scholarly journals Diketopyrrolopyrrole (DPP)-based polytriazoles: Synthesis and Immobilization by click reaction†

Author(s):  
debasis samanta ◽  
P Ramar ◽  
V Raghavendra

Diketopyrrolopyrrole-based polymers are generally immobilized to various surfaces for device fabrications and sensor applications. preparative methods as well as Immobilization processes play a significant role for device efficacy. In this paper, we demonstrated that while "click" polymerization can be conveniently used for the preparation of diketopyrrolopyrrole DPP-based polymer, self-assembled monolayer (SAM) formation technique is convenient for efficient Immobilization to surfaces. Computational models have been used to theoretically calculate various energy parameters. Finally, some of those surfaces have been used as reusable photocatalytic chips, in line with mechanistically similar photovoltaic chips

Molecules ◽  
2018 ◽  
Vol 23 (11) ◽  
pp. 2998 ◽  
Author(s):  
Shanshan Li ◽  
Qingying Luo ◽  
Zhiqing Zhang ◽  
Guanghui Shen ◽  
Hejun Wu ◽  
...  

We investigated the permselectivity and interfacial electron transfers of an amphiphilic branch-tailed fluorosurfactant self-assembled monolayer (FS-SAM) on a gold electrode by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The FS-SAM was prepared by a self-assembly technique and a “click” reaction. The barrier property and interfacial electron transfers of the FS-SAM were also evaluated using various probes with different features. The FS-SAM allowed a higher degree of permeation by small hydrophilic (Cl− and F−) electrolyte ions than large hydrophobic (ClO4− and PF6−) ones. Meanwhile, the redox reaction of the Fe(CN)63− couple was nearly completely blocked by the FS-SAM, whereas the electron transfer of Ru(NH3)63+ was easier than that of Fe(CN)63−, which may be due to the underlying tunneling mechanism. For hydrophobic dopamine, the hydrophobic bonding between the FS-SAM exterior fluoroalkyl moieties and the hydrophobic probes, as well as the hydration resistance from the interior hydration shell around the oligo (ethylene glycol) moieties, hindered the transport of hydrophobic probes into the FS-SAM. These results may have profound implications for understanding the permselectivity and electron transfers of amphiphilic surfaces consisting of molecules containing aromatic groups and branch-tailed fluorosurfactants in their structures.


2012 ◽  
Vol 48 (99) ◽  
pp. 12068 ◽  
Author(s):  
Debasis Samanta ◽  
P. Murugan ◽  
Soundaram Jeevarathinam Ananthakrishnan ◽  
Narayanasastri Somanathan ◽  
Sujoy K. Das ◽  
...  

2019 ◽  
Author(s):  
Luke Clifton ◽  
Nicoló Paracini ◽  
Arwel V. Hughes ◽  
Jeremy H. Lakey ◽  
Nina-Juliane Seinke ◽  
...  

<p>We present a reliable method for the fabrication of fluid phase unsaturated bilayers which are readily self-assembled on charged self-assembled monolayer (SAM) surfaces producing high coverage floating supported bilayers where the membrane to surface distance could be controlled with nanometer precision. Vesicle fusion was used to deposit the bilayers onto anionic SAM coated surfaces. Upon assembly the bilayer to SAM solution interlayer thickness was 7-10 Å with evidence suggesting that this layer was present due to SAM hydration repulsion of the bilayer from the surface. This distance could be increased using low concentrations of salts which caused the interlayer thickness to enlarge to ~33 Å. Reducing the salt concentration resulted in a return to a shorter bilayer to surface distance. These accessible and controllable membrane models are well suited to a range of potential applications in biophysical studies, bio-sensors and Nano-technology.</p><br>


2021 ◽  
Author(s):  
Lidia Rosado Piquer ◽  
Jan Dreiser ◽  
E. Carolina Sañudo

The heterometallic 3d-4f SMM [Co4Dy(OH)2(SALOH)5(chp)4(MeCN)(H2O)2] (1) has been deposited onto iron oxide nanoparticles (NP) with an oleate self-assembled monolayer (SAM) as surfactant. The hybrid molecular-inorganic system 1-NP has been thoroughly...


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