Functionalization of hybrid poly(n-isopropylacrylamide) hydrogels forEscherichia colicell capture via adsorbed intermediate dye molecule

2014 ◽  
Vol 132 (10) ◽  
pp. n/a-n/a ◽  
Author(s):  
Jarod Gregory ◽  
Jonathon Cannell ◽  
Matthew Kofron ◽  
Lilit Yeghiazarian ◽  
Vasile Nistor
2021 ◽  
Vol 118 (20) ◽  
pp. 204002
Author(s):  
Pietro Lombardi ◽  
Maja Colautti ◽  
Rocco Duquennoy ◽  
Ghülam Murtaza ◽  
Prosenjit Majumder ◽  
...  
Keyword(s):  

Author(s):  
Jin Sun ◽  
Zongling Ding ◽  
Yuanqin Yu ◽  
WanZhen Liang

The nonlinear Fano effects on the absorption of hybrid systems composed of a silver nanosphere and an indoline dye molecule have been systematically investigated by the hybrid approach, which combines...


2017 ◽  
Vol 53 (63) ◽  
pp. 8842-8845 ◽  
Author(s):  
Silvia Sonzini ◽  
Jade A. McCune ◽  
Peter Ravn ◽  
Oren A. Scherman ◽  
Christopher F. van der Walle

A supramolecular colorimetric assay utilising the macrocyclic host cucurbit[7]uril with a commercial dye molecule, neutral red, was evaluated as a novel method for drug detection in urine of a model therapeutic peptide drug Octreotide.


2003 ◽  
Vol 21 (5) ◽  
pp. 439-449 ◽  
Author(s):  
Yoshiaki Shimizu ◽  
Atsushi Taga ◽  
Hitoshi Yamaoka

Novel chitosan-based adsorbent materials with a higher fatty diacid diglycidyl as the crosslinking agent were synthesized and the adsorption abilities of the resulting polymers evaluated towards typical acid dyes. The successful formation of a crosslinked structure was confirmed via infrared spectroscopic measurements and the solubility of the polymer towards 10% aqueous solutions of acetic and formic acids determined. At higher dye concentrations, the adsorption abilities of the crosslinked chitosan towards hydrophilic CI Acid Orange 7 and CI Acid Red 1 increased with decreasing degree of substitution. However, at lower dye concentrations, the crosslinked chitosan with the lowest degree of substitution exhibited the lowest adsorption capability. With such hydrophilic acid dyes, the extent of adsorption decreased significantly as the pH of the solution increased. On the other hand, CI Acid Red 138, which contains a dodecyl group in the chemical structure, was adsorbed to a considerable extent even at higher pH values, suggesting hydrophobic interaction between the alkyl group in the dye molecule and the hydrophobic crosslinker.


ACS Omega ◽  
2018 ◽  
Vol 3 (5) ◽  
pp. 4878-4883 ◽  
Author(s):  
Christophe Pin ◽  
Shutaro Ishida ◽  
Genta Takahashi ◽  
Kota Sudo ◽  
Tuyoshi Fukaminato ◽  
...  
Keyword(s):  

Polymers ◽  
2021 ◽  
Vol 13 (20) ◽  
pp. 3517
Author(s):  
Horst Berneth ◽  
Friedrich Karl Bruder ◽  
Thomas Fäcke ◽  
Sven Hansen ◽  
Koichi Kawamura ◽  
...  

Versatile substituted electron-deficient trichloromethylarenes can easily be synthesized and combined with a Safranine O/triarylalkylborate salt to form a highly efficient three-component photo-initiation system that starts free radical polymerization to finally form holographic gratings with a single-pulsed laser. The mechanism of this photo-initiation most likely relies on an electron transfer from the borate salt into the semi-occupied HOMO of the excited dye molecule Safranine O, which after fragmentation generates an initiating alkyl radical and longer-lived dye radical species. This dye radical is most probably oxidized by the newly introduced trichloromethylarene derivative as an electron acceptor. The two generated radicals from one absorbed photon initiate the photopolymerization and form index gratings in a suitable holographic recording material. This process is purely photonic and does not require further non-photonic post treatments.


2021 ◽  
Author(s):  
Devin Douglas Machin

The dye-sensitized solar cell (DSSC) represents one of the most promising next-generation photovoltaic technologies. In addition, the DSSC manifold provides an exceptional platform to further appreciate photoinduced electron transfer and the fundamental features required for light-harvesting. The dye molecule is a key component in the DSSC and has achieved minor success utilizing both an organic and inorganic photosensitizers. DSSC’s show great promise owing to their inexpensive synthesis tunable optical and electrochemical properties, and a plethora of design possibilities. The typical anatomy of organic and inorganic DSSC dyes are comprised of a redox-active donor/chromophore (D) that is connected, through a conjugated linker (π), to an acceptor (A) capable of anchoring to titania (TiO2). Fine tuning each of these components can shift the absorption spectrum increasing the overall device efficiency. Boron-dipyrromethene (BODIPY) is an attractive moiety to integrate into DSSC dyes. BODIPY’s rigid organic framework should be able to improve dye stability while the high extinction coefficients of BODIPY based molecules have the potential to increase device performance. Herein, we explore the synthesis and physicochemical properties of BODIPY in an attempt to synthesize efficient DSSC dye molecules and efficient photovoltaic technologies.


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