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University of Illinois at Urbana-Champaign

Folding-Driven Synthesis of Dynamic Covalent Oligomers Joined by Imine Linkages

Abstract

dc:description

The incorporation of folding features into the imine oligomers increases the kinetic stability under hydrolysis conditions by burying the labile imine bond. The imine bond in the imine dodecamer shows an order of magnitude longer half-life compared with the imine tetramer. The folding process could affect either the protonation or attack of water in the hydrolysis mechanism. Similar trends were observed for imine reduction experiments.

Degree

thesis:*
Name thesis:degree_name
Ph.D.
Level thesis:degree_level
Dissertation
Discipline thesis:degree_discipline
Chemistry
Grantor
University of Illinois at Urbana-Champaign
Date dc:date
10000-01-01

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Oh, Keunchan
Contributors dc:contributor
  • Moore, Jeffrey S.

Subjects

dc:subject × 1

Rights

Language dc:language
eng

Identifiers

dc:identifier.*
Identifier
(MiAaPQ)AAI3130993
OAI identifier oai:identifier
oai:www.ideals.illinois.edu:2142/84138

Chain of custody

source
Harvested from
University of Illinois - Urbana-Champaign
Base URL
www.ideals.illinois.edu/oai-pmh
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

Oh, Keunchan. Folding-Driven Synthesis of Dynamic Covalent Oligomers Joined by Imine Linkages. Dissertation thesis, University of Illinois at Urbana-Champaign, http://hdl.handle.net/2142/84138