scholarly journals 9-Aryl-phenalenones: Bioinspired thermally reversible photochromic compounds for photoswitching applications in the pico-to milliseconds range

2021 ◽  
Vol 186 ◽  
pp. 109060
Author(s):  
Roger Bresolí-Obach ◽  
Walter A. Massad ◽  
Abasi Abudulimu ◽  
Larry Lüer ◽  
Cristina Flors ◽  
...  
2007 ◽  
Vol 20 (11) ◽  
pp. 1007-1020 ◽  
Author(s):  
V. A. Barachevsky ◽  
Yu. P. Strokach ◽  
Yu. A. Puankov ◽  
M. M. Krayushkin

1994 ◽  
Vol 83 (2) ◽  
pp. 147-151 ◽  
Author(s):  
G. Baillet ◽  
M. Campredon ◽  
R. Guglielmetti ◽  
G. Giusti ◽  
C. Aubert

2004 ◽  
Vol 13 (03n04) ◽  
pp. 423-426 ◽  
Author(s):  
L. SANGUINET ◽  
S. AHMED ◽  
J. L. POZZO ◽  
V. RODRIGUEZ ◽  
F. ADAMIETZ

New acidochromic and photochromic compounds with nonlinear optical properties have been designed and synthesized. The hyperpolarizabilities of the zwitterionic colored forms have been quantified with polarized hyper-Rayleigh scattering experiments. The static value of oxazolidino-indoline 2 is found to be as high as Disperse Red One. This opens the way to novel multi-addressable NLO-systems.


2014 ◽  
Vol 1003 ◽  
pp. 23-26
Author(s):  
Hong Jing Jia ◽  
Ying Long Fu ◽  
Cong Bin Fan

A new unsymmetrical photochromic diarylethene1o, which is named [1-(2-methyl-benzothiophene)-2-(2-cyano-1,5-dimethyl-4-pyrryl)]perfluorocyclopentene, was synthesized. We used it to accomplish recording by optical storage technology as memory medium. Then its photochromic both in hexane solution and in PMMA film and kinetics experiment were investigated in detail. The result indicated that this diarylethene had good thermal stability and exhibited reversible photochromism, changing the color from colorless to violet in hexane solution upon appropriate irradiation with 297 nm UV light, respectively. What is more, the kinetic experiments illustrated that the cyclization/cycloreversion process of this compound was determined to be the zeroth/first reaction. The results demonstrated that the unsymmetrical diarylethene compound1o, which we have synthesized, had attractive properties for potential application in optical storage.


Author(s):  
Hina Javed ◽  
Kalsoom Fatima ◽  
Zareen Akhter ◽  
Muhammad Arif Nadeem ◽  
Muhammad Siddiq ◽  
...  

We have investigated the attachment of azobenzene photochromic switches on the modified surface of cadmium sulfide (CdS) quantum dots (QDs). The modification of CdS QDs is done by varying the concentration of the capping agent (mercaptoacetic acid) and NH 3 in order to control the size of the QDs. The X-ray diffraction studies revealed that the crystallite size of CdS QDs ranged from 6 to 10 nm. The azobenzene photochromic derivatives bis(4-hydroxybenzene-1-azo)4,4′(1,1′ diphenylmethane) (I) and 4,4′-diazenyldibenzoic acid (II) were synthesized and attached with surface-modified CdS QDs to make fluorophore–photochrome CdS-(I) and CdS-(II) dyad assemblies. Upon UV irradiation, the photochromic compounds (I) and (II) undergo a reversible trans – cis isomerization. The photo-induced trans – cis transformation helps to transfer photo-excited electrons from the conduction band of the CdS QDs to the lowest unoccupied molecular orbital of cis isomer of photochromic compounds (I) and (II). As a result, the fluorescence of CdS-(I) and CdS-(II) dyads is suppressed approximately five times compared to bare CdS QDs. The fluorescence modulation in such systems could help to design luminescent probes for bioimaging applications.


Author(s):  
Robert J. Tombari ◽  
Jeremy Ryan Tuck ◽  
Noah Yardeny ◽  
Phillip W. Gingrich ◽  
Dean J Tantillo ◽  
...  

Azobenzenes are widely used as dyes and photochromic compounds, with the Baeyer-Mills reaction serving as the most common method for their preparation. This transformation is often plagued by low yields...


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