Persistent Link:
http://hdl.handle.net/10150/185838
Title:
A reevaluation of distortional isomerism.
Author:
Desrochers, Patrick John.
Issue Date:
1992
Publisher:
The University of Arizona.
Rights:
Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.
Abstract:
The blue and green forms of MoOCl₂(PMe₂Ph)₃ and [LWOCl₂]PF₆ (L = 1,4,7-trimethyltriazacyclononane) are not examples of distortional isomerism. For both systems, the blue form is pure and the green form is a mixture of the blue complex and other components. Characterizations of the green material of each indicates that green "MoOCl₂(PMe₂Ph)₃" is a mixture of MoOCl₂(PMe₂Ph)₃ and MoCl₃(PMe₂Ph)₃ and that green "[LWOCl₂]PF₆" is a mixture of [LWOCl₂]PF₆ and two other species; one is a W(IV) and the other a W(VI) compound. Both solid state (XPS, Raman, infrared, powder X-ray diffraction) and solution phase (¹H NMR, UV-visible, EPR, cyclic voltammetry) measurements were applied to the respective green materials, presenting a consistent description of their composite nature. A single crystal X-ray structure determination of a crystal of green "MoOCl₂(PMe₂Ph)₃" allowed the compositional disorder to be partially resolved in this case, due to the high composition of MoOCl₃(PMe₂Ph)₃ in the sample (ca. 0.30 mole percent by XPS and visible spectroscopies). The single crystal X-ray diffraction data from the original single crystal study of green "[LWOCl₂]PF₆" were reinvestigated to ascertain whether compositional disorder could also be implicated in this system. Several composite models were applied to these data, resulting in improved fits to the observed data. This indicated that the original data collected for the crystal of green "[LWOCl₂]PF₆" could not support distortional isomerism in green "[LWOCl₂]PF₆". X-ray structure calculations on models of the compositional disorder in both systems illustrated the pronounced effect of disordering chlorine electron density on the derived metal-oxo bond lengths. A calibration curve of Mo-Cl bond length versus composition calculated from these models resulted in a favorable comparison of this present theoretical work with other experimental X-ray studies of the MoOCl₂(PMe₂Ph)₃ system. Other examples of mixtures mistaken for pure materials are also discussed as well as a recent resurgence of distortional isomerism in certain niobium complexes. The nature of the compositional disorder characterized for the MoOCl₂ (PMe₂Ph)₃ and [LWOCl₂]PF₆ systems has profound implications for metal-ligand distances determined by X-ray crystallography.
Type:
text; Dissertation-Reproduction (electronic)
Keywords:
Dissertations, Academic.; Isomerism.; Chemistry.
Degree Name:
Ph.D.
Degree Level:
doctoral
Degree Program:
Chemistry; Graduate College
Degree Grantor:
University of Arizona
Advisor:
Enemark, John H.

Full metadata record

DC FieldValue Language
dc.language.isoenen_US
dc.titleA reevaluation of distortional isomerism.en_US
dc.creatorDesrochers, Patrick John.en_US
dc.contributor.authorDesrochers, Patrick John.en_US
dc.date.issued1992en_US
dc.publisherThe University of Arizona.en_US
dc.rightsCopyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.en_US
dc.description.abstractThe blue and green forms of MoOCl₂(PMe₂Ph)₃ and [LWOCl₂]PF₆ (L = 1,4,7-trimethyltriazacyclononane) are not examples of distortional isomerism. For both systems, the blue form is pure and the green form is a mixture of the blue complex and other components. Characterizations of the green material of each indicates that green "MoOCl₂(PMe₂Ph)₃" is a mixture of MoOCl₂(PMe₂Ph)₃ and MoCl₃(PMe₂Ph)₃ and that green "[LWOCl₂]PF₆" is a mixture of [LWOCl₂]PF₆ and two other species; one is a W(IV) and the other a W(VI) compound. Both solid state (XPS, Raman, infrared, powder X-ray diffraction) and solution phase (¹H NMR, UV-visible, EPR, cyclic voltammetry) measurements were applied to the respective green materials, presenting a consistent description of their composite nature. A single crystal X-ray structure determination of a crystal of green "MoOCl₂(PMe₂Ph)₃" allowed the compositional disorder to be partially resolved in this case, due to the high composition of MoOCl₃(PMe₂Ph)₃ in the sample (ca. 0.30 mole percent by XPS and visible spectroscopies). The single crystal X-ray diffraction data from the original single crystal study of green "[LWOCl₂]PF₆" were reinvestigated to ascertain whether compositional disorder could also be implicated in this system. Several composite models were applied to these data, resulting in improved fits to the observed data. This indicated that the original data collected for the crystal of green "[LWOCl₂]PF₆" could not support distortional isomerism in green "[LWOCl₂]PF₆". X-ray structure calculations on models of the compositional disorder in both systems illustrated the pronounced effect of disordering chlorine electron density on the derived metal-oxo bond lengths. A calibration curve of Mo-Cl bond length versus composition calculated from these models resulted in a favorable comparison of this present theoretical work with other experimental X-ray studies of the MoOCl₂(PMe₂Ph)₃ system. Other examples of mixtures mistaken for pure materials are also discussed as well as a recent resurgence of distortional isomerism in certain niobium complexes. The nature of the compositional disorder characterized for the MoOCl₂ (PMe₂Ph)₃ and [LWOCl₂]PF₆ systems has profound implications for metal-ligand distances determined by X-ray crystallography.en_US
dc.typetexten_US
dc.typeDissertation-Reproduction (electronic)en_US
dc.subjectDissertations, Academic.en_US
dc.subjectIsomerism.en_US
dc.subjectChemistry.en_US
thesis.degree.namePh.D.en_US
thesis.degree.leveldoctoralen_US
thesis.degree.disciplineChemistryen_US
thesis.degree.disciplineGraduate Collegeen_US
thesis.degree.grantorUniversity of Arizonaen_US
dc.contributor.advisorEnemark, John H.en_US
dc.contributor.committeememberLichtenberger, Dennis L.en_US
dc.contributor.committeememberWigley, David E.en_US
dc.contributor.committeememberBates, Robert B.en_US
dc.contributor.committeememberSalzman, William R.en_US
dc.identifier.proquest9229834en_US
dc.identifier.oclc712672699en_US
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