Supramolecular polymerization in water harnessing both hydrophobic effects and hydrogen bond formation

C.M.A. Leenders; L. Albertazzi; T. Mes; M.M.E Koenigs; A.R.A. Palmans; E.W. Meijer

doi:10.1039/c3cc38949a

Supramolecular polymerization in water harnessing both hydrophobic effects and hydrogen bond formation

C.M.A. Leenders
, L. Albertazzi
, T. Mes
, M.M.E Koenigs
, A.R.A. Palmans
, E.W. Meijer

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

165 Citations (Scopus)

213 Downloads (Pure)

Abstract

The formation of supramolecular polymers in water through rational design of a benzene-1,3,5-tricarboxamide (BTA) motif is presented. Intermolecular hydrogen bonding and hydrophobic effects cooperate in the self-assembly into long fibrillar aggregates. Minimal changes in molecular structure significantly affect the internal packing of the aggregates.

Original language	English
Pages (from-to)	1963-1965
Number of pages	3
Journal	Chemical Communications, ChemComm
Volume	49
Issue number	19
DOIs	https://doi.org/10.1039/c3cc38949a
Publication status	Published - 2013

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title = "Supramolecular polymerization in water harnessing both hydrophobic effects and hydrogen bond formation",

abstract = "The formation of supramolecular polymers in water through rational design of a benzene-1,3,5-tricarboxamide (BTA) motif is presented. Intermolecular hydrogen bonding and hydrophobic effects cooperate in the self-assembly into long fibrillar aggregates. Minimal changes in molecular structure significantly affect the internal packing of the aggregates.",

author = "C.M.A. Leenders and L. Albertazzi and T. Mes and M.M.E Koenigs and A.R.A. Palmans and E.W. Meijer",

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AU - Leenders, C.M.A.

AU - Albertazzi, L.

AU - Mes, T.

AU - Koenigs, M.M.E

AU - Palmans, A.R.A.

AU - Meijer, E.W.

PY - 2013

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N2 - The formation of supramolecular polymers in water through rational design of a benzene-1,3,5-tricarboxamide (BTA) motif is presented. Intermolecular hydrogen bonding and hydrophobic effects cooperate in the self-assembly into long fibrillar aggregates. Minimal changes in molecular structure significantly affect the internal packing of the aggregates.

AB - The formation of supramolecular polymers in water through rational design of a benzene-1,3,5-tricarboxamide (BTA) motif is presented. Intermolecular hydrogen bonding and hydrophobic effects cooperate in the self-assembly into long fibrillar aggregates. Minimal changes in molecular structure significantly affect the internal packing of the aggregates.

U2 - 10.1039/c3cc38949a

DO - 10.1039/c3cc38949a

M3 - Article

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SN - 1359-7345

VL - 49

SP - 1963

EP - 1965

JO - Chemical Communications, ChemComm

JF - Chemical Communications, ChemComm

IS - 19

ER -

Supramolecular polymerization in water harnessing both hydrophobic effects and hydrogen bond formation

Abstract

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