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Solution structural characterization of an array of nanoscale aqueous inorganic Ga(13–x)In(x) (0 ≤ x ≤ 6) clusters by (1)H-NMR and QM computations
NMR spectroscopy is the go-to technique for determining the solution structures of organic, organometallic, and even macromolecular species. However, structure determination of nanoscale aqueous inorganic clusters by NMR spectroscopy remains an unexplored territory. The few hydroxo-bridged inorganic...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707482/ https://www.ncbi.nlm.nih.gov/pubmed/29218173 http://dx.doi.org/10.1039/c5sc00776c |
Sumario: | NMR spectroscopy is the go-to technique for determining the solution structures of organic, organometallic, and even macromolecular species. However, structure determination of nanoscale aqueous inorganic clusters by NMR spectroscopy remains an unexplored territory. The few hydroxo-bridged inorganic species well characterized by (1)H Nuclear Magnetic Resonance spectroscopy ((1)H-NMR) do not provide enough information for signal assignment and prediction of new samples. (1)H-NMR and quantum mechanical (QM) computations were used to characterize the NMR spectra of the entire array of inorganic flat-Ga(13–x)In(x) (0 ≤ x ≤ 6) nanoscale clusters in solution. A brief review of the known signals for μ(2)-OH and μ(3)-OH bridges gives expected ranges for certain types of protons, but does not give enough information for exact peak assignment. Integration values and NOESY data were used to assign the peaks of several cluster species with simple (1)H-NMR spectra. Computations agree with these hydroxide signal assignments and allow for assignment of the complex spectra arising from the remaining cluster species. This work shows that (1)H-NMR spectroscopy provides a variety of information about the solution behavior of inorganic species previously thought to be inaccessible by NMR due to fast ligand and/or proton exchange in wet solvents. |
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