Bernd Fritzinger

Surface chemistry of colloidal PbSe nanocrystals

Solution nuclear magnetic resonance spectroscopy (NMR) is used to identify and quantify the organic capping of colloidal PbSe nanocrystals (Q-PbSe). We find that the capping consists primarily of tightly bound oleic acid ligands. Only a minor part of the ligand shell (0-5% with respect to the number of oleic acid ligands) is composed of tri- n-octylphosphine. As a result, tuning of the Q-PbSe size during synthesis is achieved by varying the oleic acid concentration. By combining the NMR results with inductively coupled plasma mass spectrometry, a complete Q-PbSe structural model of semiconductor core and organic ligands is constructed. The nanocrystals are nonstoichiometric, with a surface that is composed of lead atoms. The absence of surface selenium atoms is in accordance with an oleic acid ligand shell. NMR results on a Q-PbSe suspension, stored under ambient conditions, suggest that oxidation leads to the loss of oleic acid ligands and surface Pb atoms, forming dissolved lead oleate.

Utilizing Self-Exchange To Address the Binding of Carboxylic Acid Ligands to CdSe Quantum Dots

We use solution NMR techniques to analyze the organic/inorganic interface of CdSe quantum dots (Q-CdSe) synthesized using oleic acid as a surfactant. It is shown that the resulting Q-CdSe are stabilized by tightly bound oleic acid species that only exchange upon addition of free oleic acid. The NMR analysis points toward a two-step exchange mechanism where free ligands are initially physisorbed within the ligand shell to end up as bound, chemisorbed ligands in a second step. Importantly, we find that every ligand is involved in this exchange process. By addition of oleic acid with a deuterated carboxyl headgroup, we demonstrate that the bound ligands are oleate ions and not oleic acid molecules. This explains why a dynamic adsorption/desorption equilibrium only occurs in the presence of excess free oleic acid, which donates the required proton. Comparing the number of oleate ligands to the excess cadmium per CdSe quantum dot, we find a ratio of 2:1. This completes the picture of Q-CdSe as organic/inorganic entities where the surface excess of Cd(2+) is balanced by a double amount of oleate ligands, yielding overall neutral nanoparticles.

In Situ Observation of Rapid Ligand Exchange in Colloidal Nanocrystal Suspensions Using Transfer NOE Nuclear Magnetic Resonance Spectroscopy

Recently, solution NMR-based approaches have been developed that represent useful new tools for the in situ characterization of the capping ligand in colloidal nanocrystal dispersions. So far, this development has focused mainly on tightly bound ligands (no exchange) or ligands in slow exchange with the nanocrystal surface. In such systems, the ligand can be identified and its amount and interaction quantified via 1D (1)H NMR, (1)H-(13)C HSQC, and DOSY spectra. Here, we explore the case where capping ligands are in fast exchange with the nanocrystal surface. Using dodecylamine-stabilized CdTe (Q-CdTe|DDA) and octylamine-stabilized ZnO (Q-ZnO|OctA) nanoparticles, we first show that the NMR methods developed so far fail to evidence the bound ligand when the effect of the latter on the exchange-averaged parameters is marginalized by an excess of free ligand. Next, transfer NOE spectroscopy, a well-established technique in biomolecular NMR, is introduced to demonstrate and characterize the interaction of a ligand with the nanocrystal surface. Using Q-PbSe nanocrystals capped with oleic acids as a reference system, we show that bound and free ligands have strongly different NOE spectra wherein only bound ligands develop strong and negative NOEs. For the Q-CdTe|DDA system, transfer NOE spectra show a similar rapid appearance of strong, negative NOEs, thereby unambiguously demonstrating that DDA molecules spend time at the nanocrystal surface. In the case of Q-ZnO|OctA, where a more complex mixture is analyzed, transfer NOE spectroscopy allows distinguishing capping from noncapping molecules, thereby demonstrating the screening potential offered by this technique for colloidal quantum dot dispersions.

Hydrogel Network Formation Revised: High-Resolution Magic Angle Spinning Nuclear Magnetic Resonance as a Powerful Tool for Measuring Absolute Hydrogel Cross-Link Efficiencies

In the present work, high-resolution magic angle spinning (hr-MAS) NMR spectroscopy is applied as a straightforward nondestructive technique to quantify unreacted methacrylamide functionalities in cross-linked gelatin hydrogels. By adjusting several cross-linking parameters including the ultraviolet (UV) irradiation time and the photo-initiator concentration, the cross-linking degree can be easily varied. Remarkably, under all experimental conditions typically applied for hydrogel development, no more than 40% of the methacrylamide moieties present have reacted. The hr-MAS based approach to determine the cross-linking efficiency is shown to provide an innovative and more convenient alternative to the well-established classical techniques. In addition, the results obtained are in good correlation with mechanical analysis data.

