Search results for "aqueous solution"
showing 10 items of 1610 documents
Interactions between non-volatile water-soluble molecules and aroma compounds in Camembert cheese
2002
Abstract Interactions between selected aroma compounds and non-volatile water-soluble molecules were studied using dynamic headspace-gas chromatography. A model water-soluble extract (MWSE), previously constructed in gustatory and physico-chemical accordance with the crude Camembert cheese WSE, allowed the contribution of non-volatiles to the headspace composition of volatile compounds to be assessed. The presence of the MWSE increased the headspace concentration of 2-heptanone, 1-octen-3-ol and 3-methylbutanol, showing that these three volatile compounds were released by MWSE. Omission tests performed on MWSE allowed for the impact of each MWSE component on aroma compounds release to be de…
Stabilization of an ?-helical conformation in an isolated hexapeptide inhibitor of calmodulin
2001
The conformational properties of two hexapeptides, Ac-LWRILW-NH(2) and its D-amino acid counterpart Ac-lwrilw-NH(2), identified as calmodulin inhibitors using mixture-based synthetic combinatorial library approaches, have been characterised by NMR and CD spectroscopy. The peptides fold into an alpha-helical conformation in aqueous solution. The observed short- and medium-range nuclear Overhauser effects were consistent with the formation of an alpha-helical structure and a reasonably well-defined set of structures was obtained by using restraints from the NMR data in simulated annealing calculations. Analysis of glycine-substitution analogues demonstrated that all the amino acids that make …
Hierarchical structure formation of cylindrical brush polymer-surfactant complexes.
2009
The complex formation of cylindrical brush polymers with poly(l-lysine) side chains (PLL) and sodium dodecyl sulfate (SDS) can induce a helical conformation of the cylindrical brush polymer in aqueous solution (Gunari, N.; Cong, Y.; Zhang, B.; Fischer, K.; Janshoff, A.; Schmidt, M. Macromol. Rapid Commun. 2008, 29, 821-825). Herein, we have systematically investigated the influence of surfactant, salt, and pH on the supramolecular structure formation. The cylindrical brush polymers and their complexes with surfactants were directly visualized by atomic force microscopy in air and in aqueous solution. The alkyl chain length (measured by the carbon number, n) of the surfactant plays a key rol…
PNIPAM Copolymers Containing Light-Responsive Chromophores: A Method Toward Molecular Logic Gates
2010
A series of thermo-responsive PNIPAM copolymers containing different amounts of fulgimide moieties has been synthesized via a polymer analogous reaction of poly(pentafluorophenyl acrylate). All copolymers were designed to exhibit a lower critical solution temperature (LCST) in water, which was only weakly dependent on the amount of incorporated chromophoric fulgimide groups. The copolymers showed a photocyclization of the fulgimide side groups upon irradiation with UV-light accompanied with a color change. The closed form of the chromophore had a halftime of 136 min for the visible reisomerization and did not affect the LCST of the polymer. This led to the realization of a logic "NOT A" for…
Temperature- and Light-Responsive Polyacrylamides Prepared by a Double Polymer Analogous Reaction of Activated Ester Polymers
2009
Two different series of polyacrylamides containing different amounts of salicylideneaniline moieties have been synthesized via a double polymer analogous reaction of poly(pentafluorophenyl acrylate) (PPFPA). All copolymers were designed to exhibit a lower critical solution temperature (LCST) in aqueous solution, which was dependent on (i) the amount of incorporated chromophoric salicylideneaniline groups and (ii) the isomerization state of the respective salicylideneaniline group. Higher LCST values were measured for UV-irradiated solutions of the copolymers in comparison to the nonirradiated copolymer solutions. A maximum difference in the LCST of up to 13 °C was found for poly(N-cycloprop…
Amphiphilic derivatives of a polyaspartamide: their aggregation and solubilization ability
2006
Abstract The self-aggregation and solubilization capability of a series of amphiphilic copolymers obtained by derivatisation of polymeric chain of α,β-poly(N-2-hydroxyethyl)- dl -aspartamide (PHEA) with polyethylene glycols (PEG, being different molecular weight 2000 or 5000 Da, PEG2000 and PEG5000, respectively) and/or hexadecylamine alkyl chain (C16), namely PHEA–PEG2000, PHEA–PEG5000, PHEA–C16, PHEA–PEG2000–C16 and PHEA–PEG5000–C16, have been evidenced by performing systematic tensiometric and spectrophotometric studies. All measurements have been performed at 25.0 °C over a wide copolymer concentration range. The tensiometric results have shown that, for all copolymers studied, the surf…
Characterization of poly(N-alkylanilines) by Raman spectroscopy
2007
Abstract Thin films of poly( N -alkylaniline) were synthesized in acidic aqueous solution and in mixtures of aqueous and organic solvents. The polymer films (alkyl = methyl, ethyl, propyl and butyl) were characterized by Raman spectroscopy with the excitation wavelengths of 514.5, 632.8 and 780 nm. The main Raman bands have been characterized for the leucoemeraldine, emeraldine and pernigraniline oxidation states between −0.2 and 0.8 V (vs. Ag|AgCl). This fundamental study shows that the structure of the half-oxidized emeraldine form contains quinoid units, which supports the commonly accepted oxidation and reduction scheme of poly( N -alkylanilines).
