This work was supported by the University of Helsinki and the Jane and Aatos Erkko Foundation. S.H. thanks Erasmus+ EU funds for the fellowship.

1. Synthesis of Ag-Pd/ZrO2 NPs 
NOTE: In this procedure, the Pd mol% in Ag-Pd corresponded to 1%, and the Ag-Pd loading on ZrO2 corresponded to 3 wt.%.
<ol>
	<li>Place 1 g of ZrO2 powder in a 250 mL beaker.</li>
	<li>Add 50 mL of an AgNO3 (aq) (0.0059 mol/L) and 9.71 mL of a K2PdCl4 (aq) (0.00031 mol/L) solutions to the beaker under vigorous magnetic stirring (500 rpm) at room temperature.</li>
	<li>Add 10 mL of lysine (0.53 M) aqueous solution.</li>
	<li>Keep the mixture under vigorous stirring (500 rpm) for 20 min.</li>
	<li>After 20 min, use a pipette to add to the suspension 10 mL of a freshly prepared NaBH4 (aq) (0.035 M) solution dropwise, at a rate of 1 mL/min. Keep the suspension under stirring (500 rpm) throughout the process.</li>
	<li>Let the mixture stir for 30 min at room temperature.</li>
</ol>
2. Separation and purification of the catalyst
<ol>
	<li>Transfer the suspension to centrifuge tubes and separate the solids from the mixture by centrifugation at 3,260 x g for 10 min.</li>
	<li>Carefully remove the liquid phase with a pipette and add 15 mL deionized water to the tubes.
	<ol>
		<li>Shake vigorously until dispersion of the solid is obtained. If good dispersion is not achieved, place the tubes in an ultrasonic bath for 5 min.</li>
		<li>Centrifuge the dispersion at 3,260 x g for 10 min.</li>
	</ol>
	</li>
	<li>Repeat the washing steps (2.2. to 2.2.2.) two more times using deionized water, then once using ethanol instead of water.</li>
	<li>Remove the ethanol and dry the solid in an oven at 60 &#176;C for 12 h.</li>
	<li>Characterize the prepared Ag-Pd/ZrO2 NPs by a variety of microscopy, elemental, and spectroscopic techniques.</li>
</ol>
3. Synthesis of Ag/ZrO2 NPs 
NOTE: In this procedure, Ag loading on ZrO2 corresponded to 3 wt.%.
<ol>
	<li>Place 1 g of ZrO2 powder in a 250 mL beaker.</li>
	<li>Add 50 mL of an AgNO3 (aq) (0.0059 mol/L) solution to the beaker under vigorous magnetic stirring (500 rpm) at room temperature.</li>
	<li>Add 10 mL of lysine (0.53 M) aqueous solution.</li>
	<li>Keep the mixture under vigorous stirring (500 rpm) for 20 min.</li>
	<li>After 20 min, use a pipette to add to the suspension 10 mL of a freshly prepared NaBH4 (aq) (0.035 M) solution dropwise, at a rate of 1 mL/min. Keep the suspension under stirring (500 rpm) throughout the process.</li>
	<li>Let the mixture stir for 30 min under room temperature.</li>
</ol>
4. Separation and purification of the catalyst
<ol>
	<li>Transfer the suspension to centrifuge tubes and separate the solids from the mixture by centrifugation at 3,260 x g for 10 min.</li>
	<li>Carefully remove the liquid phase with a pipette and add 15 mL deionized water to the tubes.
	<ol>
		<li>Shake vigorously until the dispersion of the solid is observed. If good dispersion is not achieved, place the tubes in an ultrasonic bath for 5 min.</li>
		<li>Centrifuge the dispersion at 3,260 x g for 10 min.</li>
	</ol>
	</li>
	<li>Repeat the washing steps (4.2. to 4.2.2.) two more times using deionized water, then once using ethanol instead of water.</li>
	<li>Remove the ethanol and dry the solid in an oven at 60 &#176;C for 12 h.</li>
	<li>The prepared Ag/ZrO2 NPs can then be characterized by a variety of microscopy, elemental, and spectroscopic techniques.</li>
</ol>
5. Investigation of plasmonic catalytic performance towards the nitrobenzene reduction under LSPR excitation (light illumination)
<ol>
	<li>Place 30 mg of catalyst in a 25 mL round-bottom flask along with a magnetic stirring bar.</li>
	<li>Add 5 mL of a solution of nitrobenzene (0.03 mol/L) in isopropyl alcohol (IPA) to the reactor.</li>
	<li>Then, add 11.22 mg of KOH powder (0.0002 mol).</li>
	<li>Purge the reactor by bubbling the suspension with an argon flow for 1 min. Immediately after purging, seal the flask.</li>
	<li>Place the reactor in an oil bath heated at 70 &#176;C above a temperature-controlled magnetic stirrer (500 rpm).</li>
	<li>Irradiate the tube using 4 LED lamps with a wavelength of 425 nm as the light source, and a light intensity of 0.5 W/cm2. The distance from the lamps to the reaction flask should be 7 cm.</li>
	<li>Let the reaction proceed for 2.5 h at 70 &#176;C under vigorous magnetic stirring (500 rpm).</li>
	<li>Then, turn the light off, open the reactor and use a syringe and a needle to collect a 1 mL sample. Filter it through a 0.45 &#956;m filter, to remove the catalyst particulates, into a gas chromatography vial.</li>
</ol>
6. Reaction in the absence of LSPR excitation (dark conditions)
<ol>
	<li>Follow the same steps as described in 5, but without light irradiation. Wrap the reaction tube with aluminium foil to prevent any light exposure.</li>
</ol>
7. Gas chromatography (GC) analysis preparation
<ol>
	<li>Prepare an IPA solution containing approximately 30 mmol/L nitrobenzene (NB), 30 mmol/L of aniline (AN), and 30 mmol/L of azobenzene (AB).</li>
	<li>Run a GC analysis of the solution using a suitable method. Different methods can be tested by varying the column temperature and gas flow programs. The selected method should be able to separate the peaks corresponding to IPA, NB, AN, and AB in the minimum period of retention time.</li>
	<li>Once the method has been selected, prepare a set of solutions of 50 mM, 25 mM, 10 mM, 5 mM and 2.5 mM NB in IPA, and another set of solutions of AN and AB in IPA with the same concentrations.</li>
	<li>Run a GC analysis of the prepared solutions. Each chromatogram should present 2 peaks: the higher one corresponds to IPA and the lower one corresponds to NB, AN, or AB. For each chromatogram, note down the retention time and peak area of all the peaks.</li>
	<li>Trace the calibration curves of NB, AN, and AB by plotting the concentration versus peak area of each sample.</li>
</ol>
8. GC analysis
<ol>
	<li>Run a GC analysis on the samples collected in steps 5. and 6. with the same method used for steps 7.2. and 7.4.</li>
	<li>For each chromatogram, note down the retention time and peak area and use the calibration curves plotted previously to determine the concentration of NB, AN, and AB in the samples.</li>
	<li>Calculate the nitrobenzene conversion as well as the aniline and azobenzene selectivity using the equations: 
	<img alt="Equation 1" src="/files/ftp_upload/61712/61712eq1.jpg" /> 
	<img alt="Equation 2" src="/files/ftp_upload/61712/61712eq2.jpg" /> 
	<img alt="Equation 3" src="/files/ftp_upload/61712/61712eq3.jpg" /> 
	Where <img alt="Equation 4" src="/files/ftp_upload/61712/61712eq4.jpg" /> is the initial NB concentration (0.03 mol/L), and CNB, CAN, CAB&#160; correspond to the NB, AN, and AB concentrations, respectively, after 2.5 hours reaction by the GC analysis.</li>
</ol>

