K. Tabayashi, T. Yamanaka, H. Namatame, M. Taniguchi
{"title":"硝基甲烷团簇在氧k边的内壳激发和破碎","authors":"K. Tabayashi, T. Yamanaka, H. Namatame, M. Taniguchi","doi":"10.1142/S1793617908000197","DOIUrl":null,"url":null,"abstract":"Inner-shell excitation spectra and fragmentation of nitromethane (NM) clusters have been studied in the oxygen K-edge region under cluster beam conditions. Besides the protonated clusters (NM)n · H+, we identified the production of series of mixed fragment-cluster cations, [(NM)n · X+, (X = CH3, NO, NO2)] in time-of-flight spectra of the NM clusters. \"Cluster-specific\" excitation spectra could be generated without contribution of free molecules by monitoring partial-ion-yield spectra of the fragments originating from the clusters. Comparison of the \"cluster-specific\" band with \"monomer\" band revealed that the first resonance ${\\rm O}1s \\to \\pi^*_{\\rm NO}$ band of clusters shifts to a high energy by ~ 0.1 eV. The core-excitation spectrum to the antibonding state compared well with theoretical prediction. The band-shift of the first ${\\rm O}1s \\to \\pi ^*_{\\rm NO}$ was interpreted as being due to the weak hydrogen-bond interaction formed upon clustering. Fragmentation mechanism of the core-excited NM cluster...","PeriodicalId":166807,"journal":{"name":"Advances in Synchrotron Radiation","volume":"80 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2008-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"INNER-SHELL EXCITATION AND FRAGMENTATION OF NITROMETHANE CLUSTERS AT THE OXYGEN K-EDGE\",\"authors\":\"K. Tabayashi, T. Yamanaka, H. Namatame, M. Taniguchi\",\"doi\":\"10.1142/S1793617908000197\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Inner-shell excitation spectra and fragmentation of nitromethane (NM) clusters have been studied in the oxygen K-edge region under cluster beam conditions. Besides the protonated clusters (NM)n · H+, we identified the production of series of mixed fragment-cluster cations, [(NM)n · X+, (X = CH3, NO, NO2)] in time-of-flight spectra of the NM clusters. \\\"Cluster-specific\\\" excitation spectra could be generated without contribution of free molecules by monitoring partial-ion-yield spectra of the fragments originating from the clusters. Comparison of the \\\"cluster-specific\\\" band with \\\"monomer\\\" band revealed that the first resonance ${\\\\rm O}1s \\\\to \\\\pi^*_{\\\\rm NO}$ band of clusters shifts to a high energy by ~ 0.1 eV. The core-excitation spectrum to the antibonding state compared well with theoretical prediction. The band-shift of the first ${\\\\rm O}1s \\\\to \\\\pi ^*_{\\\\rm NO}$ was interpreted as being due to the weak hydrogen-bond interaction formed upon clustering. Fragmentation mechanism of the core-excited NM cluster...\",\"PeriodicalId\":166807,\"journal\":{\"name\":\"Advances in Synchrotron Radiation\",\"volume\":\"80 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2008-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advances in Synchrotron Radiation\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1142/S1793617908000197\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in Synchrotron Radiation","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1142/S1793617908000197","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
INNER-SHELL EXCITATION AND FRAGMENTATION OF NITROMETHANE CLUSTERS AT THE OXYGEN K-EDGE
Inner-shell excitation spectra and fragmentation of nitromethane (NM) clusters have been studied in the oxygen K-edge region under cluster beam conditions. Besides the protonated clusters (NM)n · H+, we identified the production of series of mixed fragment-cluster cations, [(NM)n · X+, (X = CH3, NO, NO2)] in time-of-flight spectra of the NM clusters. "Cluster-specific" excitation spectra could be generated without contribution of free molecules by monitoring partial-ion-yield spectra of the fragments originating from the clusters. Comparison of the "cluster-specific" band with "monomer" band revealed that the first resonance ${\rm O}1s \to \pi^*_{\rm NO}$ band of clusters shifts to a high energy by ~ 0.1 eV. The core-excitation spectrum to the antibonding state compared well with theoretical prediction. The band-shift of the first ${\rm O}1s \to \pi ^*_{\rm NO}$ was interpreted as being due to the weak hydrogen-bond interaction formed upon clustering. Fragmentation mechanism of the core-excited NM cluster...