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dc.contributor.authorLin, Yi-Shiueen_US
dc.contributor.authorTsai, Cheng-Chengen_US
dc.contributor.authorLin, Huei-Ruen_US
dc.contributor.authorHsieh, Tsung-Linen_US
dc.contributor.authorChen, Jien-Lianen_US
dc.contributor.authorHu, Wei-Pingen_US
dc.contributor.authorNi, Chi-Kungen_US
dc.contributor.authorLiu, Chen-Linen_US
dc.date.accessioned2015-12-02T02:59:10Z-
dc.date.available2015-12-02T02:59:10Z-
dc.date.issued2015-06-18en_US
dc.identifier.issn1089-5639en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.jpca.5b04415en_US
dc.identifier.urihttp://hdl.handle.net/11536/127885-
dc.description.abstractThe controlled breaking of a specific chemical bond with photons in complex molecules remains a major challenge in chemistry. In principle, using the K-edge absorption of a particular atomic element, one might excite selectively a specific atomic entity in a molecule. We report here highly selective dissociation of the peptide bonds in N-methylformamide and N-methylacetamide on tuning the X-ray wavelength to the K-edge absorption of the atoms connected to (or near) the peptide bond. The high selectivity (56-71%) of this cleavage arises from the large energy shift of X-ray absorption, a large overlap of the Is orbital and the valence pi* orbital that is highly localized on a peptide bond with antibonding character, and the relatively low bond energy of the peptide bonds. These characteristics indicate that the high selectivity on bond dissociation following core excitation could be a general feature for molecules containing peptide bonds.en_US
dc.language.isoen_USen_US
dc.titleHighly Selective Dissociation of a Peptide Bond Following Excitation of Core Electronsen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/acs.jpca.5b04415en_US
dc.identifier.journalJOURNAL OF PHYSICAL CHEMISTRY Aen_US
dc.citation.volume119en_US
dc.citation.issue24en_US
dc.citation.spage6195en_US
dc.citation.epage6202en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000356753600006en_US
dc.citation.woscount1en_US
Appears in Collections:Articles