Category: 146370-51-6

On August 14, 2017, Makkad, Sarabjot Kaur; Asha, S. K. published an article.Computed Properties of 146370-51-6 The title of the article was π-Conjugated Chromophore Incorporated Polystyrene Nanobeads as Single Optical Agent for Three-Channel Fluorescent Probe in Bioimaging Application. And the article contained the following:

Fluorescent polystyrene (PS) nanobeads in the size range ∼70-120 nm incorporating perylene bisimide (PBI-PS) and/or oligo(p-phenylenevinylene) (OPV-PS) were developed by the miniemulsion polymerization technique. A dye loading content (DLC) of <3% was sufficient to impart high fluorescence emission capability to the PS beads. OPV-PS exhibited emission in the range 400-550 nm with peak emission at 450 nm (λex = 350 nm; φFL = 26%); PBI-PS showed emission from 520-650 nm with peak emission at 545 nm (λex = 490 nm; φFL = 9.7%) in 1× PBS buffer, whereas OPV(PBI)-PS nanobeads incorporating both the fluorophores exhibited multicolor emission capabilities (λex from 350 to 490 nm). The nanoparticles were characterized by field-emission SEM (FESEM), TEM and dynamic light scattering (DLS) for size and zeta potential for surface charge. For bioimaging applications, the PS nanoparticles were incubated with HeLa cells. Cell viability anal. involving HeLa cells showed >90% cell viability confirming the biocompatibility of the PS beads. The cellular uptake of the nanoparticles was confirmed by flow cytometry anal. and confocal laser scanning microscopy (CLSM) images. The subcellular localization of the nanoparticles in the cytoplasm could be precisely established by their simultaneous multicolor emission. The PS-based single optical agent presented here that can function as three-channel fluorescent probe to meet the requirements for multicolor bioimaging is advantageous. The experimental process involved the reaction of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene(cas: 146370-51-6).Computed Properties of 146370-51-6

The Article related to conjugated chromophore polystyrene nanobead fluorescent probe bioimaging, bioimaging, fluorescent polystyrene nanobeads, oligo (p-phenylenevinylene), perylene bisimide, Biochemical Methods: Spectral and Related Methods and other aspects.Computed Properties of 146370-51-6

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Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Xie, Chen; Zhen, Xu; Miao, Qingqing; Lyu, Yan; Pu, Kanyi published an article in 2018, the title of the article was Self-Assembled Semiconducting Polymer Nanoparticles for Ultrasensitive Near-Infrared Afterglow Imaging of Metastatic Tumors.Synthetic Route of 146370-51-6 And the article contains the following content:

Detection of metastatic tumor tissues is crucial for cancer therapy; however, fluorescence agents that allow to do share the disadvantage of low signal-to-background ratio due to tissue autofluorescence. The development of amphiphilic poly(p-phenylenevinylene) derivatives that can self-assemble into the nanoagent (SPPVN) in biol. solutions and emit near-IR afterglow luminescence after cessation of light irradiation for ultrasensitive imaging of metastatic tumors in living mice is herein reported. As compared with the counterpart nanoparticle (PPVP) prepared from the hydrophobic PPV derivate, SPPVN has smaller size, higher energy transfer efficiency, and brighter afterglow luminescence. Moreover, due to the higher PEG d. of SPPVN relative to PPVP poly(ethylene glycol), SPPVN has a better accumulation in tumor. Such a high sensitivity and ideal biodistribution allow SPPVN to rapidly detect xenograft tumors with the size as small as 1 mm3 and tiny peritoneal metastatic tumors that are almost invisible to naked eye, which is not possible for PPVP. Moreover, the oxygen-sensitive afterglow makes SPPVN potentially useful for in vivo imaging of oxygen levels. By virtue of enzymic biodegradability and ideal in vivo clearance, these organic agents can serve as a platform for the construction of advanced afterglow imaging tools. The experimental process involved the reaction of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene(cas: 146370-51-6).Synthetic Route of 146370-51-6

The Article related to semiconducting polymer nanoparticle ir afterglow imaging metastatic tumor, lymph node imaging, optical imaging, semiconducting polymer nanoparticles, tumor imaging, Biochemical Methods: Spectral and Related Methods and other aspects.Synthetic Route of 146370-51-6

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On February 7, 2019, Pu, Kanyi; Miao, Qingqing published a patent.Related Products of 146370-51-6 The title of the patent was Polymer nanoparticles for afterglow molecular imaging. And the patent contained the following:

Disclosed herein are semiconducting polymers of formula (I) and polymeric composite materials containing said polymer, where said polymer displays near-IR afterglow luminescence. The polymers of formula I have the following structure, where n, m, o, p, A and R1 to R7 are as defined herein, and r is used to denote a random order to the repeating units. The experimental process involved the reaction of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene(cas: 146370-51-6).Related Products of 146370-51-6

The Article related to polymer semiconductor nanoparticle afterglow luminescence imaging, Pharmaceuticals: Prosthetics and Medical Goods and other aspects.Related Products of 146370-51-6

