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Query: UMLS:C0267964 (PAA)
 2,561 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Interactions between poly(acrylic acid) labeled with pyrene (PAA-Py) and succinylated calfskin collagen (type I) (SCSC) were studied by fluorescence spectroscopy. PAA-Py exhibits a strong emission from pyrene monomer (intensity, I(M)) when it exists in an extended conformation. It exhibits another broad emission from pyrene excimer (intensity, I(E)) when it adopts a collapsed globule conformation. At pH 3, a value that is lower than the isoelectric point of SCSC, the ratio I(E)/I(M) value decreased cooperatively with increasing concentration of SCSC at constant PAA-Py concentration, under salt-free condition. On the other hand, this effect was not observed in the presence of 0.1 M NaCl. At pH 7, a value higher than the isoelectric point of SCSC, the ratio I(E)/I(M) was not affected by the presence of SCSC in the absence and presence of salt. From electrophoretic light scattering experiments, it was found that at pH 3 PAA-Py was negatively charged, while SCSC had a positive charge. Thus it is strongly suggested that the two polymers interact by electrostatic attraction at low pH where they are oppositely charged, and that PAA-Py adopts an extended conformation in the complex formed with SCSC. Similar interactions are believed to occur between dentinal collagen and the polycarboxylate component of glass-ionomer cements.
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PMID:Interaction of water-soluble collagen with poly(acrylic acid). 1065 24

The interaction between pentaethylene glycol n-octyl ether (C8E5) and low-molecular-weight poly(acrylic acid) (PAA, M(w)=2000) in aqueous solution has been investigated by various experimental techniques at constant polymer concentration (0.1% w/w) with varying surfactant molality. Spectrofluorimetry, using pyrene as molecular probe, shows (i) the formation of surfactant-polymer aggregates at a surfactant molality (T(1)) lower than the critical micelle concentration (cmc) of C8E5 in water and (ii) the formation of free micelles at a surfactant molality (T(2)) slightly higher than the cmc. Fluorescence quenching measurements indicate that the presence of PAA induces a lowering of the C8E5 aggregation number. Calorimetry confirms spectrofluorimetric evidence; in addition, it shows the presence of weak interactions below T(1) between monomeric surfactant molecules and the polymer chains. Tensiometry shows that, above T(1), only a low fraction of surfactant molecules interact with the polymer and that free micelle formation occurs before polymer saturation. The peculiarities of the interaction between surfactants and low-molecular-weight polymers have been discussed.
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PMID:Interaction between pentaethylene glycol n-octyl ether and low-molecular-weight poly(acrylic acid). 1469 17

Novel probes represented connection of pyrene as chromophore and sterically hindered amine stabilizers (HAS) in the form of esters of 2-(1-pyrenyl)acrylic acid were synthesized. HAS was in the form of parent amine (PAP) as well as stable nitroxyl radical form (PAP-NO.). Photophysics of these probes were compared with their precursor as 2-(1-pyrenyl)acrylic acid (PAA) and its methyl ester (PAM). The fluorescence spectrum of PAA strongly depends on the acidity of the solution. The spectrum in neutral methanol indicates that it originates from the anionic form -COO(-). Changes of acidity or basicity of methanol solution resulted in the changes of shape, position as well as the intensity of fluorescence band. This is due to the presence of protolytic equilibria, either in the ground state or in the singlet excited state, leading to the formation of molecular form -COOH and the cationic form -COOH(2) (+). The ester analogues did not show any changes in various pH conditions. Fluorescence of all probes depends on the polarity of solvents and the presence of oxygen. Intermolecular quenching was studied with external quenchers TEMPO and oxygen and the data were compared with the intramolecular quenching using 1'-oxo-2',2',6',6'-tetramethyl-4'-piperidinyl-2-(1-pyrenyl)acrylate (PAP-NO.).
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PMID:Preparation and photophysics of 2-(1-pyrenyl)acrylic acid and its methyl and 2',2',6',6'-tetramethyl-4'-piperidyl esters. 1598 51

