The Effect of Head-Group on Selective Counterion Binding to Cationic Surfactants

1997 ◽  
Vol 193 (2) ◽  
pp. 312-314 ◽  
Author(s):  
Leoni Kellaway ◽  
Gregory G. Warr
Author(s):  
Mohammad Rashidi-Alavijeh ◽  
Soheila Javadian ◽  
Hussein Gharibi ◽  
Morteza Moradi ◽  
Ali Reza Tehrani-Bagha ◽  
...  

2013 ◽  
Vol 575-576 ◽  
pp. 245-248 ◽  
Author(s):  
Zong Cheng Miao ◽  
Yi Wei Wang ◽  
Xing Zhang ◽  
Lei Zhang ◽  
Zhi Xue Wang ◽  
...  

Gemini surfactants generally exhibit superior properties to those of their single-chain analogues with a similar chain length and head group, especially for gemini cationic surfactants. Gemini cationic surfactants have recently attracted considerable attention due to the increasing microbial resistance to common quaternary ammonium compounds. A novel symmetrical gemini cationic surfactant based onn-hexadecyldimethylamine was synthesized through epichlorohydrin andn-hexadecyldimethylamine as rude materials. The chemical structure of the product was confirmed using1H-NMR and FT-IR. The minimum inhibitory concentration of the surfactant toescherichia colirises to 100 ppm, and a higher concentration surely contributes to increase its effect, butstaphylococcus aureusis immune to this surfactant.


2018 ◽  
Vol 42 (18) ◽  
pp. 14914-14925 ◽  
Author(s):  
Biman Kumar Patel ◽  
Nayim Sepay ◽  
Suparna Rudra ◽  
Ambikesh Mahapatra

We decipher the mode of binding of surfactants with hemoglobin and their release by β-cyclodextrin.


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