Quantitative determination of nonylphenol polyethoxylate surfactants in marine sediment using normal-phase liquid chromatography-electrospray mass spectrometry.

A new comprehensive analytical method based on normal-phase liquid chromatography-electrospray ionization mass spectrometry (LC-ESI-MS) has been developed for the quantitative determination of individual nonylphenol ethoxylate (NPEO) surfactants in complex environmental matrices. Clean-up of sample extracts was performed on cyanopropyl silica solid-phase extraction cartridges. Complete NPEO oligomer separation was achieved by using normal-phase LC. Because the non-polar solvents used in normal-phase LC are incompatible with ESI, unique LC-ESI-MS interface conditions were adopted that provided a functional interface and also enhanced the detection response of NPEOs. These provided enhanced ESI signal intensity and stability and facilitated the detection of NPEOs as sodium adducts at parts-per-billion concentration levels. The overall analytical method was validated for accuracy and precision by analyzing sediment samples spiked with known amounts of NPEOs. The method is superior to those currently used for NPEO analysis (LC-UV, LC-fluorescence, LC-thermospray-MS, LC-field desorption-MS, LC-particle beam-MS and GC-MS) in terms of detection limits, specificity and speed of analysis. The validated method was successfully applied to determine levels of NPEOs in sediments from the Strait of Georgia, British Columbia. This work also demonstrates that by proper selection of normal-phase LC-ESI-MS interface conditions this technique is capable of solving separation problems which are not amenable with reversed-phase LC-ESI-MS.     

Solid-state 93Nb and 13C NMR investigations of half-sandwich niobium(I) and niobium(V) cyclopentadienyl complexes

Solid-state 93Nb and 13C NMR experiments, in combination with theoretical calculations of NMR tensors, and single-crystal and powder X-ray diffraction experiments, are applied for the comprehensive characterization of structure and dynamics in a series of organometallic niobium complexes. Half-sandwich niobium metallocenes of the forms Cp'Nb(I)(CO)4 and CpNb(V)Cl4 are investigated, where Cp = C5H5- and Cp' = C5H4R- with R = COMe, CO2Me, CO2Et, and COCH2Ph. Anisotropic quadrupolar and chemical shielding (CS) parameters are extracted from 93Nb MAS and static NMR spectra for seven different complexes. It is demonstrated that 93Nb NMR parameters are sensitive to changes in temperature and Cp' ring substitution in the Cp'Nb(I)(CO)4 complexes. There are dramatic differences in the 93Nb quadrupolar coupling constants (C(Q)) between the Nb(I) and Nb(V) complexes, with C(Q) between 1.0 and 12.0 MHz for Cp'Nb(CO)4 and C(Q) = 54.5 MHz for CpNbCl4. The quadrupolar Carr-Purcell Meiboom-Gill (QCPMG) pulse sequence is applied to rapidly acquire, in a piecewise fashion, a high signal-to-noise ultra-wide-line 93Nb NMR spectrum of CpNbCl4, which has a breadth of ca. 400 kHz. Solid-state 93Nb and 13C NMR spectra and powder XRD data are used to identify a new metallocene adduct coordinated at the axial position of the metal site by a THF molecule: CpNb(V)Cl4.THF. 13C MAS and CP/MAS NMR experiments are used to assess the purity of samples, as well as for measuring carbon CS tensors and the rare instance of one-bond 93Nb, 13C J-coupling, 1J(93Nb,13C). Theoretically calculated CS and electric field gradient (EFG) tensors are utilized to determine relationships between tensor orientations, the principal components, and molecular structures.     

Study of the self‐diffusion of poly(ethylene glycol)s in poly(vinyl alcohol) aqueous systems

We have measured the self‐diffusion coefficients of a series of oligo‐ and poly(ethylene glycol)s with molecular weights ranging from 150 to 10,000, in aqueous solutions and gels of poly(vinyl alcohol) (PVA), using the pulsed‐gradient spin‐echo NMR techniques. The PVA concentrations varied from 0 to 0.38 g/mL which ranged from dilute solutions to polymer gels. Effects of the diffusant size and polymer concentration on the self‐diffusion coefficients have been investigated. The temperature dependence of the self‐diffusion coefficients has also been studied for poly(ethylene glycol)s with molecular weights of 600 and 2,000. Several theoretical models based on different physical concepts are used to fit the experimental data. The suitability of these models in the interpretation of the self‐diffusion data is discussed. © 1999 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 37: 2396–2403, 1999