Category: 146370-51-6

On December 6, 2001, Kido, Junji; Nakada, Hitoshi; Tohma, Teruo; Murayama, Ryuji; Yuki, Toshinao published a patent.COA of Formula: C15H24O2 The title of the patent was Organic electroluminescent display device and chemical compounds for liquid crystals. And the patent contained the following:

The new organic electroluminescent display device has a carrier-transporting layer and/or an organic luminous layer composed of a nematic liquid crystal or a liquid crystal dispersing a carrier-transporting low-mol. therein. When the organic luminous layer is to be bestowed with faculty as a liquid crystal, it is made of a nematic liquid crystal. Both the carrier-transporting layer and the organic luminous layer may be bestowed with faculty as a liquid crystal. Since the liquid crystal is incorporated in the carrier-transporting layer and/or the organic luminous layer, the display device can be driven as a liquid crystal display device in a dark place by charging with a voltage lower than a light emission initiating potential. Of course, it is driven as an electroluminescent display device when it is charged with a voltage higher than the light emission initiating potential. Use of an electroluminescent liquid crystal as an organic luminous layer enables omission of a carrier-transporting layer. 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 organic electroluminescent display nematic liquid crystal, Radiation Chemistry, Photochemistry, and Photographic and Other Reprographic Processes: Other and other aspects.COA of Formula: C15H24O2

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On January 7, 2003, Khan, Muhammad S.; Al-Suti, Mohammed K.; Al-Mandhary, Muna R. A.; Ahrens, Birte; Bjernemose, Jens K.; Mahon, Mary F.; Male, Louise; Raithby, Paul R.; Friend, Richard H.; Koehler, Anna; Wilson, Joanne S. published an article.Application In Synthesis of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene The title of the article was Synthesis and characterization of new acetylide-functionalized aromatic and hetero-aromatic ligands and their dinuclear platinum complexes. And the article contained the following:

A new series of rigid rod protected and terminal dialkynes with extended èŸ?conjugation through aromatic and hetero-aromatic linker units in the backbone, 2,5-bis(trimethylsilylethynyl)-1-(2-ethylhexyloxy)-4-methoxybenzene 1a, 2,5-bis(ethynyl)-1-(2-ethylhexyloxy)-4-methoxybenzene 1b, 5,8-bis(trimethylsilylethynyl)quinoline 2a, 5,8-bis(ethynyl)quinoline 2b, 2,3-diphenyl-5,8-bis(trimethylsilylethynyl)quinoxaline 3a, 2,3-diphenyl-5,8-bis(ethynyl)quinoxaline 3b, 4,7-bis(trimethysilylethynyl)-2,1,3-benzothiadiazole 4a and 4,7-bis(ethynyl)-2,1,3-benzothiadiazole 4b, has been synthesized. Treatment of the complex trans-[Pt(Ph)(Cl)(Et3P)2] with half equivalent of the diterminal alkynes 1b-4b in iPr2NH-CH2Cl2, in the presence of CuI, at room temperature, afforded the platinum(ii) di-yne complexes trans-[(Et3P)2(Ph)Pt-C顚咰-R-C顚咰-Pt(Ph)(Et3P)2] [R = 1-(2-ethylhexyloxy)-4-methoxybenzene-2,5-diyl 1c, quinoline-5,8-diyl 2c, 2,3-diphenylquinoxaline-5,8-diyl 3c, 2,1,3-benzothiadiazole-4,7-diyl 4c] in good yields. The new acetylide-functionalized ligands and the platinum(ii) èŸ?acetylide complexes have been characterized by anal. and spectroscopic methods and x-ray single crystal structure determinations for 2c-4c. The absorption spectra of the complexes 2c-4c show substantial donor-acceptor interaction between the platinum(ii) centers and the conjugated ligands. The photoluminescence spectra of 1c-3c show characteristic singlet (S1) and triplet (T1) emissions. Both the singlet and triplet emissions as well as the absorption decrease in energy with increasing electronegativity of the spacer groups along the series 1c-4c. 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 acetylide functionalized hetero aromatic ligand preparation reaction platinum complex, crystal structure hetero aromatic acetylide functionalized platinum diynyl complex, Organometallic and Organometalloidal Compounds: Group Viii – Co, Ni, Ru, Rh, Pd, Os, Ir, Pt and other aspects.Application In Synthesis of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene

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Ether – Wikipedia,
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On June 1, 2001, Ram, M. K.; Sarkar, N.; Bertoncello, P.; Sarkar, A.; Narizzano, R.; Nicolini, C. published an article.HPLC of Formula: 146370-51-6 The title of the article was Fabrication and characterization of poly[(2-methoxy-5-(2′-ethyl-hexyloxy)phenylene vinylene] (MEH-PPV) Langmuir-Schaefer films and their application as photoelectrochemical cells. And the article contained the following:

The Langmuir monolayer behavior of poly[2-methoxy-5-(2′-ethyl-hexyloxy)phenylenevinylene] (MEH-PPV) conducting polymer in a subphase containing various anions was investigated at the air-water interface. The Langmuir-Schaefer (LS) films were prepared in deionized water that showed the min. area per mol., and were found to be essential for the formation of Langmuir monolayer at the air-water interface of MEH-PPV conjugated polymer. The LS films of MEH-PPV were investigated by using UV-VIS absorption, electrochem. and at. force microscopic techniques. A uniform deposition of monolayers was shown by optical technique, whereas a higher number of monolayers resulted in the tiny island morphol. in MEH-PPV LS films. The influence of concentration of anions on the redox properties of the LS films was studied by cyclic voltammetric measurements. The nature of anions in electrochem. investigation revealed the significant changes in the redox properties of the MEH-PPV LS films. The photoelectrochem. current transient of MEH-PPV LS films was compared with those obtained by the solution cast technique. This work also focused on the influence of the nature of the electrolytes, the applied potential, the type of the film and the presence of dissolved oxygen on the photoelectrochem. properties of MEH-PPV conducting polymer. The experimental process involved the reaction of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene(cas: 146370-51-6).HPLC of Formula: 146370-51-6

The Article related to polyphenylenevinylene langmuir schaefer film photoelectrochem cell, Plastics Manufacture and Processing: Preparation Of Resins and other aspects.HPLC of Formula: 146370-51-6

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Cheng, Faxiang; Ma, Haihong; Ren, Fengmei; Ouyang, Gaoyuan; Zhou, Zhengfa; Xu, Weibing published an article in 2010, the title of the article was Poly(2-methoxy-5-(2′-ethylhexyloxy)-p-phenylene vinylene) synthesized by bromine methylation.Product Details of 146370-51-6 And the article contains the following content:

Poly[2-methoxy-5-(2′-ethylhexyloxy)-p-phenylene vinylene] (MEH-PPV) was successfully synthesized using p-methoxy phenol and 1-bromo-2-ethylhexane through the reactions of etherification, bromine methylation and de-hydrogen bromide. The number average mol. weight of MEH-PPV was 5.7è„?04. The structure of intermediates and MEH-PPV were characterized by FTIR, 1HNMR and UV-Vis. The structure of intermediates and MEH-PPV was consistent with the reported in the literature. 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 methoxyethylhexyloxyphenylene vinylene bromine methylation synthesis, Industrial Organic Chemicals, Leather, Fats, and Waxes: Manufacture Of Industrial Organic Chemicals and other aspects.Product Details of 146370-51-6

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On July 27, 2005, Xu, Liangheng; Li, Xiang; Yao, Hongbing; Li, Xiaoying; Gao, Yun published a patent.Quality Control of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene The title of the patent was Preparation and application of poly(p-phenylenevinylene) derivatives. And the patent contained the following:

Poly(p-phenylenevinylene) derivatives are prepared by polymerization of CN- or halogen-containing benzene derivatives at 1.0-2.0 MPa and -80 to +150° for 1.0-18 h. The product has high relative mol. weight, low dispersion degree, good thermal stability, solubility, photoluminescence, and electroluminescence efficiency. The product is useful for light-emitting component, diode, photoemissive element, light activated element and various elec. pole unit. The experimental process involved the reaction of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene(cas: 146370-51-6).Quality Control of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene

