6 research outputs found
Highly Active, Selective, and Reusable RuO<sub>2</sub>/SWCNT Catalyst for Heck Olefination of Aryl Halides
Very
fine RuO<sub>2</sub> nanoparticles (RuO<sub>2</sub>NPs) with
a mean diameter of about 0.9 nm were decorated on single-walled carbon
nanotubes (SWCNTs) by a straightforward âdry synthesisâ
method. TEM images and the Raman spectrum of the resultant material
(RuO<sub>2</sub>/SWCNT) revealed excellent adhesion and homogeneous
dispersion of the RuO<sub>2</sub>NPs on anchoring sites of the SWCNTs.
The surface area of RuO<sub>2</sub>/SWCNT was found to be 416 m<sup>2</sup> g<sup>â1</sup>. The SEMâEDS results showed
that the weight percentage of Ru in RuO<sub>2</sub>/SWCNT was 13.8%.
The oxidation state of Ru in RuO<sub>2</sub>/SWCNT was +4, as confirmed
by XPS and XRD analyses. After the complete characterization, a 0.9
mol % loading of RuO<sub>2</sub>/SWCNT was used as a nanocatalyst
for the Heck olefination of a wide range of aryl halides to yield
products in excellent yields with good turnover numbers and turnover
frequencies. Less reactive bromo- and chloroarenes were also used
for the formation of coupled products in good yields. RuO<sub>2</sub>/SWCNT is regioselective, chemoselective, heterogeneous in nature,
and reusable. The stability of RuO<sub>2</sub>/SWCNT was also studied
by means of TEM, ICP-MS, SEMâEDS, and XPS analyses
Human Hair: A Suitable Platform for Catalytic Nanoparticles
Human
hair (HH) has been utilized as a support for Au and Ag nanoparticles
(NPs) for the very first time. Initially, a very fine human hair powder
(HHP) was obtained from HH by a simple ball milling method. The HHP
after chemical treatment (e-HHP) was used to prepare two different
nanocatalysts, Ag NPs immobilized e-HHP (Ag/HHP) and Au NPs decorated
e-HHP (Au/HHP). Influence of e-HHP on the morphology of nanocatalyts
and metalâsupport interactions were studied. Merit of Ag/HHP
and Au/HHP was realized from its excellent yields in cyclo addition
and <i>aza</i>-Michael reactions, respectively. Reusability
and heterogeneity tests of the nanocatalysts were also performed
Industrial-Quality Graphene Oxide Switched Highly Efficient Metal- and Solvent-Free Synthesis of βâKetoenamines under Feasible Conditions
Metal-
and solvent-free industrial-quality graphene oxide (IQGO)-based
highly efficient carbocatalytic system has been developed for the
synthesis of β-ketoenamines. Initially, physicochemical properties
of IQGO are briefly discussed by means of various microscopic and
spectroscopic techniques. The present system accessed a wide range
of substrates to yield β-ketoenamines in an excellent yield
(86â100%) with 100% selectivity. Catalytic activity of IQGO
is compared with other carbon materials such as carbon nanotubes,
carbon nanofibers, and graphene nanoplatelets. Cost effective recovery,
high level reusability, chemoselective nature, possible scale reaction,
and sustainability of IQGO are demonstrated. Based upon experimental
results and earlier reports, possible reaction mechanism has been
proposed for the synthesis of β-ketoenamines
Sustainable and Versatile CuO/GNS Nanocatalyst for Highly Efficient Base Free Coupling Reactions
A CuO
nanoparticles (CuO NPs)/graphene nanosheet (GNS) hybrid was
prepared by a very simple method and employed as a nanocatalyst (CuO/GNS)
for base free coupling reactions, namely, A<sup>3</sup>-coupling and <i>aza</i>-Michael reactions. TEM shows that CuO NPs of below âź35
nm size are homogeneously dispersed on the GNS. Strong adhesion between
CuO NPs and GNS was acknowledged by a high Raman <i>I</i><sub>D</sub>/<i>I</i><sub>G</sub> ratio and XPS result.
