Excited-State and Two-Photon Absorption in Salicylidene Molecules: The Role of Zn(II) Planarization

2016 ◽  
Vol 120 (7) ◽  
pp. 4032-4039 ◽  
Author(s):  
Marcelo G. Vivas ◽  
José Carlos Germino ◽  
Cristina A. Barboza ◽  
Pedro A. M. Vazquez ◽  
Leonardo De Boni ◽  
...  
Author(s):  
Alessio Cesaretti ◽  
Anna Spalletti ◽  
Fausto Elisei ◽  
Paolo FOGGI ◽  
Raimondo Germani ◽  
...  

Two symmetric quadrupolar cationic push-pull compounds with a central electron-acceptor (N+-methylpyrydinium, A+) and different lateral electron-donors, (N,N-dimethylamino and N,N-diphenylamino, D) in a D-π-A+-π-D arrangement, were investigated together with their dipolar...


2015 ◽  
Vol 56 (1) ◽  
pp. 236-242 ◽  
Author(s):  
Yulong Gong ◽  
Yao Lu ◽  
Zhenqiang Wang ◽  
Shengtao Zhang ◽  
Ziping Luo ◽  
...  

2019 ◽  
Vol 15 ◽  
pp. 2438-2446 ◽  
Author(s):  
Alessandro Iagatti ◽  
Baihao Shao ◽  
Alberto Credi ◽  
Barbara Ventura ◽  
Ivan Aprahamian ◽  
...  

In this work we apply a combination of steady state and time resolved luminescence and absorption spectroscopies to investigate the excited-state dynamics of a recently developed molecular photoswitch, belonging to the hydrazone family. The outstanding properties of this molecule, involving fluorescence toggling, bistability, high isomerization quantum yield and non-negligible two-photon absorption cross section, make it very promising for numerous applications. Here we show that the light induced Z/E isomerization occurs on a fast <1 ps timescale in both toluene and acetonitrile, while the excited state lifetime of the Z-form depends on solvent polarity, suggesting a partial charge transfer nature of its low lying excited state. Time-resolved luminescence measurements evidence the presence of a main emission component in the 500–520 nm spectral range, attributed to the Z-isomer, and a very short living blue-shifted emission, attributed to the E-isomer. Finally, transient absorption measurements performed upon far-red excitation are employed as an alternative method to determine the two-photon absorption cross-section of the molecule.


2000 ◽  
Vol 09 (02) ◽  
pp. 217-225 ◽  
Author(s):  
P. SREERAMANA AITHAL ◽  
P. PREM KIRAN ◽  
D. NARAYANA RAO

Optical limiting characteristics of pure and 150 ppm Fe-doped Bi 12 SiO 20 (BSO:Fe) crystals are studied at high intensity nanosecond pulse regime. When the input light is at 532 nm and at 595 nm with 6 ns pulse duration, a good optical limiting behavior is observed due to simultaneous effect of trap assisted excited state absorption and two photon absorption. The precise role of the internal defects due to impurity centers present in the crystal lattice is explained on the basis of a four level model. This study reveal that the increased nonlinear absorption due to iron incorporation in BSO makes it an excellent passive optical limiter.


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