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Hydroxyl-functionalized polymers using initiator solubility

An example of a functional organolithium initiator is p-lithiophenoxide. It acts both as a carrier of hydroxyl functionality and as an initiator for polymerization (122). Unfortunately, p-lithiophenoxide has a low solubility, even in such polar solvents as THF, and up to 30% of the initiator is initially inactive toward polymerization. It is difficult to control polymer molecular weights when such initiators are used (123). Trepka (124) improved the solubility of p-lilhiophenoxide by the introduction of alkyl... [Pg.91]


See other pages where Hydroxyl-functionalized polymers using initiator solubility is mentioned: [Pg.36]    [Pg.450]    [Pg.312]    [Pg.362]    [Pg.47]    [Pg.566]    [Pg.179]    [Pg.456]    [Pg.107]    [Pg.11]    [Pg.12]    [Pg.12]    [Pg.147]    [Pg.158]    [Pg.4]    [Pg.71]    [Pg.421]    [Pg.80]    [Pg.501]    [Pg.70]    [Pg.210]    [Pg.179]   
See also in sourсe #XX -- [ Pg.75 , Pg.76 ]




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Hydroxyl functionalities

Hydroxyl functions

Hydroxyl-functionalized polymers

Hydroxyl-functionalized polymers using

Hydroxylated polymers

Hydroxylation solubility

Initiators functional

Polymers solubility

Solubility function

Soluble polymers

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