Structural Aspects of Photochromism of the Internally H-Bonded Schiff Bases. "A Minimal Chromophore" |
A. Grabowska, K. Kownacki Institute of Physical Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland and Ł. Kaczmarek Pharmaceutical Research Institute, Rydygiera 8, 01-793 Warsaw, Poland |
Dedicated to Professor Zdzisław Ruziewicz on the occasion of his 70th birthday |
Received: July 4, 1995 |
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The final limiting stage of structural simplification of photochromic Schiff base was reached by the following statement: two molecules, salicylidene methylamine and its butyl analogue, show transient absorption bands (at room temperature) peaking at ≈ 22000 cm-1. These bands are characteristic of the phenomenon of photochromism. They are similar to the corresponding spectra detected earlier for several larger, symmetric systems belonging to the same family. Experimental characterization of both molecules was compared with the theoretical calculations: geometry optimization and transition energies, performed for enol, keto, and the photochromic form of salicylidene methylamine. |
DOI: 10.12693/APhysPolA.88.1081 PACS numbers: 33.10.-n, 33.50.-j |