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24 relations: Azulene, Carbene, Chemical formula, Conjugated system, Deprotonation, Diazo, Diels–Alder reaction, Dimer (chemistry), Double bond, Ferrocene, Fulvalenes, Hydrocarbon, Isomer, Journal of the American Chemical Society, Kelvin, Molecular symmetry, N-Butyllithium, Naphthalene, Organic semiconductor, Photodissociation, Sodium cyclopentadienide, Tetrathiafulvalene, Ultraviolet–visible spectroscopy, William von Eggers Doering.
Azulene
Azulene is an organic compound and an isomer of naphthalene.
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Carbene
In chemistry, a carbene is a molecule containing a neutral carbon atom with a valence of two and two unshared valence electrons.
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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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Conjugated system
In chemistry, a conjugated system is a system of connected p-orbitals with delocalized electrons in molecules which are conventionally represented as having alternating single and multiple bonds, which in general may lower the overall energy of the molecule and increase stability.
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Deprotonation
Deprotonation is the removal (transfer) of a proton (a hydrogen cation, H+) from a Brønsted–Lowry acid in an acid-base reaction.
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Diazo
Diazo refers to a type of organic compound called diazo compound that has two linked nitrogen atoms (azo) as a terminal functional group.
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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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Dimer (chemistry)
A dimer (di-, "two" + -mer, "parts") is an oligomer consisting of two monomers joined by bonds that can be either strong or weak, covalent or intermolecular.
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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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Ferrocene
Ferrocene is an organometallic compound with the formula Fe(C5H5)2.
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Fulvalenes
A fulvalene is a hydrocarbon obtained by formally cross-conjugating two rings through a common exocyclic double bond.
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Hydrocarbon
In organic chemistry, a hydrocarbon is an organic compound consisting entirely of hydrogen and carbon.
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Isomer
An isomer (from Greek ἰσομερής, isomerès; isos.
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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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Kelvin
The Kelvin scale is an absolute thermodynamic temperature scale using as its null point absolute zero, the temperature at which all thermal motion ceases in the classical description of thermodynamics.
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Molecular symmetry
Molecular symmetry in chemistry describes the symmetry present in molecules and the classification of molecules according to their symmetry.
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N-Butyllithium
n-Butyllithium (abbreviated n-BuLi) is an organolithium reagent.
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Naphthalene
Naphthalene is an organic compound with formula.
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Organic semiconductor
Organic semiconductors are solids whose building blocks are pi-bonded molecules or polymers made up by carbon and hydrogen atoms and – at times – heteroatoms such as nitrogen, sulfur and oxygen.
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Photodissociation
Photodissociation, photolysis, or photodecomposition is a chemical reaction in which a chemical compound is broken down by photons.
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Sodium cyclopentadienide
Sodium cyclopentadienide is an organosodium compound with the formula C5H5Na.
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Tetrathiafulvalene
Tetrathiafulvalene is an organosulfur compound with the formula (H2C2S2C)2.
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Ultraviolet–visible spectroscopy
Ultraviolet–visible spectroscopy or ultraviolet–visible spectrophotometry (UV–Vis or UV/Vis) refers to absorption spectroscopy or reflectance spectroscopy in the ultraviolet-visible spectral region.
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William von Eggers Doering
William von Eggers Doering (June 22, 1917 – January 3, 2011) was a Professor Emeritus at Harvard University and the former Chair of its Chemistry Department.
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Redirects here:
Bicyclopentadienylidene, Fulvalene complex, Pentafulvalene.
References
[1] https://en.wikipedia.org/wiki/Fulvalene
