The effects of reagent diversification of dye formation were
examined by combining different diazonium salts with different aromatic
coupling reagents in order to observe the dye on fabric and the maximum
wavelength produced. The structure of the diazonium ion has little effect on
the dye produced because no matter which position the SO3H group is attached
at, the bond always forms at the nitrogen. The structure of the aromatic
coupling reagent affects the active position (α, β, or γ) in which the bond forms
between the diazonium ion and the coupling reagent. The SO3H group attached to
each diazonium ion is electron withdrawing and the OH group attached to each
coupling reagent is electron donating. The color observed on the dyed fabric
strips depends on conjugated double bonds, as in the aromatic rings of the
structures. This is what absorbs energy from light. The wavelength depends on
how much energy is required to reach the new energy state; therefore, lower
energy results in longer wavelength. More conjugation in the structure of the
dye compliments less energy required to move electrons. The intensity of color
on the fabric is dependent upon the functional groups that are attached to the
structures. The polarity of the groups, such as an oxygen or nitrogen, has a
partial charge. Partial charges are responsible for stronger chemical bonds
between the dye and the fabric—thus, more color intensity. Wool and nylon work
best because their structures contain both oxygen and nitrogen. The partial
charges on their oxygen and nitrogen atoms allow the opportunity for a stronger
bond to the partial charges on the dye structures. For the reaction of
naphthalen-2-ol with 4-, 3-, and 2- aminobenzene sulfonic acid, the λmax values
were 580, 768, and 756 nm, respectively. The dye colors were shades of orange
and red, and the fabric strips were various shades of orange (some white if the
dye didn’t bond to the fabric). According to the visible light spectrum, these
values coordinate with colors ranging from light orange to dark red. The
reaction of naphthalen-1-ol with the aminobenzene sulfonic acids produced λmax
values of 469, 478, and 480 nm. The dye colors were shades of red, and the
fabric strips were different shades of brown and red. The values represent energy used to move
electrons in the conjugated system of the aromatic coupling reagent. The
reaction of 2-hydroxybenzoic acid with the aminobenzene sulfonic acids gave λmax
values of 400, 400, and 401 nm. The dye colors were yellow, and the fabric
strips were related colors of yellow. Although these values do not coordinate
with the yellow color in the visible light spectrum, they do represent a larger
amount of energy required to promote electrons to a higher energy state because
the structure of the aromatic coupling reagent contained less conjugation than
the other coupling reagents in this lab. For the reaction of
8-anilino-1-naphthalenesulfonic acid with the amminobenzene sulfonic acids, the
λmax values were 357, 498, and 479 nm. The dye colors were pick and red, and
the fabric strips were shades of maroon, gray, pink, and tan. These low values
correspond to the low wavelength violet region of the visible light spectrum.
In this experiment, combinatorial chemistry was examined
through the synthesis of dyes formed from diazonium salts and coupling
reagents. Because wavelength is based upon energy required to move electrons in
the structures, structures with more conjugation possessed a more visible λmax
and a lower energy requirement. The difference in colors on the fabric strip
were affected by functional groups attached to the structures that affected
intensity of color and were also responsible for chemical bonds formed to
specific fabrics. When a single diazonium salt was reacted with 4 different
coupling reagents, the result was 4 completely different dyes. When the same
coupling reagent was reacted with three different diazonium salts, the result
was three similar fabric strips—all the same color with different shades of
that one color depending on the fabric. Therefore, the structure of the
coupling reagents affected the product dye more than the structure of the
diazonium ions with reference to dye colors on the fabric strips.
Products listed on our website are either in stock or can be resynthesized within a reasonable time frame. N-octylpyridinium bis((trifluoromethyl)sulfonyl)imide
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