Two-photon absorption properties of cationic 1,4-Bis(styryl)benzene derivative and its inclusion complexes with cyclodextrins

Okhil Kumar Nag, Rati Ranjan Nayak, Chang Su Lim, In Hong Kim, Kwangseuk Kyhm, Bong Rae Cho, Han Young Woo

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

Two-photon absorption properties of 1,4-bis{4′-[N,N-bis(6″- trimethylammoniumhexyl)amino]styryl}benzene tetrabromide (C1) and its inclusion complexes (ICs) with cyclodextrins (CDs) have been studied. Upon complexation with CDs, the absorption spectra of C1 showed a slight red shift, whereas the emission spectra showed a blue shift with concomitant increase in the fluorescence quantum efficiency. A Stern-Volmer study using K 3Fe(CN)6 as a quencher revealed significant reduction in the photoinduced charge transfer quenching, in accord with the IC formation. Comparison of the spectroscopic results reveals that C1 forms increasingly more stable ICs in the order C1/β-CD < C1/γ-CD < C1/(3γ:β)-CD (γ-CD/β-CD 3:1, mole ratio). Moreover, the two-photon action cross section of C1 increased from 200 GM for C1 to 400 GM for C1/β-CD, 460 GM for C1/γ-CD, and 650 GM for C1/(3γ:β)-CD, respectively. Furthermore, the two-photon microscopy images of HeLa cells stained with C1 emitted strong two-photon excited fluorescence in the plasma membrane. These results provide a useful guideline for the development of efficient two-photon materials for bioimaging applications.

Original languageEnglish
Pages (from-to)9684-9690
Number of pages7
JournalJournal of Physical Chemistry B
Volume114
Issue number29
DOIs
Publication statusPublished - 2010 Jul 29

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Surfaces, Coatings and Films
  • Materials Chemistry

Fingerprint Dive into the research topics of 'Two-photon absorption properties of cationic 1,4-Bis(styryl)benzene derivative and its inclusion complexes with cyclodextrins'. Together they form a unique fingerprint.

  • Cite this