Literature DB >> 24279339

Structural basis for aggregation mode of oligo-p-phenylene ethynylenes with ionic surfactants.

Eric H Hill1, Dominic Sanchez, Deborah G Evans, David G Whitten.   

Abstract

In this letter, the aggregation modes of two classes of ionic p-phenylene ethynylene oligomers with oppositely charged surfactants are studied. The location of the ionic side chains was found to influence the type of aggregate formed when an equivalent number of surfactant molecules are added to solution. When the charged groups were located at the terminal ends of the molecule, strong H-aggregates were observed to form. Alternatively, when the ionic groups were both located on opposite sides of the central phenyl ring, the formation of J-aggregates was observed. Interestingly, as the surfactant concentration approaches the critical micelle concentration, the weakly bound aggregates are dissociated and the absorbance spectrum returns to what is observed in water. This study reveals the structural basis for aggregation effects between molecules based on the p-phenylene ethynylene backbone, and gives an understanding of how to influence the aggregation mode of similar compounds.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 24279339     DOI: 10.1021/la4038827

Source DB:  PubMed          Journal:  Langmuir        ISSN: 0743-7463            Impact factor:   3.882


  3 in total

1.  Detergent-induced self-assembly and controllable photosensitizer activity of diester phenylene ethynylenes.

Authors:  Patrick L Donabedian; Matthew N Creyer; Florencia A Monge; Kirk S Schanze; Eva Y Chi; David G Whitten
Journal:  Proc Natl Acad Sci U S A       Date:  2017-06-22       Impact factor: 11.205

2.  Dendritic domains with hexagonal symmetry formed by x-shaped bolapolyphiles in lipid membranes.

Authors:  Stefan Werner; Helgard Ebert; Bob-Dan Lechner; Frank Lange; Anja Achilles; Ruth Bärenwald; Silvio Poppe; Alfred Blume; Kay Saalwächter; Carsten Tschierske; Kirsten Bacia
Journal:  Chemistry       Date:  2015-05-04       Impact factor: 5.236

3.  Substituent, Charge, and Size Effects on the Fluorogenic Performance of Amyloid Ligands: A Small-Library Screening Study.

Authors:  Patrick L Donabedian; Mallory Evanoff; Florencia A Monge; David G Whitten; Eva Y Chi
Journal:  ACS Omega       Date:  2017-07-06
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.