6 article(s) from Landy, David
- Full Research Paper
- Published 05 May 2017
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Figure 1: Chemical structure of β-CD (a) and β-CD derivatives (b).
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Figure 2: Phase solubility diagrams of CD/trans-Ner inclusion complexes.
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Figure 3: Phase solubility profile of cabreuva EO obtained by the TOC method.
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Figure 4: a) 2D ROESY spectrum of β-CD/trans-Ner inclusion complex in D2O and b) representation of the most s...
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Figure 5: Photodegradation kinetics of cis-Ner (a), trans-Ner (b), the isomer mixture Ner (c) in the absence ...
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- Full Research Paper
- Published 08 Jan 2016
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Figure 1: Chemical structures, logP values and molecular volumes (V) of carvacrol (1) and thymol (2). ahttp:/...
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Figure 2: Phase solubility profiles of (a) CD/carvacrol (1) and (b) CD/thymol (2) inclusion complexes. Inset:...
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Figure 3: 2D DOSY NMR spectra of (a) β-CD, carvacrol (1) and β-CD/carvacrol (1) inclusion complex and (b) β-C...
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Figure 4: Representation of chemical shifts variations (Δδ) of a) carvacrol (1) and c) thymol (2) protons and...
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Figure 5: 2D ROESY plots of β-CD/carvacrol (1) complex in D2O showing the NOEs between the H-3 and H-5 proton...
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Figure 6: 2D ROESY plots of β-CD/thymol (2) complex in D2O showing the NOEs between the H-3 and H-5 protons o...
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Figure 7: Representation of the most stable CD/guest inclusion complex conformers.
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Figure 8: Effects of β-CD and HP-β-CD on the TEAC (μmol Trolox/ g of guest) of carvacrol (1) and thymol (2) b...
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- Full Research Paper
- Published 11 Nov 2014
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Figure 1: Non-competitive ITC isotherms for the β-CD-IBU complex at 298 K. Each protocol (from A to H) is def...
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Figure 2: Theoretical uncertainty on K (left) and ΔH (right) as a function of log K for titration (red curve)...
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Figure 3: Theoretical uncertainty on K (left) and ΔH (right) as a function of Log K for titration-titration (...
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Figure 4: Competitive ITC isotherms for the HPβ-CD-β-CD-IBU system at 283 K. Each protocol (from I to P) is d...
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- Full Research Paper
- Published 06 Oct 2014
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Figure 1: Chemical structure of studied phenylpropanoids (PPs).
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Figure 2: Phase solubility profiles of (a) CD/trans-anethole and (b) CD/p-coumaric acid inclusion complexes.
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Figure 3: Solubility enhancement (log (St/S0)) as a function of the solubility (log (S0)) of studied phenylpr...
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Figure 4: Representation of the most stable CD/trans-anethole inclusion complex conformers resulting from the...
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Figure 5: DPPH radical scavenging activity (%) of studied PPs alone or in presence of CD.
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- Full Research Paper
- Published 19 Jun 2013
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Figure 1: Chemical structures of β-CD 1, hydroxypropyl-β-CD 2, and β-CD-thioethers 3 and 4.
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Figure 2: Chemical structures of the benzene and cyclohexane derivatives, with their calculated molecular vol...
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Figure 3: Chromatogram obtained by HS-GC for a mixture of aromatic guests (1 ppm) in water (black) and 10 mM ...
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Figure 4: Gibbs free energy of formation of the inclusion compound of benzene derivatives, and cyclohexane de...
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Figure 5: Gibbs free energy of formation of the inclusion compounds of benzene and cyclohexane derivatives in...
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Figure 6: Gibbs free energy of formation of the inclusion compounds of benzene derivatives in host 4 as a fun...
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Figure 7: Free binding enthalpy for benzene, toluene, ethylbenzene, cumene, and tert-butylbenzene, in host 4 ...
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- Full Research Paper
- Published 06 Sep 2012
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Figure 1: Water-soluble phosphanes 1–4.
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Figure 2: 2D T-ROESY NMR spectrum of a stoichiometric mixture of β-CD and 4 (3 mM each) in D2O at 20 °C.
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Figure 3: Effect of increasing concentrations of β-CD (solid lines) and RAME-β-CD (dotted lines) on the surfa...
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Figure 4: Equilibria in a phosphane-based micelle/RAME-β-CD mixture.
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Scheme 1: Tsuji–Trost reaction mediated by a phosphane-based micelle/RAME-β-CD combination.
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Figure 5: Turnover frequency (TOF) as a function of the RAME-β-CD/phosphane ratio in the Pd-catalyzed cleavag...
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