1,8-Bis(dimethylamino)naphthalene

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1,8-Bis(dimethylamino)naphthalene
Proton sponge.svg
Proton-Sponge-from-xtal-1999-3D-balls-A.png
Names
IUPAC name
N,N,N',N'-tetramethylnaphthalene-1,8-diamine
Other names
Proton Sponge
Identifiers
20734-58-1 N
ChemSpider 80012 YesY
Jmol 3D model Interactive image
Interactive image
PubChem 88675
  • InChI=1S/C14H18N2/c1-15(2)12-9-5-7-11-8-6-10-13(14(11)12)16(3)4/h5-10H,1-4H3 YesY
    Key: GJFNRSDCSTVPCJ-UHFFFAOYSA-N YesY
  • InChI=1/C14H18N2/c1-15(2)12-9-5-7-11-8-6-10-13(14(11)12)16(3)4/h5-10H,1-4H3
    Key: GJFNRSDCSTVPCJ-UHFFFAOYAM
  • CN(C)C1=CC=CC2=C1C(=CC=C2)N(C)C
  • c1(cccc2cccc(N(C)C)c12)N(C)C
Properties
C14H18N2
Molar mass 214.31 g·mol−1
Melting point 47.8 °C (118.0 °F; 320.9 K)
Acidity (pKa) 12.1 (in water)[1]

18.62 (in acetonitrile)[2]
(acidity of the conjugate acid C14H18N2H+)
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

1,8-Bis(dimethylamino)naphthalene is a chemical compound that was first prepared in 1968[1] by Roger Alder FRS at the University of Bristol. It is often referred by the trade name Proton Sponge, a trademark of Sigma-Aldrich.[3][4] This compound is a diamine in which the two dimethylamino groups are attached on the same side or peri position of a naphthalene system. Proton-sponge has several very interesting properties; one is its very high basicity; another is its spectroscopic properties.

Structure and properties

With a pKa of 12.34 [1] for its conjugate acid in aqueous solution, 1,8-bis(dimethylamino)naphthalene is one of the strongest amine bases known, although it only absorbs protons 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 pairs.[3][5] However, the molecule is sterically hindered, making it a weak nucleophile. Because of this combination of properties, it has been used in organic synthesis as a highly selective non-nucleophilic base.

The spectroscopic properties of Proton-sponge are very interesting for researchers of molecular chemistry and have been researched for a long time. Proton-sponge emits a double fluorescence in various solutions due to the mixture of two ground state species.[4]

Preparation

This compound is commercially available; it may be prepared by the methylation of 1,8-diaminonaphthalene with iodomethane or dimethyl sulfate.[6]

Reactions

Proton-sponge is methylated by using dimethyl sulfate. The pKa of trimethylated Proton-sponge is 6.43 in aqueous solution.[citation needed]

Other proton sponges

Second generation proton sponges are known with even higher basicity. 1,8-bis(hexamethyltriaminophosphazenyl)naphthalene or HMPN[7] is prepared from 1,8-diaminonaphthalene by reaction with tris(dimethylamino)bromophosphonium bromide in the presence of triethylamine. HMPN has a pKBH+ of 29.9 in acetonitrile which is more than 11 orders of magnitude higher than Proton Sponge.

References

  1. ↑ 1.0 1.1 1.2 Lua error in package.lua at line 80: module 'strict' not found.
  2. ↑ I. Kaljurand, A. Kütt, L. Sooväli, T. Rodima, V. Mäemets, I. Leito, I. A. Koppel. Extension of the Self-Consistent Spectrophotometric Basicity Scale in Acetonitrile to a Full Span of 28 pKa Units: Unification of Different Basicity Scales. J. Org. Chem., 2005, 70, 1019–1028. doi:10.1021/jo048252w
  3. ↑ 3.0 3.1 Lua error in package.lua at line 80: module 'strict' not found.
  4. ↑ 4.0 4.1 Lua error in package.lua at line 80: module 'strict' not found.
  5. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  6. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  7. ↑ Lua error in package.lua at line 80: module 'strict' not found.

External links

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