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Nickel(II) Bis(acetylacetonate)
Nickel(II) bis(acetylacetonate) is a coordination complex with the formula [Ni(acac)2]3, where acac is the Ion, anion derived from deprotonation of acetylacetone. It is a dark green Paramagnetism, paramagnetic solid that is soluble in organic solvents such as toluene. It reacts with water to give the blue-green Metal aquo complex, diaquo complex Ni(acac)2(H2O)2. Structure and properties Anhydrous nickel(II) acetylacetonate exists as molecules of Ni3(acac)6. The three nickel atoms are approximately collinear and each pair of them is Bridging ligand, bridged by two μ2 oxygen atoms. Each nickel atom has Octahedral molecular geometry#Jahn–Teller effect, tetragonally distorted octahedral geometry, caused by the difference in the length of the Ni–O bonds between the bridging and non-bridging oxygens. Ni3(acac)6 molecules are almost Molecular symmetry, centrosymmetric, despite the non-centrosymmetric point group of the ''cis''-Ni(acac)2 "monomers," which is uncommon. The Trimer (che ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Coordination Complex
A coordination complex is a chemical compound consisting of a central atom or ion, which is usually metallic and is called the ''coordination centre'', and a surrounding array of chemical bond, bound molecules or ions, that are in turn known as ''ligands'' or complexing agents. Many metal-containing chemical compound, compounds, especially those that include transition metals (elements like titanium that belong to the periodic table's d-block), are coordination complexes. Nomenclature and terminology Coordination complexes are so pervasive that their structures and reactions are described in many ways, sometimes confusingly. The atom within a ligand that is bonded to the central metal atom or ion is called the donor atom. In a typical complex, a metal ion is bonded to several donor atoms, which can be the same or different. A Ligand#Polydentate and polyhapto ligand motifs and nomenclature, polydentate (multiple bonded) ligand is a molecule or ion that bonds to the central atom ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Magnetic Moment
In electromagnetism, the magnetic moment or magnetic dipole moment is the combination of strength and orientation of a magnet or other object or system that exerts a magnetic field. The magnetic dipole moment of an object determines the magnitude of torque the object experiences in a given magnetic field. When the same magnetic field is applied, objects with larger magnetic moments experience larger torques. The strength (and direction) of this torque depends not only on the magnitude of the magnetic moment but also on its orientation relative to the direction of the magnetic field. Its direction points from the south pole to the north pole of the magnet (i.e., inside the magnet). The magnetic moment also expresses the magnetic force effect of a magnet. The magnetic field of a magnetic dipole is proportional to its magnetic dipole moment. The dipole component of an object's magnetic field is symmetric about the direction of its magnetic dipole moment, and decreases as the inverse ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Dean–Stark Apparatus
upDean–Stark apparatus setup for an azeotrope with a solvent whose density is ''less than'' that of water: The Marcusson apparatus, Dean-Stark apparatus, Dean–Stark receiver, distilling trap, or Dean–Stark Head is a piece of laboratory glassware used in synthetic chemistry to collect water (or occasionally other liquid) from a reactor. It is used in combination with a reflux condenser and a distillation flask for the separation of water from liquids. This may be a continuous removal of the water that is produced during a chemical reaction performed at reflux temperature, such as in esterification reactions. The original setup by Julius Marcusson (invented in 1905) was refined by the American chemists Ernest Woodward Dean (1888–1959) and David Dewey Stark (1893–1979) in 1920 for determination of the water content in petroleum. Function left, A Dean–Stark apparatus in use; aluminium foil is used to reduce heat losses Two types of Dean–Stark traps exist – one ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Base (chemistry)
In chemistry, there are three definitions in common use of the word "base": '' Arrhenius bases'', '' Brønsted bases'', and '' Lewis bases''. All definitions agree that bases are substances that react with acid An acid is a molecule or ion capable of either donating a proton (i.e. Hydron, hydrogen cation, H+), known as a Brønsted–Lowry acid–base theory, Brønsted–Lowry acid, or forming a covalent bond with an electron pair, known as a Lewis ...s, as originally proposed by Guillaume-François Rouelle, G.-F. Rouelle in the mid-18th century. In 1884, Svante Arrhenius proposed that a base is a substance which dissociates in aqueous solution to form hydroxide ions OH−. These ions can react with Hydron (chemistry), hydrogen ions (H+ according to Arrhenius) from the dissociation of acids to form water in an acid–base reaction. A base was therefore a metal hydroxide such as NaOH or Calcium hydroxide, Ca(OH)2. Such aqueous hydroxide solutions were also described by ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Nickel Nitrate
Nickel (II) nitrate is the inorganic compound Ni(NO3)2 or any hydrate thereof. In the hexahydrate, the nitrate anions are not bonded to nickel. Other hydrates have also been reported: Ni(NO3)2.9H2O, Ni(NO3)2.4H2O, and Ni(NO3)2.2H2O. It is prepared by the reaction of nickel oxide with nitric acid: : NiO + 2 HNO3 + 5 H2O → Ni(NO3)2.6H2O The anhydrous nickel nitrate is typically not prepared by heating the hydrates. Rather it is generated by the reaction of hydrates with dinitrogen pentoxide or of nickel carbonyl with dinitrogen tetroxide: : Ni(CO)4 + 2 N2O4 → Ni(NO3)2 + 2 NO + 4 CO The hydrated nitrate is often used as a precursor to supported nickel catalysts. Structure Nickel(II) compounds with oxygenated ligands often feature octahedral coordination geometry. Two polymorphs of the tetrahydrate Ni(NO3)2.4H2O have been crystallized. In one the monodentate nitrate ligands are trans while in the other they are cis. Reactions and uses Nickel(II) nitr ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Ni(acac)2
