998 results about "Rhodamine" patented technology

The present invention provides novel, water-soluble, red-emitting fluorescent rhodamine dyes and red-emitting fluorescent energy-transfer dye pairs, as well as labeled conjugates comprising the same and methods for their use. The dyes, energy-transfer dye pairs and labeled conjugates are useful in a variety of aqueous-based applications, particularly in assays involving staining of cells, protein binding, and / or analysis of nucleic acids, such as hybridization assays and nucleic acid sequencing.

The present invention provides novel, water-soluble, red-emitting fluorescent rhodamine dyes and red-emitting fluorescent energy-transfer dye pairs, as well as labeled conjugates comprising the same and methods for their use. The dyes, energy-transfer dye pairs and labeled conjugates are useful in a variety of aqueous-based applications, particularly in assays involving staining of cells, protein binding, and / or analysis of nucleic acids, such as hybridization assays and nucleic acid sequencing.

Novel rhodamine dye compounds, labelled conjugates comprising the dyes are described, together with methods for their use. The dyes and labelled conjugates are useful as molecular probes in a variety of applications, such as in assays involving staining of cells, protein binding, and analysis of nucleic acids, such as hybridization assays and nucleic acid sequencing.

There are described novel rhodamine dye compounds and imaging members and imaging methods, including thermal imaging members and imaging methods, utilizing the compounds. The dye compounds exhibit a first color when in the crystalline form and a second color, different from the first color, when in the liquid, amorphous form.

The invention discloses a high-efficiency graphene / silver phosphate composite visible light photocatalyst and a preparation method thereof, belonging to the technical field of composite materials and environmental management photocatalysis. The preparation method comprises the following steps: dissolving graphene oxide in water, and carrying out ultrasonic treatment to obtain a graphene oxide dispersed liquid; dissolving silver nitrate in deionized water, gradually and dropwisely adding into the graphene oxide dispersed liquid while stirring to obtain a mixed solution, uniformly stirring, and aging; dropwisely adding a prepared disodium hydrogen phosphate or sodium dihydrogen phosphate solution into the graphene oxide-silver nitrate mixed solution, continuing stirring, transferring into a hydrothermal reaction kettle, carrying out hydrothermal reaction, and cooling to room temperature; and washing the reaction product, and carrying out vacuum drying to obtain the visible light photocatalyst. The invention has the advantages of wide material sources and simple preparation process; and the obtained composite material has the advantages of controllable structure and regular pattern, and has high-efficiency degradation effect on organic dyes rhodamine B and methylene blue with certain concentration under the visible light irradiation.

Systems and methods providing for the introduction of a dye, particularly a xanthene dye, and more particularly a rhodamine dye, to liquid anhydrous ammonia to discourage theft of the anhydrous ammonia and provide for leak detection in storage vessels. The dye will stain objects which come into contact with the liquid anhydrous ammonia allowing for the detection of such contact. Generally, the staining will be visible to the naked eye, but may also fluoresce when exposed to a particular light source such as ultra violet (UV) light.

Three-, and four-dimensional ("3-D" and "4-D") volume radiation memories store multiple binary bits of information-typically about five to ten and more typically eight such bits-in the same physical volumes on several different photochromic chemicals co-located in the volume. Each of the multiple photochromic chemicals is individually selectively written with an individually associated pair of radiation beams of an appropriate combined frequency-i.e., a "color"-and energy by a process of two-photon ("2-P") absorption. All the multiple information bits that are stored within all the photochromic chemicals in each addressable domain are read in common, and induced to simultaneously fluoresce, again by process of 2-P absorption. The fluorescence of each of different photochromic chemical in each addressed domain-which fluorescence is selective in accordance with the written state of each such photochromic chemical-is separated from, and is separately detected from, the fluorescence of all other photochromic chemicals because it is of a unique color, and is spatially steered to an associated detector array, normally a Charge Coupled Device (CCD), by a monochromator, normally a prism. Exemplary fluorescent photochromic chemicals are spirobenzopyran, rhodamine, cumarin and anthracene. Suitable groups of photochromic chemicals are formed from individual photochromic chemicals exhibiting narrow, sharp, separate spectra of absorption and of emission suitably distinct from each other, and where no chemical's fluorescent emission energy overlaps the absorption energies of any other chemicals.

