|
|
|
|
| LEADER |
03134nmm a2200301 u 4500 |
| 001 |
EB000613852 |
| 003 |
EBX01000000000000000466934 |
| 005 |
00000000000000.0 |
| 007 |
cr||||||||||||||||||||| |
| 008 |
140122 ||| eng |
| 020 |
|
|
|a 9780306470707
|
| 100 |
1 |
|
|a Lakowicz, Joseph R.
|e [editor]
|
| 245 |
0 |
0 |
|a Topics in Fluorescence Spectroscopy
|h Elektronische Ressource
|b Nonlinear and Two-Photon-Induced Fluorescence
|c edited by Joseph R. Lakowicz
|
| 250 |
|
|
|a 1st ed. 2002
|
| 260 |
|
|
|a New York, NY
|b Springer US
|c 2002, 2002
|
| 300 |
|
|
|a XVI, 544 p. 135 illus
|b online resource
|
| 505 |
0 |
|
|a The Theory of Two-Photon-Induced Fluorescence Anisotropy -- Anisotropy Decays Induced by Two-Photon Excitation -- Multiphoton Excitation of Biochemical Fluorophores -- Two-Photon Excitation and Anisotropy Decays in Membranes and Oriented Systems -- Two-Photon Induced Fluorescence of Proteins -- Fluorescence and Multiwave Mixing Induced by Photon Absorption of Excited Molecules -- Ultrafast Stimulated Emission Spectroscopy -- Fluorescence Quenching by Stimulated Emission -- Increasing the Resolution of Far-Field Fluorescence Light Microscopy by Point-Spread-Function Engineering -- Time-Resolved Stimulated-Emission and Transient-Absorption Microscopy and Spectroscopy -- Multiphoton Excitation of Molecular Fluorophores and Nonlinear Laser Microscopy
|
| 653 |
|
|
|a Physical chemistry
|
| 653 |
|
|
|a Analytical chemistry
|
| 653 |
|
|
|a Physical Chemistry
|
| 653 |
|
|
|a Analytical Chemistry
|
| 041 |
0 |
7 |
|a eng
|2 ISO 639-2
|
| 989 |
|
|
|b SBA
|a Springer Book Archives -2004
|
| 490 |
0 |
|
|a Topics in Fluorescence Spectroscopy
|
| 028 |
5 |
0 |
|a 10.1007/b115592
|
| 856 |
4 |
0 |
|u https://doi.org/10.1007/b115592?nosfx=y
|x Verlag
|3 Volltext
|
| 082 |
0 |
|
|a 543
|
| 520 |
|
|
|a Fluorescence spectroscopy continues its advance to more sophisticated methods and applications. As one looks over the previous decades, its appears that the first practical instruments for time-resolved measurements appeared in the 1970’s. The instrumentation and analysis methods for time-resolved fluorescence advanced rapidly throughout the 1980’s. Since 1990 we have witnessed a rapid migration of the principles of time-resolved fluorescence to cell biology and clinical appli- tions. Most recently, we have seen the introduction of multi-photon excitation, pump-probe and stimulated emission methods for studies of biological mac- molecules and for cellular imaging. These advanced topics are the subject of the present volume. Two-photon excitation was first predicted by Maria Goppert-Mayer in 1931, but was not experimentally observed until 1961. Observation of two-photon excitation required the introduction of lasers which provided adequate photon density for multi-photon absorption. Since the early observations of two-photon excitation in the 1960s, multi-photon spectroscopy has been limited to somewhat exotic applications of chemical physics, where it is used to study the electronic symmetry of small molecules. Placing one’s self back in 1980, it would be hard to imagine the use of multi-photon excitation in biophysics or cellular imaging
|