Strong Dual-Compartment Microcapsules Loaded with High Cargo Contents.

Compartmentalized microcapsules are useful for the release of multiple cargos in medicine, agriculture, and advanced responsive materials. Although several encapsulation strategies that involve more than one cargo have been proposed, dual- or multicompartment capsules with high cargo loadings and sufficient mechanical stability are rarely reported. Here, we propose a single-step emulsification route for the preparation of strong dual-compartment capsules that can host the main cargo in their core in combination with another liquid cargo stored within their thick shell. Capsules are produced through the polymerization of the middle oil phase of water-oil-water double emulsions made by microfluidics. Compartmentalization results from the phase separation of monomers within the middle phase of the double emulsion. We investigate the effect of such phase separation process on the microstructure and mechanical properties of the capsules and eventually illustrate the potential of this approach by creating thermosensitive capsules with programmable bursting temperature. The large variety of possible mixtures of monomers and cargos that can be added in the oil and aqueous phases of the double emulsion templates makes this encapsulation approach a promising route for the fabrication of robust microcapsules for on-demand release of multiple cargos.

Strong Microcapsules with Permeable Porous Shells Made through Phase Separation in Double Emulsions.

Microcapsules for controlled chemical release and uptake are important in many industrial applications but are often difficult to produce with the desired combination of high mechanical strength and high shell permeability. Using water-oil-water double emulsions made in microfluidic devices as templates, we developed a processing route to obtain mechanically robust microcapsules exhibiting a porous shell structure with controlled permeability. The porous shell consists of a network of interconnected polymer particles that are formed upon phase separation within the oil phase of the double emulsion. Porosity is generated by an inert diluent incorporated in the oil phase. The use of undecanol and butanol as inert diluents allows for the preparation of microcapsules covering a wide range of shell-porosity and force-at-break values. We found that the amount and chemical nature of the diluent influence the shell porous structure by changing the mechanism of phase separation that occurs during polymerization. In a proof-of-concept experiment, we demonstrate that the mechanically robust microcapsules prepared through this simple approach can be utilized for the on-demand release of small molecules using a pH change as exemplary chemical trigger.

Tunable phosphorescent NIR oxygen indicators based on mixed benzo- and naphthoporphyrin complexes.

A series of π-extended phosphorescent palladium(II) and platinum(II) porphyrin complexes were synthesized, in which additional benzene rings are fused radially onto at least one of the four peripheral benzo groups. The photophysical properties of the metalloporphyrins palladium(II)-meso-tetra-(4-fluorophenyl)mononaphthotribenzoporphyrin (Pd1NF), cis-palladium(II)-meso-tetra-(4-fluorophenyl)dibenzodinaphthoporphyrin (Pd2NF), and palladium(II)-meso-tetra-(4-fluorophenyl)monobenzotrinaphthoporphyrin (Pd3NF) and the corresponding platinum(II) compounds (Pt1NF, cis-Pt2NF, Pt3NF) were investigated. The compounds under investigation absorb intensively in the near-infrared region (628-691 nm) and emit at room temperature at 815-882 nm. Phosphorescence quantum yields of the platinum(II) porphyrins range from 25 to 53% with luminescence decay times of 21 to 44 µs in deoxygenated toluene solutions at room temperature. The corresponding palladium(II) complexes exhibit quantum yields in the range of 7 to 18% with lifetimes of 106 to 206 µs. Density functional theory (DFT) calculations revealed nonplanar geometries for all complexes and corroborate the absorption characteristics. The subsequent π extension of the porphyrin system leads to near-infrared absorbing oxygen indicators with tailor-made luminescence properties as well as tunable oxygen sensitivity.

Heteroleptic platinum(II) complexes of 8-quinolinolates bearing electron withdrawing groups in 5-position.

A series of novel luminescent platinum(II) complexes bearing orthometalated 2-phenylpyridine ligands (C N), namely 2-phenylpyridine (4) and 3-hexyloxy-2-phenylpyridine (5), and several 5-substituted quinolinolate ligands (5-X-Q), where X = NO2 (a), X = CHO (b), X = Cl (bearing another Cl in 7-position of the Q-ligand) (c) and X = H (d) have been synthesized, characterized and their photophysical properties were studied. All complexes were obtained as a single isomer with N atoms of the C N and Q ligands trans-coordinated to the platinum center as evidenced using single-crystal X-ray crystallography and NMR spectroscopy. Absorbance, luminescence as well as lifetime measurements in solution and in the solid state have been performed to establish a qualitative relationship between structure and luminescence properties. The compounds under investigation absorb intensively via an intraligand charge transfer (ILCT) in the visible range (460-480 nm) and emit from fluid solution and in the solid state at room temperature at 600-630 nm. The complexes show quantum yields up to 25% and lifetimes in the range of 20-30 micros in deoxygenated organic solvents at room temperature. The emitting state can be best described as a triplet intraligand charge-transfer state localized mainly on the quinolinolate ligand. In these complexes the phenylpyridine ligand can be essentially regarded as an ancillary ligand. Density functional theory (DFT) calculations were carried out on both the ground (singlet) and excited (triplet) states of these complexes and revealed the influence of the substitution of the quinolinolate ligand on the HOMO/LUMO energies and the oscillator strengths. Substitution on 3-position of the phenylpyridine ligand does not impact on the transition energies, and is thus suited to introduce other functional moieties, such as a solubilizing hexyloxy group.

1,5-anhydro-D-fructose from D-fructose.

1,5-anhydro-D-fructose was efficiently prepared from D-fructose via regiospecific 1,5-anhydro ring formation of 2,3-O-isopropylidene-1-O-methyl(tolyl)sulfonyl-D-fructopyranose and subsequent deprotection.