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39 relations: Acetonitrile, Acyl group, Aminolysis, Base (chemistry), Benzene, Bicyclic molecule, Bifunctional catalyst, Caprolactone, Carbanion, Carboxylic acid, Degree of polymerization, Deprotonation, Dispersity, Ditungsten tetra(hpp), End-group, Epimer, Ester, Ether, Guanidine, Horner–Wadsworth–Emmons reaction, Hydrogen bond, Journal of the American Chemical Society, Knoevenagel condensation, Ligand, Michael reaction, Monomer, Nitroaldol reaction, Phenol, Polycaprolactone, Polymerization, Pyrene, Radical initiator, Ring-opening polymerization, Sigma-Aldrich, Tautomer, Tetrahydrofuran, Transesterification, Ultraviolet–visible spectroscopy, Wittig reaction.
Acetonitrile
Acetonitrile is the chemical compound with the formula.
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Acyl group
An acyl group is a moiety derived by the removal of one or more hydroxyl groups from an oxoacid, including inorganic acids.
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Aminolysis
Aminolysis is any chemical reaction in which a molecule is split into two parts by reacting with a molecule of ammonia or an amine.
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Base (chemistry)
In chemistry, bases are substances that, in aqueous solution, release hydroxide (OH−) ions, are slippery to the touch, can taste bitter if an alkali, change the color of indicators (e.g., turn red litmus paper blue), react with acids to form salts, promote certain chemical reactions (base catalysis), accept protons from any proton donor, and/or contain completely or partially displaceable OH− ions.
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Benzene
Benzene is an important organic chemical compound with the chemical formula C6H6.
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Bicyclic molecule
A bicyclic molecule (bi.
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Bifunctional catalyst
A bifunctional catalyst is term coined to refer to a specific set of hydrogenation catalysts containing Lewis acid and Lewis base.
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Caprolactone
ε-Caprolactone or simply caprolactone is a lactone (a cyclic ester) possessing a seven-membered ring.
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Carbanion
A carbanion is an anion in which carbon is threevalent (forms three bonds) and bears a formal negative charge in at least one significant mesomeric contributor (resonance form).
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Carboxylic acid
A carboxylic acid is an organic compound that contains a carboxyl group (C(.
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Degree of polymerization
The degree of polymerization, or DP, is the number of monomeric units in a macromolecule or polymer or oligomer molecule.
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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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Dispersity
A monodisperse, or uniform, polymer is composed of molecules of the same mass.
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Ditungsten tetra(hpp)
Tetrakis(hexahydropyrimidinopyrimidine)ditungsten(II), known as ditungsten tetra(hpp), is the name of the coordination compound with the formula W2(hpp)4.
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End-group
End groups are an important aspect of polymer synthesis and characterization.
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Epimer
In stereochemistry, an epimer is one of a pair of stereoisomers.
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Ester
In chemistry, an ester is a chemical compound derived from an acid (organic or inorganic) in which at least one –OH (hydroxyl) group is replaced by an –O–alkyl (alkoxy) group.
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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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Guanidine
Guanidine is the compound with the formula HNC(NH2)2.
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Horner–Wadsworth–Emmons reaction
The Horner–Wadsworth–Emmons (HWE) reaction is a chemical reaction used in organic chemistry of stabilized phosphonate carbanions with aldehydes (or ketones) to produce predominantly E-alkenes.
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Hydrogen bond
A hydrogen bond is a partially electrostatic attraction between a hydrogen (H) which is bound to a more electronegative atom such as nitrogen (N), oxygen (O), or fluorine (F), and another adjacent atom bearing a lone pair of electrons.
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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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Knoevenagel condensation
The Knoevenagel condensation reaction is an organic reaction named after Emil Knoevenagel.
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Ligand
In coordination chemistry, a ligand is an ion or molecule (functional group) that binds to a central metal atom to form a coordination complex.
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Michael reaction
The Michael reaction or Michael addition is the nucleophilic addition of a carbanion or another nucleophile to an α,β-unsaturated carbonyl compound.
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Monomer
A monomer (mono-, "one" + -mer, "part") is a molecule that "can undergo polymerization thereby contributing constitutional units to the essential structure of a macromolecule".
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Nitroaldol reaction
The Henry Reaction (also referred to as the nitro-aldol reaction) is a classic carbon–carbon bond formation reaction in organic chemistry.
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Phenol
Phenol, also known as phenolic acid, is an aromatic organic compound with the molecular formula C6H5OH.
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Polycaprolactone
Polycaprolactone (PCL) is a biodegradable polyester with a low melting point of around 60 °C and a glass transition temperature of about −60 °C.
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Polymerization
In polymer chemistry, polymerization is a process of reacting monomer molecules together in a chemical reaction to form polymer chains or three-dimensional networks.
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Pyrene
Pyrene is a polycyclic aromatic hydrocarbon (PAH) consisting of four fused benzene rings, resulting in a flat aromatic system.
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Radical initiator
In chemistry, radical initiators are substances that can produce radical species under mild conditions and promote radical reactions.
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Ring-opening polymerization
In polymer chemistry, ring-opening polymerization (ROP) is a form of chain-growth polymerization, in which the terminal end of a polymer chain acts as a reactive center where further cyclic monomers can react by opening its ring system and form a longer polymer chain (see figure).
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Sigma-Aldrich
Sigma-Aldrich Corporation is an American chemical, life science and biotechnology company owned by Merck KGaA.
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Tautomer
Tautomers are constitutional isomers of organic compounds that readily interconvert.
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Tetrahydrofuran
Tetrahydrofuran (THF) is an organic compound with the formula (CH2)4O.
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Transesterification
In organic chemistry, transesterfication is the process of exchanging the organic group R″ of an ester with the organic group R′ of an alcohol.
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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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Wittig reaction
The Wittig reaction or Wittig olefination is a chemical reaction of an aldehyde or ketone with a triphenyl phosphonium ylide (often called a Wittig reagent) to give an alkene and triphenylphosphine oxide.
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References
[1] https://en.wikipedia.org/wiki/Triazabicyclodecene
