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35 relations: Acetylacetone, Aldehyde, Aldol reaction, Aliphatic compound, Amine, Aromaticity, Atomic nucleus, Atomic orbital, Butyl group, Catalysis, Chemical compound, Chemical shift, Conjugate acid, Coordination complex, Denticity, Diels–Alder reaction, Diene, Dihydropyran, Electron configuration, Endogeny (biology), Ether, Europium, Heptafluorobutyric acid, Hexafluoroacetylacetone, HSAB theory, Journal of the American Chemical Society, Lanthanide, Lewis acids and bases, Metal acetylacetonates, Nuclear magnetic resonance spectroscopy, Paramagnetic nuclear magnetic resonance spectroscopy, Paramagnetism, Spectrometer, Stereoselectivity, TRISPHAT.
Acetylacetone
Acetylacetone is an organic compound that exists in two tautomeric forms that interconvert rapidly and are treated as a single compound in most applications.
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Aldehyde
An aldehyde or alkanal is an organic compound containing a functional group with the structure −CHO, consisting of a carbonyl center (a carbon double-bonded to oxygen) with the carbon atom also bonded to hydrogen and to an R group, which is any generic alkyl or side chain.
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Aldol reaction
The aldol reaction is a means of forming carbon–carbon bonds in organic chemistry.
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Aliphatic compound
In organic chemistry, hydrocarbons (compounds composed of carbon and hydrogen) are divided into two classes: aromatic compounds and aliphatic compounds (G. aleiphar, fat, oil) also known as non-aromatic compounds.
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Amine
In organic chemistry, amines are compounds and functional groups that contain a basic nitrogen atom with a lone pair.
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Aromaticity
In organic chemistry, the term aromaticity is used to describe a cyclic (ring-shaped), planar (flat) molecule with a ring of resonance bonds that exhibits more stability than other geometric or connective arrangements with the same set of atoms.
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Atomic nucleus
The atomic nucleus is the small, dense region consisting of protons and neutrons at the center of an atom, discovered in 1911 by Ernest Rutherford based on the 1909 Geiger–Marsden gold foil experiment.
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Atomic orbital
In quantum mechanics, an atomic orbital is a mathematical function that describes the wave-like behavior of either one electron or a pair of electrons in an atom.
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Butyl group
In organic chemistry, butyl is a four-carbon alkyl radical or substituent group with general chemical formula −C4H9, derived from either of the two isomers of butane.
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Catalysis
Catalysis is the increase in the rate of a chemical reaction due to the participation of an additional substance called a catalysthttp://goldbook.iupac.org/C00876.html, which is not consumed in the catalyzed reaction and can continue to act repeatedly.
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Chemical compound
A chemical compound is a chemical substance composed of many identical molecules (or molecular entities) composed of atoms from more than one element held together by chemical bonds.
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Chemical shift
In nuclear magnetic resonance (NMR) spectroscopy, the chemical shift is the resonant frequency of a nucleus relative to a standard in a magnetic field.
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Conjugate acid
A conjugate acid, within the Brønsted–Lowry acid–base theory, is a species formed by the reception of a proton (H+) by a base—in other words, it is a base with a hydrogen ion added to it.
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Coordination complex
In chemistry, a coordination complex consists of a central atom or ion, which is usually metallic and is called the coordination centre, and a surrounding array of bound molecules or ions, that are in turn known as ligands or complexing agents.
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Denticity
Denticity refers to the number of donor groups in a single ligand that bind to a central atom in a coordination complex.
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Diels–Alder reaction
The Diels–Alder reaction is an organic chemical reaction (specifically, a cycloaddition) between a conjugated diene and a substituted alkene, commonly termed the dienophile, to form a substituted cyclohexene derivative.
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Diene
In organic chemistry a diene or diolefin is a hydrocarbon that contains two carbon double bonds.
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Dihydropyran
Dihydropyran is a heterocyclic compound with the formula C5H8O.
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Electron configuration
In atomic physics and quantum chemistry, the electron configuration is the distribution of electrons of an atom or molecule (or other physical structure) in atomic or molecular orbitals.
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Endogeny (biology)
Endogenous substances and processes are those that originate from within an organism, tissue, or cell.
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Ether
Ethers are a class of organic compounds that contain an ether group—an oxygen atom connected to two alkyl or aryl groups.
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Europium
Europium is a chemical element with symbol Eu and atomic number 63.
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Heptafluorobutyric acid
Heptafluorobutyric acid (HFBA) is an organofluorine compound with the formula C3F7CO2H.
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Hexafluoroacetylacetone
Hexafluoroacetylacetone is the chemical compound with the nominal formula CF3C(O)CH2C(O)CF3 (often abbreviated as hfacH).
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HSAB theory
HSAB concept is an initialism for "hard and soft (Lewis) acids and bases".
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Journal of the American Chemical Society
The Journal of the American Chemical Society (also known as JACS) is a weekly peer-reviewed scientific journal that was established in 1879 by the American Chemical Society.
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Lanthanide
The lanthanide or lanthanoid series of chemical elements comprises the 15 metallic chemical elements with atomic numbers 57 through 71, from lanthanum through lutetium.
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Lewis acids and bases
A Lewis acid is a chemical species that contains an empty orbital which is capable of accepting an electron pair from a Lewis base to form a Lewis adduct.
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Metal acetylacetonates
Metal acetylacetonates are coordination complexes derived from the acetylacetonate anion and metal ions, usually transition metals.
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Nuclear magnetic resonance spectroscopy
Nuclear magnetic resonance spectroscopy, most commonly known as NMR spectroscopy or magnetic resonance spectroscopy (MRS), is a spectroscopic technique to observe local magnetic fields around atomic nuclei.
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Paramagnetic nuclear magnetic resonance spectroscopy
Paramagnetic NMR spectroscopy refers to NMR spectroscopy of paramagnetic compounds.
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Paramagnetism
Paramagnetism is a form of magnetism whereby certain materials are weakly attracted by an externally applied magnetic field, and form internal, induced magnetic fields in the direction of the applied magnetic field.
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Spectrometer
A spectrometer is a scientific instrument used to separate and measure spectral components of a physical phenomenon.
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Stereoselectivity
In chemistry, stereoselectivity is the property of a chemical reaction in which a single reactant forms an unequal mixture of stereoisomers during the non-stereospecific creation of a new stereocenter or during the non-stereospecific transformation of a pre-existing one.
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TRISPHAT
Tributylammonium TRISPHAT is an organic salt with the formula +. The anion features phosphorus(V) bonded to three tetrachlorocatecholate (C6Cl4O22−) ligands.
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Redirects here:
Chiral shift reagent, Eu(dpm)3, Eu(fod)3, Eufod.
References
[1] https://en.wikipedia.org/wiki/EuFOD