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The authors have nothing to disclose.

The &#64257;ndings described in this method demonstrate that the intrinsic catalytic activity of Pd (or other catalytic but not plasmonic metal) can be signi&#64257;cantly enhanced by LSPR excitation via visible-light irradiation in bimetallic alloyed NPs35. In this case, Ag (or another plasmonic metal) is capable of harvesting energy from visible-light irradiation via LSPR excitation. The LSPR excitation leads to the formation of hot charge carriers (hot electrons and holes) and localized heating...

Among the several applications of metal nanoparticles (NPs), catalysis deserves special attention. Catalysis plays a central role in a sustainable future, contributing to less energy consumption, better utilization of raw materials, and enabling cleaner reaction conditions1,2,3,4. Thus, progress in catalysis can provide tools for enhancing the atomic efficiency of chemical processes, making them cleaner, more economically viable, and more environmentally friendly. Metal NPs encompassing silver (Ag), gold (Au) or copper (Cu) can display interesting optical properties in the visible range that arise from the unique way these systems interact with light at the nanoscale via the localized surface plasmon resonance (LSPR) excitation5,6,7,8. In these NPs, referred to as plasmonic NPs, the LSPR comprises the resonant interaction between the incident photons (from an incoming electromagnetic wave) with the collective motion of electrons5,6,7,8. This phenomenon takes place at a characteristic frequency which is dependent on the size, shape, composition, and dielectric constant of the environment9,10,11. For example, for Ag, Au, and Cu, these frequencies can range from the visible to the near-IR, opening up possibilities for the utilization of solar energy to excite their LSPR5,6,7,8,12,13.
Recently, it has been demonstrated that the LSPR excitation in plasmonic NPs can contribute to accelerate the rates and control the selectivity of molecular transformations5,14,15,16,17,18,19. This gave birth to a field called plasmonic catalysis, which focus on using energy from light to accelerate, drive, and/or control chemical transformations5,14,15,16,17,18,19. In this context, it has been established that the LSPR excitation in plasmonic NPs can lead to the formation of energetic hot electrons and holes, referred to as LSPR-excited hot carriers. These carriers can interact with adsorbed species through electronic or vibrational activation15,16. In addition to increased reaction rates, this process can also provide alternative reaction pathways not accessible via traditional thermochemically-driven processes, opening up new avenues for the control over reaction selectivity20,21,22,23,24,25. Importantly, it is worth noting that the plasmon decay can also lead to thermal dissipation, leading to a temperature increase in the vicinity of the NPs which can also contribute to speed up reaction rates15,16.
Due to these interesting features, plasmonic catalysis has been successfully employed towards a variety of molecular transformations18. Nevertheless, an important challenge remains. While plasmonic NPs such as Ag and Au display excellent optical properties in the visible and near-IR ranges, their catalytic properties are limited in terms of the scope of transformations. In other words, they do not display good catalytic properties for several of transformations. Additionally, metals that are important in catalysis, such as palladium (Pd) and platinum (Pt), do not support LSPR excitation in the visible or near-IR ranges. To bridge this gap, bimetallic NPs containing a plasmonic and catalytic metal represents an effective strategy20,26,27,28,29. In these systems, the plasmonic metal can be employed as an antenna to harvest energy from the light excitation through the LSPR, which is then used to drive, accelerate, and control molecular transformations at the catalytic metal. Therefore, this strategy enables us to extend plasmonic catalysis beyond traditional plasmonic metal NPs20,26,27,28,29.
This protocol describes the facile synthesis of bimetallic silver-palladium (Ag-Pd) alloyed NPs supported on ZrO2 (Ag-Pd/ZrO2) that can act as a plasmonic-catalytic system for plasmonic catalysis. The Ag-Pd/ZrO2 NPs were prepared by co-impregnation of the corresponding metal precursors on the ZrO2 support followed by simultaneous reduction30. This approach led to the formation of bimetallic NPs around 10 nm in size (diameter) directly at the surface of the ZrO2 support. The NPs were composed of 1 mol% of Pd to minimize the utilization of the catalytic metal while maximizing the optical properties of the resulting Ag-Pd NPs. A protocol for the application of the Ag-Pd/ZrO2 NPs in plasmonic catalysis was demonstrated for the reduction of nitrobenzene. We employed 425 nm LED illumination for the LSPR excitation. Gas chromatography was performed to monitor the conversion and selectivity of the reduction reaction under the dark and light irradiation conditions. LSPR excitation led to enhanced catalytic performance and control over selectivity in Ag-Pd/ZrO2 NPs relative to purely thermally driven conditions. The method described in this protocol is based on a simple photocatalytic reaction setup coupled with gas chromatography and can be adapted to a wide range of molecular transformations and NPs compositions. Thus, this method makes possible the characterization of photocatalytic activity, in terms of conversion and reaction selectivity, of different NPs and for a myriad of liquid-phase transformations. We believe this article will provide important guidelines and insights to both newcomers and more experienced scientists in the field.

