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21 relations: Angewandte Chemie, Aromatic hydrocarbon, Aromatic ring current, Aromaticity, Bond length, Chemical formula, Chemical shift, Cyclodecapentaene, Double bond, Hückel's rule, Homoaromaticity, Journal of the American Chemical Society, Methylene bridge, Naphthalene, Organic Syntheses, Proton nuclear magnetic resonance, Resonance (chemistry), Single bond, Springer Nature, X-ray crystallography, 1,5-Methano(10)annulene.
Angewandte Chemie
Angewandte Chemie (meaning "Applied Chemistry") is a weekly peer-reviewed scientific journal that is published by Wiley-VCH on behalf of the German Chemical Society (Gesellschaft Deutscher Chemiker).
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Aromatic hydrocarbon
An aromatic hydrocarbon or arene (or sometimes aryl hydrocarbon) is a hydrocarbon with sigma bonds and delocalized pi electrons between carbon atoms forming a circle.
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Aromatic ring current
An aromatic ring current is an effect observed in aromatic molecules such as benzene and naphthalene.
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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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Bond length
In molecular geometry, bond length or bond distance is the average distance between nuclei of two bonded atoms in a molecule.
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Chemical formula
A chemical formula is a way of presenting information about the chemical proportions of atoms that constitute a particular chemical compound or molecule, using chemical element symbols, numbers, and sometimes also other symbols, such as parentheses, dashes, brackets, commas and plus (+) and minus (−) signs.
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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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Cyclodecapentaene
Cyclodecapentaene or annulene is an annulene with molecular formula C10H10.
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Double bond
A double bond in chemistry is a chemical bond between two chemical elements involving four bonding electrons instead of the usual two.
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Hückel's rule
In organic chemistry, Hückel's rule estimates whether a planar ring molecule will have aromatic properties.
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Homoaromaticity
Homoaromaticity, in organic chemistry, refers to a special case of aromaticity in which conjugation is interrupted by a single sp3 hybridized carbon atom.
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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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Methylene bridge
In organic chemistry, a methylene bridge, methylene spacer, or methanediyl group is any part of a molecule with formula --; namely, a carbon atom bound to two hydrogen atoms and connected by single bonds to two other distinct atoms in the rest of the molecule.
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Naphthalene
Naphthalene is an organic compound with formula.
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Organic Syntheses
Organic Syntheses is a peer-reviewed scientific journal that was established in 1921.
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Proton nuclear magnetic resonance
Proton nuclear magnetic resonance (proton NMR, hydrogen-1 NMR, or 1H NMR) is the application of nuclear magnetic resonance in NMR spectroscopy with respect to hydrogen-1 nuclei within the molecules of a substance, in order to determine the structure of its molecules.
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Resonance (chemistry)
In chemistry, resonance or mesomerism is a way of describing delocalized electrons within certain molecules or polyatomic ions where the bonding cannot be expressed by one single Lewis structure.
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Single bond
In chemistry, a single bond is a chemical bond between two atoms involving two valence electrons.
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Springer Nature
Springer Nature is an academic publishing company created by the May 2015 merger of Springer Science+Business Media and Holtzbrinck Publishing Group's Nature Publishing Group, Palgrave Macmillan, and Macmillan Education.
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X-ray crystallography
X-ray crystallography is a technique used for determining the atomic and molecular structure of a crystal, in which the crystalline atoms cause a beam of incident X-rays to diffract into many specific directions.
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1,5-Methano(10)annulene
1,5-Methanoannulene, 1,5-methanoazulene or homoazulene is a hydrocarbon with chemical formula C11H12.
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1,6-Methanonaphthalene, 1,6-methano(10)annulene, Homonaphthalene.
References
[1] https://en.wikipedia.org/wiki/1,6-Methano(10)annulene