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Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Lee, Chang-Soo; Chang, Hee Hyun; Jung, Juyeon; Lee, No Ah; Song, Nam Woong; Chung, Bong Hyun published an article in 2012, the title of the article was A novel fluorescent nanoparticle composed of fluorene copolymer core and silica shell with enhanced photostability.COA of Formula: C15H24O2 And the article contains the following content:

A variety of fluorescent nanoparticles have been developed for demanding applications such as optical biosensing and fluorescence imaging in live cells. Silica-based fluorescent nanoparticles offer diverse advantages for biol. applications. For example, they can be used as labeling probes due to their low toxicity, high sensitivity, resolution, and stability. In this research, a new class of highly fluorescent, efficient nanoparticles composed of a newly synthesized poly[di(2-methoxy-5-(2-ethylhexyloxy))-2,7-(9,9-dioctyl-9H-fluorene)] (PDDF) core and a silica shell (designated as PDDF@SiO2) were prepared using a simple reverse micelle method, and their fluorescent properties were evaluated using methods such as single-dot photoluminescence measurements. The enhanced photostability of the particles and their potential applications for bioanal. are discussed in this article. The morphol., size, and fluorescent properties for prepared PDDF@SiO2 nanoparticles were characterized using transmission electron microscopy (TEM), SEM (SEM) and photoluminescence spectroscopy. The prepared particles size, which was approx. 60 nm, resulted in an excellent colloidal stability in a physiol. environment. The photobleaching dynamics, total numbers of emitted photons (TNEP) and statistical measurements of individual nanoparticles were observed using laser scanning fluorescence microscopy to assess the structure and photostability of PDDF@SiO2 nanoparticles. Addnl., PDDF@SiO2 nanoparticles were used in cell toxicity and permeation tests for biol. analyses, demonstrating a great potential for use as powerful, novel materials within the emerging fields of biosensing and biomedical engineering. The experimental process involved the reaction of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene(cas: 146370-51-6).COA of Formula: C15H24O2

The Article related to fluorescent nanoparticle fluorene copolymer silica photostability, Pharmaceuticals: Prosthetics and Medical Goods and other aspects.COA of Formula: C15H24O2

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Ether – Wikipedia,
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On June 13, 2002, Li, Xiao-Chang Charles; Ueno, Kazunori published a patent.Recommanded Product: 146370-51-6 The title of the patent was Deuterated semiconducting organic compounds used for optoelectronic devices. And the patent contained the following:

Organic semiconductors are described which comprise a linear conjugated organic compound or a polymer, a cyclic ring, a fused cyclic ring, a heterocyclic ring, a fused heterocyclic ring, a chelate or organometallic material described by the general formula CaMb (C = conjugated chromophore; M = Li, Na, K, Be, Mg, Ca, Ti, Cr, Mo, Mn, Fe, Ru, Os, Co, Rh, Ir, Ni, Pd, Pt, Cu, Zn, Cd, B, Al, Ga, In, Si, N, or P; and a and b = independently 1-10) wherein protons linked to the conjugated bonds are partially or fully deuterated. Preferably, the chromophore has ≥5 conjugated bonds. The semiconductor may be luminescent or promote energy transfer and it may have charge injection, hole blocking, or exciton blocking properties. Organic electroluminescent devices employing the semiconductors are also described. The experimental process involved the reaction of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene(cas: 146370-51-6).Recommanded Product: 146370-51-6

The Article related to deuterated conjugated chromophore semiconductor, organic electroluminescent device deuterated conjugated chromophore semiconductor, Electric Phenomena: Semiconductor Junctions and Devices and other aspects.Recommanded Product: 146370-51-6

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Ether – Wikipedia,
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On October 22, 2001, Yang, Chunhe; He, Gufeng; Sun, Qingjiang; Li, Yongfang published an article.SDS of cas: 146370-51-6 The title of the article was Polymer light-emitting electrochemical cells with 1-methoxy-4-(2-ethylhexyloxy)benzene as salt carrier. And the article contained the following:

The electro-active, 1-methoxy-4-(2-ethylhexyloxy)benzene (MEH-benzene) is employed as ion carrier and redox shuttle in the polymer light-emitting electrochem. cell (LEC). The corresponding LECs with MEH-PPV can be driven within 10 V without failure. The LEC characteristics are clearly shown by the current-voltage curves and the ac impedance spectroscopy. The experimental process involved the reaction of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene(cas: 146370-51-6).SDS of cas: 146370-51-6

The Article related to polymer light emitting electrochem cell methoxyethylhexyloxybenzene, Electrochemistry: Electrochemical Cells and Systems and other aspects.SDS of cas: 146370-51-6

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Ether – Wikipedia,
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On February 29, 2012, Zhao, Lifeng; Li, Shengbiao; Tao, Haiyan; Su, Jinjin; Wang, Zhenjiang; Wang, Hongli; Huang, Wei published an article.Application In Synthesis of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene The title of the article was Novel hyperbranched poly (phenylene vinylene) s containing four arms: Synthesis, characterization and properties of photophysics. And the article contained the following:

