Issue 7, 2010

Mechanochemical preparation of adducts (co-crystals and molecular salts) of 1,4-diazabicyclo-[2.2.2]-octane with aromatic polycarboxylic acids

Abstract

Solid-state adducts (co-crystals and molecular salts) of 1,4-diazabicyclo-[2.2.2]-octane (DABCO) with aromatic polycarboxylic acids (isophthalic acid, isoH2, dinicotinic acid, dinH2 and dipicolinic acid, dipH2) were prepared in the solid state by grinding and kneading techniques, and fully characterized via X-ray diffraction. The polycarboxylic acids differ for the presence/absence and position of a nitrogen atom in the aromatic ring; the extent of proton transfer, from the carboxylic groups on the acids to the nitrogen atoms on DABCO, reflects the trend of solution acidity of the three polycarboxylic acids.

Graphical abstract: Mechanochemical preparation of adducts (co-crystals and molecular salts) of 1,4-diazabicyclo-[2.2.2]-octane with aromatic polycarboxylic acids

Supplementary files

Article information

Article type
Paper
Submitted
02 nov. 2009
Accepted
15 janv. 2010
First published
03 févr. 2010

CrystEngComm, 2010,12, 2107-2112

Mechanochemical preparation of adducts (co-crystals and molecular salts) of 1,4-diazabicyclo-[2.2.2]-octane with aromatic polycarboxylic acids

S. Marivel, D. Braga, F. Grepioni and G. I. Lampronti, CrystEngComm, 2010, 12, 2107 DOI: 10.1039/B922915A

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