Patent classifications
C09B57/001
COLOR MATCHED AND BRIGHT FLUORESCENT MATERIALS COMPOSED OF SMALL-MOLECULE IONIC LATTICES
The present disclosure concerns the design, formulations, preparations and optical properties of compounds of Formulas (I) and (VI):
(charged dye.sup.m+).sub.x.Math.(counterion.sup.n−).sub.y.Math.(counterion receptor).sub.z (I) and
(charged dye.sup.m−).sub.x.Math.(counterion.sup.n+)y.Math.(counterion receptor).sub.z (VI).
The charged dye.sup.m+ is a cationic dye, counterion.sup.n− is an anion, and counterion receptor is a binding ligand for the counterion.sup.n−, wherein m, n, x and y are integers greater than or equal to 1, and products of x.Math.n and m.Math.y are identical for formula (I).
The charged dye.sup.m− is a anionic dye, counterion.sup.n+ is a cation, and counterion receptor is a binding ligand for the counterion.sup.n+, wherein m, n, x and y are integers greater than or equal to 1, and products of x.Math.n and m.Math.y are identical for formula (VI).
Fluorogenic calcium ion indicators and methods of using the same
The present disclosure provides fluorogenic compounds useful for preparing fluorescent calcium ion indicators, the fluorescent indicators themselves, and the use of the fluorescent indicators in methods of detection, discrimination and quantification of metal ions. The subject fluorogenic compounds and fluorescent ion indicators can include a chelating group based on a 2-aminophenoxyethylene glycol 2-aminoethyl ether, N,N,N′,N′-tetraacetic acid (PEGTA) moiety or precursor thereof where the phenyl group of the PEGTA is substituted with or fused with a fluorophore moiety of interest. The subject methods find use in the detection of intracellular calcium ions. Also provided are kits for use in practicing the subject methods.
Fluorescent compounds
The present invention relates to fluorescent dyes. The present invention provides a wide range of fluorescent dyes and kits containing the same, which are applicable for labeling a variety of biomolecules, cells and microorganisms. In one aspect, the invention provides a compound having a maximal fluorescence excitation wavelength, wherein the compound has a structure of Formula II: ##STR00001##
wherein Z.sup.− is a counterion, Y is a bridge unit permitting electron delocalization between F and Ψ, and F is a moiety having the structure: ##STR00002## The present invention also provides various methods of using the fluorescent dyes for research and development, forensic identification, environmental studies, diagnosis, prognosis, and/or treatment of disease conditions.
Pyrene compound and organic light emitting diode device including the same
A pyrene compound and an organic light emitting diode device including the same are disclosed. The organic light emitting diode device includes at least two stacks provided between a first electrode and a second electrode, and a charge generation layer provided between the stacks and including an N type charge generation layer and a P type charge generation layer, wherein the N type charge generation layer is made of the pyrene compound.
Organic light-emitting device
An organic light-emitting device including a first electrode; a second electrode; an organic layer between the first electrode and the second electrode and including an emission layer; and an electron transport region between the second electrode and the emission layer, the electron transport region including a charge control layer, wherein the charge control layer includes a first compound represented by Formula 1 and a second compound represented by Formula 2: ##STR00001##
COMPOUNDS AND ORGANIC ELECTRONIC DEVICE USING THE SAME
The present specification relates to an organic electronic device in which a novel compound that may improve a life-span, efficiency, a driving voltage drop, and stability of the organic electronic device is contained in an organic material layer.
Organic light-emitting devices
An organic light-emitting device including a first electrode; a second electrode; and an organic layer between the first electrode and the second electrode, the organic layer including an emission layer, wherein the emission layer includes a first host represented by Formula 1 and a second host represented by one of Formulae 2-1 to 2-3: ##STR00001##
Organic electroluminescent device
An organic electroluminescence device including at least an anode, an emitting layer, an electron-transporting region and a cathode in sequential order, wherein the emitting layer contains a host and a dopant which gives fluorescent emission of which the main peak wavelength is 550 nm or less; the affinity Ad of the dopant is equal to or larger than the affinity Ah of the host; the triplet energy E.sup.T.sub.d of the dopant is larger than the triplet energy E.sup.T.sub.h of the host; and a blocking layer is provided within the electron-transporting region such that it is adjacent to the emitting layer, and the triplet energy E.sup.T.sub.b of the blocking layer is larger than E.sup.T.sub.h.
Organic electroluminescent element, compound and material for organic electroluminescent element, used in the same, and light emitting device, display device and illumination device, using the element
An organic electroluminescent element comprising a substrate, a pair of electrodes including an anode and a cathode, disposed on the substrate, and at least one organic layer which is arranged between the electrodes and which includes a light emitting layer, wherein the organic layer contains a compound represented by general formula (1) in at least one layer. The organic electroluminescent element has a high luminous efficiency, excellent blue color purity, and little chromaticity change due to drive deterioration. (In the formula, the two Xs either both represent an O atom or both represent an S atom, and R.sup.1-R.sup.10 each independently represents a hydrogen atom or a substituent group).
Water soluble fluorescent or colored dyes and methods for their use
Compounds useful as fluorescent or colored dyes are disclosed. The compounds have the following structure (I): including stereoisomers, salts and tautomers thereof, wherein R.sup.1, R.sup.2, R.sup.3, L.sup.1, L.sup.2, L.sup.3, L.sup.4, L.sup.5, L.sup.6, M.sup.1, M.sup.2, A, q, w and n are as defined herein. Methods associated with preparation and use of such compounds are also provided. ##STR00001##