Theses and Dissertations
Issuing Body
Mississippi State University
Advisor
Rowland, Gerald
Committee Member
Pittman, Charles U., Jr.
Committee Member
Walters, Keisha B.
Committee Member
Wipf, David
Date of Degree
5-17-2014
Document Type
Graduate Thesis - Open Access
Major
Chemistry
Degree Name
Master of Science
College
College of Arts and Sciences
Department
Department of Chemistry
Abstract
The utilization of renewable sources as alternatives for petroleum and natural gas products has immense commercial, health and global warming significance. D-Isosorbide (2) is a bifunctional, polar, chiral and rigid molecule, which is produced from renewable sources. Synthesis of new polymers containing 2 is of interest for polymers and in drug delivery. The aim of the present work is to synthesize various polymers (homo- and copolymers) containing 2 via the olefin metathesis routes, ring-opening metathesis polymerization (ROMP) and acyclic-diene metathesis polymerization (ADMET). N-Phenyl-7-oxanorbornene-dicarboximide, and norbornene functionalized onto 2 were used as the monomers for ROMP. These monomers were polymerized using Grubbs’ catalysts to generate a series of homo-, co-, block and cross-linked-polymers. These polymers were characterized using GPC, NMR, and IR. In addition, ADMET polymerization of a terminal diolefinunctionalized D-isosorbide (2) was also conducted to produce ADMET polymers.
URI
https://hdl.handle.net/11668/19302
Recommended Citation
Yalamanchili, Chinni, "Synthesis of Bio-Based Polymers Containing D-Isosorbide by Ring-Opening Metathesis Polymerization" (2014). Theses and Dissertations. 4190.
https://scholarsjunction.msstate.edu/td/4190
Comments
Ring-opening metathesis polymerization||Isosorbide||ROMP||ADMET||Acyclic diene metathesis||Norbornene||GPC||block copolymers||ampiphilic block||replacement||Bisphenol A