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Transition-metal nanoclusters: fundamental studies of the factors controlling formation, stabilization, and subsequent catalytic activity

dc.contributor.authorOtt, Lisa Starkey, author
dc.contributor.authorFinke, Richard G., advisor
dc.contributor.authorChen, Eugene Y. X., committee member
dc.contributor.authorParkinson, Bruce A., committee member
dc.contributor.authorRickey, Dawn, committee member
dc.contributor.authorBelfiore, Laurence A., committee member
dc.date.accessioned2026-03-16T18:25:17Z
dc.date.issued2006
dc.description.abstractFollowing a critical review of the relevant nanocluster stabilization literature, the research presented herein primarily studies prototype Ir(0)n nanoclusters, including: (i) an evaluation of nanoclusters putatively stabilized by solvents plus the effects of weakly coordinating anions, (ii) an evaluation of five common polymeric nanocluster stabilizers, (iii) the first explicity study of the halide series for their individual efficacies in the formation and stabilization of nanoclusters, (iv) an investigation into the true source of nanocluster stabilization in imidazolium-based ionic liquids, and (v) a demonstration that added imidazolium-based ionic liquids serve to poison catalytically active Ir(0)n nanoclusters in the test reaction of acetone hydrogenation at room temperature and mild H2 pressure. The broad focus of this dissertation concerns the formation and stabilization of transition-metal nanocluster, specifically Ir nanoclusters. The extant literature in the area of transition-metal nanocluster stabilizers is voluminous and in general not to the level of precision that modern science requires. The emphasis on compositionally well-defined nanoclusters and careful studies which follow aim to resolve some of the confusion in the nanocluster stabilization literature. Four detailed investigations on claimed stabilizers—solvents, polymers, halides, and imidazolium-based ionic liquids—have been performed with an emphasis on the formation of multiple alternative hypotheses as the most efficient method for scientific investigation. The approach of multiple alternative hypotheses led to the validation of the DLVO theory of colloidal stability for the specific case of BF4- in high dielectric constant solvents. Additionally, BF4- is shown to be important for nanocluster stabilization even in the presence of polymers or halides. The method of multiple alternative hypotheses also led to the identification of N-heterocyclic carbenes as the likely nanocluster stabilizer generated in ionic liquids. Finally, imidazolium-based ionic liquids have also been probed with regard to their role in catalytic acetone hydrogenation reactions, and it was found that these ionic liquids poison previously active Ir(0)n nanoclusters at room temperature and mild pressure.
dc.format.mediumdoctoral dissertations
dc.identifier.urihttps://hdl.handle.net/10217/243740
dc.identifier.urihttps://doi.org/10.25675/3.026460
dc.languageEnglish
dc.language.isoeng
dc.publisherColorado State University. Libraries
dc.relation.ispartof2000-2019
dc.rightsCopyright and other restrictions may apply. User is responsible for compliance with all applicable laws. For information about copyright law, please see https://libguides.colostate.edu/copyright.
dc.rights.licensePer the terms of a contractual agreement, all use of this item is limited to the non-commercial use of Colorado State University and its authorized users.
dc.subjectchemistry
dc.subjectinorganic chemistry
dc.titleTransition-metal nanoclusters: fundamental studies of the factors controlling formation, stabilization, and subsequent catalytic activity
dc.typeText
dcterms.rights.dplaThis Item is protected by copyright and/or related rights (https://rightsstatements.org/vocab/InC/1.0/). You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s).
thesis.degree.disciplineChemistry
thesis.degree.grantorColorado State University
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy (Ph.D.)

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