Novel PPVs derivates were designed and successfully synthesized through Gilch reaction. The reaction intermediates and polymers were characterized by 1H NMR, GC-MS or GPC and Elemental Anal. (EA). Their optical properties, thermal properties, electrochem. properties were investigated. These polymers were soluble in common organic solvents and they have good thermal stability. The onset weights loss temperature of the three polymers were found to be 371.7, 386.6 and 391.8掳C for P1, P2 and P3, resp. Compared with their spectra absorption in chloroform, the absorption bands of polymers P1, P2 and P3 in thin films were red-shifted. These polymers would be promising materials for luminescent materials or solar cells. The experimental process involved the reaction of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene(cas: 146370-51-6).Application In Synthesis of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene

The Article related to poly phenylene vinylene synthesis characterization photophysic, Optical, Electron, and Mass Spectroscopy and Other Related Properties: Electronic Spectroscopy and other aspects.Application In Synthesis of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene

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Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

On May 23, 2000, Kwon, Hyung Ki; Kim, Yoon Hee; Shin, Dong Chul; Yoo, Han Sung; Cho, Sung Woo; Kim, Dong Geun; Cho, Sung Gun published a patent.Related Products of 146370-51-6 The title of the patent was Blue light-emitting compounds, light-emitting elements, and light-emitting display devices. And the patent contained the following:

Light-emitting compounds I [Ar1-5 = (un)substituted Ph, naphthalene, anthracene, diphenylanthracene, phenanthrene, indene, acenaphthene, biphenyl, fluorene, carbazole, thiophene, pyridine, oxadiazole, oxazole, triazole, benzothiophene, dibenzofuran, thiadiazole; R1-4 = H, ethylenoxy, C1-20 alkyl, C1-20 alkoxy, aryl, trimethylsilyl, trimethylsilylaryl, cyano] are claimed. Further specifications of Ar1-5 are also given. Light-emitting elements and displays comprising the compounds are also claimed. Blue light-emitting elements showing high luminosity are obtained. The experimental process involved the reaction of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene(cas: 146370-51-6).Related Products of 146370-51-6

The Article related to electroluminescent device blue light emitting compound, display electroluminescent device, anthracene derivative electroluminescent compound, Radiation Chemistry, Photochemistry, and Photographic and Other Reprographic Processes: Other and other aspects.Related Products of 146370-51-6

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Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

On May 26, 2000, Kwon, Soon Ki; Kim, Yoon Hee; Shin, Dong Chul; Ahn, Joon Hwan; Yoo, Han Sung; Soh, Sung Hyun published a patent.Product Details of 146370-51-6 The title of the patent was Blue-emitting luminescent comound, organic electroluminescent device, and imaging device thereof. And the patent contained the following:

The luminescent compound is shown as [Ar1C(Ar2R3):C(Ar3R1)(Ar4)l[C(Ar5R5):C(Ar6R6)Ar7]k]m (I; Ar1-Ar7 = chem. bond, phenylene, divalent group derived from naphthalene, anthracene, diphenylanthracene, etc.; R1-R6 = H, ethylene oxyalkyl, ethylene oxyalkylene, C1-20 alkyl, alkoxy, etc.; l, k = 0, 1; m = 10-200 integer). Organic electroluminescent device involves I-containing organic films, which may be a luminescent or a charge-transfer layer, between a pair of electrodes. The imaging device uses I as a luminescent material. Luminescence efficiency is improved. The experimental process involved the reaction of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene(cas: 146370-51-6).Product Details of 146370-51-6

The Article related to blue emitting luminescent compound imaging device, electroluminescent device blue emitting luminescent compound, Radiation Chemistry, Photochemistry, and Photographic and Other Reprographic Processes: Other and other aspects.Product Details of 146370-51-6

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Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

On June 30, 2003, Plavich, M. L.; Zubov, V. P.; Borisov, A. G.; Korsakov, V. S. published an article.Category: ethers-buliding-blocks The title of the article was Information display devices based on organic luminophors. And the article contained the following:

The development and properties of light-emitting devices based on the organic luminophors have been studied in the State Research University of Phys. Problems named after F.V. Lukin for more than 7 yr. The development of such devices is a relatively new field of optoelectronics, and some problems which encountered in this field are discussed in the present paper. The description of matrix monochrome indicator having 16è„?6 pixels size based on the recent studies is given. Exptl. elec. current-potential relationships and elec. current-brightness relationships for different light-emitting materials are considered. The experimental process involved the reaction of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene(cas: 146370-51-6).Category: ethers-buliding-blocks

The Article related to organic luminophor display material elec current potential brightness relationship, Radiation Chemistry, Photochemistry, and Photographic and Other Reprographic Processes: Other and other aspects.Category: ethers-buliding-blocks

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem