In this study, two formazans were synthesized by coupling cinnamaldehyde phenyl hydrazone which was obtained by activation of cinnamaldehyde with phenylhydrazone, with diazonium salts of anthranilic acid and sulfonilic acid. The complexes of Co+2, Ni+2, Cu2+ salts of these formazans were also synthesized. These compounds were characterized by elemental analysis, infrared (IR), ultraviolet–visible (UV–vis),1H nuclear magnetic resonance (1H-NMR) and 13C-NMR spectra datas. Investigation of availability of these compounds as dyes were carried out for this purpose. In the present experimental approach, we applied two methods; The first one was direct dyeing with these complexes, and the other one was complex formation on the fibres. Finally, an investigation was carried out for the fastness values (test) and it was found higher values, which was quite better and different from the other workers / researcher working in the same field.
In this study,
two formazans were synthesized by coupling cinnamaldehyde phenyl hydrazone
which was obtained by activation of cinnamaldehyde with phenylhydrazone, with
diazonium salts of anthranilic acid and sulfonilic acid. The complexes of Co+2,
Ni+2, Cu2+ salts of these formazans were also
synthesized. These compounds were characterized by elemental analysis, infrared
(IR), ultraviolet–visible (UV–vis),1H nuclear magnetic resonance (1H-NMR) and 13C-NMR spectra datas. Investigation of availability of
these compounds as dyes were
carried out for this purpose. In the present experimental approach, we
applied two methods; The first one was direct dyeing with these complexes, and
the other one was complex formation on the fibres. Finally, an
investigation was carried out for the fastness
values (test) and it was found higher values, which was quite better and
different from the other workers / researcher working in the same field.
Primary Language | English |
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Subjects | Engineering |
Journal Section | Articles |
Authors | |
Publication Date | December 31, 2018 |
Published in Issue | Year 2018 |