Grafting of amphiphilic polymers containing quaternary ammonium group on SiO2 surface via surface-initiated ATRP

2012 ◽  
Vol 19 (2) ◽  
Author(s):  
Wenping Wang ◽  
Jiayuan Tang ◽  
Zhongqi Jia ◽  
Xiaoxuan Li ◽  
Zhenghui Xiao
ChemSusChem ◽  
2008 ◽  
Vol 1 (1-2) ◽  
pp. 103-109 ◽  
Author(s):  
Łukasz Gułajski ◽  
Anna Michrowska ◽  
Joanna Narożnik ◽  
Zuzanna Kaczmarska ◽  
Leszek Rupnicki ◽  
...  

Soft Matter ◽  
2018 ◽  
Vol 14 (3) ◽  
pp. 387-395 ◽  
Author(s):  
Mintai P. Hwang ◽  
Xiaochu Ding ◽  
Jin Gao ◽  
Abhinav P. Acharya ◽  
Steven R. Little ◽  
...  

Betaine, a naturally occurring amino acid, is conjugated onto a polyester backbone, in which the quaternary ammonium group imparts additional functionality to the resulting polycation (B-PED). B-PED demonstrates excellentin vitroandin vivobiocompatibility and is also assessed for its effect on angiogenesis, anti-bacterial activity, and complex coacervation.


1982 ◽  
Vol 37 (3-4) ◽  
pp. 282-288 ◽  
Author(s):  
Gieren Gieren ◽  
Michail Kokkinidis

Abstract The crystal structure of Trimethyl(4-oxopentyl)ammonium-chloride ([(CH3)3N+-(CH2)3COCH3]Cl-) (1) was determined by an X-ray structure analysis. 1 crystallizes in the orthorhombic space group P212121 with a = 10.440 (3), b = 14.600 (9), c = 6.804 (9) Å and with four formula units per unit cell. The structure was solved by a Patterson and a successive Fourier synthesis. The least squares refinement yielded an R-value of 0.064 for 1077 observed reflections. The cation of 1 is derived from acetylcholine by replacement of the ester oxygen with a CH2 group. It shows a potent nicotinic activity and a significant difference in conformation as compared with acetylcholine. In the crystal structure the anions are oriented stereospecifically with respect to the tetrahedron of the quaternary ammonium group. The geometry of two triangles formed by the quaternary nitrogen atom, the oxygen atom of the carbonyl group, and by either of the two anions nearest to the quaternary ammonium group is characteristic for the nicotinic activity of 1.


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