Nickel(II) bis(acetylacetonate) is a coordination complex with the formula i(acac)2sub>3, where acac is the anion derived from deprotonation of acetylacetone. It is a dark green paramagnetic solid that is soluble in organic solvents such as toluene. It reacts with water to give the blue-green diaquo complex Ni(acac)2(H2O)2. Structure and properties Anhydrous nickel(II) acetylacetonate exists as molecules of Ni3(acac)6. The three nickel atoms are approximately collinear and each pair of them is bridged by two μ2 oxygen atoms. Each nickel atom has tetragonally distorted octahedral geometry, caused by the difference in the length of the Ni–O bonds between the bridging and non-bridging oxygens. Ni3(acac)6 molecules are almost centrosymmetric, despite the non-centrosymmetric point group of the ''cis''-Ni(acac)2 "monomers," which is uncommon. The trimeric structure allows all nickel centers to achieve an octahedral coordination. The trimer is only formed if intramolecular sharing ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Pyridine-N-oxide
Pyridine-''N''-oxide is the heterocyclic compound with the chemical formula, formula C5H5NO. This colourless, hygroscopic solid is the product of the oxidation of pyridine. Its synthesis was first reported by Jakob Meisenheimer, who used peroxybenzoic acid as the oxidant. The compound is used infrequently as an oxidizing reagent in organic synthesis. Structure The structure of pyridine-''N''-oxide is very similar to that of pyridine with respect to the parameters for the ring. The molecule is planar. The N–O distance is 1.34Å. The C–N–C angle is 124°, 7° wider than in pyridine. Synthesis The oxidation of pyridine can be achieved with a number of peroxy acids, including peracetic acid and peroxybenzoic acid. Oxidation can also be effected by a modified Dakin reaction using a urea–hydrogen peroxide complex, and sodium perborate or, using methylrhenium trioxide () as catalyst, with sodium percarbonate. Reactions Pyridine ''N''-oxide is five orders of magnitude less ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Inorganica Chimica Acta
''Inorganica Chimica Acta'' is a peer-reviewed scientific journal published since 1967 that covers original research and reviews of fundamental and applied aspects of inorganic chemistry. See also * List of scientific journals in chemistry This is a list of scientific journals in chemistry and its various subfields. For journals mainly about materials science, see List of materials science journals. A B * ''Beilstein Journal of Organic Chemistry'' * ''Biochemical Journal'' * ''B ... External links * Elsevier academic journals Inorganic chemistry journals Academic journals established in 1967 English-language journals Journals published between 13 and 25 times per year {{chem-journal-stub ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Cis–trans Isomerism
''Cis''–''trans'' isomerism, also known as geometric isomerism, describes certain arrangements of atoms within molecules. The prefixes "''cis''" and "''trans''" are from Latin: "this side of" and "the other side of", respectively. In the context of chemistry, ''cis'' indicates that the functional groups (substituents) are on the same side of some plane, while ''trans'' conveys that they are on opposing (transverse) sides. ''Cis''–''trans'' isomers are stereoisomers, that is, pairs of molecules which have the same formula but whose functional groups are in different orientations in three-dimensional space. ''Cis'' and ''trans'' isomers occur both in organic molecules and in inorganic coordination complexes. ''Cis'' and ''trans'' descriptors are not used for cases of conformational isomerism where the two geometric forms easily interconvert, such as most open-chain single-bonded structures; instead, the terms "''syn''" and "''anti''" are used. According to IUPAC, "geome ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Coordination Sphere
In coordination chemistry, the first coordination sphere refers to the array of molecules and ions (the ligands) directly attached to the central metal atom. The second coordination sphere consists of molecules and ions that attached in various ways to the first coordination sphere. First coordination sphere The first coordination sphere refers to the molecules that are attached directly to the metal. The interactions between the first and second coordination spheres usually involve hydrogen-bonding. For charged complexes, ion pairing is important. In hexamminecobalt(III) chloride ( o(NH3)6l3), the cobalt cation plus the 6 ammonia ligands comprise the first coordination sphere. The coordination sphere of this ion thus consists of a central MN6 core "decorated" by 18 N−H bonds that radiate outwards. Second coordination sphere Metal ions can be described as consisting of series of two concentric coordination spheres, the first and second. More distant from the second coo ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Steric Effects
Steric effects arise from the spatial arrangement of atoms. When atoms come close together there is generally a rise in the energy of the molecule. Steric effects are nonbonding interactions that influence the shape (conformational isomerism, conformation) and chemical reaction, reactivity of ions and molecules. Steric effects complement electronic effects, which dictate the shape and reactivity of molecules. Steric repulsive forces between overlapping electron clouds result in structured groupings of molecules stabilized by the way that opposites attract and like charges repel. Steric hindrance Steric hindrance is a consequence of steric effects. Steric hindrance is the slowing of chemical reactions due to steric bulk. It is usually manifested in ''intermolecular reactions'', whereas discussion of steric effects often focus on ''intramolecular interactions''. Steric hindrance is often exploited to control selectivity, such as slowing unwanted side-reactions. Steric hindran ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
