The present invention relates to a compound of the following formula (I). The invention also relates to uses thereof as a chromophore as such or for building pigments displaying special optical effects, including metal-like reflection. ##STR00001##

Provided herein are dyes, dye-sensitized solar cells, and sequential series multijunction dye-sensitized solar cell devices. The dyes include an electron deficient acceptor moiety, a medium electron density ?-bridge moiety, and an electron rich donor moiety comprising a biaryl, a substituted biaryl, or an R1, R2, R3 substituted phenyl where each of R1, R2, and R3 independently comprises H, aryl, multiaryl, alkyl substituted aryl, alkoxy substituted aryl, alkyl substituted multiaryl, alkoxy substituted multiaryl, OR4, N(R5)2, or a combination thereof; each R4 independently comprises H, alkyl, aryl, alkyl substituted aryl, alkoxy substituted aryl, or a combination thereof; and each R5 independently comprises aryl, multiaryl, alkyl substituted aryl, alkoxy substituted aryl, alkyl substituted multiaryl, alkoxy substituted multiaryl, or a combination thereof. The solar cells include a glass substrate, a dye-sensitized active layer, and a redox shuttle. The devices include at least two dye-sensitized solar cells connected in series. ##STR00001##

Provided herein are dyes, dye-sensitized solar cells, and sequential series multijunction dye-sensitized solar cell devices. The dyes include an electron deficient acceptor moiety, a medium electron density ?-bridge moiety, and an electron rich donor moiety comprising a biaryl, a substituted biaryl, or an R1, R2, R3 substituted phenyl where each of R1, R2, and R3 independently comprises H, aryl, multiaryl, alkyl substituted aryl, alkoxy substituted aryl, alkyl substituted multiaryl, alkoxy substituted multiaryl, OR4, N(R5)2, or a combination thereof; each R4 independently comprises H, alkyl, aryl, alkyl substituted aryl, alkoxy substituted aryl, or a combination thereof; and each R5 independently comprises aryl, multiaryl, alkyl substituted aryl, alkoxy substituted aryl, alkyl substituted multiaryl, alkoxy substituted multiaryl, or a combination thereof. The solar cells include a glass substrate, a dye-sensitized active layer, and a redox shuttle. The devices include at least two dye-sensitized solar cells connected in series. ##STR00001##

A copolymer useful as an ingredient of a colored resin composition, comprising a structural unit derived from an aromatic carboxylic acid having an ethylenically unsaturated bond, a structural unit (Ab) represented by formula (Z), and a structural unit (Ac) derived from an unsaturated compound having a cyclic ether structure having 2 to 4 carbon atoms, wherein L represents a single bond or a divalent linking group, A represents a phenyl group optionally having a substituent other than a carboxy group or a naphthyl group optionally having a substituent other than a carboxy group, R.sup.a represents a hydrogen atom, or an alkyl group having 1 to 4 carbon atoms, and a hydrogen atom contained in the alkyl group is optionally replaced by a hydroxy group. ##STR00001##

This disclosure relates to advanced image signal processing technology including encoded signals and digital watermarking. One implementation is directed a printed object comprising: a substrate comprising a first area; a first colored ink or design printed within the first area, the first colored ink or design comprising a spectral reflectivity of less than or equal to 20% at or around 660 nm; a colored ink mixture printed over the first colored ink or design at a first plurality of spatial locations within the first area, the colored ink mixture printed such that the first area comprises a second plurality of spatial locations without the colored ink mixture, the colored ink mixture comprising opaque white ink and a first colorant, wherein the color ink mixture comprises a spectral reflectivity greater than the first colored ink or design at or around 660 nm, and wherein colored ink mixture comprises a spectral reflectivity less than the first colored ink or design in the range of 495 nm-570 nm; in which the first plurality of spatial locations is arranged in a pattern conveying an encoded signal, and in which the first colored ink or design and the colored ink mixture comprise a spectral reflectivity difference at or around 660 nm in a difference range of 8%-30%. Of course, other objects, methods, packages, labels, containers, systems and apparatus are described in this patent document.

