4.5 Article

Spatially Heterogeneous Nature of Self-Catalytic Reaction in Hetero-Double Helix Formation of Helicene Oligomers

Journal

CHEMPHYSCHEM
Volume 17, Issue 20, Pages 3283-3288

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cphc.201600627

Keywords

circular dichroism; heterogeneous solutions; imaging; self-catalysis; UV; Vis spectroscopy

Funding

  1. Ministry of Education, Culture, Sports, Science and Technology (MEXT) [15H00981]
  2. Uehara Memorial Foundation
  3. JSPS [257424]
  4. Grants-in-Aid for Scientific Research [15H00981, 15K18825] Funding Source: KAKEN

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A 1:1 mixture of pseudoenantiomeric aminomethylenehelicene oligomers, (P)-tetramer and (M)-pentamer, in fluorobenzene show a self-catalytic phenomenon in the formation of hetero-double helices from random coils. This study visualizes the spatially heterogeneous nature of the self-catalytic reaction in dilute solution. UV/Vis imaging analysis of the mixture at 70 degrees C, containing random coils, exhibits a homogeneous bright area. When the solution is cooled from 70 to 30 degrees C and held at that temperature, dark domains of approximately 1mm in size appear, which move approximately at a rate of 1mmmin(-1). The dark domains indicate that weaker UV/Vis absorption results from the formation of hetero-double helices, which is supported by circular dichroism (CD) imaging experiments. Then a homogeneous mixture is regenerated upon heating to 55 degrees C, as shown by CD imaging. Under self-catalytic conditions, a homogeneous solution spontaneously changed to a heterogeneous solution in the process of hetero-double-helix formation.

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