Widening the view on dispersant-pigment interactions in colloidal dispersions with saturation transfer difference NMR spectroscopy.

The application of Saturation Transfer Difference (STD) NMR spectroscopy for the characterization of dispersant particle interactions is introduced. STD NMR has hitherto been applied, with great success, to the characterization of ligand-protein interactions and is currently a standard tool in biomolecular NMR spectroscopy. Nevertheless, the STD NMR technique has so far not yet crossed the boundaries of the biomolecular field. Here, we demonstrate that in spite of clear differences between a protein binding site and the surface of a pigment nanoparticle, the latter can also be subjected to STD NMR analysis, allowing us to detect (screen for) binding ligands, discriminate ligand from nonligand, and obtain information on the binding epitope. The approach should be generally applicable as long as the nanoparticle is comprised of a dense network of hydrogens, implicating almost all organic molecular nanocrystals. Thus it provides a novel investigative tool for the study of dispersions that is highly complementary to existing ones.

Ligands for Nanoparticles

This chapter deals with ligands of colloidal nanoparticles. In the first section, it provides an understanding of the many different ways ligands act as a go between in nanoparticle (NP) science and technology, emphasizing their role in NP synthesis, colloid stability, and chemical functionalization of NPs. In the second section, special attention is paid to the experimental in situ study of NP ligands with nuclear magnetic resonance (NMR) spectroscopy. We show how a combination of regular one-dimensional (1D) proton NMR in solution with more advanced 2D techniques, such as diffusion NMR and nuclear Overhauser effect (NOE)-based NMR, leads to a clear identification of ligands bound to colloidal nanoparticles. The so-called tightly bound ligands feature broadened resonances in the 1D 1 H spectrum, have the diffusion coefficient that agrees with the hydrodynamic radius of the entire nanoparticle, and show strongly negative NOE cross-peaks. Next, we show that adsorption/desorption of ligands manifests itself in deviations from this tightly bound ligand behavior. If the exchange is slow on the NMR timescale, bound and free ligands are observed simultaneously, enabling the analysis of the thermodynamics of the adsorption/desorption process. If the exchange is fast on the NMR timescale, the kinetics of the adsorption/desorption process can be studied. In the chapter, these different situations are illustrated by experimental examples of various colloidal nanoparticle systems.

Sandwich-ELISE NMR: Reducing the sample volume of NMR samples

We present Sandwich-ELISE, a concatenated version of our previously proposed Experimental LIquid SEaling (ELISE) protocol, in which an aqueous sample is effectively sealed by the addition of a small layer of mineral oil, or, alternatively, a chloroform sample was sealed by a water layer. With Sandwich-ELISE, a triple layered geometry composed of deuterated chloroform/aqueous buffer/mineral oil can be used to limit the sample to the active coil volume, effectively replacing the popular Shigemi tubes. Importantly, this procedure is readily applicable to smaller diameter tubes, for which no Shigemi tubes are available. We further present spectra of a 1 microl protein sample sandwiched between the chloroform and Nujol phases in a 1mm tube, demonstrating thereby that the volume of the aqueous phase of interest can be reduced even further.

Ranking high affinity ligands of low solubility by NMR spectroscopy.

Cyclosporine A (CsA) and its chemical analogues EthVal4Cs, MeVal4Cs, and Me(d-Ala)3EthVal4Cs (Alisporivir) all interact with cyclophilin A (CypA). The latter Alisporivir is a nonimmunosuppressive CsA derivative that has potent anti-HCV properties in clinical trials. We show here that NMR spectroscopy can be used to rank this series of related pharmacological molecules despite their high affinity for the target protein and low solubility in water. The novel method is based on the possibility to detect distinct NMR signals from the different protein complexes in a mixture. The method has enabled us to distinguish subtle effects of discrete chemical modifications of the parent molecule on the affinity of the ligands for the target protein.

Intermolecular interaction studies using small volumes.

We present the use of 1‐mm room‐temperature probe technology to perform intermolecular interaction studies using chemical shift perturbation methods and saturation transfer difference (STD) spectroscopy using small sample volumes. The use of a small sample volume (5–10 µl) allows for an alternative titration protocol where individual samples are prepared for each titration point, rather than the usual protocol used for a 5‐mm probe setup where the ligand is added consecutively to the solution containing the protein or host of interest. This allows for considerable economy in the consumption and cost of the protein and ligand amounts required for interaction studies. For titration experiments, the use of the 1‐mm setup consumes less than 10% of the ligand amount required using a 5‐mm setup. This is especially significant when complex ligands that are only available in limited quantities, typically because they are obtained from natural sources or through elaborate synthesis efforts, need to be investigated. While the use of smaller volumes does increase the measuring time, we demonstrate that the use of commercial small volume probes allows the study of interactions that would otherwise be impossible to address by NMR. Copyright