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快原子轰击质谱电离机理研究 Title:MechanisticInvestigationsonFastAtomBombardmentMassSpectrometryIonization Introduction: FastAtomBombardmentMassSpectrometry(FAB-MS)isapowerfultechniqueusedfortheanalysisofbiomolecules,pharmaceuticalcompounds,andotherorganicmolecules.FAB-MSallowsfortheionizationandanalysisofnon-volatileorthermallylabilecompounds,whicharedifficulttoanalyzeusingtraditionalelectronionizationtechniques.ThispaperaimstoprovideanoverviewoftheionizationmechanisminvolvedinFAB-MSanddiscussthevariousfactorsinfluencingtheefficiencyandselectivityofionization. IonizationMechanism: TheionizationmechanisminFAB-MSinvolvesthebombardmentofthesamplewithabeamofhigh-energyatoms.Typically,aliquidmatrixcompoundisusedasasolventtodissolveandfacilitatetheionizationoftheanalytemolecules.Thehigh-energyatomsinthebeamcollidewiththemoleculesinthesample,transferringenergyandcausingtheionizationoftheanalyte.Thisionizationcanoccurthroughseveraldifferentprocesses,includingprotontransfer,chargeexchange,andradicalcationformation. ProtonTransfer: OneoftheprimaryionizationmechanismsinFAB-MSisprotontransfer.Inthisprocess,aprotonistransferredfromthematrixcompoundtotheanalytemolecule,formingapositivelychargedanalyteion.ThismechanismiscommonlyobservedinFAB-MSofsmallpolarandacidiccompounds.Theextentofprotontransferdependsonseveralfactors,suchasthepKaoftheanalyte,theacidityofthematrixcompound,andthecollisionenergy. ChargeExchange: ChargeexchangereactionsalsoplayasignificantroleinFAB-MSionization.Inthisprocess,aprotonfromthematrixcompoundistransferredtotheanalytemolecule,whileacorrespondingionfromtheanalytemoleculeistransferredtothematrixcompound.Thisresultsintheformationofachargedanalyteionandaneutralmatrixmolecule.Chargeexchangereactionsareobservedforbothpolarandnon-polarcompoundsandareinfluencedbyfactorssuchastheionizationpotentialoftheanalyteandtheelectronaffinityofthematrixcompound. RadicalCationFormation: TheformationofradicalcationsisanotherimportantionizationmechanisminFAB-MS.Inthisprocess,theanalytemol