Delayed fluorescence of chlorella in the microsecond range

G. Laczko, P. Maróti, A. Ringler, L. Szalay

Research output: Contribution to journalArticle

Abstract

A multi-exponential analysis is made of the fall in the intensity of delayed fluorescence produced by nanosecond light pulses from a nitrogen laser between the 40th and 550th μsec from the moment of switching off the exciting radiation at room temperature. The multi-component character of the disappearance of fluorescence is due to the different paths of transition of the reaction centre of the pigment of the second photochemical system of photosynthesis from the oxidized to the reduced state. A description is given of a laser phosphoroscope with a time resolution of 20 μsec. Delayed fluorescence in intact samples is characterized by two components with lifetimes in the excited state of 30 and 150 μsec. Treatment of the preparations with 3(3,4-dichlorophenyl)-1, 1-dimethylurea (DCU) causes quenching but does not change the kinetic characteristics of fluorescence. Hydroxylamine (NH2OH) in low concentrations increases the intensity of fluorescence while high ones lead to quenching; the component with a lifetime 150 μsec disappears. The findings confirm the model according to which delayed fluorescence in the microsecond range is due to the presence in the system of heterogeneous centres.

Original languageEnglish
Pages (from-to)549-555
Number of pages7
JournalBiophysics
Volume25
Issue number3
Publication statusPublished - 1980

Fingerprint

Chlorella
Fluorescence
Diuron
Hydroxylamine
Gas Lasers
Photosynthesis
Lasers
Radiation
Light
Temperature

ASJC Scopus subject areas

  • Biophysics

Cite this

Laczko, G., Maróti, P., Ringler, A., & Szalay, L. (1980). Delayed fluorescence of chlorella in the microsecond range. Biophysics, 25(3), 549-555.

Delayed fluorescence of chlorella in the microsecond range. / Laczko, G.; Maróti, P.; Ringler, A.; Szalay, L.

In: Biophysics, Vol. 25, No. 3, 1980, p. 549-555.

Research output: Contribution to journalArticle

Laczko, G, Maróti, P, Ringler, A & Szalay, L 1980, 'Delayed fluorescence of chlorella in the microsecond range', Biophysics, vol. 25, no. 3, pp. 549-555.
Laczko G, Maróti P, Ringler A, Szalay L. Delayed fluorescence of chlorella in the microsecond range. Biophysics. 1980;25(3):549-555.
Laczko, G. ; Maróti, P. ; Ringler, A. ; Szalay, L. / Delayed fluorescence of chlorella in the microsecond range. In: Biophysics. 1980 ; Vol. 25, No. 3. pp. 549-555.
@article{49db127063664a1ea294859d4ca40a87,
title = "Delayed fluorescence of chlorella in the microsecond range",
abstract = "A multi-exponential analysis is made of the fall in the intensity of delayed fluorescence produced by nanosecond light pulses from a nitrogen laser between the 40th and 550th μsec from the moment of switching off the exciting radiation at room temperature. The multi-component character of the disappearance of fluorescence is due to the different paths of transition of the reaction centre of the pigment of the second photochemical system of photosynthesis from the oxidized to the reduced state. A description is given of a laser phosphoroscope with a time resolution of 20 μsec. Delayed fluorescence in intact samples is characterized by two components with lifetimes in the excited state of 30 and 150 μsec. Treatment of the preparations with 3(3,4-dichlorophenyl)-1, 1-dimethylurea (DCU) causes quenching but does not change the kinetic characteristics of fluorescence. Hydroxylamine (NH2OH) in low concentrations increases the intensity of fluorescence while high ones lead to quenching; the component with a lifetime 150 μsec disappears. The findings confirm the model according to which delayed fluorescence in the microsecond range is due to the presence in the system of heterogeneous centres.",
author = "G. Laczko and P. Mar{\'o}ti and A. Ringler and L. Szalay",
year = "1980",
language = "English",
volume = "25",
pages = "549--555",
journal = "Biophysics (Russian Federation)",
issn = "0006-3509",
publisher = "Maik Nauka-Interperiodica Publishing",
number = "3",

}

TY - JOUR

T1 - Delayed fluorescence of chlorella in the microsecond range

AU - Laczko, G.

AU - Maróti, P.

AU - Ringler, A.

AU - Szalay, L.

PY - 1980

Y1 - 1980

N2 - A multi-exponential analysis is made of the fall in the intensity of delayed fluorescence produced by nanosecond light pulses from a nitrogen laser between the 40th and 550th μsec from the moment of switching off the exciting radiation at room temperature. The multi-component character of the disappearance of fluorescence is due to the different paths of transition of the reaction centre of the pigment of the second photochemical system of photosynthesis from the oxidized to the reduced state. A description is given of a laser phosphoroscope with a time resolution of 20 μsec. Delayed fluorescence in intact samples is characterized by two components with lifetimes in the excited state of 30 and 150 μsec. Treatment of the preparations with 3(3,4-dichlorophenyl)-1, 1-dimethylurea (DCU) causes quenching but does not change the kinetic characteristics of fluorescence. Hydroxylamine (NH2OH) in low concentrations increases the intensity of fluorescence while high ones lead to quenching; the component with a lifetime 150 μsec disappears. The findings confirm the model according to which delayed fluorescence in the microsecond range is due to the presence in the system of heterogeneous centres.

AB - A multi-exponential analysis is made of the fall in the intensity of delayed fluorescence produced by nanosecond light pulses from a nitrogen laser between the 40th and 550th μsec from the moment of switching off the exciting radiation at room temperature. The multi-component character of the disappearance of fluorescence is due to the different paths of transition of the reaction centre of the pigment of the second photochemical system of photosynthesis from the oxidized to the reduced state. A description is given of a laser phosphoroscope with a time resolution of 20 μsec. Delayed fluorescence in intact samples is characterized by two components with lifetimes in the excited state of 30 and 150 μsec. Treatment of the preparations with 3(3,4-dichlorophenyl)-1, 1-dimethylurea (DCU) causes quenching but does not change the kinetic characteristics of fluorescence. Hydroxylamine (NH2OH) in low concentrations increases the intensity of fluorescence while high ones lead to quenching; the component with a lifetime 150 μsec disappears. The findings confirm the model according to which delayed fluorescence in the microsecond range is due to the presence in the system of heterogeneous centres.

UR - http://www.scopus.com/inward/record.url?scp=49149146306&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=49149146306&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:49149146306

VL - 25

SP - 549

EP - 555

JO - Biophysics (Russian Federation)

JF - Biophysics (Russian Federation)

SN - 0006-3509

IS - 3

ER -