Multinuclear magnetic resonance investigations of structure and order in borates and metal cyanides

The local information provided by nuclear magnetic resonance (NMR) makes it an ideal method for the structural investigations of materials lacking extended long-range ordering. This work focuses on investigations of two types of materials possessing very different types of disorder. The first sectio...

Full description

Bibliographic Details
Main Author: Aguiar, Pedro Miguel
Other Authors: Kroeker, Scott (Chemistry)
Language:en_US
Published: 2007
Subjects:
Online Access:http://hdl.handle.net/1993/2823
id ndltd-MANITOBA-oai-mspace.lib.umanitoba.ca-1993-2823
record_format oai_dc
spelling ndltd-MANITOBA-oai-mspace.lib.umanitoba.ca-1993-28232014-01-31T03:31:29Z Multinuclear magnetic resonance investigations of structure and order in borates and metal cyanides Aguiar, Pedro Miguel Kroeker, Scott (Chemistry) Ratcliffe, Christopher (Steacie Institute for Molecular Science, National Research Council) Hawthorne, Frank (Geological Sciences) Freund, Michael (Chemistry) O'Neil, Joseph (Chemistry) Solid-State NMR Glasses Cyanides MQMAS Nuclear Waste Magic-angle spinning The local information provided by nuclear magnetic resonance (NMR) makes it an ideal method for the structural investigations of materials lacking extended long-range ordering. This work focuses on investigations of two types of materials possessing very different types of disorder. The first section involves investigations of alkali borate glasses and the application of solid-state NMR techniques to probe short- and medium-range ordering in such glasses. Differences between the various alkali borates over a wide compositional range are probed using one and two-dimensional techniques. The use of double-resonance dipolar recoupling techniques to investigate cesium-boron distances is investigated. The second section probes a series of transition-metal cyanide coordination polymers. The bidentate nature of the cyanide ligand allows for the possibility of forming numerous isomers. Information about the isomer(s) present is gained via the various NMR parameters available, such as the chemical shifts, shift anisotropies and J-couplings. This is then extended to the characterization of paramagnetic transition-metal cyanides, where strong electron-nuclear interactions are shown to significantly increase spin-lattice relaxation rates allowing the acquisition of spectra without the need of typically employed enhancement techniques, yet often yielding spectra of better quality. Variable-temperature experiments allow a measure of the electron-nuclear interaction, which can be related to spatial proximity, and provide “diamagnetic” chemical shifts allowing comparison with other cyanides. J-couplings and chemical shift anisotropies are shown to be applicable in much the same fashion as with diamagnetic systems. 2007-09-14T17:08:17Z 2007-09-14T17:08:17Z 2007-09-14T17:08:17Z P.M. Aguiar, S. Kroeker, “Boron Speciation and Non-bridging Oxygens in High-Alkali Borate Glasses”. Journal of Non-Crystalline Solids, 353, 2007, 1834-1839 M.J. Katz, P.M. Aguiar, R.J. Batchelor, A.A. Bokov, Z-G Ye, S. Kroeker, D.B. Leznoff. “Structure and Multinuclear Solid-State NMR of a Highly Birefringent Lead-Gold Cyanide Coordination Polymer”. Journal of the American Chemical Society, 128(11), 2006, 3669–3676 L. Ouyang, P.M. Aguiar, R.J. Batchelor, S. Kroeker, D.B. Leznoff. “Preparation, Structure and Solid-State NMR Characterization of a Paramagnetic CuI/CuII/ZnII Coordination Polymer with Multiple CN-Binding Modes”. Chemical Communications, (7), 2006, 744-746 S. Kroeker, P.M. Aguiar, A. Cerquiera, J. Okoro, W. Clarida, J. Doerr, M. Olesiuk, G. Ongie, M. Affatigato and S.A. Feller. “Alkali Dependence of Tetrahedral Boron in Alkali Borate Glasses”. Physics and Chemistry of Glasses: European Journal of Glass Science and Technology Part B, 47(4), 2006, 393-396 P.M. Aguiar, S. Kroeker, “Medium-Range Order in Cesium Borate Glasses Probed by Double-Resonance NMR”. Solid-State Nuclear Magnetic Resonance, 27, 2005, 10-15 N.D. Draper, R.J. Batchelor, P.M. Aguiar, S. Kroeker, D.B. Leznoff. “Factors Affecting the Solid-State Structure and Dimensionality of Mercury Cyanide/Chloride Double Salts, and NMR Characterization of Coordination”. Inorganic Chemistry, 43, 2004, 6557-6567 http://hdl.handle.net/1993/2823 en_US
collection NDLTD
language en_US
sources NDLTD
topic Solid-State NMR
Glasses
Cyanides
MQMAS
Nuclear Waste
Magic-angle spinning
spellingShingle Solid-State NMR
Glasses
Cyanides
MQMAS
Nuclear Waste
Magic-angle spinning
Aguiar, Pedro Miguel
Multinuclear magnetic resonance investigations of structure and order in borates and metal cyanides
description The local information provided by nuclear magnetic resonance (NMR) makes it an ideal method for the structural investigations of materials lacking extended long-range ordering. This work focuses on investigations of two types of materials possessing very different types of disorder. The first section involves investigations of alkali borate glasses and the application of solid-state NMR techniques to probe short- and medium-range ordering in such glasses. Differences between the various alkali borates over a wide compositional range are probed using one and two-dimensional techniques. The use of double-resonance dipolar recoupling techniques to investigate cesium-boron distances is investigated. The second section probes a series of transition-metal cyanide coordination polymers. The bidentate nature of the cyanide ligand allows for the possibility of forming numerous isomers. Information about the isomer(s) present is gained via the various NMR parameters available, such as the chemical shifts, shift anisotropies and J-couplings. This is then extended to the characterization of paramagnetic transition-metal cyanides, where strong electron-nuclear interactions are shown to significantly increase spin-lattice relaxation rates allowing the acquisition of spectra without the need of typically employed enhancement techniques, yet often yielding spectra of better quality. Variable-temperature experiments allow a measure of the electron-nuclear interaction, which can be related to spatial proximity, and provide “diamagnetic” chemical shifts allowing comparison with other cyanides. J-couplings and chemical shift anisotropies are shown to be applicable in much the same fashion as with diamagnetic systems.
author2 Kroeker, Scott (Chemistry)
author_facet Kroeker, Scott (Chemistry)
Aguiar, Pedro Miguel
author Aguiar, Pedro Miguel
author_sort Aguiar, Pedro Miguel
title Multinuclear magnetic resonance investigations of structure and order in borates and metal cyanides
title_short Multinuclear magnetic resonance investigations of structure and order in borates and metal cyanides
title_full Multinuclear magnetic resonance investigations of structure and order in borates and metal cyanides
title_fullStr Multinuclear magnetic resonance investigations of structure and order in borates and metal cyanides
title_full_unstemmed Multinuclear magnetic resonance investigations of structure and order in borates and metal cyanides
title_sort multinuclear magnetic resonance investigations of structure and order in borates and metal cyanides
publishDate 2007
url http://hdl.handle.net/1993/2823
work_keys_str_mv AT aguiarpedromiguel multinuclearmagneticresonanceinvestigationsofstructureandorderinboratesandmetalcyanides
_version_ 1716628589015728128