Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Charles M. Leir"'
Telechelic siloxanes with hydrogen-bonded polymerizable end groups. I. Liquid rubbers and elastomers
Publikováno v:
Journal of Applied Polymer Science. 117:756-766
Functional siloxanes are widely used in the synthesis of model networks used in rubber elasticity studies, and various functional siloxanes are also used in the synthesis of silicone rubbers. We present here the results of studies of two classes of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::baef90a1d318f19a7590b6e7ab83a7c9
https://doi.org/10.1002/app.31757
https://doi.org/10.1002/app.31757
Publikováno v:
Journal of Applied Polymer Science. 117:982-995
Hydrogen-bonding phenomena in amides and ureas are of great practical and theoretical importance. In this article, we report on infrared temperature studies aimed at the elucidation of the hydrogen-bonding phenomena of (meth)acrylamide groups directl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d8232c79da56bcb75d22db5259a85cb
https://doi.org/10.1002/app.31553
https://doi.org/10.1002/app.31553
Autor:
Kyle J. Lindstrom, Philip D. Heppner, Daniel J Willie, Michael E. Danielson, Charles M. Leir, Joshua R. Wurst, Gregory D. Lundquist, Sonja S. Mackey, Tushar A. Kshirsagar, Chad A. Haraldson, David S. Hays, Karl E. Benson
Publikováno v:
The Journal of Organic Chemistry. 72:4570-4573
The deprotonation and regioselective reaction of 2H-pyrazolo[3,4-c]quinolines with a variety of electrophiles is described. Electrophiles include benzaldehyde, DMF, carbon dioxide, and iodine. This method provides a direct route to a class of pharmac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b0237f06064236349491db0ad2186ef
https://doi.org/10.1021/jo070392t
https://doi.org/10.1021/jo070392t
Publikováno v:
Journal of Macromolecular Science: Part A - Chemistry. 26:1151-1181
A series of segmented ionene polymers with polytetramethyleneoxide (PTMO) soft segments and dibromoxylene hard segments have been studied by small-angle x-ray scattering (SAXS) and by transmission electron microscopy (TEM). As detected by SAXS, these
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb9c22e9251aebabb02de383b6331beb
https://doi.org/10.1080/00222338908052040
https://doi.org/10.1080/00222338908052040
Autor:
John E. Stark, Charles M. Leir
Publikováno v:
Journal of Applied Polymer Science. 38:1535-1547
The reaction of α,ω-bis(dimethylamino) polytetramethylene oxide with various dihalides provided a series of elastomeric ionenes. The influence of dihalide structure on the reaction was studied and a number of substituents were found which dramatica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8a25e306e660d55bce674b0e632b312
https://doi.org/10.1002/app.1989.070380810
https://doi.org/10.1002/app.1989.070380810
Publikováno v:
Journal of Applied Polymer Science. 38:1549-1565
A series of segmented ionene polymers based on the reaction of α,ω-bis(dimethyl amino)polytetramethylene oxide with various dihalide compounds were investigated with respect to their structure–property behavior. The placement of quaternary ammoni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b082eae91adb2a6fb6b424ca73f9e160
https://doi.org/10.1002/app.1989.070380811
https://doi.org/10.1002/app.1989.070380811
Autor:
Charles M. Leir
Publikováno v:
The Journal of Organic Chemistry. 42:911-913
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d463e1f5acbab5c0dcc0f25e0298d33
https://doi.org/10.1021/jo00425a036
https://doi.org/10.1021/jo00425a036
Autor:
Charles M. Leir
Publikováno v:
The Journal of Organic Chemistry. 35:3203-3205
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3e3b97502de7d558d9710c5c805a8de
https://doi.org/10.1021/jo00835a001
https://doi.org/10.1021/jo00835a001
Autor:
Charles M. Leir
Publikováno v:
The Journal of Organic Chemistry. 37:887-889
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a495eec10f9b77e437ff5da30e960f4e
https://doi.org/10.1021/jo00971a016
https://doi.org/10.1021/jo00971a016
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