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		<col />
		<col />
		<col />
		<col />
	</colgroup>
	<tbody>
		<tr height="42">
			<td height="42" style="height:42px;width:427px;">2-Propanol (anhydrous, 99.5%)</td>
			<td style="width:96px;">Sigma-Aldrich</td>
			<td style="width:114px;">278475</td>
			<td style="width:89px;">CAS Number 67-63-0</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:427px;">Aniline (for synthesis)</td>
			<td style="width:96px;">Sigma-Aldrich</td>
			<td style="width:114px;">8.22256</td>
			<td style="width:89px;">CAS Number 62-53-3</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:427px;">Azobenzene (98%)</td>
			<td style="width:96px;">Sigma-Aldrich</td>
			<td style="width:114px;">424633</td>
			<td style="width:89px;">CAS Number 103-33-3</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:427px;">Ethanol</td>
			<td style="width:96px;">Honeywell</td>
			<td style="width:114px;">32221</td>
			<td style="width:89px;">CAS Number 64-17-5</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:427px;">Hydrochloric acid (37%)</td>
			<td style="width:96px;">VWR</td>
			<td style="width:114px;">PRLSMC310066</td>
			<td style="width:89px;">CAS Number 7647-01-0</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:427px;">L-Lysine (crystallized, &#8805;98.0% (NT))</td>
			<td style="width:96px;">Sigma-Aldrich</td>
			<td style="width:114px;">62840</td>
			<td style="width:89px;">CAS Number 56-87-1</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:427px;">Nitric acid (65%)</td>
			<td style="width:96px;">Merck</td>
			<td style="width:114px;">100456</td>
			<td style="width:89px;">CAS Number 7697-37-2</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:427px;">Nitrobenzene</td>
			<td style="width:96px;">Sigma-Aldrich</td>
			<td style="width:114px;">8.06770</td>
			<td style="width:89px;">CAS Number 98-95-3</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:427px;">Potassium hydroxide</td>
			<td style="width:96px;">Fisher</td>
			<td style="width:114px;">10448990</td>
			<td style="width:89px;">CAS Number 1310-58-3</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:427px;">Potassium tetrachloropalladate (II) (98%)</td>
			<td style="width:96px;">Sigma-Aldrich</td>
			<td style="width:114px;">205796</td>
			<td style="width:89px;">CAS Number 10025-98-6</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:427px;">Silver nitrate (ACS reagent, &#8805;99.0%)</td>
			<td style="width:96px;">Sigma-Aldrich</td>
			<td style="width:114px;">209139</td>
			<td style="width:89px;">CAS Number 7761-88-8</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:427px;">Sodium borohydride (fine granular for synthesis)</td>
			<td style="width:96px;">Sigma-Aldrich</td>
			<td style="width:114px;">8.06373</td>
			<td style="width:89px;">CAS Number 16940-66-2</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:427px;">Zirconium (IV) oxide (nanopowder, &#60;100 nm particle size (TEM))</td>
			<td style="width:96px;">Sigma-Aldrich</td>
			<td style="width:114px;">544760</td>
			<td style="width:89px;">CAS Number 1314-23-4</td>
		</tr>
	</tbody>
</table>

preparation of silver-palladium alloyed nanoparticles for plasmonic catalysis under visible-light illumination

Localized surface plasmon resonance (LSPR) in plasmonic nanoparticles (NPs) can accelerate and control the selectivity of a variety of molecular transformations. This opens possibilities for the use of visible or near-IR light as a sustainable input to drive and control reactions when plasmonic nanoparticles supporting LSPR excitation in these ranges are employed as catalysts. Unfortunately, this is not the case for several catalytic metals such as palladium (Pd). One strategy to overcome this limitation is to employ bimetallic NPs containing plasmonic and catalytic metals. In this case, the LSPR excitation in the plasmonic metal can contribute to accelerate and control transformations driven by the catalytic component. The method reported herein focuses on the synthesis of bimetallic silver-palladium (Ag-Pd) NPs supported on ZrO2 (Ag-Pd/ZrO2) that acts as a plasmonic-catalytic system. The NPs were prepared by co-impregnation of corresponding metal precursors on the ZrO2 support followed by simultaneous reduction leading to the formation of bimetallic NPs directly on the ZrO2 support. The Ag-Pd/ZrO2 NPs were then used as plasmonic catalysts for the reduction of nitrobenzene under 425 nm illumination by LED lamps. Using gas chromatography (GC), the conversion and selectivity of the reduction reaction under the dark and light irradiation conditions can be monitored, demonstrating the enhanced catalytic performance and control over selectivity under LSPR excitation after alloying non-plasmonic Pd with plasmonic metal Ag. This technique can be adapted to a wide range of molecular transformations and NPs compositions, making it useful for the characterization of the plasmonic catalytic activity of different types of catalysis in terms of conversion and selectivity.

Figure 1A shows digital photographs of the solid samples containing the pure ZrO2 oxide (left) and the Ag-Pd/ZrO2 NPs (right). This change in color from white (in ZrO2) to brown (Ag-Pd/ZrO2) provides the initial qualitative evidence on the deposition of Ag-Pd NPs at the ZrO2 surface. Figure 1B shows the UV-visible absorption spectra from the Ag-Pd/ZrO2 NPs (blue trace) as well as ZrO2 (...

Watch this Scientific Journal Video about Preparation of Silver-Palladium Alloyed Nanoparticles for Plasmonic Catalysis under Visible-Light Illumination at JoVE.com

Preparation of Silver-Palladium Alloyed Nanoparticles for Plasmonic Catalysis under Visible-Light Illumination

Presented here is a protocol for the synthesis of silver-palladium (Ag-Pd) alloy nanoparticles (NPs) supported on ZrO2 (Ag-Pd/ZrO2). This system allows for harvesting energy from visible light irradiation to accelerate and control molecular transformations. This is illustrated by nitrobenzene reduction under light irradiation catalyzed by Ag-Pd/ZrO2 NPs.

