scholarly journals Front Cover: Theoretical and Experimental Studies on the Near‐Infrared Photoreaction Mechanism of a Silicon Phthalocyanine Photoimmunotherapy Dye: Photoinduced Hydrolysis by Radical Anion Generation (ChemPlusChem 9/2020)

ChemPlusChem ◽  
2020 ◽  
Vol 85 (9) ◽  
pp. 1949-1949
Author(s):  
Masato Kobayashi ◽  
Mei Harada ◽  
Hideo Takakura ◽  
Kanta Ando ◽  
Yuto Goto ◽  
...  
2018 ◽  
Vol 20 (28) ◽  
pp. 19030-19036 ◽  
Author(s):  
Erin D. Anderson ◽  
Stacey Sova ◽  
Joseph Ivanic ◽  
Lisa Kelly ◽  
Martin J. Schnermann

The near-IR light induced ligand exchange of silicon phthalocyanines involves a critical radical anion intermediate and is dependent on hypoxia and a reductant.


ChemNanoMat ◽  
2018 ◽  
Vol 4 (3) ◽  
pp. 243-243
Author(s):  
Christopher M. Andolina ◽  
Scott E. Crawford ◽  
Ashley M. Smith ◽  
Kathryn A. Johnston ◽  
Patrick J. Straney ◽  
...  

2006 ◽  
Vol 3 (2) ◽  
pp. 312-314 ◽  
Author(s):  
John R. H. Xie ◽  
Chiu Fung Cheung ◽  
Jijun Zhao

Gao, Bulusu and Zeng have recently reported a new series of isoelectronic, sub-nanometer gold-caged metal systems M@Au14 which have large energy gaps than icosahedral W@Au12 and Au32 and tetrahedral Au20. In this communication, we propose a "tuning" scheme, substitutional-doping, to achieve the tunable optical excitation and emission of M@Au14 over a broad wavelength region. For example, the optical absorption gaps of isoelectronic M@Au14 could be tuned from the near infrared to green by substituting the metal M with group IIIB, IVB, and VB constituents in the periodic table. Our results provide basic guidelines for further experimental studies on the spectral properties of M@Au14 as well as for the development of M@Au14-based tunable optoelectronic devices.


2010 ◽  
Vol 132 (48) ◽  
pp. 17157-17173 ◽  
Author(s):  
Shang-U Kim ◽  
Yangping Liu ◽  
Kevin M. Nash ◽  
Jay L. Zweier ◽  
Antal Rockenbauer ◽  
...  

2003 ◽  
Vol 57 (5) ◽  
pp. 580-587 ◽  
Author(s):  
S. D. Harvey ◽  
T. J. Peters ◽  
B. W. Wright

Raman spectroscopy is often considered a nondestructive analytical technique; however, this is not always the case. The 300-mW 785-nm near-infrared (NIR) laser source used with many commercially available instruments has sufficient power to burn samples. This destructive potential is of special concern if the sample is irreplaceable (e.g., fine art, forensic evidence, or for in vivo medical diagnostics) or a hazardous energetic material (explosive or pyrophoric samples). This study quantifies the heat resulting from illuminating an extensive color array with a 785-nm NIR laser and relates these values to the hazards associated with Raman analysis. In general, darker colors were found to be more problematic. Since visible colors are not ideally correlated with absorptive characteristics at 785 nm, predictions based on thermography are not perfect; however, this approximation gives a useful method for predicting the thermal response of unknown samples to NIR exposure. Additionally, experimental studies evaluated the analysis of flammable organic solvents, propellants, military explosives, mixtures containing military explosives, shock-sensitive explosives, and gunpowders (i.e., smokeless, black, and Pyrodex powders). Safety guidelines for analysis are presented.


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