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NEXAFS spectra and specific dissociation of oligo-peptide model molecules

dc.citation.epage0en_US
dc.citation.issue8en_US
dc.citation.spage0en_US
dc.citation.volume9en_US
dc.citation.woscount0en_US
dc.contributor.authorChiang, Yu-Juen_US
dc.contributor.authorHuang, Wan-Chouen_US
dc.contributor.authorNi, Chi-Kungen_US
dc.contributor.authorLiu, Chen-Linen_US
dc.contributor.authorTsai, Cheng-Chengen_US
dc.contributor.authorHu, Wei-Pingen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2019-10-05T00:08:46Z
dc.date.available2019-10-05T00:08:46Z
dc.date.issued2019-08-01en_US
dc.description.abstractTotal-ion-yield near-edge X-ray absorption fine-structure (NEXAFS) spectra of three oligo-peptide model molecules were recorded. The NEXAFS spectra were also calculated with time-dependent density functional theory; the calculated spectra are consistent with the experimental measurements. The ionic products from core-excited molecules and their branching ratios as functions of excitation energy show branching ratios 42%-75% of dissociation of the peptide bond, especially at resonant excitations. The major destination orbitals assigned at these excitation energies show significant antibonding character along peptide bonds, which causes large probabilities of bond cleavage. (C) 2019 Author(s).en_US
dc.identifier.doi10.1063/1.5112151en_US
dc.identifier.issn2158-3226en_US
dc.identifier.journalAIP ADVANCESen_US
dc.identifier.urihttp://dx.doi.org/10.1063/1.5112151en_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/152857
dc.identifier.wosnumberWOS:000483883400072en_US
dc.language.isoen_USen_US
dc.titleNEXAFS spectra and specific dissociation of oligo-peptide model moleculesen_US
dc.typeArticleen_US

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