Photophysical and electrochemical investigations of the fluorescent probe, 4,4'-bis(2-benzoxazolyl)stilbene.

In solution, 4,4'-bis(2-benzoxazolyl)stilbene (BBS) was found to exhibit consistently high absolute fluorescence quantum yields (Φ(fl) ≥ 0.88) and a monoexponential lifetime, both independent of BBS concentration. The BBS steady-state and time-resolved photophysics were investigated by different techniques to understand the various deactivation pathways. Nonradiative deactivation of BBS singlet excited state by intersystem crossing was found to be negligible. Other than fluorescence, the excited state of BBS was found to be deactivated by trans-cis photoisomerization. At low concentrations (≈5 µg/mL), UV spectroscopy and laser flash photolysis showed concordant results that the photoinduced cis isomer gradually replaced the original absorption spectrum of the pure trans isomer. However, at high concentrations (≈0.2 mg/mL), (1)H NMR and DOSY measurements confirmed that irradiating BBS at 350 nm induced a conversion from the trans-BBS into its cis isomer by photoisomerization. It was further found that the stilbene moiety of both isomers was photocleaved. The resulting photoproduct was an aldehyde that was oxidized under ambient conditions to its corresponding carboxylic acid, i.e., 4-(1,3-benzoxazol-2-yl)benzoic acid. The structure of the photoproduct was unequivocally confirmed by X-ray diffraction. Spectroscopic investigation of BBS showed a limited photoisomerization after irradiation at 350 nm of a trans solution. The BBS electrochemistry showed irreversible oxidation, resulting in an unstable and highly reactive radical cation. Similarly, the cathodic process was also found to be irreversible, giving rise to a radical anion and showing its n-doping character.

Polymer-grafted-nanoparticle surfactants.

We have studied the surface behavior of nanoparticles, which are lightly grafted with polymer chains, when they are mixed with matrix chains of the same architecture as the grafts. We consider the particular case where the nanoparticle core and the grafted polymer chains energetically dislike each other and show that the extent of surface segregation of these "hairy" nanoparticles and their self-assembly into a variety of structures can be tuned by varying the number and the length of the grafted chains and the matrix chain length. These results unequivocally show that grafted nanoparticles in polymer matrices behave akin to block copolymers (or amphiphiles) in selective solvents, with readily controllable surface behavior.

Aminated linear and star-shape poly(glycerol methacrylate)s: synthesis and self-assembling properties.

Over the past 10 years, polyglycerols and their structurally related analogs have received considerable attention in the biomedical field. Poly(glycidyl methacrylate) (PGMA) is a versatile polymer because its pendant epoxide groups can be opened with different functional groups to generate poly(glycerol methacrylate)s (PGOHMA) derivatives. In this work, linear and star-shape PGMAs were synthesized by atom transfer radical polymerization and then functionalized with four different amines by ring-opening addition. This resulted in the formation of polyglycerol-like polymers having both hydroxyl and amine moieties and different water-solubility. The water-insoluble polymers could form pH-sensitive nanoassemblies, while the soluble derivatives efficiently complexed a short strand polynucleotide. The aminated polyglycerol interacted more avidly with the oligonucleotide than the control poly(ethyleneimine), and high transfection efficacy could be obtained with the linear derivative. Such polymers could find practical applications for the delivery of drugs and nucleic acids.

(E)-4,4'-Bis(1,3-benzoxazol-2-yl)stilbene at 150 and 375 K.

The title compound, a chromophore of formula C(28)H(18)N(2)O(2), crystallizes with the molecule lying on an inversion centre to give one-half of a crystallographically independent molecule in the asymmetric unit. The molecule is almost planar, with slight deviation of the benzene rings from the mean molecular plane. The structure is characterized by a herringbone packing arrangement arising from C-H...pi and pi-pi intermolecular interactions. The benzoxazole group is disordered between two orientations, with occupancy factors of 0.669 (10) and 0.331 (10) at 150 K [0.712 (7) and 0.288 (7) at 375 K].

Robust Superhydrophobic Cotton Fibers Prepared by Simple Dip-Coating Approach Using Chemical and Plasma-Etching Pretreatments.