The invention relates to fluorescence immune chromatography test paper which is formed by mutually and sequentially overlapping a sample pad, a combination pad, an antibody carrying film and water absorbing paper on a lining board with adhesive, wherein the combination pad is coated with a fluorescence material antibody 1 composite, a fluorescence-marked material is fluorescein granules or fluorescence material converted by rare earth, the antibody carrying film is a cellulose nitrate film or a nylon film and is respectively connected with an antibody 2 and the T line and the C line of a secondary antibody, the fluorescence material is fluorescein granules or the fluorescence granules converted by the rare earth, and the fluorescein granules are selected from isosulfocyanic acid fluorescein or tetramethyl isosulfocyanic acid rhodamine or tetraethyl rhodamine, and the surface of the fluorescence-marked material is aminated and combined with the antibody by cross-linking reaction. The fluorescence quantitative measuring system is used for detecting the fluorescence strength of the areas of the T line and the C line, and the quantitative detection is completed by the standard curve of the antigen concentration. The invention is suitable for the immune detection of tumor marked objects of urinal fiber-connected protein, and the like.

The invention relates to a silver-modified carbon nitride composite photocatalytic material and a preparation method thereof. The preparation method comprises: dissolving dicyanodiamide or melamine in deionized water or dimethyl sulfoxide and performing ultrasonic dispersing, so as to obtain a dicyanodiamide or melamine dispersion liquid; dissolving silver nitrate in deionized water and stirring uniformly, so as to obtain a silver nitrate solution; slowly dropwise adding the silver nitrate solution into the above dicyanodiamide or melamine dispersion liquid under the condition of magnetic stirring, and continuing stirring the solution, so as to obtain a mixed precursor solution; using anhydrous ethanol and deionized water repeatedly wash the obtained mixed precursor solution for multiple times, and performing vacuum drying; and putting the obtained product in a proper crucible and covering, putting in a high-temperature furnace, and sintering for a period under the condition of nitrogen protection, so as to obtain a powdery sample. The advantages comprise that the raw material source is wide, the preparation technology is simple and practicable, and the cost is relatively low; and the prepared composite photocatalytic material has relatively good photocatalytic degradation effect on organic dye rhodamine B under irradiation of visible light.

The invention discloses a top silver-cladding gold nanorod array and a preparation method and application thereof. In the array, a gold film is provided with a gold nanorod array of which the top end is cladded with silver nanoparticles with the diameters of between 60 and 90nm, and the bottom surface is provided with an organic matter substrate with the thickness of between 50 and 100 mu m. The method comprises the following steps of: evaporating the gold film on one side of a nano through-hole alumina template, and growing the gold nanorod array in the hole of the template, particularly coating a liquid organic matter on the gold film on one side on which the gold nanorod array does not grow; evaporating the gold film on one side after the liquid organic matter is cured; placing the alumina template of which the hole is deposited with the gold nanorod array and the gold film is coated with the organic matter in acid or alkali solution; etching off the template; and evaporating silver on the top of the gold nanorod array by film evaporating technology to obtain the top silver-cladding gold nanorod array. A trace amount of organic matter rhodamine or 2,3,3'-trichlorodiphenyl can be detected by using the surface enhanced raman scattering effect of the top silver-cladding gold nanorod array.

The invention relates to a preparation method of TiO2 photocatalyst by loading TiO2 to diatomite formed in advance and doping rare earth, and belongs to the technical field of photocatalysis. The preparation method comprises the steps of: pickling original diatomite, roasting the pickled diatomite, and uniformly mixing the roasted diatomite, a binder, a fluxing agent and the like so as to obtain molded diatomite; and using tetrabutyl orthotitanate and dehydrated alcohol as raw materials, preparing TiO2 and rare earth doped TiO2 sol by a sol-gel method, macerating the preformed diatomite in the sol, drying the macerated diatomite, and calcining the dried diatomite so as to obtain the load type photocatalyst. The photocatalyst can prevent the TiO2 from running off; besides, the rare earth is doped, so that the utilization rate of visible light by the TiO2 is increased; when a mercury-vapor lamp is used for 3 hours, 95% of a rhodamine b solution can be degraded; when the photocatalyst is illuminated for an hour under sunlight, escherichia coli can be thoroughly killed; when the photocatalyst is illuminated for 24 hours by common daylight lamps, 92% of methanal can be degraded; the photocatalyst is excellent in photocatalytic property and stability, which indicates that the photocatalyst has favorable application prospects in the respects of waste water treatment, sanitation and sterilization, air purification and the like.

