Molecular-scale characterisation of humic substances using isotope-filtered nD NMR spectroscopy
dc.contributor.advisor
Uhrin, Dusan
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dc.contributor.advisor
Graham, Margaret
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dc.contributor.author
Bell, Nicholle Georgina Anneke
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dc.date.accessioned
2017-05-15T15:26:01Z
dc.date.available
2017-05-15T15:26:01Z
dc.date.issued
2016-06-28
dc.description.abstract
Humic substances (HS), the complex mixture of organic molecules produced by microbial and
abiotic degradation of plant and animals residues, are the major components of organic matter in
soil and natural waters. As such, they are vital to the integrity of soil, play important roles in
nutrient biogeochemical cycling and determine the mobility and fate of both nutrients and
contaminants. How HS enact their varied roles, however, is largely unknown due to the lack of
comprehension of their molecular make-up. What is known is that they contain aromatic (e.g.
phenols, condensed aromatics) and aliphatic (e.g. carbohydrates, lipids) molecules with
prevailing carboxyl and hydroxyl functionalities.
As for other complex chromatographically inseparable mixtures, high-resolution analytical
techniques such as Fourier Transform Ion Cyclotron Resonance Mass Spectrometry (FT-ICR MS)
as well as Nuclear Magnetic Resonance (NMR) spectroscopy have been applied to study HS
composition at the molecular level. While FT-ICR MS can provide molecular formulae, it is only
NMR that can unveil structures. Until now, however, very few unambiguous structures of
individual molecules have emerged from standard NMR experiments. This is because purposely
designed multidimensional NMR experiments are required to achieve ‘spectroscopic separation’
where chromatography fails.
In this work, ‘spectroscopic separation’ was accomplished with the aid of chemical modification
in the form of 13C methylation of COOH and OH groups. 13C containing tags allow the
observation of signals only from molecules carrying these tags. In combination with purposelydesigned
isotope-filtered NMR experiments, these tags act as spies reporting on their
surrounding structure. This is achieved by utilising scalar and dipolar couplings to transfer the
polarisation between protons and carbons of the 13CH3O groups and nuclei of the parent
molecules. The necessary spectral resolution is attained using 3D/4D NMR experiments. This
approach provides access to an array of correlated chemical shifts of HS molecules and represents
a paradigm shift in the use of tags in investigations of complex mixtures: instead of focusing only
on the tags, they are used to obtain structural information from the molecules they are attached
to.
The compounds at the centre of this investigation are the phenols of HS. These molecules are
thought to be important in many of the key processes in organic matter rich soils, particularly
peat. For example, their accumulation is thought to impair the activity of extracellular enzymes
essential for the degradation of peat HS. Understanding the nature and source of phenols would
provide a more fundamental framework for rationalising their role in peat, as well as other carbon
rich soils.
The developed methodology was initially tested on model mixtures containing 3 or 9 phenolic
compounds before applying it to a operational fraction of HS, fulvic acid, extracted from a
Scottish raised peat bog. For this fulvic acid, over 30 major phenolic molecules/moieties were
identified, many of which can be directly traced to the flora prevalent in the vicinity of the
sampling site. For the first time in 150 years of HS research, a novel analytical methodology has
yielded unambiguous structural information, providing the first steps towards understanding
the various roles of HS in natural systems.
en
dc.identifier.uri
http://hdl.handle.net/1842/21994
dc.language.iso
en
dc.publisher
The University of Edinburgh
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dc.relation.hasversion
N.G.A. Bell, L. Murray, M.C. Graham, D. Uhrín, NMR methodology for complex mixture ‘separation’, Chem. Commun. 50, 1694-1697, 2014.
en
dc.relation.hasversion
N.G.A. Bell, A.A.L. Michalchuk, J.W.T. Blackburn, M.C. Graham, D. Uhrín, Isotope-Filtered 4D NMR Spectroscopy for Structure Determination of Humic Substances, Angew. Chem. Int. 29, 8382-8385, 2015.
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dc.subject
peat
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dc.subject
FT-ICR MS
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dc.subject
NMR
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dc.subject
spectroscopic separation
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dc.subject
organic matter rich soils
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dc.subject
phenolic molecules
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dc.title
Molecular-scale characterisation of humic substances using isotope-filtered nD NMR spectroscopy
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dc.type
Thesis or Dissertation
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dc.type.qualificationlevel
Doctoral
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dc.type.qualificationname
PhD Doctor of Philosophy
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