Molecules 2011-01-01

Li⁺ selective podand-type fluoroionophore based on a diphenyl sulfoxide derivative bearing two pyrene groups.

Yukihiro Nishimura, Tetsuo Takemura, Sadao Arai

Index: Molecules 16(8) , 6844-57, (2011)

Full Text: HTML

Abstract

New podand-type fluoroionophores having two pyrene moieties: 2,2´-bis(1-pyrenylacetyloxy)diphenyl sulfide (3), 2,2´-bis(1-pyrenylacetyloxy)diphenyl sulfoxide (4), and 2,2´-bis(1-pyrenylacetyloxy)diphenyl sulfone (5), have been synthesized by connecting two 1-pyrenecarbonylmethyl groups with the two hydroxy groups of 2,2´-dihydroxydiphenyl sulfide, sulfoxide, and sulfone, respectively. Their complexation behavior toward alkali metal ions was examined by fluorescence spectroscopy. Among these fluoroionophores, compound 4, having a sulfinyl group, showed high selectivity toward Li⁺.


Related Compounds

Related Articles:

[A novel synthetic approach of tryptophan-containing cystine peptides by regioselective disulfide bond-forming reaction using the silyl chloride-sulfoxide system].

2000-02-01

[Yakugaku Zasshi 120(2) , 197-205, (2000)]

Disposition of diphenyl sulphoxide in rat.

1998-07-01

[Xenobiotica 28(7) , 715-22, (1998)]

Fluorescence emission mechanism and fluorescence properties of ternary Tb(III) complex with diphenyl sulphoxide and bipyridine.

2011-01-01

[Luminescence 26(6) , 754-61, (2011)]

[Fluorescence enhancement character of terbium perchlorate and thulium perchlorate with phenylcarboxymethyl sulfoxide coordination compounds].

2002-12-01

[Guang Pu Xue Yu Guang Pu Fen Xi 22(6) , 905-7, (2002)]

Ph2SO/Tf2O: a powerful promotor system in chemoselective glycosylations using thioglycosides.

2003-05-01

[Org. Lett. 5(9) , 1519-22, (2003)]

More Articles...