학술논문

Picosecond phase shift measurements at 358 MHz using synchrotron radiation
Document Type
Conference
Author
Source
Conference: Meeting on picosecond phenomena, Hilton Head, SC, USA, 24 May 1978
Subject
43 PARTICLE ACCELERATORS
74 ATOMIC AND MOLECULAR PHYSICS
59 BASIC BIOLOGICAL SCIENCES ATOMS
FLUORESCENCE SPECTROSCOPY
MOLECULES
SPEAR
SYNCHROTRON RADIATION
USES
TRYPTOPHAN
FLUORESCENCE
LIFETIME
MEASURING METHODS
MHZ RANGE 100-1000
PHASE SHIFT
AMINO ACIDS
AZOLES
BREMSSTRAHLUNG
CARBOXYLIC ACIDS
ELECTROMAGNETIC RADIATION
EMISSION SPECTROSCOPY
FREQUENCY RANGE
HETEROCYCLIC ACIDS
HETEROCYCLIC COMPOUNDS
INDOLES
LUMINESCENCE
MHZ RANGE
ORGANIC ACIDS
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
PYRROLES
RADIATIONS
SPECTROSCOPY
STORAGE RINGS 430400* -- Particle Accelerators-- Storage Rings
640305 -- Atomic, Molecular & Chemical Physics-- Atomic & Molecular Theory-- (-1987)
550200 -- Biochemistry
Language
English
Abstract
Properties of synchrotron radiation from SPEAR are reviewed. The power--frequency spectrum of source and photomultiplier tube is measured with a spectrum analyzer. The decay time of a single fluorescent species can be deduced by measuring the phase delay between excitation and fluorescence radiation modulated at a single suitable frequency. It is possible to characterize completely the time (impulse) response or the complex frequency response of a linear system with only phase measurements. A number of test experiments were made by using apparatus designed for time-resolved fluorescence emission anisotropy studies of tryptophan in proteins. Phase shifts were produced by insertion of water-filled quartz cells into the beam and by the introduction of a thick glass slab. The total optical path length could also be altered by linear motion of the phototube. The results yielded 4.7 +- 0.5 degrees per cm of motion. It was concluded that this procedure can be used to study short atomic and molecular fluorescence lifetimes. 3 figures. (RWR)