scholarly journals Correction: Photophysical properties of the intramolecular excited charge-transfer states of π-expanded styryl phenanthrimidazoles – effect of solvent polarity

RSC Advances ◽  
2016 ◽  
Vol 6 (87) ◽  
pp. 83709-83709
Author(s):  
V. Thanikachalam ◽  
A. Arunpandiyan ◽  
J. Jayabharathi ◽  
P. Ramanathan
Keyword(s):  
Charge Transfer ◽  
Photophysical Properties ◽  
Solvent Polarity ◽  
Effect Of Solvent

Correction for ‘Photophysical properties of the intramolecular excited charge-transfer states of π-expanded styryl phenanthrimidazoles – effect of solvent polarity’ by V. Thanikachalam et al., RSC Adv., 2014, 4, 6790–6806.

Experimental and theoretical insights on the effect of solvent polarity on the photophysical properties of a benzanthrone dye

2019 ◽  
Vol 218 ◽  
pp. 221-228 ◽  
Author(s):  
Shivraj ◽  
B. Siddlingeshwar ◽  
Anup Thomas ◽  
Elena M. Kirilova ◽  
Darshan Devang Divakar ◽  
...  
Keyword(s):  
Photophysical Properties ◽  
Solvent Polarity ◽  
Effect Of Solvent

Effect of solvent polarity on the photophysical properties of coumarin-1 dye

2003 ◽  
Vol 119 (19) ◽  
pp. 10202-10208 ◽  
Author(s):  
Atanu Barik ◽  
Sukhendu Nath ◽  
Haridas Pal
Keyword(s):  
Photophysical Properties ◽  
Solvent Polarity ◽  
Effect Of Solvent ◽  
Coumarin 1

scholarly journals Effect of solvent polarity on the photophysical properties of chalcone derivatives

RSC Advances ◽  
2017 ◽  
Vol 7 (39) ◽  
pp. 24204-24214 ◽  
Author(s):  
Rekha Kumari ◽  
Anitha Varghese ◽  
Louis George ◽  
Sudhakar Y. N.
Keyword(s):  
Excited State ◽  
Organic Solvents ◽  
Ground State ◽  
Photophysical Properties ◽  
Solvent Polarity ◽  
Chalcone Derivatives ◽  
Effect Of Solvent

The photophysical properties were studied for FNPO, AFPO and FHPO in different organic solvents. The excited state of the molecules were found to be more polar than the ground state.

scholarly journals Synthesis and Photophysical Properties of a Series of Dimeric Indium Quinolinates

Molecules ◽  
2020 ◽  
Vol 26 (1) ◽  
pp. 34
Author(s):  
Sang Woo Kwak ◽  
Ju Hyun Hong ◽  
Sang Hoon Lee ◽  
Min Kim ◽  
Yongseog Chung ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Nmr Spectroscopy ◽  
1H Nmr Spectroscopy ◽  
Photophysical Properties ◽  
Emission Spectra ◽  
Solvent Polarity ◽  
Low Energy ◽  
Quantum Yields ◽  
Absorption Bands ◽  
Indium Complexes

A novel class of quinolinol-based dimeric indium complexes (1–6) was synthesized and characterized using 1H and 13C(1H) NMR spectroscopy and elemental analysis. Compounds 1–6 exhibited typical low-energy absorption bands assignable to quinolinol-centered π–π* charge transfer (CT) transition. The emission spectra of 1–6 exhibited slight bathochromic shifts with increasing solvent polarity (p-xylene < tetrahydrofuran (THF) < dichloromethane (DCM)). The emission bands also showed a gradual redshift, with an increase in the electron-donating effect of substituents at the C5 position of the quinoline groups. The absolute emission quantum yields (ΦPL) of compounds 1 (11.2% in THF and 17.2% in film) and 4 (17.8% in THF and 36.2% in film) with methyl substituents at the C5 position of the quinoline moieties were higher than those of the indium complexes with other substituents.

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