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University of Illinois at Urbana-Champaign

Picosecond studies of free radical reactions in solution

Abstract

dc:description

The 2,7-dihalofluorenylidenes were examined. Electron paramagnetic resonance (EPR) spectroscopy shows that these carbenes are ground-state triplets. These carbenes react with methanol to form 9-methoxy ethers. The absence of a heavy atom effect in this reaction suggests that intersystem crossing is not involved in the rate-determining step, and that diaryl carbenes react with methanol via their singlet states.

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
Year dc:date
2011

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Falvey, Daniel Edward
Contributors dc:contributor
  • Schuster, Gary B.

Subjects

dc:subject × 1

Rights

dc:rights
Statement dc:rights
  • Copyright 1989 Falvey, Daniel Edward
Language dc:language
eng

Identifiers

dc:identifier.*
Identifier
AAI8916245
(UMI)AAI8916245
OAI identifier oai:identifier
oai:www.ideals.illinois.edu:2142/19350

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

Falvey, Daniel Edward. Picosecond studies of free radical reactions in solution. Dissertation thesis, University of Illinois at Urbana-Champaign, 2011. http://hdl.handle.net/2142/19350