Abstract: A photochemical method for chemical modification of a hydrophilic material to provide the surface of the material with hydrophobic properties. The method comprises functionalizing the surface to provide an amine group thereon, and then functionalizing the surface photo-catalytically to provide perfluoroalkanamide thereon. Alternatively, the method comprises reacting a silane moiety functional group on the surface of the material with a perfluoroalkylhalide in the presence of a photo-catalyst and light.

Abstract: An apparatus, a system, sensor, and a method for determining dissolved oxygen content in air and aqueous medium are disclosed herein. The dissolved oxygen content may be determined by irradiating the sensor comprising at least a photo-oxidizable compound by a light irradiation source, wherein the irradiation enables the photo-oxidizable compound to change its luminescent properties based upon photo-oxidation thereby enabling the quantification of the dissolved oxygen content in the medium. The dissolved oxygen content may be captured via the impedance response generated by interdigitated conducting electrode patterns included in the sensor. The dissolved oxygen content registered by the interdigitated conducting electrode patterns may be transmitted to a user device via a short range or long-range communication via an electronic circuit embedded within the sensor.

Abstract: Molecularly imprinted polymers (MIPs) capable of binding acetate and other target molecules, processes for their production, pharmaceutical compositions comprising the MIPs, and methods of using the MIPs and pharmaceutical compositions for binding target molecules and for treating conditions associated with accumulation of acetate and other target molecules.

Abstract: Molecularly imprinted polymers (MIPs) capable of binding acetate and other target molecules, processes for their production, pharmaceutical compositions comprising the MIPs, and methods of using the MIPs and pharmaceutical compositions for binding target molecules and for treating conditions associated with accumulation of acetate and other target molecules.

Abstract: Diarylethene-containing ligands and their coordination compounds are described. The ligands display photochromism with UV excitation, while the coordination compounds display photochromism with both excitation in the UV region and excitation into lower energy absorption bands characteristic of the coordination compounds, through which the excitation wavelengths for the photocyclization can be extended from ??340 nm to wavelengths beyond 470 nm. Switching of the luminescence properties of the compounds has also been achieved through photochromic reactions.

Abstract: Diarylethene-containing ligands and their coordination compounds are described. The ligands display photochromism with UV excitation, while the coordination compounds display photochromism with both excitation in the UV region and excitation into lower energy absorption bands characteristic of the coordination compounds, through which the excitation wavelengths for the photocyclization can be extended from ??340 nm to wavelengths beyond 470 nm. Switching of the luminescence properties of the compounds has also been achieved through photochromic reactions.

Abstract: Diarylethene-containing ligands and their coordination compounds are described. The ligands display photochromism with UV excitation, while the coordination compounds display photochromism with both excitation in the UV region and excitation into lower energy absorption bands characteristic of the coordination compounds, through which the excitation wavelengths for the photocyclization can be extended from ??340 nm to wavelengths beyond 470 nm. Switching of the luminescence properties of the compounds has also been achieved through photochromic reactions.

Abstract: Diarylethene-containing ligands and their coordination compounds are described. The ligands display photochromism with UV excitation, while the coordination compounds display photochromism with both excitation in the UV region and excitation into lower energy absorption bands characteristic of the coordination compounds, through which the excitation wavelengths for the photocyclization can be extended from ??340 nm to wavelengths beyond 470 nm. Switching of the luminescence properties of the compounds has also been achieved through photochromic reactions.

Abstract: Diarylethene-containing ligands and their coordination compounds are described. The ligands display photochromism with UV excitation, while the coordination compounds display photochromism with both excitation in the UV region and excitation into lower energy absorption bands characteristic of the coordination compounds, through which the excitation wavelengths for the photocyclization can be extended from ??340 nm to wavelengths beyond 470 nm. Switching of the luminescence properties of the compounds has also been achieved through photochromic reactions.

Abstract: Diarylethene-containing ligands and their coordination compounds are described. The ligands display photochromism with UV excitation, while the coordination compounds display photochromism with both excitation in the UV region and excitation into lower energy absorption bands characteristic of the coordination compounds, through which the excitation wavelengths for the photocyclization can be extended from ??340 nm to wavelengths beyond 470 nm. Switching of the luminescence properties of the compounds has also been achieved through photochromic reactions.