Localized surface plasmon resonance (LSPR) in plasmonic nanoparticles (NPs) can accelerate and control the selectivity of a variety of molecular ...

preparation-silver-palladium-alloyed-nanoparticles-for-plasmonic

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JoVE Journal

Chemistry

5.4K Views.  University of Helsinki. Presented here is a protocol for the synthesis of silver-palladium (Ag-Pd) alloy nanoparticles (NPs) supported on ZrO2 (Ag-Pd/ZrO2). This system allows for harvesting energy from visible light irradiation to accelerate and control molecular transformations. This is illustrated by nitrobenzene reduction under light irradiation catalyzed by Ag-Pd/ZrO2 NPs.

Video: Preparation of Silver-Palladium Alloyed Nanoparticles for Plasmonic Catalysis under Visible-Light Illumination

Gyroid Nickel Nanostructures from Diblock Copolymer Supramolecules

Nanoporous metal foams possess a unique combination of properties - they are catalytically active, thermally and electrically conductive, and furthermore, have high porosity, high surface-to-volume and strength-to-weight ratio. Unfortunately, common approaches for preparation of metallic nanostructures render materials with highly disordered architecture, which might have an adverse effect on their mechanical properties. Block copolymers have the ability to self-assemble into ordered nanostructures and can be applied as templates for the preparation of well-ordered metal nanofoams. Here we describe the application of a block copolymer-based supramolecular complex - polystyrene-block-poly(4-vinylpyridine)(pentadecylphenol) PS-b-P4VP(PDP) - as a precursor for well-ordered nickel nanofoam. The supramolecular complexes exhibit a phase behavior similar to conventional block copolymers and can self-assemble into the bicontinuous gyroid morphology with two PS networks placed in a P4VP(PDP) matrix. PDP can be dissolved in ethanol leading to the formation of a porous structure that can be backfilled with metal. Using electroless plating technique, nickel can be inserted into the template&#39;s channels. Finally, the remaining polymer can be removed via pyrolysis from the polymer/inorganic nanohybrid resulting in nanoporous nickel foam with inverse gyroid morphology.

This article describes the preparation of well-ordered nickel nanofoams via electroless metal deposition onto nanoporous templates obtained from self-assembled diblock copolymer based supramolecules.

Nanoporous metal foams possess a unique combination of properties - they are catalytically active, thermally and electrically conductive, and furthermore, ...

Preparation of Silica Nanoparticles Through Microwave-assisted Acid-catalysis

Microwave-assisted synthetic techniques were used to quickly and reproducibly produce silica nanoparticle sols using an acid catalyst with nanoparticle diameters ranging from 30-250 nm by varying the reaction conditions. Through the selection of a microwave compatible solvent, silicic acid precursor, catalyst, and microwave irradiation time, these microwave-assisted methods were capable of overcoming the previously reported shortcomings associated with synthesis of silica nanoparticles using microwave reactors. The siloxane precursor was hydrolyzed using the acid catalyst, HCl. Acetone, a low-tan &#948; solvent, mediates the condensation reactions and has minimal interaction with the electromagnetic field. Condensation reactions begin when the silicic acid precursor couples with the microwave radiation, leading to silica nanoparticle sol formation. The silica nanoparticles were characterized by dynamic light scattering data and scanning electron microscopy, which show the materials&#39; morphology and size to be dependent on the reaction conditions. Microwave-assisted reactions produce silica nanoparticles with roughened textured surfaces that are atypical for silica sols produced by St&#246;ber&#39;s methods, which have smooth surfaces.

Silica nanoparticles were prepared using acid-catalysis of a siloxane precursor and microwave-assisted synthetic techniques resulting in the controlled growth of nanomaterials ranging from 30-250 nm in diameter. The growth dynamics can be controlled by varying the initial silicic acid concentration, time of the reaction, and temperature of reaction.

Microwave-assisted synthetic techniques were used to quickly and reproducibly produce silica nanoparticle sols using an acid catalyst with nanoparticle ...

