−. Tetracyanonickelate(III) can add two more cyanide groups to form hexacyanonickelate(III). In combination with alkyldiamines, and other metal ions, tetracyanonickelate ions can form cage structure that can ac ...
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Potassium Tetracyanonickelate
Potassium tetracyanonickelate is the inorganic compound with the formula K2Ni(CN)4. It is usually encountered as the monohydrate but the anhydrous salt is also known. Both are yellow, water-soluble, diamagnetic solids. The salt consists of potassium ions and the tetracyanonickelate coordination complex, which is square planar. ICSD number 24099 Preparation Potassium tetracyanonickelate is prepared by treating aqueous solutions of nickel(II) salts with potassium cyanide. The synthesis is often conducted stepwise, precipitating the nickel dicyanide coordination polymer first. This route allows removal of excess potassium salts: : Ni2+ + 2KCN → Ni(CN)2 + 2K+ : Ni(CN)2 + 2KCN → K2 i(CN)4This procedure yields the monohydrate. That solid dehydrates at 100 °C. Reactions The N-terminus of the cyanide ligand is basic and nucleophilic. The complex binds four equivalents of boron trifluoride Boron trifluoride is the inorganic compound with the formula BF3. This pungent, colourle ...
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Hofmann Clathrates
In inorganic chemistry, Hofmann clathrates refers to materials with the formula Ni(CN)2(NH3)(C6H6). These materials are a type of coordination polymer. They have attracted attention because they can be used to separate xylenes. On a conceptual level, Hofmann clathrates can be viewed as forerunners to metal-organic frameworks (MOFs). Structures The empirical formula Ni(CN)2(NH3)(C6H6) reflects the presence of two types of nickel(II) centers, one of which is the square-planar tetracyanonickelate, i(CN)4sup>2-. The second kind of nickel site consists of i(NH3)2sup>2+ groups that are connected to the Ni-CN nitrogens. Thus cyanide serves as a bridging ligand. The linking of the i(CN)4sup>2- and ''trans''- i(NH3)2sup>2+ subunits results in a sheet-like polymer. Voids between these sheets, defined by the ammonia ligands, are occupied by benzene molecules. Variations Many variations of Hofmann clathrates have been reported. The ammonia ligands can be replaced by diamines. Tetra ...
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Hofmann Clathrate
In inorganic chemistry, Hofmann clathrates refers to materials with the formula Ni(CN)2(NH3)(C6H6). These materials are a type of coordination polymer. They have attracted attention because they can be used to separate xylenes. On a conceptual level, Hofmann clathrates can be viewed as forerunners to metal-organic frameworks (MOFs). Structures The empirical formula Ni(CN)2(NH3)(C6H6) reflects the presence of two types of nickel(II) centers, one of which is the square-planar tetracyanonickelate, i(CN)4sup>2-. The second kind of nickel site consists of i(NH3)2sup>2+ groups that are connected to the Ni-CN nitrogens. Thus cyanide serves as a bridging ligand. The linking of the i(CN)4sup>2- and ''trans''- i(NH3)2sup>2+ subunits results in a sheet-like polymer. Voids between these sheets, defined by the ammonia ligands, are occupied by benzene molecules. Variations Many variations of Hofmann clathrates have been reported. The ammonia ligands can be replaced by diamines. Tetra ...
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Potassium Tetracyanonickelate Solution
Potassium is the chemical element with the symbol K (from Neo-Latin ''kalium'') and atomic number19. Potassium is a silvery-white metal that is soft enough to be cut with a knife with little force. Potassium metal reacts rapidly with atmospheric oxygen to form flaky white potassium peroxide in only seconds of exposure. It was first isolated from potash, the ashes of plants, from which its name derives. In the periodic table, potassium is one of the alkali metals, all of which have a single valence electron in the outer electron shell, that is easily removed to create an ion with a positive charge – a cation, that combines with anions to form salts. Potassium in nature occurs only in ionic salts. Elemental potassium reacts vigorously with water, generating sufficient heat to ignite hydrogen emitted in the reaction, and burning with a lilac- colored flame. It is found dissolved in sea water (which is 0.04% potassium by weight), and occurs in many minerals such as orthoclase, a c ...
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Nickel
Nickel is a chemical element with symbol Ni and atomic number 28. It is a silvery-white lustrous metal with a slight golden tinge. Nickel is a hard and ductile transition metal. Pure nickel is chemically reactive but large pieces are slow to react with air under standard conditions because a passivation layer of nickel oxide forms on the surface that prevents further corrosion. Even so, pure native nickel is found in Earth's crust only in tiny amounts, usually in ultramafic rocks, and in the interiors of larger nickel–iron meteorites that were not exposed to oxygen when outside Earth's atmosphere. Meteoric nickel is found in combination with iron, a reflection of the origin of those elements as major end products of supernova nucleosynthesis. An iron–nickel mixture is thought to compose Earth's outer and inner cores. Use of nickel (as natural meteoric nickel–iron alloy) has been traced as far back as 3500 BCE. Nickel was first isolated and classified as an e ...
