37results about How to "Strong fluorescence emission properties" patented technology

The invention discloses a ratio-dependent fluorescent probe for detecting hydrogen peroxide. The ratio-dependent fluorescent probe is an anthocyanin-like derivative, has the chemical structure as shown in the formula (1) and is particularly 2-(3-(7-diethylamino) coumarin)-4-(2-phenmethyl)-7-diethylamino-benzopyran perchlorate. The probe disclosed by the invention is cheap and available, convenient to use, capable of specifically reacting together with hydrogen peroxide to generate a coumarin derivative with stronger fluorescence emission capacity, free of interference from other related oxides in the process of detecting hydrogen peroxide, favorable in hydrogen peroxide selectivity and capable of accurately detecting hydrogen peroxide in living cells.

The invention discloses a near-infrared fluorescent probe for detecting thiophenol and a synthesis method and application thereof, and belongs to the technical field of chemical analysis and detection. The near-infrared fluorescent probe is obtained by reaction between a dicyano-substituted isophorone large pi system and 2,4-dinitrofluorobenzene, and has the following structure (being defined as in the specification). Fluorophore of the probe is the dicyano-substituted isophorone large pi system, and a response group to thiophenol is 2,4-dinitrophenoxy. Molecules of the probe have high selectivity and sensitivity to thiophenol, the detection range is 0.5-10 [mu]mol.L<-1>, and the limit of detection is 23 nmol.L<-1>. The probe can be used for detecting thiophenol in water bodies, soil and cells.

The invention discloses a solid broadband blue-light transmitting organic luminescent material shown in a formula I and a preparation method thereof. R is H or OCH3. Two functional structural units such as the quinoxaline group and the pyridazinone group are effectively combined to form a pyridazinone-type organic luminescent molecule with quinoxaline being functionalized. The two-heterocyclic-ring pyridazinone compound provided by the invention is stable in structure and easy to store, a good ultraviolet absorption property and a strong fluorescent transmitting property in a chloroform solution can be realized, and the solid broadband blue-light transmitting organic luminescent compound is expected to become a novel organic material obtaining the white light. The preparation method is simple, the luminescent material is good in stability and can be used in the fields such as luminescent devices, white light luminescence or fluorescent probes. By adopting the solid broadband blue-light transmitting organic luminescent material and the preparation method thereof, the research and application field of the quinoxaline pyridazinone compound can be enlarged.

The invention provides a stable method for preparing a nitrogen-doped graphene quantum dot material. The preparation method comprises the following steps: dispersing networked reduced graphene oxide in concentrated nitric acid, and heating in an oil bath to a temperature of 140-160 DEG C while magnetic stirring, and reacting at a constant temperature for 12-48 hours under circulating water condensation; removing circulating condensate water, continuously evaporating at the constant temperature for 2-3 hours, and cooling to a room temperature; adding ultrapure water for ultrasonic dispersion, filtering, performing rotary evaporation and concentration on the filtrate, and filling in a dialysis bag of 3000-8000Da to dialyze for 24-48 hours; and performing rotary evaporation and concentrationon the dialysate again, and performing vacuum freeze drying, thereby obtaining the nitrogen-doped graphene quantum dots. The luminous stability of the nitrogen-doped graphene quantum dot is improved to a certain degree, and complicated passivating treatment and mixed element doping processes in the traditional process of preparing the doped quantum dots are effectively simplified. Moreover, the charge transfer capacity of the quantum dots is effectively improved, and the application potential in more fields such as photoelectricity, biomedicine and the like is facilitated.

The invention discloses a preparation method of an ultrathin nano belt structure perovskite single crystal. The preparation method comprises the following steps: 1) dissolving AX and PbX2 in a precursor solvent according to a molar ratio of n: 1, heating and stirring to obtain a precursor solution of three-dimensional perovskite APbX3; 2) dropping a proper amount of the precursor solution of the three-dimensional perovskite APbX3 on a substrate, placing the substrate in a vessel containing an anti-solvent, and sealing the opening of the vessel, placing the vessel in a drying oven, and standingto grow the crystal, thereby obtaining the ultrathin strip-shaped perovskite single crystal, wherein AX is selected from one or more of methylamine bromine, formamidine bromine and cesium bromide; Xis a halogen anion, and n is 1-2.2. The optimal light emitting wavelength of the obtained ultrathin perovskite single crystal is 508-512 nm, and low-threshold laser lasing at the room temperature andcontinuous optical pumping laser lasing at the liquid nitrogen temperature are achieved.

