The gelator molecule triethylammonium
5-(3,5-bis((1H-tetrazol-5-yl)carbamoyl)benzamido)tetrazol-1-ide
(G7) has been studied in our previous work, where G7 formed
an organogel, metallogels, and silver nanocomposite which was used
as a catalyst for the reduction of nitroaromatics. During the catalytic
study of the nanocomposite M
1
G7AgNPs, it was found that the recyclability of the
catalyst decreases with the increasing number of catalytic cycles
due to the aggregation of silver nanoparticles. From there, the motivation
is to increase the strength of the gel network so that the synthesis
of a more stabilized nanocomposite can be obtained. To increase the
strength of organogel G7 and study the effect of this
modification on the catalytic activity of its nanocomposite catalyst,
a molecule with H-bonding donor and acceptor sites, N
2,N
4,N
6-tri(pyridin-2-yl)-1,3,5-triazine-2,4,6-triamine (TPTT), has been synthesized and characterized by spectroscopic techniques. TPTT (or T) and G7 formed a reinforced
gel in a DMSO:H2O mixture and exhibited an effect of strong
hydrogen bond formation on the rheological and catalytic properties
of the organogel and metallogel of G7T. The combined
gelator system fabricated three metallogels: M
1
G7T, M
2
G7T, and M
3
G7T (M1 = Fe(III), M2 = Cu(II),
and M3 = Ag(I)). Among these, M
1
G7T has been used for the production and
stability of silver nanoparticles and formed M
1
G7TAg nanocomposites. This dual metal
system has been used as a catalyst to reduce nitro substituents, i.e.
4-nitrophenol, 4-nitroaniline, 2-amino-5-nitrobenzonitrile, etc.,
into their respective amine products. Here, during the reaction the
substrate which contained adjacent nitrile and amine functional groups
shows indazole formation, which is a very important part of organic
transformations. The recyclability of the catalyst has been done with
the conversion of 4-nitrophenol to 4-aminophenol and it was found
that it can be unchanged even with five repeating reactions. The organogels
and metallogels of the combined G7 and T molecule show enhancement in storage modulus from 586 to 3091 Pa,
showing that after the combination of the T molecule
with G7, a strong hydrogen-bond interaction increases;
therefore, the strength of organogels and metallogels also increases.
Additionally, M
1
G7TAg demonstrates the fabrication of metallogels using G7 and T, exhibiting thixotropic behavior that is validated
by time oscillation sweep studies. Therefore, the work shows major
changes in the rheological properties of G7T as compared
to the G7 organogel. Due to increasing strength, the
stabilization of silver nanoparticles inside the metallogel network
(M
1
G7T) increases,
increasing the recyclability of nanocomposite catalyst M
1
G7TAg.