Please use this identifier to cite or link to this item: http://hdl.handle.net/2289/8462
Title: D-A-π-D Synthetic approach for thienyl chalcones – NLO – a structure activity study
Authors: Tejkiran, P J
Teja, M S Brahma
Kumar, P Sai Siva
Sankar, Pranitha
Philip, Reji
Naveen, S
Lokanath, N K
Rao, G Nageswara
Keywords: Thienyl chalcones
Z-Scan
Nonlinear optical properties (NLO)
Three photon absorption
Second harmonic generation (SHG)
Issue Date: Mar-2016
Publisher: Journal of Photochemistry and Photobiology A: Chemistry
Citation: Journal of Photochemistry and Photobiology A: Chemistry, 2016, Vol.324, p33-39
Abstract: With the growing interest for organic molecules in Nonlinear Optical (NLO) applications, we have synthesized nine novel thienyl chalcones based on the D-A-π-D design. In order to establish the identity, these have been characterized in detail. Having followed the design based synthetic route, we have focused on two prime criteria for comparison; namely second harmonic generation (SHG) and non-linear absorption. In this work the role of the electron withdrawing groups, electron donating groups and extended conjugation, have been extensively studied vis-à-vis the NLO properties. The change in these properties by virtue of the molecular structure has been elucidated in this work as the structure activity relationship. Optical nonlinearity is studied using ultrafast (100 fs) laser pulses at 800 nm, employing the open aperture Z-scan technique. The compounds exhibit large effective three-photon absorption (3PA) coefficients, in the order of 10−28 m3/W2. These observations show that these compounds possess potential for application in all-optical limiting and switching devices.
Description: Open Access.
URI: http://hdl.handle.net/2289/8462
ISSN: 1010-6030
1873-2666 (online)
Alternative Location: http://dx.doi.org/10.1016/j.jphotochem.2016.03.009
Copyright: 2016 Elsevier B.V.
Additional information: • Based on D-A-π-D SYNTHETIC APPROACH we could synthesize nine novel thienyl chalcones with high effective 3 photon absorption coefficient (3 PA) of order 10−28 m3/W2. • Of these, T-CHL-NDM was found to have the highest 3PA coefficient of about 105.0 × 10−28 m3/W2. • Structure activity relationship based on the functional group vis-à-vis its NLO properties was established, and making minor modifications in the structure of the chalcones, desired 3PA values could be obtained. • Structures of all compounds have been characterized adequately. • These compounds will be useful in various applications like optical devices, communications, etc.
Appears in Collections:Research Papers (LAMP)

Files in This Item:
File Description SizeFormat 
2016_J of Photochemistry and Photobiology A_Vol.324_p33-39.pdf
  Restricted Access
1.4 MBAdobe PDFView/Open Request a copy
Supplementary_copy_2016_J of Photochemistry and Photobiology A_Vol.324_p33-39.pdf
  Restricted Access
650.51 kBAdobe PDFView/Open Request a copy


Items in RRI Digital Repository are protected by copyright, with all rights reserved, unless otherwise indicated.