Linear and Nonlinear Optical Properties of a Macrocyclic Trichromophore Bundle with Parallel-Aligned Dipole Moments

2006 ◽  
Vol 110 (11) ◽  
pp. 5434-5438 ◽  
Author(s):  
Yi Liao ◽  
Kimberly A. Firestone ◽  
Sanchali Bhattacharjee ◽  
Jingdong Luo ◽  
Marnie Haller ◽  
...  
RSC Advances ◽  
2015 ◽  
Vol 5 (103) ◽  
pp. 84643-84656 ◽  
Author(s):  
Sarbjeet Kaur ◽  
Sugandha Dhoun ◽  
Griet Depotter ◽  
Paramjit Kaur ◽  
Koen Clays ◽  
...  

Thermally stable ferrocene-DPP dyads exhibit non-zero dipole moments as well as negative solvatochromism and show structure dependent second-order nonlinear polarizabilities.


2018 ◽  
Vol 4 (4) ◽  
Author(s):  
Siddheshwar D. Jadhav ◽  
Ponnadurai Ramasami ◽  
Nagaiyan Sekar

Abstract Effects of alkylamino and bromo substituents on imidazo[1,2-a]pyridines containing donor-π-acceptor type groups were comprehensively investigated for their linear and nonlinear optical properties by solvatochromic and DFT (CAM-B3LYP and BHandHLYP) methods. The difference between the ground and excited dipole moments as well as their ratios obtained by solvatochromic analysis indicate that the excited state is more polar than the ground state for both the bromo and diethyl amino derivative. More than twofold enhancement in the excited state dipole moments was observed as revealed by the difference and ratio of dipole moment upon the introduction of alkylamino donor group and these suggest large intramolecular charge transfer in the dyes. Stabilization energy above 20 kJ/mol was observed for large number of electron donor–acceptor interactions in Natural Bonding Orbital (NBO) analysis. Bond length alternation (BLA) and Bond order alternation (BOA) values tend to zero suggesting a high degree of polarization in the dyes. Enhancement in mean polarizability (α0), first hyperpolarizability (β0) and second static hyperpolarizabilities ( $\bar \gamma$) were observed by the introduction of alkylamino and bromo group in place of chloro in spite of the fact that Hammett constant of chloro and bromo are the same. The dyes have fundamental and intrinsic properties within the Hamiltonian limits. The two-photon absorption cross section value (≈100 GM) is comparable with LDS-698, a commercial TPA dye. This investigation is important for understanding the electronic structure of imidazo[1,2-a]pyridine with active functional groups and extending the potential for optical applications.


2004 ◽  
Vol 97-98 ◽  
pp. 201-206 ◽  
Author(s):  
A. Pugžlys ◽  
P.R. Hania ◽  
C. Didraga ◽  
J. Knoester ◽  
K. Duppen

The linear and nonlinear optical properties of pure 3,3'-bis(3-carboxypropyl)-5,5',6,6'- tetrachloro-1,1'-dioctylbenzimidacarbocyanine (C8O3) aggregates as well as of C8O3 aggregates in the presence of PVA are studied at room temperature. The obtained results reveal that absorption spectra of both aggregates are governed by four absorption bands. Three of these represent transitions having dipole moments oriented parallel to the axis of the aggregate and one oriented perpendicular to it. The two lower energy parallel transitions are found to be weakly coupled which suggests that they represent two excitons located on different walls of the double-wall cylinder. In contrast, the lowest energy parallel transition and the transition having a transition dipole moment oriented perpendicular to the aggregate axis share the same ground state which reveals that they belong to the same exciton band. The manner of modification of the linear absorption with addition of PVA as well as the similarity of the pump-probe spectra of the two investigated aggregates suggests that this exciton band originates from the inner wall of the double-wall cylinder.


1990 ◽  
Author(s):  
Tapio T. Rantala ◽  
Mark I. Stockman ◽  
Daniel A. Jelski ◽  
Thomas F. George

Author(s):  
Francisco Germán Mejía-Hernández ◽  
Oscar Javier Hernández-Ortíz ◽  
Francisco Misael Muñoz-Pérez ◽  
Armando Irving Martínez-Pérez ◽  
Rosa Angeles Vázquez-García ◽  
...  

2021 ◽  
Vol 573 (1) ◽  
pp. 52-62
Author(s):  
Siddique Aneesa-Fatema ◽  
Y. B. Rasal ◽  
R. N. Shaikh ◽  
M. D. Shirsat ◽  
S. S. Hussaini ◽  
...  

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