This paper describes the preparation and Langmuir-Blodgett (LB) monomolecular film formation of H2
Cu
Ni
Co
and Zn phthaloeyanine compounds with p-vinyiphenoxy peripheral substituent on each benzo ring at either 2- or 3- position [i.e.
tetra (p-vinylphenoxy) substituted isomer mixture]. These phthalocyanine derivatives form stable LB films at the film pressures greater than 10 dynes/cm. The surface pressure-area isotherms indicate that the phthalocyanine units are densely packed with a eofacial orientation.Schottky cells of [Indium-Tin Oxide/LB film/Al] were prepared and their electronic properties were examined.Much better rectifying properties
diode parameter
break-down potential and mechanical strength were notified by the post-polymerization of LB-layers.On exposing the polymerized films to tetrahydrofuran vapor
the absorption maxima of Q-band shift bathochromically by about 100nm
being sensitive to diode laser light.
Abstract
This paper describes the preparation and Langmuir-Blodgett (LB) monomolecular film formation of H2
Cu
Ni
Co
and Zn phthaloeyanine compounds with p-vinyiphenoxy peripheral substituent on each benzo ring at either 2- or 3- position [i.e.
tetra (p-vinylphenoxy) substituted isomer mixture]. These phthalocyanine derivatives form stable LB films at the film pressures greater than 10 dynes/cm. The surface pressure-area isotherms indicate that the phthalocyanine units are densely packed with a eofacial orientation.Schottky cells of [Indium-Tin Oxide/LB film/Al] were prepared and their electronic properties were examined.Much better rectifying properties
diode parameter
break-down potential and mechanical strength were notified by the post-polymerization of LB-layers.On exposing the polymerized films to tetrahydrofuran vapor
the absorption maxima of Q-band shift bathochromically by about 100nm
being sensitive to diode laser light.
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