Synthesis and Characterization of a Fluorinated Schiff Base from Benzimidazole and Its Metal Complexes for Antimicrobial and UV-Protective Cotton Fabrics
Coatings,
Год журнала:
2025,
Номер
15(4), С. 380 - 380
Опубликована: Март 24, 2025
Due
to
the
lack
of
UV-protective
properties
for
cotton
textiles
and
potential
cause
microbes
their
users,
we
synthesized
benzimidazole
Schiff
base
derivative
(BZI)
namely
N-((1H-benzo[d]imidazol-2-yl)methyl)-1-(4-fluorophenyl)methanimine
V(III),
Fe(III),
Co(II),
Ni(II),
Cu(II)
complexes
as
UV
protection
antimicrobial
agents
textile.
Several
techniques
investigated
these
compounds:
1H,
13C
NMR,
IR,
UV–Vis,
elemental
analysis,
DTA,
TGA.
The
ligand
behaved
a
bidentate
ligand.
prepared
its
are
used
treat
fabrics
(CFs)
by
immersing
fabric
in
solution
samples
under
ultrasonic.
treated
were
using
IR
SEM-EDX
analysis.
UPF
values
obtained.
results
showed
that
with
Fe(III)
had
excellent
50+.
disc
diffusion
method
evaluated
fabric’s
activity.
antifungal
activities
CFs
demonstrated
Co(II)-BZI-CF
was
active
on
C.
albicans
an
inhibition
zone
12
mm,
while
other
inactive
A.
flavus.
V(III)-BZI-CF
Fe(III)-BZI-CF
no
activity
against
S.
aureus
E.
coli
bacteria
gave
between
10
17
mm.
Unlike
previous
studies
primarily
focused
either
or
metal
separately,
this
research
integrates
both
functionalities
synthesizing
applying
them
textiles,
demonstrating
enhanced
selective
Язык: Английский
Nickel (II) Macrocyclic Complexes: Template Synthesis, Spectroscopic Investigations, Electrochemical Behavior, DFT Studies, and Biological Evaluation
ChemistrySelect,
Год журнала:
2025,
Номер
10(15)
Опубликована: Апрель 1, 2025
Abstract
A
novel
series
of
tetraaza
nickel
(II)
macrocyclic
complexes
was
prepared
via
template
condensation
involving
the
ligand
2‐[4‐bromo‐2‐(2‐oxo‐1,2‐diphenyl‐ethylideneamino)‐phenylimino]‐1,2‐diphenyl‐ethanone
(ML)
and
selected
diamines,
such
as
4‐chloro
1,2‐phenylenediamine,
4‐bromo
1,2‐diaminotoluene,
4‐nitro
1,2‐diaminopropane,
ethylenediamine,
in
presence
NiCl
2
.6H
O.
The
its
resulting
were
characterized
through
elemental
analysis,
molecular
weight
determination,
a
range
spectral
techniques,
including
IR,
electronic
spectra,
1
H
NMR,
mass
spectrometry,
X‐ray
powder
diffraction,
DFT‐assisted
structural
characterization.
DFT
(TDDFT/B3LYP/6–311g(d)
method)
analysis
representative
Ni(II)
supports
plausible
structures
proposed
based
on
spectroscopic
studies.
These
analyses
suggest
that
each
complex
adopts
six‐coordinated
octahedral
geometry.
Their
redox
behavior
examined
detail
using
cyclic
voltammetry
(CV).
Furthermore,
new
tested
for
their
antimicrobial,
antioxidant,
antidiabetic,
antituberculosis
activities.
Antimicrobial
tests
conducted
against
E.
coli,
B.
subtilis,
A.
niger
,
P.
chrysogenum
synthesized
compounds.
antioxidant
properties
assessed
DPPH
assay
showed
[Ni(C
41
29
BrCl
N
4
)]
exhibited
highest
activity,
with
an
IC
50
value
89.13
mg/mL.
Additionally,
antimycobacterial
where
40
3
demonstrated
significant
effectiveness
inhibiting
growth
Mycobacterium
tuberculosis
.
Язык: Английский