Literature DB >> 11667384

Lithium and Cesium Ion-Pair Acidities of Dibenzyl Ketone. Aggregation of Lithium and Cesium Ion Pairs of the Enolate Ion and Dianion(1)(,).

Roustam Gareyev1, James C. Ciula, Andrew Streitwieser.   

Abstract

Spectral study of the cesium and lithium enolates of dibenzyl ketone (DBK) showed that both salts exist as contact ion pairs in THF solutions. The spectral data for the dicesium salt of DBK indicate that it exists as triple ions in which both cations are in contact with the dianion. The dilithium salt of DBK forms triple ions of two types in THF: in one, both cations are in contact with the DBK dianion, in the other, one of the lithium cations is solvent-separated. Evidence for dimerization of the ion pairs was obtained for both lithium and cesium enolates of DBK from UV-vis spectral (blue shift of the absorbance band at higher concentrations) and acidity (the decrease of pK at higher concentrations) studies. The dimerization constant for the cesium enolate of DBK obtained from the acidity data (3.5 x 10(3) M(-)(1)) is considered to be more accurate than that from the spectral analysis (1.7 x 10(3) M(-)(1)). The lithium enolate is much less dimerized than its cesium counterpart with a dimerization constant from acidity data of 4.2 x 10(2) M(-)(1). The first and second cesium pK values of DBK are 18.07 and 33.70, respectively, compared to the first lithium pK of 11.62.

Entities:  

Year:  1996        PMID: 11667384     DOI: 10.1021/jo960013o

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  10 in total

1.  Ion pair aggregates and reactions; experiment and theory.

Authors:  Andrew Streitwieser
Journal:  J Mol Model       Date:  2005-12-09       Impact factor: 1.810

2.  Enediolate-dilithium amide mixed aggregates in the enantioselective alkylation of arylacetic acids: structural studies and a stereochemical model.

Authors:  Yun Ma; Craig E Stivala; Ashley M Wright; Trevor Hayton; Jun Liang; Ivan Keresztes; Emil Lobkovsky; David B Collum; Armen Zakarian
Journal:  J Am Chem Soc       Date:  2013-05-31       Impact factor: 15.419

3.  Structure determination using the method of continuous variation: lithium phenolates solvated by protic and dipolar aprotic ligands.

Authors:  Laura L Tomasevich; David B Collum
Journal:  J Org Chem       Date:  2013-07-15       Impact factor: 4.354

4.  Azaaldol condensation of a lithium enolate solvated by N,N,N',N'-tetramethylethylenediamine: dimer-based 1,2-addition to imines.

Authors:  Timothy S De Vries; Angela M Bruneau; Lara R Liou; Hariharaputhiran Subramanian; David B Collum
Journal:  J Am Chem Soc       Date:  2013-03-04       Impact factor: 15.419

Review 5.  Perspectives on computational organic chemistry.

Authors:  Andrew Streitwieser
Journal:  J Org Chem       Date:  2009-06-19       Impact factor: 4.354

6.  Lithium phenolates solvated by tetrahydrofuran and 1,2-dimethoxyethane: structure determination using the method of continuous variation.

Authors:  Timothy S De Vries; Anandarup Goswami; Lara R Liou; Jocelyn M Gruver; Emily Jayne; David B Collum
Journal:  J Am Chem Soc       Date:  2009-09-16       Impact factor: 15.419

7.  Structures of beta-amino ester enolates: new strategies using the method of continuous variation.

Authors:  Lara R Liou; Anne J McNeil; Gilman E S Toombes; David B Collum
Journal:  J Am Chem Soc       Date:  2008-12-24       Impact factor: 15.419

8.  Lithium Enolates Derived from Pyroglutaminol: Mechanism and Stereoselectivity of an Azaaldol Addition.

Authors:  Michael J Houghton; Christopher J Huck; Stephen W Wright; David B Collum
Journal:  J Am Chem Soc       Date:  2016-08-08       Impact factor: 15.419

9.  Lithium enolates of simple ketones: structure determination using the method of continuous variation.

Authors:  Lara R Liou; Anne J McNeil; Antonio Ramirez; Gilman E S Toombes; Jocelyn M Gruver; David B Collum
Journal:  J Am Chem Soc       Date:  2008-03-13       Impact factor: 15.419

10.  Lithium Enolates Derived from Pyroglutaminol: Aggregation, Solvation, and Atropisomerism.

Authors:  Michael J Houghton; Naomi A Biok; Christopher J Huck; Russell F Algera; Ivan Keresztes; Stephen W Wright; David B Collum
Journal:  J Org Chem       Date:  2016-04-25       Impact factor: 4.354

  10 in total

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