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Title: Structural characterization of Langmuir-Blodgett films derived from multisulfur heterocycles

Journal Article · · Journal of Physical Chemistry
DOI:https://doi.org/10.1021/jp961128z· OSTI ID:380904
; ; ;  [1]
  1. Univ. of Illinois, Urbana, IL (United States)

A novel multisulfur heterocyclic compound with alkyl chains, C{sub 3}S{sub 5}(C{sub 18}H{sub 37}){sub 2} (4,5,-bis(octadecylthio)-1,3-dithiole-2-thione), has been synthesized and fabricated into Langmuir-Blodgett (LB) films. The structure of this film on SiO{sub 2} slides has been studied using X-ray photoelectron spectroscopy (XPS) and IR and UV transmission linear dichroism (LD) measurements. From the isotherm, it is known that the Langmuir film at the air-water interface is a bilayer. Angle-resolved XPS of films transferred to SiO{sub 2} show that the alkyl chains of the molecule form the topmost layer of the film, with the C{sub 3}S{sub 5} ring underneath the alkyl layer. Electronic structure calculations indicate that the transition moment associated with the observed UV band lies coincident with the C{sub 2} axis of the C{sub 3}S{sub 5} ring group. In order to properly interpret the polarized absorption data, a simple model addressing the local field effect in LD measurements was developed. Incorporating measured information on the polarizability of the chromophore, UV and IR LD measurements showed the ring plane and the chains to be stacked at 69{degree} and 20{degree}, respectively, relative to the surface normal. These data coupled with the XPS results permitted a structural model to be constructed which accounts for the multilayer structure of the transferred film. 31 refs., 8 figs., 1 tab.

DOE Contract Number:
FG02-91ER45439
OSTI ID:
380904
Journal Information:
Journal of Physical Chemistry, Vol. 100, Issue 32; Other Information: PBD: Aug 1996
Country of Publication:
United States
Language:
English