Excited-state multiplicity for the direct photochemical isomerization of azomethine dyes

1976 ◽  
Vol 98 (20) ◽  
pp. 6210-6218 ◽  
Author(s):  
William G. Herkstroeter
Keyword(s):  
Excited State ◽  
Photochemical Isomerization ◽  
State Multiplicity

The role of the excited-state geometry in the photochemical isomerization of bis(glycinato) platinum (II)

1967 ◽  
Vol 1 ◽  
pp. 76-80 ◽  
Author(s):  
F. Scandola ◽  
O. Traverso ◽  
V. Balzani ◽  
G.L. Zucchini ◽  
V. Carassiti
Keyword(s):  
Excited State ◽  
Photochemical Isomerization

scholarly journals EXCITED STATE MULTIPLICITY INVOLVED IN PHOTOCYCLOADDITION OF POLYMETHYLENE DICINNAMATES AS STUDIED BY QUENCHING EXPERIMENTS

1985 ◽  
Vol 14 (10) ◽  
pp. 1467-1470 ◽  
Author(s):  
Masayuki Kuzuya ◽  
Naohisa Yokota ◽  
Mitsushi Tanaka ◽  
Takachiyo Okuda
Keyword(s):  
Excited State ◽  
State Multiplicity

Renilla Bioluminescence: A Morphologic Approach to the Location of Photocytes

1974 ◽  
Vol 32 ◽  
pp. 208-209
Author(s):  
Ben O. Spurlock ◽  
Milton J. Cormier
Keyword(s):  
Excited State ◽  
Ground State ◽  
Molecular Basis ◽  
Light Emission ◽  
Chemical Basis ◽  
Electronic Excited State ◽  
Colonial Form ◽  
The Common ◽  
Eighteenth And Nineteenth Centuries ◽  
Catalyzed Oxidation

The phenomenon of bioluminescence has fascinated layman and scientist alike for many centuries. During the eighteenth and nineteenth centuries a number of observations were reported on the physiology of bioluminescence in Renilla, the common sea pansy. More recently biochemists have directed their attention to the molecular basis of luminosity in this colonial form. These studies have centered primarily on defining the chemical basis for bioluminescence and its control. It is now established that bioluminescence in Renilla arises due to the luciferase-catalyzed oxidation of luciferin. This results in the creation of a product (oxyluciferin) in an electronic excited state. The transition of oxyluciferin from its excited state to the ground state leads to light emission.

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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