Process for the synthesis of hydroxyl-end group functionalized polybutadienes.

  • Peters M
N/ACitations
Citations of this article
1Readers
Mendeley users who have this article in their library.

Abstract

The process for the prepn. of an hydroxyl end-group functionalized, linear, non-crosslinked polyolefin without pendant chain branched groups comprises (I) polymg. (A) a cyclic olefin monomer with (B) a chain transfer agent in the presence of (C) a metathesis polymn. catalyst; thereby forming a protected end-group functionalized polyolefin, (II) sapong. the protected end-group functionalized polyolefin by adding (D) a mixt. comprising water and caustic, to the protected end-group functionalized polyolefin to remove the protecting end-groups. Thus, a hydroxyl-terminated polybutadiene was prepd. by polymg. 1,5-cyclooctadiene using 1,4-diacetoxy-2-butene in the presence of bis(tricyclohexylphosphine)benzylidene-ruthenium dichloride, then sapong. in potassium hydroxide soln., and finally neutralizing in sulfuric acid soln. [on SciFinder(R)]

Cite

CITATION STYLE

APA

Peters, M. A. (2002, May 21). Process for the synthesis of hydroxyl-end group functionalized polybutadienes. U.S. Bayer Corporation, USA .

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free