Anionic Synthesis of α-Functionalized Polymers by Combination of 1,1-Diphenylethylene and Hydrosilation Chemistry

2013 ◽  
Vol 325-326 (1) ◽  
pp. 77-88 ◽  
Author(s):  
Roderic P. Quirk ◽  
Sujata Sahoo
1990 ◽  
Vol 32 (1) ◽  
pp. 47-59 ◽  
Author(s):  
Roderic P. Quirk ◽  
Jian Yin ◽  
Shao-Hua Guo ◽  
Xiao-Wei Hu ◽  
Gabriel Summers ◽  
...  

2000 ◽  
Vol 161 (1) ◽  
pp. 37-44 ◽  
Author(s):  
Roderic P. Quirk ◽  
Jing-Jing Ma ◽  
Gilda Lizarraga ◽  
Qing Ge ◽  
Hiroaki Hasegawa ◽  
...  

1992 ◽  
Vol 50 (0) ◽  
pp. 23-41 ◽  
Author(s):  
Roderic P. Quirk ◽  
Toshiki Takizawa ◽  
Glida Lizarraga ◽  
Lin-Fang Zhu

2003 ◽  
Vol 76 (4) ◽  
pp. 812-831 ◽  
Author(s):  
Roderic P. Quirk ◽  
Deanna L. Gomochak

Abstract Recent developments are reviewed for the applications of reactions of polymeric organolithium compounds with epoxides and oxetane to obtain the corresponding ω-hydroxy chain-end functionalized polymers. State-of-the-art characterization methods for ω-functionalized polymers are also reviewed. Investigations of the usefulness of functionalization reactions of polymeric organolithium compounds with ethylene oxide, propylene oxide, 1-butene oxide, styrene oxide, oxetane, 3,4-epoxy-1-butene, 3-glycidoxypropyltrimethoxysilane and other epoxides are described. In general, these functionalization reactions are very efficient (> 90% yields of ω-hydroxy-functionalized polymers). The use of substituted epoxides is shown to provide an efficient methodology for attachment of a variety of groups at the polymer chain end.


2008 ◽  
Vol 81 (1) ◽  
pp. 77-95 ◽  
Author(s):  
Roderic P. Quirk ◽  
Manuela Ocampo ◽  
Rebecca L. King ◽  
Michael J. Polce ◽  
Chrys Wesdemiotis

Abstract A new general functionalization methodology (GFM) is applied to the synthesis of trimethoxysilyl-functionalized polymers. This GFM involves (a) the preparation of a well-defined polymeric organolithium compound (PLi) using alkyllithium-initiated anionic polymerization; (b) quantitative silyl hydride-functionalization of PLi with chlorodimethylsilane to form PSi(CH3)2H; (c) hydrosilation of PSi(CH3)2H with vinyltrimethoxysilane in the presence of Karstedt's catalyst. The desired PSi(OCH3)3 was obtained in > 80% yield. The product was characterized by SEC, 1H and 13C NMR and MALDI-TOF mass spectrometry.


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