Laser photoelectron spectroscopic determination of electronic states of Fe atoms produced in multiphoton dissociation of Fe(CO)5 in the gas phase

1986 ◽  
Vol 84 (3) ◽  
pp. 1063-1070 ◽  
Author(s):  
Yatsuhisa Nagano ◽  
Yohji Achiba ◽  
Katsumi Kimura
Keyword(s):  
Gas Phase ◽  
Electronic States ◽  
Spectroscopic Determination ◽  
Multiphoton Dissociation

scholarly journals Determination of Excited State Molecular Structures from Time-Resolved Gas-Phase X-Ray Scattering

2020 ◽  
Author(s):  
Haiwang Yong ◽  
Andrés Moreno Carrascosa ◽  
Lingyu Ma ◽  
Brian Stankus ◽  
Michael P Minitti ◽  
...  
Keyword(s):  
Excited State ◽  
Gas Phase ◽  
Electronic States ◽  
Molecular Structures ◽  
Excited Electronic States ◽  
Comprehensive Investigation ◽  
Time Resolved ◽  
X Ray ◽  
X Ray Scattering

We present a comprehensive investigation of a recently introduced method to determine transient structures of molecules in excited electronic states with sub-Ångstrom resolution from time-resolved gas-phase scattering signals. The method,...

Infrared Spectroscopy of Gas-Phase Cr+Coordination Complexes:  Determination of Binding Sites and Electronic States

2005 ◽  
Vol 127 (19) ◽  
pp. 7243-7254 ◽  
Author(s):  
David T. Moore ◽  
Jos Oomens ◽  
John R. Eyler ◽  
Gert von Helden ◽  
Gerard Meijer ◽  
...  
Keyword(s):  
Infrared Spectroscopy ◽  
Gas Phase ◽  
Binding Sites ◽  
Electronic States ◽  
Coordination Complexes

Integration of Core-Edge Spectroscopy Methods for the Study of Polymers

1996 ◽  
Vol 54 ◽  
pp. 154-155
Author(s):  
E. G. Rightor
Keyword(s):  
Excited State ◽  
Polymer Blends ◽  
Gas Phase ◽  
Spatial Resolution ◽  
High Spatial Resolution ◽  
Electronic States ◽  
Core Electron ◽  
Bulk Solids ◽  
Development Application

Core edge spectroscopy methods are versatile tools for investigating a wide variety of materials. They can be used to probe the electronic states of materials in bulk solids, on surfaces, or in the gas phase. This family of methods involves promoting an inner shell (core) electron to an excited state and recording either the primary excitation or secondary decay of the excited state. The techniques are complimentary and have different strengths and limitations for studying challenging aspects of materials. The need to identify components in polymers or polymer blends at high spatial resolution has driven development, application, and integration of results from several of these methods.

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