ORDER-DISORDER TRANSITION IN LANGMUIR-BLODGETT-FILMS OF IOCTADECYLAMINO)PHENYLAZO)-N-METHYLBENZOTHIAZOLIUM PERCHLORATE STUDIED BY INFRARED,VISIBLE ABSORPTION, AND RESONANCE RAMAN SPECTROSCOPIES

Citation
N. Katayama et al., ORDER-DISORDER TRANSITION IN LANGMUIR-BLODGETT-FILMS OF IOCTADECYLAMINO)PHENYLAZO)-N-METHYLBENZOTHIAZOLIUM PERCHLORATE STUDIED BY INFRARED,VISIBLE ABSORPTION, AND RESONANCE RAMAN SPECTROSCOPIES, Journal of physical chemistry, 97(26), 1993, pp. 6880-6884
Citations number
21
Categorie Soggetti
Chemistry Physical
ISSN journal
00223654
Volume
97
Issue
26
Year of publication
1993
Pages
6880 - 6884
Database
ISI
SICI code
0022-3654(1993)97:26<6880:OTILOI>2.0.ZU;2-8
Abstract
Infrared transmission, visible absorption, and resonance Raman spectra of 15-monolayer Langmuir-Blodgett (LB) films of ioctadecylamino)pheny lazo)-N-methylbenzothiazolium perchlorate (Azo II) have been measured at elevated temperatures, and the order-disorder transition of the fil ms has been investigated. Upward shifts of CH2 antisymmetric and symme tric stretching bands of the hydrocarbon chains suggest that the order -disorder transition of the tail groups occurs around 70-degrees-C in the films. Prior to the transition, the two CH2 stretching bands show broadening (50 approximately 70-degrees-C), indicating that the alkyl chain mobility begins to increase before their conformational disorder occurs. The visible absorption and resonance Raman spectra of the LB films of Azo Il undergo marked changes in the same temperature range a s the infrared bands due to the CH2 stretching modes show the broadeni ng. The spectral changes in the visible absorption and resonance Raman spectra are indicative of the conversion from an H-aggregate to monom ers in the chromophoric part of Azo II, and therefore, it seems likely that the conversion is linked with the increase in the mobility of th e hydrocarbon chains. Cyclic thermal treatment experiments in the infr ared spectra of the Azo II LB film show that not only bands due to the chromophoric part but also the CH2 stretching bands do not return to original spectral features after the temperature is cycled to 70-degre es-C. This result indicates that the orientation and/or aggregation in the head groups do not recover upon the cyclic thermal treatment to 7 0-degrees-C and that the remaining disorder in the head groups hinders reversible order-disorder transition in the alkyl tails.