The invention discloses a method for degrading organic waste water by photo-assisted activation of potassium hydrogen persulfate through bismuth ferrite, belonging to the technical field of waste water treatment. A perovskite structure BiFeO3 in the invention has a spherical morphology and is prepared by adding a certain amount of a surface active agent under hydrothermal conditions; the specific surface area is high; and the prepared BiFeO3 self can degrade organic pollutants by photocatalysis under the irradiation of visible light. According to the method disclosed by the invention, BiFeO3 is applied to degrading the organic pollutants by activating potassium hydrogen persulfate; the methyl orange degradation rate within 15 min is 94%; the methyl blue degradation rate within 40 min is 90%; the rhodamine degradation rate within 40 min is 65%; by means of combined use of BiFeO3 and potassium hydrogen persulfate, the organic pollutants are oxidized and degraded; the organic pollutants can be effectively degraded under better illumination conditions; the organic pollutants can also be effectively oxidized and degraded without light or under poor illumination conditions; and therefore, the method has good application prospect.

The invention discloses a silver nanometer column array erected on the orifice of a porous alumina template and a preparation method and application thereof. The silver nanometer column array is characterized in that silver nanometer columns with the heights of 30-200 nanometers and the diameters of 30-60 nanometers are sequentially hexagonally arrayed on the periphery of the orifice of the porous anodic alumina template with taper holes; and silver nanometer particles with the particle size of 5-40 nanometers are attached to the walls of the taper holes. The preparation method comprises the following steps of: firstly placing an aluminum sheet into an oxalic acid solution, and carrying out anodization at direct-current voltage for at least 2 hours; then placing into a phosphorus-chromium acid mixed solution, and soaking for at least 3 hours to obtain an intermediate product; then firstly placing the intermediate product into the oxalic acid solution, carrying out the anodization at the direct-current voltage for at least 20 seconds, then placing the intermediate product into a phosphorus acid solution, and soaking for at least 1 minute; repeating the process for at least 10 times to obtain the alumina template with the holes in the shape of the taper holes; and then placing the alumina template into an ion sputter for silver sputtering so as to prepare a target product. The silver nanometer column array disclosed by the invention can be used as an active base of surface-enhanced Raman scattering; and the content of rhodamine or tetrachlorobiphenyl which is attached to the silver nanometer column array is measured by using a laser Raman spectrometer.

The invention discloses preparation of hydrophilic polymer and application thereof in detecting mercury ions based on the change of fluorescence and color, particularly a rhodamine B hydrazide grafted hydrophilic polymer probe applied to the detection of mercury ions in aqueous medium based on the change of fluorescence and color and a kit and test paper applied to the detection of the mercury ions by using the probe, belonging to the technical field of material preparation and heavy metal ion detection. The polymer containing a rhodamine chromophore is prepared by subjecting rhodamine B hydrazide and propylene oxide on the side chain of polyvinylpyrrolidone-glycidyl methacrylate which is a water-soluble polymer to ring-opening reaction, has good water solubility and can be applied to selectively detecting the mercury ions by using visual colorimetry and fluorescence detection. The probe realizes the high-sensitivity and high-selectivity rapid quantitative or semi-quantitative detection of the trace mercury ions in the aqueous medium, has a simple synthetic route, low cost and convenience of use, is applicable to amplified synthesis and actual production and has great application prospects in the field of medicine, biology and environmental science and the like.

The present invention is drawn to dye sets for formulating ink-jet ink sets, and to specific ink sets. The dye set can comprise cyan colorant including a phthalocyanine dye; magenta colorant including a copper- or nickel-containing azo dye; and yellow colorant including at least one of Yellow 1189 dye and Yellow 104 dye yellow colorant having the structure Formula 1: wherein R1 is H, SO3M, COOM, or SO2NH2; and wherein R2 is H, SO3M, COOM, or SO2NH2; and wherein R3 is H or CH3; and wherein n and m are 2, 3, 4, 5 or 6; and wherein M is H, Na, Li, K, ammonium, ammonium substituted with alkyl or combinations thereof. Optionally, a cyan triarylmethine dye such as Acid Blue 9, or another similar cyan dye, can be blended with the phthalocyanine dye; a rhodamine dye can be blended with the copper- or nickel-containing azo dye; and / or Acid Yellow 17 or Acid Yellow 23 can be blended with Formula 1.

The invention relates to a novel visible light responding photocatalysis material and a preparation method thereof. The effect of the visible light responding photocatalysis material of the BiOBr micro sphere is obviously superior to that of TiO2 (P25, Degussa), wherein BiOBr is square crystalloid; and the diameter of the sphere is about 5mu m. The invention discusses the effects of the additive amounts of glycol and hexadecyl trimethyl ammonium bromide on the physical, chemical and photocatalytic performances of the synthesized catalyst. The preparation process is simple and environment-friendly. The catalyst can almost completely remove the organic dye rhodamine B under visible light.