This disclosure relates to advanced image signal processing technology including encoded signals and digital watermarking. One implementation is directed a printed object comprising: a substrate comprising a first area; a first colored ink or design printed within the first area, the first colored ink or design comprising a spectral reflectivity of less than or equal to 20% at or around 660 nm; a colored ink mixture printed over the first colored ink or design at a first plurality of spatial locations within the first area, the colored ink mixture printed such that the first area comprises a second plurality of spatial locations without the colored ink mixture, the colored ink mixture comprising opaque white ink and a first colorant, wherein the color ink mixture comprises a spectral reflectivity greater than the first colored ink or design at or around 660 nm, and wherein colored ink mixture comprises a spectral reflectivity less than the first colored ink or design in the range of 495 nm-570 nm; in which the first plurality of spatial locations is arranged in a pattern conveying an encoded signal, and in which the first colored ink or design and the colored ink mixture comprise a spectral reflectivity difference at or around 660 nm in a difference range of 8%-30%. Of course, other objects, methods, packages, labels, containers, systems and apparatus are described in this patent document.

Water-soluble dipyrromethene-based dyes are provided herein. In certain cases, the water-soluble dye is a dipyrromethene-boron dye. Embodiments of the subject water-soluble dipyrromethene-based dyes have a narrow absorption maxima in the yellow green range close to or at the 561 nm laser line, and are suitable for use in tandem dye systems. Embodiments of the subject dyes efficiently transfer energy to an acceptor chromophore while a second dipyrromethene-based dye of the same or different chemical structure is within energy-receiving proximity therewith. Also provided herein are tandem dyes that include the subject water-soluble dipyrromethene-based dyes, e.g., as donor chromophores. Methods of evaluating a sample for the presence of a target analyte and methods of labelling a target molecule in which the subject dyes find use are also provided. Systems and kits for practicing the subject methods are also provided.

Novel reaction media for electron donating and electron accepting components in colour-change compositions are described. The compound is of formula (VI); R.sub.1, and R.sub.2 are independently selected from an optionally substituted linear or branched alkyl group, alkenyl group, alkoxy group, aryl group and an alkylene aryl group having from 5 to 22 carbon atoms; X.sub.1 and X.sub.2 are independently selected from —OC(O)—, —CO.sub.2— and O; Y.sub.1, and Y.sub.2 are independently selected from hydrogen, halogen, R.sub.1, —OR.sub.1; y is independently 0 or 1; and suitably the groups R.sub.1X.sub.1— and —X.sub.2R.sub.2 are independently in the ortho or meta position. The compounds are useful in ink compositions, writing implements containing the compound and medical and industrial applications in which temperature sensitive colour change may be required. ##STR00001##

Novel reaction media for electron donating and electron accepting components in colour-change compositions are described. The compound is of formula (VI); R.sub.1, and R.sub.2 are independently selected from an optionally substituted linear or branched alkyl group, alkenyl group, alkoxy group, aryl group and an alkylene aryl group having from 5 to 22 carbon atoms; X.sub.1 and X.sub.2 are independently selected from —OC(O)—, —CO.sub.2— and O; Y.sub.1, and Y.sub.2 are independently selected from hydrogen, halogen, R.sub.1, —OR.sub.1; y is independently 0 or 1; and suitably the groups R.sub.1X.sub.1— and —X.sub.2R.sub.2 are independently in the ortho or meta position. The compounds are useful in ink compositions, writing implements containing the compound and medical and industrial applications in which temperature sensitive colour change may be required. ##STR00001##

An organic electronic device, preferably an organic light-emitting diode (OLED), comprising at least one metal-carbene complex comprising one, two or three specific bidentate diazabenzimidazole carbene ligands; a light-emitting layer comprising said metal-carbene complex as emitter material, preferably in combination with at least one host material; the use of said metal-carbene complex in an OLED; an apparatus selected from the group consisting of stationary visual display units, mobile visual display units, illumination units, units in items of clothing, units in handbags, units in accessories, units in furniture and units in wallpaper comprising said organic electronic device, preferably said OLED, or said light-emitting layer; the metal-carbene complex comprising one, two or three specific bidentate diazabenzimidazole carbene ligands mentioned above and a process for the preparation of said metal-carbene complex.