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Neue H-Chelate mir dualer Fluoreszenz (English shop)
Jochen Lipps (Author)Preview
Table of Contents, Datei (24 KB)
Extract, Datei (150 KB)
The reaction of 2-aminobenzaldehydes with 2-heteroarylacetonitrile derivatives yields 3-heteroaryl-substituted 2-aminoquinolines, which in most cases exhibit dual fluorescence upon protonation. In this dissertation, systematic dependencies of the intensity and spectral position of the fluorescence emissions are demonstrated by varying the heteroaromatic subsystems.
| ISBN-13 (Printausgabe) | 3867275998 |
| ISBN-13 (Hard Copy) | 9783867275996 |
| ISBN-13 (eBook) | 9783736925991 |
| Language | German |
| Page Number | 276 |
| Edition | 1 |
| Volume | 0 |
| Publication Place | Göttingen |
| Place of Dissertation | Konstanz |
| Publication Date | 2008-05-27 |
| General Categorization | Dissertation |
| Departments |
Chemistry
|
| Keywords | Acetonitrile, alkylations, aminobenzaldehydes, quinolines, dual fluorescence, ESIPT, fluorescence quantum yields, H-chelates, hydrogenations, intramolecular proton transfer, nitrations, reductions, ring-closure reactions, spectroscopy, substitution reactions on aromatics. |
