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kim,kyunghwan
나노물질및화학반응연구단
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Femtosecond X-ray solution scattering reveals that bond formation mechanism of a gold trimer complex is independent of excitation wavelength

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dc.contributor.authorKyung Hwan Kim-
dc.contributor.authorJong Goo Kim-
dc.contributor.authorKey Young Oang-
dc.contributor.authorTae Wu Kim-
dc.contributor.authorHosung Ki-
dc.contributor.authorJunbeom Jo-
dc.contributor.authorKim J.-
dc.contributor.authorSato T.-
dc.contributor.authorNozawa S.-
dc.contributor.authorAdachi S.-I.-
dc.contributor.authorHyotcherl Ihee-
dc.date.available2016-08-08T07:39:49Z-
dc.date.created2016-06-20-
dc.date.issued2016-04-
dc.identifier.issn2329-7778-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/2725-
dc.description.abstractThe [Au(CN)2 -]3 trimer in water experiences a strong van der Waals interaction between the d10 gold atoms due to large relativistic effect and can serve as an excellent model system to study the bond formation process in real time. The trimer in the ground state (S0) exists as a bent structure without the covalent bond between the gold atoms, and upon the laser excitation, one electron in the antibonding orbital goes to the bonding orbital, thereby inducing the formation of a covalent bond between gold atoms. This process has been studied by various time-resolved techniques, and most of the interpretation on the structure and dynamics converge except that the structure of the first intermediate (S1) has been debated due to different interpretations between femtosecond optical spectroscopy and femtosecond X-ray solution scattering. Recently, the excitation wavelength of 267 nm employed in our previous scattering experiment was suggested as the culprit for misinterpretation. Here, we revisited this issue by performing femtosecond X-ray solution scattering with 310 nm excitation and compared the results with our previous study employing 267 nm excitation. The data show that a linear S1 structure is formed within 500 fs regardless of excitation wavelength and the structural dynamics observed at both excitation wavelengths are identical to each other within experimental errors. © 2016 Author(s)-
dc.description.uri1-
dc.language영어-
dc.publisherAMER INST PHYSICS-
dc.titleFemtosecond X-ray solution scattering reveals that bond formation mechanism of a gold trimer complex is independent of excitation wavelength-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000383880700011-
dc.identifier.scopusid2-s2.0-84966710594-
dc.identifier.rimsid55777ko
dc.contributor.affiliatedAuthorKyung Hwan Kim-
dc.contributor.affiliatedAuthorJong Goo Kim-
dc.contributor.affiliatedAuthorKey Young Oang-
dc.contributor.affiliatedAuthorTae Wu Kim-
dc.contributor.affiliatedAuthorHosung Ki-
dc.contributor.affiliatedAuthorJunbeom Jo-
dc.contributor.affiliatedAuthorHyotcherl Ihee-
dc.identifier.doi10.1063/1.4948516-
dc.identifier.bibliographicCitationSTRUCTURAL DYNAMICS, v.3, no.4, pp.043209-
dc.citation.titleSTRUCTURAL DYNAMICS-
dc.citation.volume3-
dc.citation.number4-
dc.citation.startPage043209-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
Appears in Collections:
Center for Nanomaterials and Chemical Reactions(나노물질 및 화학반응 연구단) > 1. Journal Papers (저널논문)
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