Discriminating Among Co-monomer Sequence Distributions in Random Copolymers Using Interaction Chromatography

2009 ◽  
Vol 30 (18) ◽  
pp. 1543-1548 ◽  
Author(s):  
Junwon Han ◽  
Byung Ho Jeon ◽  
Chang Y. Ryu ◽  
James J. Semler ◽  
Young K. Jhon ◽  
...  
2007 ◽  
Vol 19 (19) ◽  
pp. 2877-2883 ◽  
Author(s):  
J. J. Semler ◽  
Y. K. Jhon ◽  
A. Tonelli ◽  
M. Beevers ◽  
R. Krishnamoorti ◽  
...  

1970 ◽  
Vol 43 (5) ◽  
pp. 1138-1153 ◽  
Author(s):  
V. D. Mochel ◽  
B. L. Johnson

Abstract A method is described for determining styrene sequence distribution in butadiene-styrene copolymers. An analog computer is used to resolve overlapped peaks in the styrene aromatic proton NMR spectrum. In n-BuLi copolymers a quite quantitative distinction can be made between “short” sequences, containing two and three styrene units, and “long” sequences, containing more than three units. With this method it is possible to determine experimentally the styrene-centered triad distributions and approximate styrene sequence distributions of butadiene—styrene copolymers. Agreement between calculated and NMR-curve analysis results is good, especially for n-butyllithium-catalyzed butadiene—styrene copolymers.


2012 ◽  
Vol 1 (9) ◽  
pp. 1128-1133 ◽  
Author(s):  
Wayne Powers ◽  
Chang Y. Ryu ◽  
Young K. Jhon ◽  
Lawrence A. Strickland ◽  
Carol K. Hall ◽  
...  

1982 ◽  
Vol 15 (5) ◽  
pp. 1402-1406 ◽  
Author(s):  
Eric T. Hsieh ◽  
James C. Randall

Author(s):  
Abraham Herzog-Arbeitman ◽  
Jeffrey Ting ◽  
Siqi Meng ◽  
Hao Wu ◽  
Matthew Tirrell

<div> <div> <div> <p>Charge-driven complexation of polyelectrolytes in water is a fundamental phase separation phenomenon that is prevalent in nature and across the high-value technology landscape. Here we describe an experimentally convenient and versatile approach to construct patterned PECs, comprising well-defined charged macromolecules with both ionic styrene and neutral maleimide units alternating in the chain sequence. </p> </div> </div> </div>


2014 ◽  
Vol 48 (1) ◽  
pp. 58-63 ◽  
Author(s):  
Yavuz Caydamli ◽  
Yi Ding ◽  
Abhay Joijode ◽  
Shanshan Li ◽  
Jialong Shen ◽  
...  

2003 ◽  
Vol 771 ◽  
Author(s):  
Petra Herguth ◽  
Joo Hyun Kim ◽  
Xuezhong Jiang ◽  
Michelle S. Liu ◽  
Alex K-Y. Jen

AbstractThe emission wavelength in conjugated copolymers is determined by the various monomers used, their sequence in the polymer backbone, the effective conjugation length of the material, and intra- and intermolecular interactions of the different units. This paper will discuss the influence of conjugation length as well as the influence of intramolecular charge-transfer on the absorption and emission properties. Fluorene, benzothiadiazole and a third comonomer (fluorene, xylene or triphenylamine) were used as building blocks. The influence of monomer sequence is probed as well by comparing sequentially random copolymers to their sequentially defined ones with identical monomer ratios. Model oligomers were also made for comparison.


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