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1180 results about "Pyrene" patented technology

Pyrene is a polycyclic aromatic hydrocarbon (PAH) consisting of four fused benzene rings, resulting in a flat aromatic system. The chemical formula is C₁₆H₁₀. This yellow solid is the smallest peri-fused PAH (one where the rings are fused through more than one face). Pyrene forms during incomplete combustion of organic compounds.

Isoreticular metal-organic frameworks, process for forming the same, and systematic design of pore size and functionality therein, with application for gas storage

The ability to design and construct solid-state materials with pre-determined structures is a grand challenge in chemistry. An inventive strategy based on reticulating metal ions and organic carboxylate links into extended networks has been advanced to a point that has allowed the design of porous structures in which pore size and functionality can be varied systematically. MOF-5, a prototype of a new class of porous materials and one that is constructed from octahedral Zn—O—C clusters and benzene links, was used to demonstrate that its 3-D porous system can be functionalized with the organic groups, —Br, —NH2, —OC3H7, —OC5H11, —H4C2, and —H4C4, and its pore size expanded with the long molecular struts biphenyl, tetrahydropyrene, pyrene, and terphenyl. The ability to direct the formation of the octahedral clusters in the presence of a desired carboxylate link is an essential feature of this strategy, which resulted in the design of an isoreticular (having the same framework topology) series of sixteen well-defined materials whose crystals have open space representing up to 91.1% of the crystal volume, and homogeneous periodic pores that can be incrementally varied from 3.8 to 28.8 angstroms. Unlike the unpredictable nature of zeolite and other molecular sieve syntheses, the deliberate control exercised at the molecular level in the design of these crystals is expected to have tremendous implications on materials properties and future technologies. Indeed, data indicate that members of this series represent the first monocrystalline mesoporous organic / inorganic frameworks, and exhibit the highest capacity for methane storage (155 cm3 / cm3 at 36 atm) and the lowest densities (0.41 to 0.21 g / cm3) attained to date for any crystalline material at room temperature.
Owner:RGT UNIV OF MICHIGAN

Isoreticular metal-organic frameworks, process for forming the same, and systematic design of pore size and functionality therein, with application for gas storage

The ability to design and construct solid-state materials with pre-determined structures is a grand challenge in chemistry. An inventive strategy based on reticulating metal ions and organic carboxylate links into extended networks has been advanced to a point that has allowed the design of porous structures in which pore size and functionality can be varied systematically. MOF-5, a prototype of a new class of porous materials and one that is constructed from octahedral Zn—O—C clusters and benzene links, was used to demonstrate that its 3-D porous system can be functionalized with the organic groups, —Br, —NH2, —OC3H7, —OC5H11, —H4C2, and —H4C4, and its pore size expanded with the long molecular struts biphenyl, tetrahydropyrene, pyrene, and terphenyl. The ability to direct the formation of the octahedral clusters in the presence of a desired carboxylate link is an essential feature of this strategy, which resulted in the design of an isoreticular (having the same framework topology) series of sixteen well-defined materials whose crystals have open space representing up to 91.1% of the crystal volume, and homogeneous periodic pores that can be incrementally varied from 3.8 to 28.8 angstroms. Unlike the unpredictable nature of zeolite and other molecular sieve syntheses, the deliberate control exercised at the molecular level in the design of these crystals is expected to have tremendous implications on materials properties and future technologies. Indeed, data indicate that members of this series represent the first monocrystalline mesoporous organic / inorganic frameworks, and exhibit the highest capacity for methane storage (155 cm3 / cm3 at 36 atm) and the lowest densities (0.41 to 0.21 g / cm3) attained to date for any crystalline material at room temperature.
Owner:RGT UNIV OF MICHIGAN

Organic electroluminescent device based on pyrene derivatives

A pyrene based compound and its use in an organic light emitting device (OLED) according to the following formula: In the above formula, Z1 represents a hydrogen atom, deuterium atom, oxygen atom, silicon atom, selenium atom, substituted or unsubstituted aryl group, substituted or unsubstituted heteroaryl group, substituted or unsubstituted aryl amine or a combination thereof, and Z2 represents a hydrogen or deuterium atom. One of Y1 and Y2 represents a hydrogen atom, deuterium atom, oxygen atom, silicon atom, selenium atom, a substituted or unsubstituted aryl group, substituted or unsubstituted heteroaryl group, substituted or unsubstituted aryl amine or a combination thereof, and the other of Y1 and Y2 represents a hydrogen or deuterium atom. X1 through X6 independently represent hydrogen atoms, deuterium atoms, alkyl groups or aryl groups, and at least one of X1 through X6 represents a bulky alkyl group or bulky aryl group. Also, at least one of X1 through X6, Y1, Y2, Z1, and Z2 represents a deuterium atom. The pyrene based compounds of this invention are useful in emissive layers, hole transport layers, or electron transport layers of an organic light emitting device (OLED). Within these layers, the pyrene based compound can serve directly to constitute the layers or as a host and / or dopant.
Owner:CANON KK

Method for functionalizing polymer on surface of nano graphene oxide

The invention relates to a method for functionalizing a polymer on the surface of nano graphene oxide. The method comprises the following specific steps: preparing graphene oxide from natural graphite powder by an improved Hummers method, utilizing methoxy polyethylene glycol and pyrene acids to carry out esterification to generate polyethylene glycol with pyrenyl as the terminal group, and finally grafting the polyethylene glycol with pyrenyl as the terminal group on the surface of graphene oxide through pi-pi interaction between pyrenyl and the surface of graphene oxide, thus obtaining the graphene oxide with the functionalized polymer on the surface. The solubility of the prepared graphene oxide with the functionalized polymer on the surface is greatly improved. The method has the following advantages: a main process adopted in the experiment is as follows: a polymer with a complex structure is designed and prepared in advance and then is grafted on the graphene oxide, and the grafting reaction can be carried out at normal temperature and pressure, so the whole experiment process is very simple and convenient. Therefore, the study provides a direct method for modifying the graphene oxide and preparing the functionalized graphene oxide-polymer complex to form a new inorganic-organic hybrid material, thereby promoting the development and application of graphene oxide-based materials.
Owner:TONGJI UNIV

Grapheme type fiber cigarette filter and preparation method thereof

InactiveCN103005712ALarge surface atomic ratioUnique adsorptionTobacco smoke filtersFiberHazardous substance
The invention discloses a grapheme type fiber cigarette filter and a preparation method thereof. The filter comprises a fiber carrier, wherein the fiber carrier is provided with a grapheme type material for absorbing harmful components in smoke. The filter loads the grapheme type material on a carbon fiber or acetate fiber carrier; and the carrier is added in the filter by adopting the binary filter production mode in the existing industries to produce a compound filter for absorbing harmful substances in the smoke which is generated when cigarettes are smoked. The filter applies unique phi absorption characteristics and higher surface active atom ratio of novel two-dimensional nanometer materials to efficiently absorb benzo [a] pyrene, volatile aldehyde ketone type cancer promoting molecules, phenol and HCN (Hydrogen Cyanide) under the condition of smaller adding quantity, so that the filter is environment-friendly and has no additional poison; as the amount is small and the effect is high, the harm of the cigarettes to human bodies is reduced under the condition of not influencing the inherent sensory quality of the cigarettes. And at the same time, the method has the advantages of simple technique, large-scale production and low cost, and has wide application foreground in the cigarette field of harm reduction and tar reduction.
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