Synthesis of Immunotargeted Magneto-plasmonic Nanoclusters

Magnetic and plasmonic properties combined in a single nanoparticle provide a synergy that is advantageous in a number of biomedical applications including contrast enhancement in novel magnetomotive imaging modalities, simultaneous capture&#160;and detection of circulating tumor cells (CTCs),&#160;and multimodal molecular imaging combined with photothermal therapy of cancer cells. These applications have stimulated significant interest in development of protocols for synthesis of magneto-plasmonic nanoparticles with optical absorbance in the near-infrared (NIR) region and a strong magnetic moment. Here, we present a novel protocol for synthesis of such hybrid nanoparticles that is based on an oil-in-water microemulsion method. The unique feature of the protocol described herein is synthesis of magneto-plasmonic nanoparticles of various sizes from primary blocks which also have magneto-plasmonic characteristics. This approach yields nanoparticles with a high density of magnetic and plasmonic functionalities which are uniformly distributed throughout the nanoparticle volume. The hybrid nanoparticles can be easily functionalized by attaching antibodies through the Fc moiety leaving the Fab portion that is responsible for antigen binding available for targeting.

Here, we describe a protocol for synthesis of magneto-plasmonic nanoparticles with a strong magnetic moment and a strong near-infrared (NIR) absorbance. The protocol also includes antibody conjugation to the nanoparticles through the Fc moiety for various biomedical applications which require molecular specific targeting.

Magnetic and plasmonic properties combined in a single nanoparticle provide a synergy that is advantageous in a number of biomedical applications ...

Preparation and Characterization of SDF-1&#945;-Chitosan-Dextran Sulfate Nanoparticles

Chitosan (CS) and dextran sulfate (DS) are charged polysaccharides (glycans), which form polyelectrolyte complex-based nanoparticles when mixed under appropriate conditions. The glycan nanoparticles are useful carriers for protein factors, which facilitate the in vivo delivery of the proteins and sustain their retention in the targeted tissue. The glycan polyelectrolyte complexes are also ideal for protein delivery, as the incorporation is carried out in aqueous solution, which reduces the likelihood of inactivation of the proteins. Proteins with a heparin-binding site adhere to dextran sulfate readily, and are, in turn, stabilized by the binding. These particles are also less inflammatory and toxic when delivered in vivo. In the protocol described below, SDF-1&#945; (Stromal cell-derived factor-1&#945;), a stem cell homing factor, is first mixed and incubated with dextran sulfate. Chitosan is added to the mixture to form polyelectrolyte complexes, followed by zinc sulfate to stabilize the complexes with zinc bridges. The resultant SDF-1&#945;-DS-CS particles are measured for size (diameter) and surface charge (zeta potential). The amount of the incorporated SDF-1&#945; is determined, followed by measurements of its in vitro release rate and its chemotactic activity in a particle-bound form.

The objective of this protocol is to incorporate SDF-1&#945;, a stem cell homing factor, into dextran sulfate-chitosan nanoparticles. The resultant particles are measured for their size and zeta potential, as well as the content, activity, and in vitro release rate of SDF-1&#945; from the nanoparticles.

Chitosan (CS) and dextran sulfate (DS) are charged polysaccharides (glycans), which form polyelectrolyte complex-based nanoparticles when mixed under ...

A Simple Method for the Size Controlled Synthesis of Stable Oligomeric Clusters of Gold Nanoparticles under Ambient Conditions

Reducing dilute aqueous HAuCl4 with sodium thiocyanate (NaSCN) under alkaline conditions produces 2 to 3 nm diameter nanoparticles. Stable grape-like oligomeric clusters of these yellow nanoparticles of narrow size distribution are synthesized under ambient conditions via two methods. The delay-time method controls the number of subunits in the oligoclusters by varying the time between the addition of HAuCl4 to alkaline solution and the subsequent addition of reducing agent, NaSCN. The yellow oligoclusters produced range in size from ~3 to ~25 nm. This size range can be further extended by an add-on method utilizing hydroxylated gold chloride (Na+[Au(OH4-x)Clx]-) to auto-catalytically increase the number of subunits in the as-synthesized oligocluster nanoparticles, providing a total range of 3 nm to 70 nm. The crude oligocluster preparations display narrow size distributions and do not require further fractionation for most purposes. The oligoclusters formed can be concentrated &#62;300 fold without aggregation and the crude reaction mixtures remain stable for weeks without further processing. Because these oligomeric clusters can be concentrated before derivatization they allow expensive derivatizing agents to be used economically. In addition, we present two models by which predictions of particle size can be made with great accuracy.

We describe a simple method for producing highly stable oligomeric clusters of gold nanoparticles via the reduction of chloroauric acid (HAuCl4) with sodium thiocyanate (NaSCN). The oligoclusters have a narrow size distribution and can be produced with a wide range of sizes and surface coats.

Reducing dilute aqueous HAuCl4 with sodium thiocyanate (NaSCN) under alkaline conditions produces 2 to 3 nm diameter nanoparticles. Stable grape-like ...

Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst

A standardized technique for atom transfer radical polymerization of vinyl monomers using perylene as a visible-light photocatalyst is presented. The procedure is performed under an inert atmosphere using air- and water-exclusion techniques. The outcome of the polymerization is affected by the ratios of monomer, initiator, and catalyst used as well as the reaction concentration, solvent, and nature of the light source. Temporal control over the polymerization can be exercised by turning the visible light source off and on. Low dispersities of the resultant polymers as well as the ability to chain-extend to form block copolymers suggest control over the polymerization, while chain end-group analysis provides evidence supporting an atom-transfer radical polymerization mechanism.

A method for the atom transfer radical polymerization of functionalized vinyl monomers using perylene as a visible-light photocatalyst is described.

A standardized technique for atom transfer radical polymerization of vinyl monomers using perylene as a visible-light photocatalyst is presented. The ...

HKUST-1 as a Heterogeneous Catalyst for the Synthesis of Vanillin

Vanillin (4-hydoxy-3-methoxybenzaldehyde) is the main component of the extract of vanilla bean. The natural vanilla scent is a mixture of approximately 200 different odorant compounds in addition to vanillin. The natural extraction of vanillin (from the orchid Vanilla planifolia, Vanilla tahitiensis and Vanilla pompon) represents only 1% of the worldwide production and since this process is expensive and very long, the rest of the production of vanillin is synthesized. Many biotechnological approaches can be used for the synthesis of vanillin from lignin, phenolic stilbenes, isoeugenol, eugenol, guaicol, etc., with the disadvantage of harming the environment since these processes use strong oxidizing agents and toxic solvents. Thus, eco-friendly alternatives on the production of vanillin are very desirable and thus, under current investigation. Porous coordination polymers (PCPs) are a new class of highly crystalline materials that recently have been used for catalysis. HKUST-1 (Cu3(BTC)2(H2O)3, BTC = 1,3,5-benzene-tricarboxylate) is a very well known PCP which has been extensively studied as a heterogeneous catalyst. Here, we report a synthetic strategy for the production of vanillin by the oxidation of trans-ferulic acid using HKUST-1 as a catalyst.

The conversion of trans-ferulic acid to vanillin was achieved by heterogeneous catalysis. HKUST-1 was employed in this synthesis and the essential step in the catalytic process was the generation of unsaturated metal sites. Thus, when the catalyst was activated under vacuum, full vanillin conversion (yield of 95%) was obtained.

Vanillin (4-hydoxy-3-methoxybenzaldehyde) is the main component of the extract of vanilla bean. The natural vanilla scent is a mixture of approximately ...

A Protocol for the Production of Gliadin-cyanoacrylate Nanoparticles for Hydrophilic Coating

This article presents a protocol for the production of protein-based nanoparticles that changes the hydrophobic surface to hydrophilic by a simple spray coating. These nanoparticles are produced by the polymerization reaction of alkyl cyanoacrylate on the surface of cereal protein (gliadin) molecules. Alkyl cyanoacrylate is a monomer that instantly polymerizes at RT when it is applied to the surface of materials. Its polymerization reaction is initiated by the trace amounts of weakly basic or nucleophilic species on the surface, including moisture. Once polymerized, the polymerized alkyl cyanoacrylates show a strong affinity with the object materials because nitrile groups are in the backbone of poly (alkyl cyanoacrylate). Proteins also work as initiator for this polymerization because they contain amine groups that can initiate the polymerization of cyanoacrylate. If aggregated protein is used as an initiator, protein aggregate is surrounded by the hydrophobic poly(alkyl cyanoacrylate) chains after the polymerization reaction of alkyl cyanoacrylate. By controlling the experimental condition, particles in the nanometer range are produced. The produced nanoparticles readily adsorb to the surface of most materials including glass, metals, plastics, wood, leather, and fabrics. When the surface of a material is sprayed with the produced nanoparticle suspension and rinsed with water, the micellar structure of nanoparticle changes its conformation, and the hydrophilic proteins are exposed to the air. As a result, the nanoparticle-coated surface changes to hydrophilic.

This article presents a protocol for the production of protein-based nanoparticles that changes the hydrophobic surface to hydrophilic. The produced nanoparticle is an assembly of gliadin-cyanoacrylate diblock copolymers. Spray coating with the produced nanoparticle changes the surface of target material to a hydrophilic surface.

This article presents a protocol for the production of protein-based nanoparticles that changes the hydrophobic surface to hydrophilic by a simple spray ...