New low and high molecular weight poly(acrylic acid), PAA, 2000 g mol(-1) and 450,000 g mol(-1), respectively, were tagged with pyrene (low and high contents of probe) and its behaviour in solution was investigated using absorption and fluorescence (steady-state and time-resolved) techniques. Fluorescence data shows that the degree and level of intramolecular association strongly depends on the molecular weight. With the short pyrene-labeled PAA chains in aqueous solution, the excimer-to-monomer fluorescence ratio I(E)/I(M) decreases with the increase of pH, oppositely to the increase in the I(E)/I(M) ratio with the increase in pH previously observed with the long chain PAA. Time-resolved data suggest that excimer formation with the short pyrene-labeled PAA polymers (ca. 28 acrylic acid monomers per chain) in water is largely due to excitation of Ground State Dimers, GSD. The increment of pH, and the consequent gradual ionization of the carboxylic groups in the chain, initially increases the fraction of GSD, possibly due to the occurrence of special micelle-like chain conformations, inside which the pyrene units are accommodated. A further increase of the pH above the pK(a) values, resulting in the full ionization of carboxylic groups, apparently destabilizes such chain conformations, which leads to a pH effect on the photophysical properties identical to that of the long chain polymers. In water, the dynamic data shows the existence of two excimers coexisting with two monomer classes. In methanol and dioxane (good solvents for the pyrene probe) at room temperature, where one excimer and two monomers are present, all rate constants could be obtained, as well as the fractions of ground-state species. It is thus shown that different types of interactions are produced with small- and long-sized PAA polymers, i.e., the size of the polymer matters.
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PMID:Dynamics of short as compared with long poly(acrylic acid) chains hydrophobically modified with pyrene, as followed by fluorescence techniques. 1734 10

The formation of binary and ternary complexes of poly(acrylic acid) (PAA) with N, N, N, N-dodecyltrimethylammonium chloride (DTAC) and/or Cu (2+) ions is investigated in dilute aqueous solution through turbidimetry, viscometry, and pyrene fluorescence probing. It is shown that the PAA-DTAC and PAA-Cu (2+) complexation as well as the formation of ternary PAA-DTAC-Cu (2+) complexes are controlled from the pH of the aqueous solution. A pronounced quenching of the emission of pyrene is observed when ternary PAA-DTAC-Cu (2+) complexes are formed, as a result of the close proximity of Cu (2+) ions (complexed along the polymer chain) and the probe (solubilized in the hydrophobic mixed polymer-surfactant aggregates), as indicated from the corresponding Stern-Volmer plots. A significant quenching is also observed when poly(sodium styrene sulfonate) is used instead of PAA, indicating that electrostatically bound Cu (2+) ions are still effective quenchers of the emission of the probes under similar conditions. Finally, it is demonstrated that the formation-deformation of the ternary PAA-DTAC-Cu (2+) complexes upon changing pH may act as a pH-controlled "on-off" switch of the emission of pyrene in aqueous solution.
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PMID:Formation of ternary poly(acrylic acid)-surfactant-Cu2+ complexes in aqueous solution: quenching of pyrene fluorescence and pH-controlled "on-off" emitting properties. 1881 24

Noncharged pyrene molecules were incorporated into multilayer films by first loading pyrene into poly(acrylic acid) (PAA)-stabilized cetyltrimethylammonium bromide (CTAB) micelles (noted as PAA&(Py@CTAB)) and then layer-by-layer (LbL) assembled with poly(diallyldimethylammonium chloride) (PDDA). The stable incorporation of pyrene into multilayer films was confirmed by quartz crystal microbalance (QCM) measurements and UV-vis absorption spectroscopy. The resultant PAA&(Py@CTAB)/PDDA multilayer films show an exponential growth behavior because of the increased surface roughness with increasing number of film deposition cycles. The present study will open a general and cost-effective avenue for the incorporation of noncharged species, such as organic molecules, nanoparticles, and so forth, into LbL-assembled multilayer films by using polyelectrolyte-stabilized surfactant micelles as carriers.
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PMID:Layer-by-layer-assembled multilayer films of polyelectrolyte-stabilized surfactant micelles for the incorporation of noncharged organic dyes. 1892 6

The association between a randomly pyrene labeled PAA polymer (PAAMePy55) and a PEO-PPO-PEO triblock copolymer (P123) in aqueous solutions of different NaCl concentrations and pHs has been studied by means of dynamic light scattering (DLS) and steady-state fluorescence spectroscopy at 40 degrees C. At acidic pH values, in the low P123/PAAMePy55 molar ratio regime (i.e., at low P123 concentrations), the relaxation time distributions retrieved from the DLS data analysis were monomodal and very similar to those obtained for the pure PAAMePy55 solution. The apparent hydrodynamic radius of PAAMePy55 at low pH is 18 nm. At higher molar ratios (i.e., at high P123 concentrations), still in the acidic pH regime, bimodal relaxation time distributions were obtained, where the fast relaxation mode is connected to the translational diffusion of free P123 micelles with a hydrodynamic radius obtained at infinite P123 dilution (R(H,P123=0)) of 10-11 nm. This value coincides perfectly with the hydrodynamic radius of the pure P123 micelles at 40 degrees C, which was found to be ca. 10 nm at all pH values. The second mode corresponds to a complex consisting of one PAAMePy55 polymer chain and about 42 P123 micelles and with a R(H,P123=0) between 35 and 36 nm depending on pH. At pH 9, the mixed system also presented bimodal relaxation time distributions. At this high pH, the intermolecular association between PAAMePy55 and P123 is less strong than at acidic pH according to the steady-state fluorescence measurements. The fast mode is also in this case attributed to free P123 micelles whereas the second mode is related to the so-called "slow mode" commonly observed for polyelectrolyte solutions. In this system, it is related to the formation of multichain domains, that is, large domains formed by several PAAMePy55 chains that move in a common electrostatic field (i.e., a structure factor effect). The presence of P123 micelles does not lead to the total disruption of these domains. They may either contain entrapped P123 micelles or hydrophilic diblock impurities (originating from the P123 sample) that associate with the PAAMePy55 chains.
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PMID:Complex formation between a fluorescently-labeled polyelectrolyte and a triblock copolymer. 1935 71

