26 relations: Agostic interaction, Alkene, Amine, Benzene, Borrowing hydrogen, Carbon dioxide, Carbon monoxide, Carboxylic acid, Coordination complex, Formic acid, Grubbs' catalyst, Homogeneous catalysis, Hydrogen, Hydrogenation, Imine, James A. Ibers, Ketone, Kharasch addition, Lewis acids and bases, Methanol, Nitro compound, Recrystallization (chemistry), Ruthenium, Ruthenium(III) chloride, Triphenylphosphine, 1,2-Bis(diphenylphosphino)ethane.
Agostic interaction
Agostic interaction is a term in organometallic chemistry for the interaction of a coordinatively-unsaturated transition metal with a C−H bond, when the two electrons involved in the C−H bond enter the empty d-orbital of a transition metal, resulting in a three-center two-electron bond.
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Alkene
In organic chemistry, an alkene is an unsaturated hydrocarbon that contains at least one carbon–carbon double bond.
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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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Benzene
Benzene is an important organic chemical compound with the chemical formula C6H6.
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Borrowing hydrogen
Borrowing hydrogen catalysis, also called hydrogen autotransfer, is an important catalytic concept.
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Carbon dioxide
Carbon dioxide (chemical formula) is a colorless gas with a density about 60% higher than that of dry air.
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Carbon monoxide
Carbon monoxide (CO) is a colorless, odorless, and tasteless gas that is slightly less dense than air.
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Carboxylic acid
A carboxylic acid is an organic compound that contains a carboxyl group (C(.
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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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Formic acid
Formic acid, systematically named methanoic acid, is the simplest carboxylic acid.
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Grubbs' catalyst
Grubbs' catalysts are a series of transition metal carbene complexes used as catalysts for olefin metathesis.
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Homogeneous catalysis
In chemistry, homogeneous catalysis is catalysis in a solution by a soluble catalyst.
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Hydrogen
Hydrogen is a chemical element with symbol H and atomic number 1.
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Hydrogenation
Hydrogenation – to treat with hydrogen – is a chemical reaction between molecular hydrogen (H2) and another compound or element, usually in the presence of a catalyst such as nickel, palladium or platinum.
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Imine
An imine is a functional group or chemical compound containing a carbon–nitrogen double bond.
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James A. Ibers
James A. Ibers is a professor of chemistry at Northwestern University.
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Ketone
In chemistry, a ketone (alkanone) is an organic compound with the structure RC(.
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Kharasch addition
The Kharasch addition is an organic reaction and a metal-catalysed free radical addition of CXCl3 compounds (X.
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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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Methanol
Methanol, also known as methyl alcohol among others, is a chemical with the formula CH3OH (a methyl group linked to a hydroxyl group, often abbreviated MeOH).
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Nitro compound
Nitro compounds are organic compounds that contain one or more nitro functional groups (−2).
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Recrystallization (chemistry)
In chemistry, recrystallization is a technique used to purify chemicals.
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Ruthenium
Ruthenium is a chemical element with symbol Ru and atomic number 44.
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Ruthenium(III) chloride
Ruthenium(III) chloride is the chemical compound with the formula RuCl3.
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Triphenylphosphine
Triphenylphosphine (IUPAC name: triphenylphosphane) is a common organophosphorus compound with the formula P(C6H5)3 - often abbreviated to PPh3 or Ph3P.
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1,2-Bis(diphenylphosphino)ethane
1,2-Bis(diphenylphosphino)ethane (dppe) is an organophosphorus compound with the formula (Ph2PCH2)2 (Ph.
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Redirects here:
RuCl2(PPh3)3, RuCl2P3, Tris(triphenylphosphine)ruthenium dichloride.
References
[1] https://en.wikipedia.org/wiki/Dichlorotris(triphenylphosphine)ruthenium(II)