Surface functionalization of two-dimensional crystals is a key path to tuning their intrinsic physical and chemical properties. However, synthetic protocols and experimental strategies to directly probe chemical bonding in modified surfaces are scarce. Introduced herein is a mild, surfacespecific protocol for the surface functionalization of few-layer black phosphorus nanosheets using a family of photolytically generated nitrenes (RN) from the corresponding azides. By embedding spectroscopic tags in the organic backbone, a multitude of characterization techniques are employed to investigate in detail the chemical structure of the modified nanosheets, including vibrational, X-ray photoelectron, solid state 31 P NMR, and UV-vis spectroscopy. To directly probe the functional groups introduced on the surface, R fragments were selected such that in conjunction with vibrational spectroscopy, 15 N-labeling experiments, and DFT methods, diagnostic P = N vibrational modes indicative of iminophosphorane units on the nanosheet surface could be conclusively identified.

We present DEIMoS: Data Extraction for Integrated Multidimensional Spectrometry, a Python application programming interface (API) and command-line tool for high-dimensional mass spectrometry data analysis workflows that offers ease of development and access to efficient algorithmic implementations. Functionality includes feature detection, feature alignment, collision cross section (CCS) calibration, isotope detection, and MS/MS spectral deconvolution, with the output comprising detected features aligned across study samples and characterized by mass, CCS, tandem mass spectra, and isotopic signature. Notably, DEIMoS operates on N-dimensional data, largely agnostic to acquisition instrumentation; algorithm implementations simultaneously utilize all dimensions to (i) offer greater separation between features, thus improving detection sensitivity, (ii) increase alignment/feature matching confidence among data sets, and (iii) mitigate convolution artifacts in tandem mass spectra. We demonstrate DEIMoS with LC-IMS-MS/MS metabolomics data to illustrate the advantages of a multidimensional approach in each data processing step.

Abstract. Earth’s biogeochemical cycles are intimately tied to the biotic and abiotic processing of organic matter (OM). Spatial and temporal variation in OM chemistry is often studied using high resolution mass spectrometry (HRMS). An increasingly common approach is to use ecological metrics (e.g., within-sample diversity) to summarize high-dimensional HRMS data, notably Fourier transform ion cyclotron resonance MS (FTICR MS). However, problems arise when HRMS peak intensity data are used in a way that is analogous to abundances in ecological analyses (e.g., species abundance distributions). Using peak intensity data in this way requires the assumption that intensities act as direct proxies for concentrations, which is often invalid. Here we discuss theoretical expectations and provide empirical evidence why concentrations do not map to HRMS peak intensities. The theory and data show that comparisons of the same peak across samples (within-peak) may carry information regarding variation in relative concentration, but comparing different peaks (between-peak) within or between samples does not. We further developed a simulation model to study the quantitative implications of both within-peak and between-peak errors that decouple concentration from intensity. These implications are studied in terms of commonly used ecological metrics that quantify different aspects of diversity and functional trait values. We show that despite the poor linkages between concentration and intensity, the ecological metrics often perform well in terms of providing robust qualitative inferences and sometimes quantitatively-accurate estimates of diversity and trait values. We conclude with recommendations for using peak intensities in an informed and robust way for natural organic matter studies. A primary recommendation is the use and extension of the simulation model to provide objective, quantitative guidance on the degree to which conceptual and quantitative inferences can be made for a given analysis of a given dataset. Without objective guidance, researchers that use peak intensities are doing so with unknown levels of uncertainty and bias, potentially leading to spurious scientific outcomes.

We describe the Mass Spectrometry Adduct Calculator (MSAC), an automated Python tool to calculate the adduct ion masses of a parent molecule. Here, adduct refers to a version of a parent molecule [M] that is charged due to addition or loss of atoms and electrons resulting in a charged ion, for example, [M + H]+. MSAC includes a database of 147 potential adducts and adduct/neutral loss combinations and their mass-to-charge ratios (m/z) as extracted from the NIST/EPA/NIH Mass Spectral Library (NIST17), Global Natural Products Social Molecular Networking Public Spectral Libraries (GNPS), and MassBank of North America (MoNA). The calculator relies on user-selected subsets of the combined database to calculate expected m/z for adducts of molecules supplied as formulas. This tool is intended to help researchers create identification libraries to collect evidence for the presence of molecules in mass spectrometry data. While the included adduct database focuses on adducts typically detected during liquid chromatography–mass spectrometry analyses, users may supply their own lists of adducts and charge states for calculating expected m/z. We also analyzed statistics on adducts from spectra contained in the three selected mass spectral libraries. MSAC is freely available at .

This article describes a method for improving 1 H NMR spectra of aqueous samples containing paramagnetic metals by precipitation of metal cations with a variety of counteranions. The addition of hydroxide, phosphate, carbonate, and arsenate to solutions of transition metals such as Fe 2+ and Mn 2+ can reduce line broadening and improve the ability of a spectrometer to lock on the signal of deuterium. The method is most effective under strongly alkaline conditions, and care must be taken to observe whether the organic substrates undergo side reactions or are themselves removed from solution upon addition of the precipitating salts. As a demonstration of the practical value of the method, we show that NMR spectroscopy can be used to monitor the transition-metal-mediated hydrolysis of glycylglycine (Gly 2 ).