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University of the Pacific

NMR characterization of a diiron macrocycle and structural characterization of a diketo derivative

Abstract

dc:description.abstract

<p>The time-dependent visible spectra and the crystal structure of [Fe<sub>2</sub>(C<sub>20</sub>H<sub>24</sub>N<sub>8</sub>O<sub>2</sub>)(CH<sub>3</sub>CN)<sub>4</sub>]&#183;PF<sub>6</sub> (diketo-dimer) were studied. The spectra showed that the most significant chemistry occurred during the initial 1.5 hours of the synthetic reaction. The starting materials 343 nm peak shifted to a lower energy, at 360 nm, and a new shoulder appeared at 490 nm. This change suggests the formation of a new intermediate whose spectrum has an exceptional resemblance to the starting materials mixed valent species, [Fe<sub>2</sub>(TIED)(Cl)<sup>4</sup>]<sup>+1</sup> (TIED = tetraiminethylene dimacrocycles). Two isosbestic points were found at 538 and 371 nm.</p><p>The diketo-dimer's crystals appear to have individual colors, a physical characteristic called pleochroism. Pleochroism is a topic in the study of optical crystallography which is discussed and applied to the diketo-dimer. The extinction angle was estimated to be 14&#176;, a value consistent for triclinic crystals. X-ray crystallography found that the diketo-dimer is triclinic, and has a space group of P-1. A noteworthy feature is the bond length, 1.406 &#197;, between the two linking bridgehead carbons. This bond length matches the value for partial double bonds of aromatic compounds. This argues for a delocalized electron circulating within the macrocycle.</p><p>The NMR spectra of a diiron macrocycle, [Fe<sub>2</sub>(TIED)(CH<sub>3</sub>CN)<sub>4</sub>]<sup>4+</sup>, were examined. Temperature dependent, pH dependent, D<sup>+</sup> substitution, selectively decoupled, and COSY <sup>1</sup>H NMR experiments were performed. Two sets of structural equilibria were found. One set is temperature dependent, and the other is pH dependent. Of particular interest are the peaks centered at 9.7 ppm and assigned to the imine carbon protons H2. Its resonance indicates an imine proton in an extensively conjugated aromatic environment with an electron deficient metal.</p>

Degree

thesis:*
Name thesis:degree_name
Master of Science (M.S.)
Level thesis:degree_level
Thesis - Pacific Access Restricted
Discipline thesis:degree_discipline
Chemistry
Year dc:date.available
2001

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Brackett, Claudia Lindblom
Contributors dc:contributor
  • Larry O. Spreer

Subjects

dc:subject × 7

Rights

dc:rights

Identifiers

dc:identifier.*
Repository record dc:identifier
https://scholarlycommons.pacific.edu/uop_etds/554
OAI identifier oai:identifier
oai:scholarlycommons.pacific.edu:uop_etds-1553

Chain of custody

source
Harvested from
University of the Pacific
Base URL
scholarlycommons.pacific.edu/do/oai/
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Brackett, Claudia Lindblom. NMR characterization of a diiron macrocycle and structural characterization of a diketo derivative. Thesis - Pacific Access Restricted thesis, 2001. https://scholarlycommons.pacific.edu/uop_etds/554