The preparation of superhydrophobic textiles with high mechanical and chemical durability is challenging. Here, facile and fluorine-free methods, using alkali and plasma-etching treatments, followed by the addition of silica nanoparticles and tetraethyl orthosilicate (TEOS), were used to prepare superhydrophobic cotton surfaces. With different input variables and etching techniques, superhydrophobic cotton fabrics with high chemical and mechanical durability were successfully prepared, with contact angles up to 173°. A control of the surface architecture at the nanoscale in combination with a homogeneous repellent layer of TEOS in the cotton surface was achieved. The repellent properties of the as-prepared cotton remain stable under accelerated laundering and abrasion test conditions. The etching pretreatment by alkali or plasma plays a key role in obtaining superhydrophobic cotton surfaces.

A new method for the time-resolved analysis of structure and orientation: polarization modulation infrared structural absorbance spectroscopy.

Polarization modulation infrared linear dichroism (PM-IRLD) is often used for measurements of molecular orientation with high sensitivity and good time resolution. However, PM-IRLD is unable to provide the structural absorbance spectrum because it does not measure separately the parallel and perpendicular spectra. Here we propose a new method, named polarization modulation infrared structural absorbance spectroscopy (PM-IRSAS), to overcome this limitation of PM-IRLD. PM-IRSAS measures the dichroic difference and structural absorbance spectra simultaneously and, therefore, allows quantitative analysis of molecular orientation and conformation with 200 ms time resolution. The PM-IRSAS method was first validated through comparison with conventional polarized FT-IR spectroscopy using drawn polymer films. Second, it was demonstrated that the PM-IRSAS method can provide a quantitative analysis of dynamic orientation and conformation changes in PET films during deformation and crystallization processes.

Morphology, Thickness, and Composition Evolution in Supramolecular Block Copolymer Films over a Wide Range of Dip-Coating Rates.

Dip-coating, an important industrial technique, has been underexploited for preparing block copolymer (BC) thin films, such that the knowledge regarding their general characteristics is limited. Here, we present an overview of the crucial factors that determine how BC film morphology evolves as a function of dip-coating rate (withdrawal speed) over a wide range, illustrated using THF solutions of a polystyrene-b-poly(4-vinyl pyridine) (PS-P4VP) diblock copolymer mixed with two small molecules, naphthol and naphthoic acid, which are hydrogen-bonders with P4VP. Key factors in determining the film morphology are the systematic variation in film thickness and, for supramolecular BCs, in film composition with dip-coating rate. The former shows a general V-shaped dependence, related to the so-called capillarity and draining regimes identified previously for dip-coated sol-gel films. The relative small molecule content in the films studied is shown to increase in the capillarity regime from low to that of the dip-coating solution and thereafter to remain constant. Together, these changes, in addition to solvent and other effects, determine the film morphology and its evolution with dip-coating rate.

Photophysical, electrochemical and crystallographic investigations of the fluorophore 2,5-bis(5-tert-butyl-benzoxazol-2-yl)thiophene.

The photophysics of 2,5-bis(5-tert-butyl-benzoxazol-2-yl)thiophene (BBT) were investigated for assessing its limitations for use as a universal fluorophore and as a viable sensor for both polymeric and solution studies. This is of importance given the limitations of currently used materials. BBT's steady-state and time-resolved fluorescence were additionally investigated to correlate its solid-state features, observed by fluorescence spectroscopy when mixed in poly(1,4-butylene succinate) (PBS) films, with its single crystal characteristics. The conjugated fluorophore was found to be highly fluorescent, with absolute quantum yields of (Φ(fl)) ≥ 0.60. The Φ(fl) values were high, regardless of solvent polarity and proticity and whether alone or in polymeric films. The major competitive fluorescence quenching pathway was found to occur by intersystem crossing to the triplet state. This was confirmed by laser flash photolysis in which the BBT triplet absorbed at 500 nm. The triplet transient was confirmed by quenching studies with 1,3-cyclohexadiene. Meanwhile, nonradiative deactivation of BBT's singlet excited state by internal conversion was found to be negligible. In solution and especially when distributed in semicrystalline PBS, BBT exhibits spectral changes and a bathochromic shift as a function of concentration due to aggregation of ground state molecules, which is present even at low BBT concentrations. Consistent monoexponential lifetimes on the order of ∼2 ns were observed regardless of solvent and independent of both the excitation wavelength and concentration. The constant excited state kinetics confirm the absence of a singlet excited state deactivation by excimer formation. The electrochemistry of BBT demonstrated that it is irreversibly oxidized and the resulting radical cation is unstable. Conversely, the cathodic process, resulting in the radical anion, is reversible, confirming its n-doping character. Crystallographic studies revealed that the planes described by the benzoxazolyl moieties are twisted from the plane described by the central thiophene. Several weak C-H···π and π-π intermolecular interactions were also observed. BBT's high solubility in common solvents combined with its measured enhanced optoelectronic properties make it a candidate as a universal fluorophore reference and smart material for both polymeric and solution studies.

