A stereoselectively deuterated supramolecular motif to probe the role of solvent during self-assembly processes

S. Cantekin; Y. Nakano; J.C. Everts; P.P.A.M. Schoot, van der; E.W. Meijer; A.R.A. Palmans

doi:10.1039/c2cc17284d

A stereoselectively deuterated supramolecular motif to probe the role of solvent during self-assembly processes

S. Cantekin
, Y. Nakano
, J.C. Everts
, P.P.A.M. Schoot, van der
, E.W. Meijer
, A.R.A. Palmans

Research output: Contribution to journal › Article › Academic › peer-review

51 Citations (Scopus)

1 Downloads (Pure)

Abstract

Small changes in the alkane solvent structure in combination with temperature effects lead to four different conformations of stereoselectively deuterated benzene-1,3,5-tricarboxamides in the aggregated state, affecting the expression of the supramolecular chirality and highlighting the role of the solvent structure in self-assembly processes.

Original language	English
Pages (from-to)	3803-3805
Journal	Chemical Communications, ChemComm
Volume	48
Issue number	32
DOIs	https://doi.org/10.1039/c2cc17284d
Publication status	Published - 2012

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abstract = "Small changes in the alkane solvent structure in combination with temperature effects lead to four different conformations of stereoselectively deuterated benzene-1,3,5-tricarboxamides in the aggregated state, affecting the expression of the supramolecular chirality and highlighting the role of the solvent structure in self-assembly processes.",

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AU - Meijer, E.W.

AU - Palmans, A.R.A.

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AB - Small changes in the alkane solvent structure in combination with temperature effects lead to four different conformations of stereoselectively deuterated benzene-1,3,5-tricarboxamides in the aggregated state, affecting the expression of the supramolecular chirality and highlighting the role of the solvent structure in self-assembly processes.

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A stereoselectively deuterated supramolecular motif to probe the role of solvent during self-assembly processes

Abstract

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