1,8-Bis(dimethylamino)naphthalene is an organic compound with the formula CH(NMe) (Me = methyl). It is classified as a

peri-naphthalene In organic chemistry, peri-naphthalenes are particular derivatives of naphthalene with the formula C10H6-1,8-X2. Owing to the rigidity of the naphthalene skeleton, these substituents on the 1- and 8-positions are constrained to be relatively close ...

, i.e. a 1,8-disubstituted derivative of

naphthalene Naphthalene is an organic compound with formula . It is the simplest polycyclic aromatic hydrocarbon, and is a white crystalline solid with a characteristic odor that is detectable at concentrations as low as 0.08 ppm by mass. As an aromati ...

. Owing to its unusual structure, it exhibits exceptional basicity. It is often referred by the trade name Proton Sponge, a trademark of

Sigma-Aldrich Sigma-Aldrich (formally MilliporeSigma) is an American chemical, life science, and biotechnology company that is owned by the German chemical conglomerate Merck Group. Sigma-Aldrich was created in 1975 by the merger of Sigma Chemical Company a ...

Structure and properties

This compound is a diamine in which the two dimethylamino groups are attached on the same side ( peri position) of a

ring. This molecule has several very interesting properties; one is its very high basicity; another is its spectroscopic properties. With a p''K'' of 12.34 for its conjugate acid in aqueous solution, 1,8-bis(dimethylamino)naphthalene is one of the strongest

organic Organic may refer to: * Organic, of or relating to an organism, a living entity * Organic, of or relating to an anatomical organ Chemistry * Organic matter, matter that has come from a once-living organism, is capable of decay or is the product ...

bases. However, it only absorbs

proton A proton is a stable subatomic particle, symbol , H+, or 1H+ with a positive electric charge of +1 ''e'' elementary charge. Its mass is slightly less than that of a neutron and 1,836 times the mass of an electron (the proton–electron mass ...

s slowly—hence the trade name. The high basicity is attributed to the relief of strain upon protonation and/or the strong interaction between the nitrogen

lone pair In chemistry, a lone pair refers to a pair of valence electrons that are not shared with another atom in a covalent bondIUPAC ''Gold Book'' definition''lone (electron) pair''/ref> and is sometimes called an unshared pair or non-bonding pair. Lone ...

s. Additionally, although many aromatic amines such as aniline show reduced basicity (due to nitrogen being sp² hybridized; its lone pair occupying a 2p

orbital Orbital may refer to: Sciences Chemistry and physics * Atomic orbital * Molecular orbital * Hybrid orbital Astronomy and space flight * Orbit ** Earth orbit Medicine and physiology * Orbit (anatomy), also known as the ''orbital bone'' * Orbito ...

and interacting and being withdrawn by the aromatic ring), this is not possible in this molecule, as the nitrogens' methyl groups prevent its substituents from adopting a planar geometry, as this would require forcing methyl groups from each nitrogen atom into one another - thus the basicity is not reduced by this factor which is found in other molecules. It is

sterically hindered Steric effects arise from the spatial arrangement of atoms. When atoms come close together there is a rise in the energy of the molecule. Steric effects are nonbonding interactions that influence the shape ( conformation) and reactivity of ions ...

, making it a weak

nucleophile In chemistry, a nucleophile is a chemical species that forms bonds by donating an electron pair. All molecules and ions with a free pair of electrons or at least one pi bond can act as nucleophiles. Because nucleophiles donate electrons, they are ...

. Because of this combination of properties, it has been used in organic synthesis as a highly selective non-nucleophilic base.Alexander F. Pozharskii and Valery A. Ozeryanskii "Proton sponges and hydrogen transfer phenomena" Mendeleev Commun., 2012, 22, 117–124. Proton sponge also exhibits a very high affinity for boron, and is capable of displacing hydride from borane to form a boronium–borohydride ion pair.

Preparation

This compound is commercially available. It may be prepared by the

methylation In the chemical sciences, methylation denotes the addition of a methyl group on a substrate, or the substitution of an atom (or group) by a methyl group. Methylation is a form of alkylation, with a methyl group replacing a hydrogen atom. These t ...

of 1,8-diaminonaphthalene with iodomethane or

dimethyl sulfate Dimethyl sulfate (DMS) is a chemical compound with formula (CH3O)2SO2. As the diester of methanol and sulfuric acid, its formula is often written as ( CH3)2 SO4 or Me2SO4, where CH3 or Me is methyl. Me2SO4 is mainly used as a methylating agent ...

Related compounds

Other proton sponges

Second generation proton sponges are known with even higher basicity. 1,8-bis(hexamethyltriaminophosphazenyl)naphthalene or HMPN is prepared from 1,8-diaminonaphthalene by reaction with tris(dimethylamino)bromophosphonium bromide in the presence of triethylamine. HMPN has a pK of 29.9 in

acetonitrile Acetonitrile, often abbreviated MeCN (methyl cyanide), is the chemical compound with the formula and structure . This colourless liquid is the simplest organic nitrile (hydrogen cyanide is a simpler nitrile, but the cyanide anion is not clas ...

which is more than 11 orders of magnitude higher than Proton Sponge.

Hydride sponge

The chemical inverse of a proton sponge would be a hydride sponge. This property is exhibited by CH(BMe), which reacts with potassium hydride to afford K H(BMe)H

References

External links

Roger Alder research page
{{DEFAULTSORT:Bis(Dimethylamino)Naphthalene, 1, 8- Naphthylamines Reagents for organic chemistry Non-nucleophilic bases Dimethylamino compounds Substances discovered in the 1960s