0000000000147535

AUTHOR

Eva ÅKesson

showing 3 related works from this author

Corrigendum to “Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans” [J. Neuroim…

2007

GeneticsLinkage disequilibriumJAG1Multiple sclerosisImmunologySusceptibility geneBiologymedicine.disease03 medical and health sciences0302 clinical medicineNeurologymedicineImmunology and AllergyNeurology (clinical)030215 immunologyJournal of Neuroimmunology
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Characterisation of Chlorophyll a and Chlorophyll b Monomers in Various Solvent Environments with Ultrafast Spectroscopy

1998

In photosynthesis the energy from the sun is captured by light harvesting chlorophyll pigments and converted to stable chemical energy, by the photochemical reaction center. Photosynthetic energy transfer in the antenna systems of green plants has previously been studied by ultrafast time resolved spectroscopy. The characteristics of the chlorophyll pigments itself is important to study in order to understand the dynamics on a femtosecond timescale. One way to study the energy transfer is to use transient absorption spectroscopy and follow the increase or decrease in the transient absorption signal with time (1). Another way to study the energy transfer is to monitor the change in dichroism…

Chlorophyll bPhysics::Biological Physics0303 health sciencesChlorophyll aMaterials scienceDichroism010402 general chemistryPhotochemistry7. Clean energy01 natural sciences0104 chemical sciencesLight-harvesting complex03 medical and health scienceschemistry.chemical_compoundchemistryChlorophyllUltrafast laser spectroscopyTime-resolved spectroscopySpectroscopy030304 developmental biology
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Dynamics of ground and excited state chlorophylla molecules in pyridine solution probed by femtosecond transient absorption spectroscopy

1999

Abstract Femtosecond pump–probe spectroscopy was used to investigate the ground and excited state dynamics of chlorophyll  a (Chl  a ) in pyridine following excitation by a 100 fs optical pulse. The transient absorption spectrum and kinetics reveal spectral evolution on two ultrafast time scales: ∼100 fs and ∼3 ps. We attribute these dynamics to ground-state transient hole-burning and solvation dynamics. Transient absorption anisotropy at early times (∼500 fs) was measured for Chl  a in pyridine and shows a pronounced wavelength dependence, where anisotropy varies between 0 and 0.5. Strong contribution from excited state absorption is the origin of the variation.

ChemistrySolvationGeneral Physics and Astronomy02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesExcited stateUltrafast laser spectroscopyFemtosecondPhysical and Theoretical ChemistryAtomic physics0210 nano-technologySpectroscopyAnisotropyUltrashort pulseExcitationChemical Physics Letters
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