Issue 31, 2005
From the journal:

CrystEngComm

Is conformational flexibility in a supramolecular reagent advantageous for high-yielding co-crystallization reactions?

Christer B. Aakeröy,a   John Despera  and  Joaquin F. Urbinaa  

a Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, USA

Abstract

A conformationally flexible tris-carboxylic acid has been employed in the construction of several co-crystals involving a variety of ditopic N-heterocyclic hydrogen-bond acceptors.

Graphical abstract: Is conformational flexibility in a supramolecular reagent advantageous for high-yielding co-crystallization reactions?

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Article information

DOI
https://doi.org/10.1039/B419029G
Article type
Paper
Submitted
20 Dec 2004
Accepted
03 Mar 2005
First published
10 Mar 2005

CrystEngComm, 2005,7, 193-201

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Is conformational flexibility in a supramolecular reagent advantageous for high-yielding co-crystallization reactions?

C. B. Aakeröy, J. Desper and J. F. Urbina, CrystEngComm, 2005, 7, 193 DOI: 10.1039/B419029G

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