Literature DB >> 20486673

Efficient two-photon absorbing acceptor-pi-acceptor polymethine dyes.

Lazaro A Padilha1, Scott Webster, Olga V Przhonska, Honghua Hu, Davorin Peceli, Trenton R Ensley, Mykhailo V Bondar, Andriy O Gerasov, Yuriy P Kovtun, Mykola P Shandura, Alexey D Kachkovski, David J Hagan, Eric W Van Stryland.   

Abstract

We present an experimental and theoretical investigation of the linear and nonlinear optical properties of a series of acceptor-pi-acceptor symmetrical anionic polymethine dyes with diethylamino-coumarin-dioxaborine terminal groups and different conjugation lengths. Two-photon absorption (2PA) cross sections (delta(2PA)) are enhanced with an increase of pi-conjugation length in the investigated series of dyes. 2PA spectra for all dyes consist of two well-separated bands. The first band, located within the telecommunications window, occurs upon two-photon excitation into the vibrational levels of the main S(0) --> S(1) transition, reaching a large delta(2PA) = 2200 GM (1 GM = 1 x 10(-50) cm(4) s/photon) at 1600 nm for the longest conjugated dye. The position of the second, and strongest, 2PA band for all anionic molecules corresponds to the second-excited final state, which is confirmed by quantum-chemical calculations and excitation anisotropy measurements. Large delta(2PA) values up to 17,000 GM at 1100 nm are explained by the combination of the large ground- and excited-state transition dipole moments. The three shortest dyes show good photochemical stability and surprisingly large fluorescence quantum yields of approximately 0.90, approximately 0.66, and approximately 0.18 at the red to near-IR region of approximately 640, approximately 730, and approximately 840 nm, respectively. The excited-state absorption spectra for all samples are also studied and exhibit intense bands throughout the visible wavelength region with peak cross section close to 5 x 10(-16) cm(2) with a corresponding red shift with increasing conjugation lengths.

Entities:  

Year:  2010        PMID: 20486673     DOI: 10.1021/jp100963e

Source DB:  PubMed          Journal:  J Phys Chem A        ISSN: 1089-5639            Impact factor:   2.781


  7 in total

1.  Coumarin-Pyrazole Hybrid with Red Shifted ESIPT Emission and AIE Characteristics - a Comprehensive Study.

Authors:  Milind R Shreykar; Nagaiyan Sekar
Journal:  J Fluoresc       Date:  2017-05-13       Impact factor: 2.217

2.  A Dual-Signaling Ferrocene-Pyrene Dyad: Triple-Mode Recognition of the Cu(II) Ions in Aqueous Medium.

Authors:  Manzoor Ahmad Wani; Mrituanjay D Pandey; Rampal Pandey; Sandeep Kumar Maurya; Debabrata Goswami
Journal:  J Fluoresc       Date:  2017-08-24       Impact factor: 2.217

3.  Red Emitting Coumarins: Insights of Photophysical Properties with DFT Methods.

Authors:  Abhinav B Tathe; Lydia Rhyman; Ponnadurai Ramasami; Nagaiyan Sekar
Journal:  J Fluoresc       Date:  2015-07-03       Impact factor: 2.217

4.  Spectroscopic Investigation and Photophysics of a D-π-A-π-D Type Styryl Pyrazine Derivative.

Authors:  Samy A El-Daly; Khalid A Alamry
Journal:  J Fluoresc       Date:  2016-01       Impact factor: 2.217

5.  Aromatic difluoroboron β-diketonate complexes: effects of π-conjugation and media on optical properties.

Authors:  Songpan Xu; Ruffin E Evans; Tiandong Liu; Guoqing Zhang; J N Demas; Carl O Trindle; Cassandra L Fraser
Journal:  Inorg Chem       Date:  2013-03-19       Impact factor: 5.165

6.  Fluorescence, Photophysical Behaviour and DFT Investigation of E,E-2,5-bis[2-(3-pyridyl)ethenyl]pyrazine (BPEP).

Authors:  Amerah M Al-Soliemy; Osman I Osman; Mahmoud A Hussein; Abdullah M Asiri; Samy A El-Daly
Journal:  J Fluoresc       Date:  2016-04-15       Impact factor: 2.217

7.  Computer aided chemical design: using quantum chemical calculations to predict properties of a series of halochromic guaiazulene derivatives.

Authors:  Adam W Woodward; Ebrahim H Ghazvini Zadeh; Mykhailo V Bondar; Kevin D Belfield
Journal:  R Soc Open Sci       Date:  2016-11-23       Impact factor: 2.963

  7 in total

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