Development of a Catalytic Protocol for Alkane Dehydrogenation by C–H Activation at Iridium(III)
Development of a Catalytic Protocol for Alkane Dehydrogenation by C–H Activation at Iridium(III)
批准号:
9395276
负责人:
Kelly Kim
金额:
$5.63万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-09-01 至 2020-08-31
关键词:
AerobicAlcoholsAldehydesAlkanesAlkenesAmidesBiologicalCarbonCatalysisChemicalsCokeComplexDependenceDevelopmentElectronicsElectronsEstersFutureGoalsHealthHigh temperature of physical objectHumanHydrocarbonsIndustrializationInsertional ActivationsInvestigationIridiumKetonesLigandsLigationMediatingMediator of activation proteinMetalsMethodsModificationMolecularNatural regenerationOctanesOrganic SynthesisOxidantsOxygenPredispositionPreparationProblem SolvingProcessProductionProtocols documentationReactionResearchSchemeScientistSystemTemperatureTransition Elementsbasecareercatalystchemical synthesiscold temperaturecomputer studiesdehydrogenationdrug discoveryimprovednovelnovel strategiesplanetary Atmosphereskills
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英文摘要
PROJECT SUMMARY
Inexpensive and abundant, unactivated alkanes are ideal precursors for the production of commodity
chemicals. Common starting materials in industrial processes and ubiquitous motifs in complex molecules,
alkenes can be produced from more readily available alkanes through transition-metal-catalyzed
dehydrogenation. While heterogeneous catalysis has proven useful in industrial dehydrogenation of low-carbon
alkanes, applications in chemical synthesis have been limited due to high temperatures, susceptibility to
catalyst-deactivating coking, and low selectivity with longer-chain alkane substrates. In contrast, homogeneous
catalytic reactions generally proceed under milder conditions and can be effective in the dehydrogenation of
higher alkanes. Extensive research has revealed pincer-ligated Ir compounds to be the optimal catalysts, and
recent studies have implicated Ir(III) complexes as promising candidates capable of circumventing many
limitations of established Ir(I) systems.
This application describes the development of a novel protocol for catalytic alkane dehydrogenation by pincer-
ligated Ir(III) complexes using the most economical oxidant available, molecular oxygen. The research strategy
builds on the previously demonstrated capabilities of a (NCN)Ir(III) complex for mediating alkane
dehydrogenation and for regenerating under aerobic conditions. To date, catalysis has remained elusive due to
the instability of the Ir(III) complex in the presence of oxygen at the high temperatures required for
dehydrogenation. Computational studies suggest that ligation of the Ir(III) metal center with electron-poor
pincer ligand frameworks will lower the energy barrier to dehydrogenation. Based on the conclusions drawn
from these experimental and computational investigations, the central hypothesis of this research plan is that
catalytic dehydrogenation can be realized by reducing the reaction temperature through strategic modification
of the pincer ligand supporting the Ir(III) metal center. The specific aims of this application are: 1) synthesis of
novel Ir(III) pincer complexes for alkane dehydrogenation, 2) Ir(III)-catalyzed alkane dehydrogenation under
aerobic conditions, and 3) dehydrogenation of functionalized organic substrates.
The development of a method for Ir(III)-catalyzed alkane dehydrogenation under aerobic conditions will
contribute a novel olefin preparation strategy invulnerable to many limitations of current processes while using
an environmentally friendly oxidant. The results of this project will greatly impact the preparation of olefin-
containing commodity chemicals and complex molecules relevant to human health or intermediates thereto.
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