By using absorption and fluorescence (steady-state and time-resolved) techniques, the interaction between a poly(acrylic acid) (PAA), randomly grafted with pyrene (Py) units (PAAMePy55), and a triblock copolymer of poly(ethylene oxide) and poly(propylene oxide) (EO(20)PO(68)EO(20), P123) was investigated. From the fluorescence data, it is shown that upon addition of P123 a decrease of the (pyrene-pyrene, Py-Py) intramolecular association, i.e., a decrease of dynamic and static excimer formation, is observed. Time-resolved fluorescence data reveal the existence of two types of monomers (monomers that are able to form excimer, MAGRE, and isolated monomers) and two excimers. Addition of P123 causes also an increase of the amount of isolated Py monomers. The overall fluorescence data suggest that the PAAMePy55 and the P123 block copolymer associate strongly at low pH, leading to the formation of P123 micelles surrounded by one PAAMePy55 chain, where the pyrene groups are located at the PPO/PEO interface of the P123 micelles. Steady-state fluorescence results also showed that an excess of P123 micelles in solution is required for the association to occur. At high pH (pH 9 and above) the situation is less clear. The steady-state (particularly in the I(1)/I(3) ratio) and time-resolved fluorescence results indicate a contact between the pyrene groups and PEO, which then would imply that there may be an interaction, but much weaker than at low pH.
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PMID:Association of a hydrophobically modified polyelectrolyte and a block copolymer followed by fluorescence techniques. 1935 73

We report herein the fluorescence response of pyrene in the presence of sodium dodecyl sulfate (SDS) micelle and poly(acrylic acid) (PAA) with Cu(2+) as an ionic quencher. Pyrene present in the PAA-SDS complex is quenched by Cu(2+) at pH approximately 2 ("off" state). Quenched pyrene emission is recovered at pH approximately 8 ("on" state). Due to easy protonation and deprotonation of the PAA chain in aqueous solution, this pH-controlled micellar ternary system exhibits a highly reversible "off-on-off" switch of the pyrene emission.
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PMID:pH-Controlled "off-on-off" switch based on Cu(2+)-mediated pyrene fluorescence in a PAA-SDS micelle aggregated supramolecular system. 1976 33

pH sensitive graphene-polymer composites have been prepared by the modification of graphene basal planes with pyrene-terminated poly(2-N,N'-(dimethyl amino ethyl acrylate) (PDMAEA) and poly(acrylic acid) (PAA) via pi-pi stacking. The pyrene-terminal PDMAEA and PAA were synthesized using reversible addition-fragmentation chain transfer (RAFT) polymerization with a pyrene-functional RAFT agent. The graphene-polymer composites were found to demonstrate phase transfer behavior between aqueous and organic media at different pH values. Atomic force microscopy (AFM) analysis revealed that the thicknesses of the graphene-polymer sheets were approximately 3.0 nm when prepared using PDMAEA (M(n): 6800 and PDI: 1.12). The surface coverage of polymer chains on the graphene basal plane was calculated to be 5.3 x 10(-11) mol cm(-2) for PDMAEA and 1.3 x 10(-10) mol cm(-2) for PAA. The graphene-polymer composites were successfully characterized using X-ray photoelectron spectroscopy (XPS), attenuated total reflection infrared (ATR-IR) spectroscopy, and thermogravimetric analysis (TGA). Self-assembly of the two oppositely charged graphene-polymer composites afforded layer-by-layer (LbL) structures as evidenced by high-resolution scanning electron microscopy (SEM) and quartz crystal microbalance (QCM) measurements.
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PMID:Synthesis, characterization, and multilayer assembly of pH sensitive graphene-polymer nanocomposites. 2042 64


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