Structure directing role of amines and water molecules in the self-assembly of polyoxomolybdates

CrystEngComm ◽  
2017 ◽  
Vol 19 (15) ◽  
pp. 2021-2035 ◽  
Author(s):  
Amanpreet Kaur Jassal ◽  
Love Karan Rana ◽  
Geeta Hundal

2020 ◽  
Vol 56 (29) ◽  
pp. 4102-4105 ◽  
Author(s):  
Pedro J. Pacheco-Liñán ◽  
Cristina Martín ◽  
Carlos Alonso-Moreno ◽  
Alberto Juan ◽  
Daniel Hermida-Merino ◽  
...  

New AIEGen was obtained (QY = 1) based on the formation of an aggregate-dimer in the ground state assisted by water molecules. The inclusion of guanidine group is crucial to open a new framework for developing more environmentally friendly AIEGen.



2020 ◽  
Vol 27 (9) ◽  
pp. 923-929
Author(s):  
Gaurav Pandey ◽  
Prem Prakash Das ◽  
Vibin Ramakrishnan

Background: RADA-4 (Ac-RADARADARADARADA-NH2) is the most extensively studied and marketed self-assembling peptide, forming hydrogel, used to create defined threedimensional microenvironments for cell culture applications. Objectives: In this work, we use various biophysical techniques to investigate the length dependency of RADA aggregation and assembly. Methods: We synthesized a series of RADA-N peptides, N ranging from 1 to 4, resulting in four peptides having 4, 8, 12, and 16 amino acids in their sequence. Through a combination of various biophysical methods including thioflavin T fluorescence assay, static right angle light scattering assay, Dynamic Light Scattering (DLS), electron microscopy, CD, and IR spectroscopy, we have examined the role of chain-length on the self-assembly of RADA peptide. Results: Our observations show that the aggregation of ionic, charge-complementary RADA motifcontaining peptides is length-dependent, with N less than 3 are not forming spontaneous selfassemblies. Conclusion: The six biophysical experiments discussed in this paper validate the significance of chain-length on the epitaxial growth of RADA peptide self-assembly.



2021 ◽  
Author(s):  
Beatriz Matarranz ◽  
Goutam Ghosh ◽  
Ramesh Kandanelli ◽  
Angel Sampedro ◽  
Kalathil K. Kartha ◽  
...  

We unravel the relationship between conjugation length and self-assembly behaviour of oligophenyleneethynylenes (OPEs).



2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Meneka Banik ◽  
Shaili Sett ◽  
Chirodeep Bakli ◽  
Arup Kumar Raychaudhuri ◽  
Suman Chakraborty ◽  
...  

AbstractSelf-assembly of Janus particles with spatial inhomogeneous properties is of fundamental importance in diverse areas of sciences and has been extensively observed as a favorably functionalized fluidic interface or in a dilute solution. Interestingly, the unique and non-trivial role of surface wettability on oriented self-assembly of Janus particles has remained largely unexplored. Here, the exclusive role of substrate wettability in directing the orientation of amphiphilic metal-polymer Bifacial spherical Janus particles, obtained by topo-selective metal deposition on colloidal Polymestyere (PS) particles, is explored by drop casting a dilute dispersion of the Janus colloids. While all particles orient with their polymeric (hydrophobic) and metallic (hydrophilic) sides facing upwards on hydrophilic and hydrophobic substrates respectively, they exhibit random orientation on a neutral substrate. The substrate wettability guided orientation of the Janus particles is captured using molecular dynamic simulation, which highlights that the arrangement of water molecules and their local densities near the substrate guide the specific orientation. Finally, it is shown that by spin coating it becomes possible to create a hexagonal close-packed array of the Janus colloids with specific orientation on differential wettability substrates. The results reported here open up new possibilities of substrate-wettability driven functional coatings of Janus particles, which has hitherto remained unexplored.



2007 ◽  
Vol 111 (51) ◽  
pp. 14233-14238 ◽  
Author(s):  
Guillaume Tresset ◽  
Wun Chet Davy Cheong ◽  
Yeng Ming Lam
Keyword(s):  
The Self ◽  


2012 ◽  
Vol 550-553 ◽  
pp. 57-61
Author(s):  
Hao Li ◽  
Yong Hong Deng ◽  
Kai Huang

Alkali lignin (AL) was used as a polyanion to form layer-by-layer self-assembled film with PDAC as a polycation. The effects of temperature and concentration on the adsorption characteristics of AL were investigated. Iodine was added into AL solutions to study the role of π-π interaction in self-assembly of AL and PDAC. Results show that the self-assembly of AL/PDAC is mainly driven by π-π interaction and electrostatic interaction. A higher temperature or a larger concentration can enhance the aggregation of lignin. I2 can form lignin–iodine charge–transfer complexes with AL to reduce the degree of aggregation of AL, so the adsorbed amount of AL decreases significantly with increasing iodine contents.



2017 ◽  
Vol 129 (43) ◽  
pp. 13473-13477 ◽  
Author(s):  
Shibaji Basak ◽  
Ishwar Singh ◽  
Annaleizle Ferranco ◽  
Jebreil Syed ◽  
Heinz-Bernhard Kraatz
Keyword(s):  


2017 ◽  
Vol 1142 ◽  
pp. 148-155 ◽  
Author(s):  
Amanpreet Kaur Jassal ◽  
Rajwinder Kaur ◽  
Nasarul Islam ◽  
Anu ◽  
Rahul Kumar Mudsainiyan




RSC Advances ◽  
2015 ◽  
Vol 5 (115) ◽  
pp. 95007-95013 ◽  
Author(s):  
A. Scelsi ◽  
B. Bochicchio ◽  
A. Smith ◽  
A. Saiani ◽  
A. Pepe

The self-assembly of an elastin-inspired triblock peptide into nanospheres highlights the important role of conformational flexibility and π–π stacking.



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