Theoretical Analysis of Solvent Polarity Effect on the Electronic and Spectroscopic Properties (IR and UV) of the Ni(CO)2(NHC)2 Complex (NHC = 1H-Imidazol-2-ylidene)

2020 ◽  
Vol 94 (2) ◽  
pp. 345-351 ◽  
Author(s):  
Mona Kiani ◽  
Reza Ghiasi ◽  
Hoda Pasdar ◽  
Behroz Mirza
2001 ◽  
Vol 3 (17) ◽  
pp. 3499-3505 ◽  
Author(s):  
Georgia M. A. Junqueira ◽  
William R. Rocha ◽  
Wagner B. De Almeida ◽  
He′lio F. Dos Santos

2020 ◽  
Vol 11 (2) ◽  
pp. 567-576 ◽  
Author(s):  
Kais Dhbaibi ◽  
Ludovic Favereau ◽  
Monika Srebro-Hooper ◽  
Cassandre Quinton ◽  
Nicolas Vanthuyne ◽  
...  

Solvent polarity effect on circularly polarized luminescence intensity was assessed in helical push–pull organic systems through excited-state symmetry breaking and interbranched exciton coupling.


1998 ◽  
Vol 76 (6) ◽  
pp. 686-694 ◽  
Author(s):  
Christian Reichardt ◽  
Stefan Löbbecke ◽  
Abdol Mohammed Mehranpour ◽  
Gerhard Schäfer

Syntheses and negative solvatochromism of two new lipophilic pentaphenyl pyridinium N-phenolate betaine dyes, substituted with seven tert-butyl groups (9) or with three tert-butyl and two 1-adamantyl groups (13) in the peripheral phenyl rings, are described in order to get zwitterionic dyes that are more soluble in nonpolar solvents such as the standard betaine dye, 1, which has been used for the construction of an empirical scale of solvent polarity, called the ET(30) scale.Key words: betaine dyes, ET(30) values, lipophilic dyes, pyridinium N-phenolate betaine dyes, solvatochromism, solvent polarity.


2010 ◽  
Vol 114 (13) ◽  
pp. 4507-4519 ◽  
Author(s):  
M. Shaikh ◽  
J. Mohanty ◽  
P. K. Singh ◽  
A. C. Bhasikuttan ◽  
R. N. Rajule ◽  
...  

Molecules ◽  
2018 ◽  
Vol 23 (4) ◽  
pp. 733
Author(s):  
Jun Hu ◽  
Shijun He ◽  
Yaozhong Zhang ◽  
Haixia Ma ◽  
Xiaoli Zhang ◽  
...  

2019 ◽  
Vol 21 (2) ◽  
pp. 915-928 ◽  
Author(s):  
Wilver A. Muriel ◽  
Rodrigo Morales-Cueto ◽  
William Rodríguez-Córdoba

TD-DFT has been used to investigate the relaxation pathways of 1- and 2-salicylideneanthrylamine in different solvent environments.


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