The invention discloses a probe reagent for concurrent selection and determination of multiple metal ions, and preparation and appliance, and belongs to the field of organic synthesis and analytical chemistry. Tri (2-aminoethyl) amine serves as a parent, wherein rhodamine B is connected to an amino chain, 2-hydroxy-1-naphthaldehyde groups are connected to other two amino chains respectively, and thus a tripod structured rhodamine-hydroxyl naphthalene derivative probe is prepared. In 1,4-dioxane / water (19 / 1, v / v, pH=7) solution, the probe respectively detects Cu2+, Co2+ and Fe3+ by utilizing rate absorption of different wavelengths, and the detection does not interfere with each other; in acetonitrile / water (19 / 1, v / v) solution, fluorescence emission of different wavelengths under different pHs is utilized, the probe respectively detects Zn2+, Al3+, Hg2+ and Cu2+, and the detection does not interfere with each other; under an ultraviolet lamp of 365 nm, Zn2+, Al3+ and Hg2+ are detected to show blue, pink and orange red fluorescence respectively, and through -Zn2+ mixture detection by the probe, Cu2+ shows blue fluorescence vanishing. The probe structure is as follows.

There are described novel rhodamine color-forming compounds. The rhodamine color-forming compounds exhibit a first color when in a crystalline form and a second color, different from the first color, when in an amorphous form. Thermal imaging members containing these color-formers are also described.

The invention relates to a fluorescent DNA-silver nanocluster, and a preparation method and application thereof. The particle size of the fluorescent DNA-silver nanocluster is 2-10nm. A water solution of the fluorescent DNA-silver nanocluster looks light pink by visual inspection, and looks shiny red under irradiation of an ultraviolet lamp with the wavelength of 360nm. The water solution is excited by light with the excitation wavelength of 530nm, the emission wavelength is 570-800nm, and high fluorescence emission strength is acquired at the wavelength of 618nm; rhodamine B is taken as a reference substance, and fluorescence quantum yield is 35.3%. A method for detecting cupric ions and pyrophosphate ions by the fluorescent DNA-silver nanocluster includes (1), drawing a response standard curve of the corresponding ions to acquire a linear regression equation; (2), substituting the detected fluorescence strength into the linear regression equation to obtain the concentration of the cupric ions or the pyrophosphate ions. The fluorescent DNA-silver nanocluster has the advantages of stable performance and environment friendliness, the detection method is rapid and simple, and the detection sensitivity is high.

The invention relates to a silicon-based rhodamine-nitrogen oxide fluorescent probe. The structures of the probe are shown in the following figures (please see the figures in the specification), wherein the Lyso-SiRB-NO in the figure II has a lysosome positioning function. The probe has the advantages that excitation and emission wavelengths of the probe are located in a near infrared light area, and when the probe is applied to biological imaging, the interference of the fluorescent background of a living body itself can be reduced; the probe is high in penetrating power and little damages tissue or cells of the living body; the probe can specifically detect nitrogen oxide molecules in lysosome, and a reliable research tool is provided for research on the physiological effect of nitrogen oxide molecules.

Color conversion films for a LCD (liquid crystal display) having RGB (red, green, blue) color filters, as well as such displays, formulations, precursors and methods are provided, which improve display performances with respect to color gamut, energy efficiency, materials and costs. The color conversion films absorb backlight illumination and convert the energy to green and / or red emission at high efficiency, specified wavelength ranges and narrow emission peaks. For example, rhodamine-based fluorescent compounds are used in matrices produced by sol gel processes and / or UV (ultraviolet) curing processes which are configured to stabilize the compounds and extend their lifetime—to provide the required emission specifications of the color conversion films. Film integration and display configurations further enhance the display performance with color conversion films utilizing various color conversion elements.

Color conversion films for a LCD (liquid crystal display) having RGB (red, green, blue) color filters, as well as such displays, formulations, precursors and methods are provided, which improve display performances with respect to color gamut, energy efficiency, materials and costs. The color conversion films absorb backlight illumination and convert the energy to green and / or red emission at high efficiency, specified wavelength ranges and narrow emission peaks. For example, rhodamine-based fluorescent compounds are used in matrices produced by sol gel processes and / or UV (ultraviolet) curing processes which are configured to stabilize the compounds and extend their lifetime - to provide the required emission specifications of the color conversion films. Film integration and display configurations further enhance the display performance with color conversion films utilizing various color conversion elements. Fluorescent emission may be enhanced by plasmon resonance of coupled nanoparticles.

