Hole-burning spectra are considered. taking into account averaging over molecular orientations. Dependence of hole-burning spectra on the polarwation of the probing laser is found. A method for findmg the correct Debye-Walk factor from hole-burning and fluorescence line-narrowing spectra is suggeste
Photochemical hole burning of ionic porphins and the deuterated analogues
β Scribed by Kazuaki Sakoda; Masayuki Maeda
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 408 KB
- Volume
- 217
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
The quantum yields of photochemical hole burning (PHB) of three ionic porphins and their deuterated analogues doped in poly (vinylalcohol) and poly (sodium 4-styrenesulfonate) were estimated. The deuterated compounds, whose two hydrogen atoms at the nitrogen sites in the porphin ring were exchanged with deuterium atoms, were synthesized by reacting the non-deuterated compounds with heavy water. The quantum yield of the deuterated porphin was 18 to 45 times smaller than that of the nondeuterated compound. Besides, the hole area did not decrease at least up to about 60 K. These two facts definitely show that the main mechanism of PHB in this system is not a photophysical process, but the tautomerization of the porphin ring.
π SIMILAR VOLUMES
Photochemlcal holc-burnmg IS uxd to detemunc rhc rclzmon woes oi vlbromc bands of the S, -So transmon of free-base porphm III ddlercnt subwwtIona1 sites oTrr-lle\~nc,rl-hcpt~c,fr-oct3nr and ,Idccmc at 1 6 K.. Tbr wbromc rc-Iaalion depends strongly on WC and host. A correlation bctaeen the rr-alka~e
Tr.msien: and photochemical hole-burning is used to determine the homqeneous linewidths of the S, + So and Su t So . transitions of a magwsium porphin-pyridine comptex in four sites of n-octane (T= 1.1-4.2 I;). Thermally induced dephas-' ins of S, .-So is consistent 1% ith "exchange" to low-frequenc