Abstract
A new series of substituted anthranilic esters derivatives linked with a 1,3-dithiolane and
benzyloximino moiety was synthesized using the simple esterfication reaction and products were
fully characterized. The isolated yields of these compounds range from 59 to 96%. 1,3-
dithiolane ester and the benzyloxy substituted diamine derivatives are white solids and stable to
air and moisture. The synthesized compounds can be exhibits UV-vis absorption properties by
their structures with a amine or amide group, It is observed that absorption maximum is excellent
for 2,6-disubstituted benzyloxy esters which can be explained by electron transfer or conjugation
is steric effect in ortho substitution from the amino group and the amide group.
Supplementary materials
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Fluorescent manuscript with endnote, submitted to chemrxiv on 6-27-2021
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Fluorescent manuscript
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20210210 Fluoroscent spectral data, ready to submit in chemrxiv
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Fluorescent spectral data
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compound 16 details submitted to CCDC-2090893
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compound 16 details submitted to CCDC-2090893
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compound-16, gd-326-cif generated by VESTA and submit in ccdc on 6-17-2021
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compound-16, gd-326-cif generated by VESTA
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compound-16, gd-326-xraydata.cif original data
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compound-16, gd-326-xraydata.cif original data
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compound 18 details submitted to CCDC-2090913
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compound 18 details submitted to CCDC-2090913
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compound-18, gd-326-cif generated by VESTA and submit in ccdc on 6-17-2021
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compound-18, gd-326-cif generated by VESTA
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compound-18, gd-333-xraydata1.cif original data
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compound-18, gd-333-xraydata1.cif original data
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