Near-infrared fluorescent organic porous crystal that responds to solvent vapors

2020 ◽  
Vol 8 (36) ◽  
pp. 12437-12444
Author(s):  
Tsutomu Ishi-i ◽  
Honoka Tanaka ◽  
Himiko Koga ◽  
Yuuma Tanaka ◽  
Taisuke Matsumoto

Creation of a near-IR porous florescent crystal by noncovalent synthesis based on the self-assembly of donor–acceptor dye and its development into a solvent vapor-responsive fluorescence system were studied.

2018 ◽  
Vol 74 (8) ◽  
pp. 1151-1154
Author(s):  
Pushpendra Singh ◽  
Harkesh B. Singh ◽  
Ray J. Butcher

In the title compound, [HgCl2(C16H28N2Se)], the primary geometry around the Se and Hg atoms is distorted trigonal–pyramidal and distorted square-pyramidal, respectively. The distortion of the molecular geometry in the complex is caused by the steric demands of the ligands attached to the Se atom. The Hg atom is coordinated through two chloride anions, an N atom and an Se atom, making up an unusual HgNSeCl2 coordination sphere with an additional long Hg...N interaction. Intermolecular C—H...Cl interactions are the only identified intermolecular hydrogen-bonding interactions that seem to be responsible for the self assembly. These relatively weak C—H...Cl hydrogen bonds possess the required linearity and donor–acceptor distances. They act as molecular associative forces that result in a supramolecular assembly along the b-axis direction in the solid state of the title compound.


2016 ◽  
Vol 52 (73) ◽  
pp. 10938-10947 ◽  
Author(s):  
Tomasz Marszalek ◽  
Mengmeng Li ◽  
Wojciech Pisula

This review discusses the role of chemical design on the self-assembly of donor–acceptor polymers on surfaces. Three major structural factors are highlighted including molecular weight, side chain engineering and backbone curvature of the polymers.


2014 ◽  
Vol 16 (36) ◽  
pp. 19402-19407 ◽  
Author(s):  
Harekrishna Ghosh ◽  
Ahmed Bouhekka ◽  
Thomas Bürgi

Germanium modified with gold nanoparticles shows a drastically increased concentration of holes near the valence band edge upon illumination with visible or near infrared light.


2017 ◽  
Vol 53 (15) ◽  
pp. 2371-2374 ◽  
Author(s):  
Sougata Datta ◽  
Nilanjan Dey ◽  
Santanu Bhattacharya

We report the electrochemical analysis of a donor–acceptor type two-component hydrogelation by an electroactive co-assembly of pyranine and n-dodecyl methyl viologen.


2021 ◽  
Vol 5 (7) ◽  
pp. 193
Author(s):  
Adrian Ionut Bercea ◽  
Corinne Champeaux ◽  
Catalin Daniel Constantinescu ◽  
Frédéric Dumas-Bouchiat

This work serves as a roadmap for the development of a Vanadium dioxide (VO2)–Iridium composite based on the self-assembly of closely packed colloidal polystyrene microspheres (P-spheres) coupled with a Pulsed Laser Deposition (PLD) process. The self-assembly of a monolayer of PS is performed on an Al2O3-c substrate, using an adapted Langmuir–Blodgett (LB) process. Then, on the substrate covered with P-spheres, a 50-nanometer Iridium layer is deposited by PLD. The Iridium deposition is followed by the removal of PS with acetone, revealing an array of triangular shaped metallic elements formed on the underlaying substrate. In a last deposition step, 50-, 100- and 200-nanometer thin films of VO2 are deposited by PLD on top of the substrates covered with the Iridium quasi-triangles, forming a composite. Adapting the size of the P-spheres leads to control of both the size of the Iridium micro-triangle and, consequently, the optical transmittance of the composite. Owing to their shape and size the Iridium micro-triangles exhibit localized surface plasmon resonance (LSPR) characterized by a selective absorption of light. Due to the temperature dependent properties of VO2, the LSPR properties of the composite can be changeable and tunable.


2012 ◽  
Vol 25 (1) ◽  
pp. 27-32 ◽  
Author(s):  
Norikatsu Sasao ◽  
Ryosuke Yamamoto ◽  
Naoko Kihara ◽  
Takuya Shimada ◽  
Akiko Yuzawa ◽  
...  

Molecules ◽  
2020 ◽  
Vol 25 (19) ◽  
pp. 4551
Author(s):  
Yongjun Zhang ◽  
Fan Zhang ◽  
Yaxin Wang

We demonstrated that the localized surface plasmon resonance (LSPR) features of Ag/TiS2 nanostructures were dependent on the sublayer thickness. The Ag/TiS2 bilayer film was obtained by the self-assembly method and magnetron sputtering. The thickness was controlled by changing the sputtering time when the sputtering powers were the same. When the Ag thickness decreased from 50 nm to 5 nm, the LSPR was tuned from the visible region to the Near Infrared (NIR) region. When the TiS2 thickness decreased from 60 nm to 2 nm, the LSPR shifted from the IR to NIR region. Analysis showed the thickness changes of Ag and TiS2 resulted in the changed carrier density, which led to the thickness-dependent shift of the LSPR.


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