Physical characterization of blends of poly(D-lactide) and LHRH (a leuprolide decapeptide analog).

Stereocomplexes between poly(D-lactide) (PDLA) and poly(L-lactide) (PLLA) have been extensively studied, including, in recent years, several reports on the stereocomplexation of PDLA with small molecules such as peptides. Here, the possible complexation between PDLA and luteinizing hormone releasing hormone (LHRH), a l-configured decapeptide, is considered for which several observations were made: (1) in calorimetry an additional endothermic peak appears at a lower temperature than the melting temperature of pure PDLA; (2) in Raman analyses a band splitting of the C=O stretching mode (not present in pure PDLA) shows up; (3) in X-ray diffraction, however, no change is observed after mixing the two species, indicating no crystal structure modification (and the absence of any stereocomplex crystal structure). The calorimetric double melting peak is merely explained by the presence of two distinct morphological forms of PDLA, whereas the spectroscopic band splitting can be due to simple differences of crystallinity. From these observations it is concluded that the LHRH modifies the crystallization of PDLA without, however, the formation of a stereocomplex.

Stereocomplex block copolymer micelles: core-shell nanostructures with enhanced stability.

Monodisperse stereocomplex block copolymer micelles were obtained through the self-assembly of equimolar mixtures of poly(ethylene glycol)-block-poly(l-lactide) and poly(ethylene glycol)-block-poly(d-lactide) in water. These micelles possessed partially crystallized cores and mean hydrodynamic diameters ranging from 31 to 56 nm, depending on the lactide content. They exhibited kinetic stability and redispersion properties superior to micelles prepared with isotactic or racemic polymers alone. This study demonstrates the advantages of stereocomplex formation in the design of stabilized water-soluble nanoparticles.

Influence of in vitro hydrolytic degradation on the morphology and crystallization behavior of poly(p-dioxanone).

We have studied the hydrolytic degradation of high molecular weight poly(p-dioxanone), PPDX, sutures. The samples were degraded either in distilled water or in a phosphate buffer at 37 degrees C, and the starting viscosity-average molecular weight was 130 kg/mol. The hydrolytic degradation of PPDX occurs in an approximate two stage process where the amorphous regions of the sample are attacked faster than the crystalline regions of the sample. The changes experienced by the samples as degradation proceeded were successfully monitored by viscosimetry, differential scanning calorimetry (DSC), weight loss, pH changes, and scanning electron microscopy (SEM). Polarized optical microscopy (POM) observations performed on PPDX films revealed that PPDX crystallizes in spherulites whose detailed morphology depends on the supercooling employed during isothermal crystallization. Changes in the spherulitic morphology as molecular weight is reduced are only pronounced when the molecular weight is equal or lower than 8 kg/mol. The dependence of lamellar thickness as a function of isothermal crystallization temperature was examined by atomic force microscopy (AFM) in thin films of PPDX together with melting point data obtained by DSC. Through the use of the Thomson-Gibbs equation, we obtained a value of 166 erg/cm2 for the fold surface free energy of PPDX. This value is in the same range as those obtained previously for similar linear polyesters. The lamellar thickness, as well as the melting point, was found to have a small decreasing dependence with the molecular weight of the samples.