Not just size and shape: spherically symmetrical d5 and d10 metal ions give different coordination nets with 4,2′:6′,4″-terpyridines
2010
Functionalized 4,2′:6′,4″-terpyridine ligands have been used to provide a divergent N,N′-donor set for the formation of coordination polymers containing {Zn2(µ-OAc)4} or {Mn3(µ-OAc)4(OAc)2} scaffolds. Single-stranded coordination polymers are produced from the reactions of 4′-(4-bromophenyl)-4,2′:6′,4″-terpyridine (1) and 4′-(4-methylthiophenyl)-4,2′:6′,4″-terpyridine (2) with Zn(OAc)2·2H2O. In [Zn2(1)(OAc)4]n and [Zn2(2)(OAc)4]n, the two outer nitrogen donors of the 4,2′:6′,4″-terpyridine ligands, bind to the axial sites of {Zn2(µ-OAc)4} units to generate coordination polymer chains which are π-stacked so that the V-shaped ligand domains are interleaved. When Mn(OAc)2·4H2O is treated with …
Interactions of metal ions with two quinolone antimicrobial agents (cinoxacin and ciprofloxacin)
2002
Several novel metal-quinolone compounds have been synthesized and characterized by analytical, spectroscopic and X-ray diffraction methods. The crystal structure of the four compounds, Na(2)[(Cd(Cx)3)(Cd(Cx)3(H2O))].12H2O, [Co(Cp)2(H2O)2].9H2O, [Zn(Cp)2(H2O)2].8H2O and [Cd(HCp)2(Cl)2].4H2O, is presented and discussed: HCx=1-ethyl-1,4-dihydro-4-oxo(1,3)-dioxolo(4,5-g)cinnoline-3-carboxylic acid and HCp=1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinoline carboxylic acid. In all these compounds the quinolone acts as a bidentate chelate ligand that binds through one carboxylate oxygen atom and the exocyclic carbonyl oxygen atom. Complexes of ciprofloxacin were screened for th…
SEVERAL COORDINATION MODES OF 5-AMINO-1,3,4-THIADIAZOLE-2-SULFONAMIDE (HATS) WITH Cu(II), Ni(II) AND Zn(II): MIMETIC TERNARY COMPLEXES OF CARBONIC AN…
2001
Abstract The coordination properties of 5-amino-1,3,4-thiadiazole-2-sulfonamide (Hats) with Cu(II), Ni(II) and Zn(II) ions, are analyzed. Although the ligand presents several donor atoms, we have only observed three coordination behaviors: (i) as a monodentate ligand through the Nsulfonamido atom, (ii) as a bridging ligand linking the metal ions through the Nsulfonamido and Nthiadizole atoms and (iii) as a bridging ligand linking metal ions through the N and O atoms of the sulfonamidate group. It is noteworthy that coordination mode (iii) is observed for the first time in heterocyclic sulfonamides complexes. In addition, the conformation of the Hats as counter-ion is analyzed and compared w…