Facile Synthesis of Worm-like Micelles by Visible Light Mediated Dispersion Polymerization Using Photoredox Catalyst

Presented herein is a protocol for the facile synthesis of worm-like micelles by visible light mediated dispersion polymerization. This approach begins with the synthesis of a hydrophilic poly(oligo(ethylene glycol) methyl ether methacrylate) (POEGMA) homopolymer using reversible addition-fragmentation chain-transfer (RAFT) polymerization. Under mild visible light irradiation (&#955; = 460 nm, 0.7 mW/cm2), this macro-chain transfer agent (macro-CTA) in the presence of a ruthenium based photoredox catalyst, Ru(bpy)3Cl2 can be chain extended with a second monomer to form a well-defined block copolymer in a process known as Photoinduced Electron Transfer RAFT (PET-RAFT). When PET-RAFT is used to chain extend POEGMA with benzyl methacrylate (BzMA) in ethanol (EtOH), polymeric nanoparticles with different morphologies are formed in situ according to a polymerization-induced self-assembly (PISA) mechanism. Self-assembly into nanoparticles presenting POEGMA chains at the corona and poly(benzyl methacrylate) (PBzMA) chains in the core occurs in situ due to the growing insolubility of the PBzMA block in ethanol. Interestingly, the formation of highly pure worm-like micelles can be readily monitored by observing the onset of a highly viscous gel in situ due to nanoparticle entanglements occurring during the polymerization. This process thereby allows for a more reproducible synthesis of worm-like micelles simply by monitoring the solution viscosity during the course of the polymerization. In addition, the light stimulus can be intermittently applied in an ON/OFF manner demonstrating temporal control over the nanoparticle morphology.

This article describes a process for producing polymeric self-assembled nanoparticles using visible light mediated dispersion polymerization. Using low energy visible light to control the polymerization allows for the reproducible formation of self-assembled worm-like micelles at high solids content.

Presented herein is a protocol for the facile synthesis of worm-like micelles by visible light mediated dispersion polymerization. This approach begins ...

Imine Metathesis by Silica-Supported Catalysts Using the Methodology of Surface Organometallic Chemistry

With this protocol, a well-defined singlesite silica-supported heterogeneous catalyst [(&#8801;Si-O-)Hf(=NMe)(&#951;1-NMe2)] is designed and prepared according to the methodology developed by surface organometallic chemistry (SOMC). In this framework, catalytic cycles can be determined by isolating crucial intermediates. All air-sensitive materials are handled under inert atmosphere (using gloveboxes or a Schlenk line) or high vacuum lines (HVLs, &#60;10-5 mbar). The preparation of SiO2-700 (silica dehydroxylated at 700 &#176;C) and subsequent applications (the grafting of complexes and catalytic runs) requires the use of HVLs and double-Schlenk techniques. Several well-known characterization methods are used, such as Fourier-transform infrared spectroscopy (FTIR), elemental microanalysis, solid-state nuclear magnetic resonance spectroscopy (SSNMR), and state-of-the-art dynamic nuclear polarization surface enhanced NMR spectroscopy (DNP-SENS). FTIR and elemental microanalysis permit scientists to establish the grafting and its stoichiometry. 1H and 13C SSNMR allows the structural determination of the hydrocarbon ligands coordination sphere. DNP SENS is an emerging powerful technique in solid characterization for the detection of poorly sensitive nuclei (15N, in our case). SiO2-700 is treated with about one equivalent of the metal precursor compared to the amount of surface silanol (0.30 mmol&#183;g-1) in pentane at room temperature. Then, volatiles are removed, and the powder samples are dried under dynamic high vacuum to afford the desired materials [(&#8801;Si-O-)Hf(&#951;2&#960;-MeNCH2)(&#951;1-NMe2)(&#951;1-HNMe2)]. After a thermal treatment under high vacuum, the grafted complex is converted into metal imido silica complex [(&#8801;Si-O-)Hf(=NMe)(&#951;1-NMe2)]. [(&#8801;Si-O-)Hf(=NMe)(&#951;1-NMe2)] effectively promotes the metathesis of imines, using the combination of two imine substrates, N-(4-phenylbenzylidene)benzylamine, or N-(4-fluorobenzylidene)-4-fluoroaniline, with N-benzylidenetert-butylamine as substrates. A significantly lower conversion is observed with the blank runs; thus, the presence of the imido group in [(&#8801;Si-O-)Hf(=NMe)(&#951;1-NMe2)] is correlated to the catalytic performance.

A new group IV metal catalyst for imine metathesis is prepared by grafting amine metal complex onto dehydroxylated silica. Surface metal fragments are characterized using FT-IR, elemental microanalysis, and solid-state NMR spectroscopy. Further dynamic nuclear polarization surface enhanced NMR spectroscopy experiments complement the determination of the coordination sphere.

With this protocol, a well-defined singlesite silica-supported heterogeneous catalyst [(&#8801;Si-O-)Hf(=NMe)(&#951;1-NMe2)] is designed and prepared ...