The invention discloses a preparation method of supermolecule composite nano particles. The method comprises the following steps of: dissolving TPE-m-COOH in an organic solvent to obtain a TPE-m-COOH solution; and mixing dendronized polymer Gn PAMAM and the TPE-m-COOH solution in the organic solvent, keeping the concentration of the TPE-m-COOH solution 1*10<-6> to 1*10<-4>M, wherein the molar ratio of amino of Gn PAMAM to carboxyl of TPE-m-COOH is definite, dispersing and standing to obtain the supermolecule composite nano particles. The supermolecule composite nano particles are strong in fluorescence emission performance; compared with tetraphenylethenes derivatives, the supermolecule composite nano particles have the advantages that fluorescence intensity is greatly enhanced, and the supermolecule composite nano particles can be used as novel luminescent materials; the preparation method is simple and mild in condition; and the supermolecule composite nano particles are easy to prepare.

The invention relates to a method for preparing fluorescent nitrogen-doped carbon nanodots by taking compost humic acid as a raw material. The preparation method comprises the following steps: uniformly mixing humic acid and a hydrogen peroxide aqueous solution at room temperature, carrying out hydrothermal reaction, and naturally cooling to room temperature to obtain a reaction solution; carryingout ultrasonic treatment, centrifugation and separation on the reaction liquid at room temperature to obtain supernatant; enabling the supernatant to pass through a water system microporous filter membrane, dialyzing, intercepting to obtain a carbon nano point aqueous solution with the molecular weight of more than 3500Da, and freeze-drying to obtain the solid nitrogen-doped carbon nanodots. According to the invention, high-value recycling of sludge can be realized, and the provided nitrogen-doped carbon nanodot synthesis method is convenient, green and efficient. The prepared nitrogen-dopedcarbon nanodot has high quantum dot yield and high fluorescence emission and can be applied to rapid detection of metal ions, and shows high selectivity and sensitivity for detection of Fe < 3 + >, and the Fe < 3 + > detection effect can be visualized by using an induction strip of a nitrogen-doped carbon nanodot matrix.

The invention relates to an anthracene main chain type polymer of intrinsic microporosity as well as a synthetic method and application thereof, and belongs to the field of polymers. The molecular weight of the polymer is 4000-400000, the molecular weight distribution is 1.15-3.50, and the specific surface area is 50-800 m<2>/g. The preparation method comprises the following steps: performing a Diels-Alder reaction on anthracene-2,6-diamine and maleimide, or performing a Diels-Alder reaction on anthracene-2,6-diamine and a maleimide derivative to obtain a dianiline monomer; performing a polycondensation reaction on the dianiline monomer by using a Troger base reaction to obtain a polymer; and performing a reverse reaction of the Diels-Alder reaction to remove the maleimide or the maleimidederivative to obtain the anthracene main chain type polymer of intrinsic microporosity. According to the method, the maleimide or the maleimide derivative is used as a protective group of an anthracene functional group, the synthesized polymer has a microporous structure, solubility and light sensitive characteristic, and can be used as a photosensitizer in the fields of organic contaminant degradation and photodynamic preparations.

The invention discloses a multi-response azacyclo-formaldehyde fluorescent probe molecule with a structure shown as a formula I and a preparation method and application thereof, the molecule realizesselective quantitative recognition of formaldehyde through a fluorescence analysis method, and formaldehyde, copper ions and sulfur ions are tested and evaluated in the fields of automotive trim materials, healthy home furnishing, biological medicines and the like. The multi-response azacyclo-formaldehyde fluorescent probe molecule can be used for fluorescence imaging of biological samples, can also be used as an ultraviolet light absorber to be applied to the technical fields of plastics, coatings, printing ink, display, illumination, glasses, daily-use chemical industry, textiles and the like, and in addition, the multi-response azacyclo-formaldehyde fluorescent probe molecule provided by the invention has relatively strong fluorescence emission performance under both solution and solidconditions; can be used as a fluorescent material in the fields of anti-counterfeiting technologies, light conversion materials, fluorescence labeling, fluorescence imaging and the like, wherein R isH or Cl, and X is CH or N.