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Cyanide
Cyanide is a naturally occurring, rapidly acting, toxic chemical that can exist in many different forms. In chemistry, a cyanide () is a chemical compound that contains a functional group. This group, known as the cyano group, consists of a carbon atom triple-bonded to a nitrogen atom. In inorganic cyanides, the cyanide group is present as the anion . Soluble salts such as sodium cyanide (NaCN) and potassium cyanide (KCN) are highly toxic. Hydrocyanic acid, also known as hydrogen cyanide, or HCN, is a highly volatile liquid that is produced on a large scale industrially. It is obtained by acidification of cyanide salts. Organic cyanides are usually called nitriles. In nitriles, the group is linked by a covalent bond to carbon. For example, in acetonitrile (), the cyanide group is bonded to methyl (). Although nitriles generally do not release cyanide ions, the cyanohydrins do and are thus rather toxic. Bonding The cyanide ion is isoelectronic with carbon monoxide a ...
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Dihedral Symmetry In Three Dimensions
In geometry, dihedral symmetry in three dimensions is one of three infinite sequences of point groups in three dimensions which have a symmetry group that as an abstract group is a dihedral group Dih''n'' (for ''n'' ≥ 2). Types There are 3 types of dihedral symmetry in three dimensions, each shown below in 3 notations: Schönflies notation, Coxeter notation, and orbifold notation. ;Chiral: *''Dn'', 'n'',2sup>+, (22''n'') of order 2''n'' – dihedral symmetry or para-n-gonal group (abstract group: ''Dihn''). ;Achiral: *''Dnh'', 'n'',2 (*22''n'') of order 4''n'' – prismatic symmetry or full ortho-n-gonal group (abstract group: ''Dihn'' × ''Z''2). *''Dnd'' (or ''Dnv''), ''n'',2+ (2*''n'') of order 4''n'' – antiprismatic symmetry or full gyro-n-gonal group (abstract group: ''Dih''2''n''). For a given ''n'', all three have ''n''-fold rotational symmetry about one axis (rotation by an angle of 360°/''n'' does not change the object), and 2-fold rotational symmetr ...
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Cyanate
Cyanate is an anion with the structural formula , usually written . It also refers to any salt containing it, such as ammonium cyanate. It is an isomer of the much less stable fulminate anion .William R. Martin and David W. Ball (2019): "Small organic fulminates as high energy materials. Fulminates of acetylene, ethylene, and allene". ''Journal of Energetic Materials'', volume 31, issue 7, pages 70-79. A cyanate ester is an organic compound containing the cyanate group. The cyanate ion is an ambidentate ligand, forming complexes with a metal ion in which either the nitrogen or oxygen atom may be the electron-pair donor. It can also act as a bridging ligand. Cyanate ion The three atoms in a cyanate ion lie on a straight line, giving the ion a linear structure. The electronic structure is described most simply as : :Ö̤−C≡N: with a single C−O bond and a triple C≡N bond. The infrared spectrum of a cyanate salt has a band at ca. 2096 cm−1; such a high frequen ...
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Diamine
A diamine is an amine with exactly two amino groups. Diamines are used as monomers to prepare polyamides, polyimides, and polyureas. The term ''diamine'' refers mostly to primary diamines, as those are the most reactive. In terms of quantities produced, 1,6-diaminohexane (a precursor to Nylon 6-6) is most important, followed by ethylenediamine. Vicinal diamines (1,2-diamines) are a structural motif in many biological compounds and are used as ligands in coordination chemistry. Aliphatic diamines Linear * 1 carbon: methylenediamine (diaminomethane) of theoretical interest only * 2 carbons: ethylenediamine (1,2-diaminoethane). Related derivatives include the N-alkylated compounds, 1,1-dimethylethylenediamine, 1,2-dimethylethylenediamine, ethambutol, tetrakis(dimethylamino)ethylene, TMEDA. File:Ethylene_diamine.png, Ethylenediamine * 3 carbons: 1,3-diaminopropane (propane-1,3-diamine) * 4 carbons: putrescine (butane-1,4-diamine) * 5 carbons: cadaverine (pentane-1,5-diamine) ...
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Amines
In chemistry, amines (, ) are compounds and functional groups that contain a basic nitrogen atom with a lone pair. Amines are formally derivatives of ammonia (), wherein one or more hydrogen atoms have been replaced by a substituent such as an alkyl or aryl group (these may respectively be called alkylamines and arylamines; amines in which both types of substituent are attached to one nitrogen atom may be called alkylarylamines). Important amines include amino acids, biogenic amines, trimethylamine, and aniline; Inorganic derivatives of ammonia are also called amines, such as monochloramine (). The substituent is called an amino group. Compounds with a nitrogen atom attached to a carbonyl group, thus having the structure , are called amides and have different chemical properties from amines. Classification of amines Amines can be classified according to the nature and number of substituents on nitrogen. Aliphatic amines contain only H and alkyl substituents. Aromatic ...
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Dimethylformamide
Dimethylformamide is an organic compound with the formula ( CH3)2NC(O)H. Commonly abbreviated as DMF (although this initialism is sometimes used for dimethylfuran, or dimethyl fumarate), this colourless liquid is miscible with water and the majority of organic liquids. DMF is a common solvent for chemical reactions. Dimethylformamide is odorless, but technical-grade or degraded samples often have a fishy smell due to impurity of dimethylamine. Dimethylamine degradation impurities can be removed by sparging samples with an inert gas such as argon or by sonicating the samples under reduced pressure. As its name indicates, it is structurally related to formamide, having two methyl groups in the place of the two hydrogens. DMF is a polar (hydrophilic) aprotic solvent with a high boiling point. It facilitates reactions that follow polar mechanisms, such as SN2 reactions. Structure and properties As for most amides, the spectroscopic evidence indicates partial double bond charact ...
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