Chemical synthesis of amino-group-containing (1 → 6)-α-D-glucan derivatives by ring-opening polymerization of 1,6-anhydroazido sugars

1983 ◽  
Vol 16 (6) ◽  
pp. 853-858 ◽  
Author(s):  
Toshiyuki Uryu ◽  
Kenichi Hatanaka ◽  
Kei Matsuzaki ◽  
Hiroyoshi Kuzuhara
2014 ◽  
Vol 513-517 ◽  
pp. 86-90
Author(s):  
Feng Hong Li ◽  
Wen Jing Zhang ◽  
San Xi Li ◽  
Yan Ming Chen ◽  
Xin Rui Zhang

The amphiphilic chitosan oligosaccharides graft copolymer (PHCSO-g-PCL) was synthesized via ring-opening polymerization (ROP) of ε-caprolactone (ε-CL) through an amino group protection route using phthaloyl chitosan oligosaccharide (PHCSO) as intermediate. The graft reaction was carried out in Pyridine at 120 °C with a chitosan oligosaccharide (CSO) initiator and a tin 2-ethylhexanoate (Sn (Oct)2) catalyst. The amphiphilic PHCSO-g-PCL nanoparticles were prepared through the self-assembled in DMF organic solvents. PHCSO-PCL copolymer was characterized by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The physicochemical properties of the hydrophobized PHCSO-g-PCL nanoparticles were investigated by using dynamic light scattering (DLS). The results of DLS showed that the hydrodynamic diameters and particle size distribution with various concentrations of PHCSO-g-PCL nanoparticles were from 69.82 nm to 195.9 nm with a narrow polydispersity factor of 0.212 to 0.172.


1991 ◽  
Vol 24 (25) ◽  
pp. 6797-6799 ◽  
Author(s):  
Masahiko Okada ◽  
Yoshitaka Yamakawa ◽  
Hiroshi Sumitomo

1986 ◽  
Vol 18 (8) ◽  
pp. 601-611 ◽  
Author(s):  
Masahiko Okada ◽  
Hiroshi Sumitomo ◽  
Takahito Hirasawa ◽  
Kiyomichi Ihara ◽  
Yoshikazu Tada

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