Synthesis and characterization of isocyanic acid,m-phenylenediiso-propylidene based poly(urethane-urea) dispersions containing different amount of 2,2-Bis(hydroxyl methyl)propionic acid

2006 ◽  
Vol 102 (6) ◽  
pp. 5737-5746 ◽  
Author(s):  
Hsien-Tang Chiu ◽  
Yi-Chin Huang ◽  
Hsiu-Yeh Hu
2004 ◽  
Vol 42 (7) ◽  
pp. 1758-1767 ◽  
Author(s):  
Michael Malkoch ◽  
Hans Claesson ◽  
Peter Löwenhielm ◽  
Eva Malmström ◽  
Anders Hult

1997 ◽  
Vol 50 (9) ◽  
pp. 939 ◽  
Author(s):  
Fang Chen ◽  
Parveen Akhtar ◽  
Leon A. P. Kane-Maguire ◽  
Gordon G. Wallace

A range of optically active pyrrole monomers have been synthesized in which a chiral sub- stituent is covalently bonded either to the pyrrole N or C3 ring position, namely (–)-(1R)-4-methyl-N-(1-phenylethyl)pyrrole-3-carboxamide, (+)-(1S)-4-methyl-N-(1-phenylethyl)pyrrole-3-carboxamide, (–)-(1R)-4-methyl-N-(1-naphthylethyl)pyrrole-3-carboxamide, (+)-(1S)-4-methyl-N-(1-naphthylethyl)pyrrole-3-carboxamide, (+)-(2S)-2-(1H-pyrrol-1-yl)propionic acid, (+)-(1S)-N-(1-phenyl-ethyl)pyrrole, and (–)-(1R)-N-(1-phenylethyl)pyrrole. Their chiroptical properties have been established by circular dichroism spectroscopy. Electropolymerization of the three N-substituted pyrrole monomers provided films of chiral conducting polymers, whose electrical and spectroscopic properties are described. Although oxidation of the C3 substituted pyrrole monomers was also facile, electrodeposition was poor and films of the associated polymers could not be obtained.


2013 ◽  
Vol 19 (4) ◽  
pp. 1226-1228
Author(s):  
Guoku Chao ◽  
Lianping Shao ◽  
Shuai Yao ◽  
Liming Hong ◽  
Dashuai Li ◽  
...  

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