scholarly journals Motion Restricted by Hydration Shell: A Self-Reporting System for Visualizing Electrolyte Interactions

Author(s):  
Hao Xing ◽  
Junkai Liu ◽  
Xiaowei Wang ◽  
Yeqing Yu ◽  
Ying Yu, ◽  
...  

<div><div><div><p>Electrolyte interaction is of pivotal importance for chemical, biochemical, and environmental processes, including cellular signal transduction, DNA attraction, and protein dynamics. Although its investigation has been at the focus of extensive research, direct visualization of electrolyte interaction at the molecular level is exceptionally challenging. Here, we report a highly sensitive and readily-accessible technique to visualize the electrolyte interactions in water through molecular design and fluorescence spectroscopy. Two water-soluble luminogens with either cationic or anionic groups are designed as electrolyte models. The hydration shell of isolated luminogens is able to restrict their intramolecular motion, which enhances the emission. Consequently, the occurred electrolyte interactions can be optically detected since they affect the reorientation dynamics of water molecules in the hydration shell and vary the restriction strength on the intramolecular motion of the luminogens. Moreover, this technology allows us to reveal how electrolyte interaction affects the internal motion of an electrolyte within its hydration shell, which has rarely been achieved through experimental approaches.</p></div></div></div>

2020 ◽  
Author(s):  
Hao Xing ◽  
Junkai Liu ◽  
Xiaowei Wang ◽  
Yeqing Yu ◽  
Ying Yu, ◽  
...  

<div><div><div><p>Electrolyte interaction is of pivotal importance for chemical, biochemical, and environmental processes, including cellular signal transduction, DNA attraction, and protein dynamics. Although its investigation has been at the focus of extensive research, direct visualization of electrolyte interaction at the molecular level is exceptionally challenging. Here, we report a highly sensitive and readily-accessible technique to visualize the electrolyte interactions in water through molecular design and fluorescence spectroscopy. Two water-soluble luminogens with either cationic or anionic groups are designed as electrolyte models. The hydration shell of isolated luminogens is able to restrict their intramolecular motion, which enhances the emission. Consequently, the occurred electrolyte interactions can be optically detected since they affect the reorientation dynamics of water molecules in the hydration shell and vary the restriction strength on the intramolecular motion of the luminogens. Moreover, this technology allows us to reveal how electrolyte interaction affects the internal motion of an electrolyte within its hydration shell, which has rarely been achieved through experimental approaches.</p></div></div></div>


2019 ◽  
Vol 10 (47) ◽  
pp. 6489-6494 ◽  
Author(s):  
Yan-Qing Fan ◽  
Qing Huang ◽  
You-Ming Zhang ◽  
Jiao Wang ◽  
Xiao-Wen Guan ◽  
...  

Two novel approaches for highly sensitive detection and efficient adsorption of aldehydes by forming a water-soluble supramolecular polymer and an AIEE hydrogel.


Polymer ◽  
2012 ◽  
Vol 53 (12) ◽  
pp. 2356-2360 ◽  
Author(s):  
Wenjun Zhang ◽  
Chen'ge Li ◽  
Jingui Qin ◽  
Chuluo Yang

2020 ◽  
Vol 24 (01n03) ◽  
pp. 362-378 ◽  
Author(s):  
Nobuyuki Matsumoto ◽  
Masahiko Taniguchi ◽  
Jonathan S. Lindsey

Chlorins provide many ideal features for use as red-region fluorophores but require molecular tailoring for solubilization in aqueous solution. A chlorin building-block bearing 18,18-dimethyl, 15-bromo and 10-[2,4,6-tris(propargyloxy)phenyl] substituents has been transformed via click chemistry with CH3(OCH2CH[Formula: see text]-N3 followed by Suzuki coupling with 3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propanoic acid, thereby installing a water-solubilization motif and a bioconjugatable handle, respectively. In toluene, [Formula: see text]-dimethylformamide (DMF) or water, the resulting facially encumbered free base chlorin exhibits characteristic chlorin absorption ([Formula: see text] [Formula: see text]412, 643 nm) and fluorescence ([Formula: see text] [Formula: see text]645 nm) spectra with only modest variation in fluorescence quantum yield ([Formula: see text] values (0.24, 0.25 and 0.19, respectively). The zinc chlorin derived therefrom exhibits similar spectral constancy ([Formula: see text] [Formula: see text]414 and 613 nm, [Formula: see text] [Formula: see text]616 nm) and [Formula: see text] 0.094, 0.10 and 0.086 in the three solvents. The results together indicate the viability of the molecular design and synthetic methodology to create red-region fluorophores for use in diverse applications.


1992 ◽  
Vol 277 ◽  
Author(s):  
Jang-Joo Kim ◽  
Do-Hoon Hwang ◽  
Shin-Woong Kang ◽  
Hong-Ku Shim

ABSTRACTPoly(CMPV-co-PV) have been synthesized via water soluble sulfonium salt precursor route and their linear and non-linear optical properties were characterized. The electro-optic response was stable up to 100°C when the materials were poled during the elimination. The thermal stability and mechanical strength of PPV and its derivatives, and easy processibility from the precursor polymers suggest a new approach for the molecular design of the 2nd order non-linear optical polymers.


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