The reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) with sodium borohydride (NaBH4) in aqueous media is by far the most widely used reaction for testing the catalytic performance of a large variety of metal nanoparticles (MNPs) using UV/vis absorption spectroscopy. Huge differences in the kinetic rate constant of the catalytic 4-NP to 4-AP conversion as a function of material composition, size, and morphology have been reported by many different groups; so far, these have been exclusively attributed to the catalytic activity of the corresponding MNPs. In this study, we study the overlooked critical role of the pH value on the kinetics of this important reaction. We observe a strong pH dependence of both rate constant and reaction order, which we attribute to the pH-dependent hydrolysis of the reducing agent NaBH4 in water. In each hydrolysis step, molecular hydrogen as a second reducing agent is produced. Overall, two competing pathways result in: slow hydride versus fast hydrogen reduction. Kinetic simulations based on a model including all relevant species are capable of quantitatively describing all experimental results for three different noble-metal nanoparticle catalysts (Au, Pt, and Pd). Most importantly, for a fair interlaboratory comparison of the catalytic performances of MNPs, we recommend to report rate constants of the 4-NP to 4-AP conversion at pH 13 by strict pH control using a strong base such as NaOH since at pH 13 the hydrolysis of NaBH4 in aqueous solution is slowed down significantly.

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Ultraviolet resonance Raman (UVRR) scattering is a highly sensitive and selective vibrational spectroscopic technique with a broad range of applications from polyaromatic hydrocarbons (PAHs) to biomolecular systems (peptides/ proteins and nucleic acids) and catalysts. The interpretation of experimental UVRR spectra is not as straightforward as in purely vibrational Raman scattering (Placzek approximation) due to the involvement of higher lying electronic states and vibronic coupling. This necessitates the comparison with theoretical UVRR spectra computed by electronic structure calculations.Anthracene is an ideal model system for such a comparison between experiment and theory because it is rigid, symmetric, and of moderate size. By taking into account Herzberg-Teller contributions including Duschinsky effects, bulk solvent effects, and anharmonic contributions, a good qualitative agreement close to the resonance condition is achieved. The present study shows that within the framework of time-dependent density functional theory (TD-DFT), a general and robust approach for the analysis and interpretation of resonance Raman spectra of medium-to large-size molecules is available.

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Ultraviolet resonance Raman (UVRR) spectroscopy is a powerful vibrational spectroscopic technique for the label-free monitoring of molecular recognition of peptides or proteins with supramolecular ligands such as guanidiniocarbonyl pyrroles (GCPs). The use of UV laser excitation enables Raman binding studies of this class of supramolecular ligands at submillimolar concentrations in aqueous solution and provides a selective signal enhancement of the carboxylate binding site (CBS). A current limitation for the extension of this promising UVRR approach from peptides to proteins as binding partners for GCPs is the UV-excited autofluorescence from aromatic amino acids observed for laser excitation wavelengths >260 nm. These excitation wavelengths are in the electronic resonance with the GCP for achieving both a signal enhancement and the selectivity for monitoring the CBS, but the resulting UVRR spectrum overlaps with the UV-excited autofluorescence from the aromatic binding partners. This necessitates the use of a laser excitation <260 nm for spectrally separating the UVRR spectrum of the supramolecular ligand from the UV-excited autofluorescence of the peptide or protein. Here, we demonstrate the use of UVRR spectroscopy with 244 nm laser excitation for the characterization of GCP as well as guanidiniocarbonyl indole (GCI), a next generation supramolecular ligand for the recognition of carboxylates. For demonstrating the feasibility of the UVRR binding studies without an interference from the disturbing UV-excited autofluorescence, benzoic acid (BA) was chosen as an aromatic binding partner for GCI. We also present the UVRR results from the binding of GCI to the ubiquitous RGD sequence (arginylglycylaspartic acid) as a biologically relevant peptide. In the case of RGD, the more pronounced differences between the UVRR spectra of the free and complexed GCI (1:1 mixture) clearly indicate a stronger binding of GCI to RGD compared with BA. A tentative assignment of the experimentally observed changes upon molecular recognition is based on the results from density functional theory (DFT) calculations.