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  2. Förster resonance energy transfer - Wikipedia

    en.wikipedia.org/wiki/Förster_resonance_energy...

    Jablonski diagram of FRET with typical timescales indicated. The black dashed line indicates a virtual photon.. Förster resonance energy transfer (FRET), fluorescence resonance energy transfer, resonance energy transfer (RET) or electronic energy transfer (EET) is a mechanism describing energy transfer between two light-sensitive molecules (chromophores). [1]

  3. Single-molecule FRET - Wikipedia

    en.wikipedia.org/wiki/Single-molecule_FRET

    Single-molecule fluorescence (or Förster) resonance energy transfer (or smFRET) is a biophysical technique used to measure distances at the 1-10 nanometer scale in single molecules, typically biomolecules. It is an application of FRET wherein a pair of donor and acceptor fluorophores are excited and detected at a single molecule level. In ...

  4. Biophotonics - Wikipedia

    en.wikipedia.org/wiki/Biophotonics

    Biophotonics can also be described as the "development and application of optical techniques, particularly imaging, to the study of biological molecules, cells and tissue". [2] One of the main benefits of using the optical techniques which make up biophotonics is that they preserve the integrity of the biological cells being examined. [3] [4]

  5. Fluorescence in the life sciences - Wikipedia

    en.wikipedia.org/wiki/Fluorescence_in_the_life...

    A simplified Jablonski diagram illustrating the change of energy levels.. The principle behind fluorescence is that the fluorescent moiety contains electrons which can absorb a photon and briefly enter an excited state before either dispersing the energy non-radiatively or emitting it as a photon, but with a lower energy, i.e., at a longer wavelength (wavelength and energy are inversely ...

  6. Fiesselmann thiophene synthesis - Wikipedia

    en.wikipedia.org/wiki/Fiesselmann_thiophene...

    The Fiesselmann thiophene synthesis is a name reaction in organic chemistry that allows for the generation of 3-hydroxy-2-thiophenecarboxylic acid derivatives from α,β-acetylenic esters with thioglycolic acid and its derivatives under the presence of a base. The reaction was developed by Hans Fiesselmann in the 1950s.

  7. Fluorescence-lifetime imaging microscopy - Wikipedia

    en.wikipedia.org/wiki/Fluorescence-lifetime...

    Hence, 2 values for the lifetime can be determined from the phase-modulation method. The lifetimes are determined through a fitting procedures of these experimental parameters. An advantage of PMT-based or camera-based frequency domain FLIM is its fast lifetime image acquisition making it suitable for applications such as live cell research. [12]

  8. Resonance (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Resonance_(chemistry)

    Contributing structures of the carbonate ion. In chemistry, resonance, also called mesomerism, is a way of describing bonding in certain molecules or polyatomic ions by the combination of several contributing structures (or forms, [1] also variously known as resonance structures or canonical structures) into a resonance hybrid (or hybrid structure) in valence bond theory.

  9. Thioester - Wikipedia

    en.wikipedia.org/wiki/Thioester

    General structure of a thioester, where R and R' are organyl groups, or H in the case of R.. In organic chemistry, thioesters are organosulfur compounds with the molecular structure R−C(=O)−S−R’.