Novel organic-inorganic hybrids of various sizes were generated by reaction of 1,8-octanediphosphonic acid (ODP) and (NH4)6Mo7O24 in aqueous solution. The formation of rodlike hybrids with variable numbers of covalently bound ODP and polyoxomolybdate (POM) units can be tuned as a function of increasing (NH4)6Mo7O24 concentration at fixed ODP concentration. The chemical structure of the ODP/POM hybrids was characterized by (1)H, (31)P, and (95)Mo NMR spectroscopy. Heteronuclear (31)P DOSY (diffusion- ordered NMR spectroscopy) and molecular mechanics (MM) calculations were applied to determine the size and shape of the nanosized hybrids generated at various ODP/POM ratios. For this purpose, the structures of ODP/POM hybrids with variable numbers of ODP and POM units were optimized by MM and then approximated as cylinder-shaped objects by using a recently described mathematical algorithm. The thus-obtained cylinder length and diameter were further used to calculate the expected diffusion coefficients of the ODP/POM hybrids. Comparison of the calculated and experimentally determined diffusion coefficients led to the most probable ODP/POM hybrid length for each sample composition. The (31)P DOSY results show that the length of the hybrids increases with increasing POM concentration and reaches a maximum corresponding to an average of 8 ODP/7 POM units per chain at a sample composition of 20 mM ODP and 14 mM POM. With excess POM, above the latter concentration, the formation of shorter-chain hybrids terminated by Mo7 clusters at one or both ends was evidenced on further increasing the POM concentration. The results demonstrate that the combination of (31)P DOSY and MM, although virtually unexplored in POM chemistry, is a powerful innovative strategy for the detailed characterization of nanosized organic-inorganic POM-based hybrids in solution.
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http://dx.doi.org/10.1002/chem.201304969 | DOI Listing |
J Phys Chem B
September 2024
Department of Chemistry, New York University, New York, New York 10003, United States.
This study reports on the conformational states of nicotinamide adenine dinucleotide (NADH) in water/DMSO mixtures and examines the influence of ion binding. We observe evidence of conformational changes through a series of NMR techniques, including P NMR relaxation ( and ), chemical exchange saturation transfer (CEST), and diffusion-ordered spectroscopy (DOSY) experiments. The observed variation of the conformational states is indicative of the solvent's influence on NADH's structural flexibility.
View Article and Find Full Text PDFInorg Chem
September 2023
Department of Chemistry, The University of Western Ontario, London, Ontario N6A 587, Canada.
Multicomponent reactions of primary phosphines (R-PH), diimines (R'-N═C(H)-R-(H)C═N-R'), and chalcogens (O, S) generate poly(α-aminophosphine chalcogenide)s (-) through step-growth polymerization. Characterization of the linear polymers using P{H} diffusion-ordered NMR spectroscopy (DOSY) experiments aided in determining the molecular weight () of the material. Subjecting the polyphosphine oxide or sulfide to reducing conditions in the presence of a Lewis acid resulted in complete depolymerization of the polymers, quantitatively releasing the 1° phosphine and diimine () starting materials, with concomitant reduction of diimine to diamine ().
View Article and Find Full Text PDFElectrophoresis
August 2023
Department of Mining and Materials Engineering, McGill University, Montreal, Quebec, Canada.
Polyacrylamide gel electrophoresis is commonly used to characterize the chain length of polyphosphates (polyP), more generally called condensed phosphates. After separation, nonradioactive, optical polyP staining is limited to chain lengths greater than 15 monomers with toluidine blue or 4',6-diamidino-2-phenylindole. PolyP chain lengths longer than 62 monomers were correlated to the shortest DNA ladders.
View Article and Find Full Text PDFElectrophoresis
October 2022
Department of Mining and Materials Engineering, McGill University, Montreal, Quebec, Canada.
Inorganic polyphosphates (polyPs) have been identified in eukaryotic and prokaryotic cells alike. Various extraction methods have been optimized as a necessary step before identification and measurement of these polymers. Three commercially available sodium polyP glasses were either dissolved or dissolved and extracted by two commonly used polyP extraction techniques - perchloric acid or buffered phenol-chloroform.
View Article and Find Full Text PDFRSC Adv
March 2021
Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education, P. R. China, School of Chemistry and Materials Science, Heilongjiang University Harbin 150080 P. R. China
Creating optically pure metal assemblies is a hot research topic in the realms of chiral supramolecules. Here, three new triple-stranded europium(iii) helicates EuL(L') [L = 4,4'-bis(4,4,4-trifluoro-1,3-dioxobutyl)diphenyl sulphide; L' = 1,10-phenanthroline (Phen) or /-2,2'-bis(diphenylphosphinyl)-1,1'-binaphthyl (/-BINAPO)] were synthesized in order to investigate the effects of ancillary ligands on controlling the stereoselective self-assembly of lanthanide helicates. X-ray single crystal structure analysis showed that EuL(Phen) crystalized in an achiral space group 1̄ with the equivalent amount of P and M helicates in one single cell.
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