The invention discloses a preparation method of a BiOBr / RGO nanometer composite and application thereof, belonging to the field of photocatalysts. The BiOBr / RGO nanometer composite has an active ingredient of BiOBr / RGO, and is characterized in that floriform BiOBr and laminar RGO are interweaved together to form a special three-dimensional structure. The preparation method comprises the following steps: weighing a certain amount of methylbenzene, hexadecyl trimethyl ammonium bromide and oleic acid, mixing at a constant temperature, adding oxidized graphene to obtain a solution A; weighing a certain amount of H2O, adding HNO3 and Bi(NO3)3.5H2O to obtain a solution B; dropping the solution B in the solution A under a mixing state, raising the temperature to 85 DEG C and reflowing for 12h; and then, cooling, washing and drying to obtain a target product. The BiOBr / RGO nanometer composite prepared by adopting the preparation method can be used as a photocatalyst for a reaction of degrading rhodamine, and has good catalysis effect and stability.

There are described thermal imaging members and thermal imaging methods utilizing unsymmetrical rhodamine compounds. The rhodamine color-forming compounds exhibit a first color when in a crystalline form and a second color, different from the first color, when in an amorphous form.

The invention discloses a synthetic method and application of a visible-light responding carbon nitride / iron sesquioxide nano composite, belongs to the fields of composite preparation technologies and photocatalysis and aims to solve the problems that a conventional carbon nitride material is small in specific surface area, high in photon-generated electron-hole recombination rate, low in solar energy utilization ratio and the like. The composite is prepared by taking melamine and iron nitrate as raw materials and methanol as a solvent and adopting the chemical reaction method and the heat treating process. Compared with carbon nitride, the prepared carbon nitride / iron sesquioxide nano composite has a wider light absorption range (expanded from the ultraviolet region to the visible region), greatly improves the solar energy utilization ratio, meanwhile, has a larger specific surface area, is low in photon-generated electron-hole recombination rate, and can effectively degrade Rhodamin B under visible light. The advantages that the preparation technology is simple, the raw material cost is low, mass production is available, and the obtained composite is large in specific surface area, high in solar energy utilization ratio, excellent in catalytic performance, and good in application prospect are achieved.

There are described novel rhodamine color-forming compounds. The rhodamine color-forming compounds exhibit a first color when in a crystalline form and a second color, different from the first color, when in an amorphous form.

The invention discloses a four-color fluorescence labeling reversible terminal and a use thereof in DNA (Deoxyribonucleic Acid) sequencing. The structural formula of the reversible terminal is as shown in a formula (I) in the specification, wherein R1 is triphosphate; R2 is H or OH; the basic group is U, C, A, G or derivatives thereof; the connecting unit is a bifunctional compound which is breakable under a mild condition; the fluorescence group is one selected from a combination of BODIPY, fluorescein, rhodamine, coumarin, xanthene, cyanin, pyrene, phthalocyanine, alexa, squarene dye and an energy transferring dye, and derivatives thereof. The reversible terminal provided by the invention can be used for DNA single-molecule sequencing; simultaneously, raw materials required by the synthesis of the reversible terminal provided by the invention are simple and easy to get and the synthesis process of the reversible terminal is completely involved with conventional chemical reactions, so that the four-color fluorescence labeling reversible terminal can be popularized and utilized to a large scale; biological evaluation results indicate that the reversible terminal is capable of completely meeting the biochemical reaction requirements of high-flux sequencing and has a good practical prospect.

The invention relates to fluorescent colorimetric analysis and discloses a colorimetric analysis method for quantitatively detecting copper ions through fluorescent equipment. The colorimetric analysis method comprises the following steps: reacting a copper ion solution and a Rhodamine fluorescent indicator synthesized in a lab to enhance fluorescence, and exciting the indicator through light with a particular wavelength of 365nm by adopting home-made fluorescent colorimetric equipment; catching fluorescence color change of the indicator before and after the copper ions are added by using electronic imaging equipment such as a scanner and a digital camera; extracting color change values of red, green and blue (RGB) channels in the image before and after color change, and establishing a standard curve between the copper ions and a concentration gradient which corresponds to the copper ions; and comparing the obtained color change values of the sample with values in the curve in a sample test process, thus quantitatively and selectively analyzing the copper ions in an unknown sample. According to the method, copper ion concentration of 10<-5>M can be detected, co-existing interference of nine ions can be effectively eliminated, and the method has high selectivity.