The BET surface area of CuO/GNS was found to be 66.26 m<sup>2</sup> g<sup>â1</sup>. The EDS and XPS investigations revealed that
the weight percentage and chemical state of Cu in CuO/GNS were 4.46%
and +2, respectively. Under mild reaction conditions, CuO/GNS exhibited
an outstanding catalytic activity in terms of yield, turnover number
(TON) and turnover frequency (TOF) toward A<sup>3</sup>-coupling reaction.
A small amount of catalyst (10 mg, 0.7 mol % of Cu) is enough to carry
out the reactions with a wide range of substrates. The CuO/GNS is
stable, heterogeneous in nature and reusable for at least five times
without any significant loses of yield. N-oxidation of tertiary amines
was also carried out to explore further the activity of CuO/GNS, and
the results are found to be excellent. Versatility of the CuO/GNS
was realized from the superior catalytic activity of used CuO/GNS
in <i>aza</i>-Michael reaction. Finally, GNS (âź95%)
and CuO (as CuCl<sub>2</sub>) were successfully recovered from the
used CuO/GNS and confirmed by TEM, Raman, XPS, XRD and SEM-EDS analyses
Utilization of Human Hair as a Synergistic Support for Ag, Au, Cu, Ni, and Ru Nanoparticles: Application in Catalysis
Human hair powder (HHP) after chemical
treatment (e-HHP) has been
successfully utilized as a unique catalyst support for immobilization
of metal nanoparticles (MNPs). Ag, Au, Cu, Ni, and Ru NPs were used
to prepare five different nanocatalysts (MNPs/e-HHP). High-resolution
transmission electron microscopy results confirmed the excellent attachment
of ultrafine MNPs on the surface of e-HHP. Actual loading of metal
in MNPs/e-HHP was determined by energy-dispersive spectroscopy and
X-ray photoelectron spectroscopy analyses. The zero-valent state of
MNPs in MNPs/e-HHP and a very strong interaction between MNPs and
e-HHP were also proven. The obtained AgNPs/e-HHP, AuNPs/e-HHP, CuNPs/e-HHP,
NiNPs/e-HHP, and RuNPs/e-HHP catalysts were employed for the self-coupling
of amines, <i>N</i>-oxidation of tertiary amines, <i>aza</i>-Michael reaction, imines synthesis, and oxidation of
alcohols, respectively. Reaction conditions were optimized, and the
scope of the catalytic systems was extended. The merit of the MNPs/e-HHP
materials is shown to be the superior catalytic activity. Advantages,
shortcomings, and future scope of the MNPs/e-HHP system are also highlighted
Ag and MoO<sub>3</sub> Nanoparticle-Containing Polyacrylonitrile Nanofiber Membranes for Wound Dressings
Herein,
we report the effect of different reducing agents
on Ag-MoO3/polyacrylonitrile nanofibers for their promising
potential
as advanced wound dressings. The nanofibers were treated with NaOH,
NaBH4, sodium citrate, and UV light, and their properties
were evaluated. Water contact angle measurements revealed that NaOH
treatment resulted in a less wettable surface, while NaBH4 and sodium citrate treatments led to more wettable surfaces. UV
light treatment induced a slight increase in the surface wettability.
Antibacterial inhibition zone tests showed that NaOH and UV treatments
exhibited significant inhibitory effects against both Escherichia
coli and Bacillus subtilis, while NaBH4 and sodium citrate treatments displayed moderate inhibitory
effects. Moreover, silver release profiles demonstrated a sustained
release of silver ions over time, with sodium citrate treatment exhibiting
a higher release rate. MoO3/polyacrylonitrile displayed
a substantially lower stress value, 73% less than that of the blank
polyacrylonitrile (PAN) nanofiber. This decrease in the stress value
is advantageous for wound dressings, as it allows for improved flexibility
and conformability to the wound site. Overall, these findings provide
insights into the surface wettability, antimicrobial properties, and
silver ion release capabilities of Ag-MoO3/polyacrylonitrile
nanofibers under different treatments, highlighting their potential
for wound dressing applications