The Article related to polyphenylenevinylene derivative preparation application photoluminescence electroluminescence, Plastics Manufacture and Processing: Preparation Of Resins and other aspects.Quality Control of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene

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Ether – Wikipedia,
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Xia, Jin; Xu, Zili; Lu, Yimin; Yang, Yingge published an article in 2008, the title of the article was Ultrasonic synthesis and structure characterization of poly(2-ethoxy-5-(2′-ethylhexyloxy)-p-phenylenevinylene).COA of Formula: C15H24O2 And the article contains the following content:

The preparation of poly(2-ethoxy-5-(2′-ethylhexyloxy)-phenylenevinylene) (MEH-PPV) was investigated with p-methoxyphenol as raw material. Gel-free soluble and high-mol.-weight (Mn) MEH-PPV was prepared by the method of ultrasonic synthesis. The molar weight of the polymer was 7.9 × 105. The structure of the polymer was identified by IR, 1H-NMR and Raman spectra. 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 polyphenylenevinylene derivative preparation characterization ultrasound methoxyphenol, Plastics Manufacture and Processing: Preparation Of Resins and other aspects.COA of Formula: C15H24O2

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Ether – Wikipedia,
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On April 8, 2004, Leatherdale, Catherine A.; Schardt, Craig R.; Thompson, D. Scott; Thompson, Wendy L. published a patent.Application In Synthesis of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene The title of the patent was Multiphoton photoreactive compositions with inorganic particles and fabricating three-dimensional structures. And the patent contained the following:

A multiphoton reactive composition includes (a) â‰? reactive species; and (b) multi-photon photoinitiator system; and (c) a plurality of substantially inorganic particles, wherein the particles have an average particle size of â‰?0 μ in diameter 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 oxide epoxy nanocomposite photoreactive fabrication three dimensional structure, Plastics Manufacture and Processing: Preparation Of Resins and other aspects.Application In Synthesis of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene

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On August 12, 2014, Resta, Claudio; Di Pietro, Sebastiano; Majeric Elenkov, Maja; Hamersak, Zdenko; Pescitelli, Gennaro; Di Bari, Lorenzo published an article.COA of Formula: C15H24O2 The title of the article was Consequences of Chirality on the Aggregation Behavior of Poly[2-methoxy-5-(2′-ethylhexyloxy)-p-phenylenevinylene] (MEH-PPV). And the article contained the following:

Poly[2-methoxy-5(2′-ethylhexoxy)-p-phenylenevinylene] (MEH-PPV) has been for the first time prepared and fully characterized in enantiopure (R) form. If the polymer mol. weight is sufficiently low, (R)-MEH-PPV assumes a helical supramol. structure in the solution aggregates, with consequences on the tendency to aggregation and on the fluorescence quenching, both of which are reduced with respect to the racemic analog. 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 chirality effect aggregation poly methoxy ethylhexyloxy phenylenevinylene, Physical Properties of Synthetic High Polymers: Polymer Structure and other aspects.COA of Formula: C15H24O2

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Ether – Wikipedia,
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On March 18, 2004, Whiteford, Jeffery A.; Buretea, Mihai A.; Scher, Erik C. published a patent.Related Products of 146370-51-6 The title of the patent was Organic species that facilitate charge transfer to or from nanostructures. And the patent contained the following:

The present invention provides compositions (small mols., oligomers and polymers) that can be used to modify charge transport across a surface or a nanostructure (e.g., nanocrystal) surface, or within a nanostructure (e.g., nanocrystal)containing matrix, as well as methods for making and using the novel compositions The compositions contain a conjugated organic species and at least one binding group capable of interacting with a nanostructure (e.g., nanocrystal) surface; during use, the compositions are coupled via the binding group to the nanostructure (e.g., nanocrystal) surface, such that the compositions are substantially conductive to electrons and/or holes being transported by/through the nanostructure (e.g., nanocrystal) (e.g., during the process of extracting or injecting the electrons or holes). The compositions of the present invention can optionally be derivatized with addnl. chem. groups, e.g., to enhance the electronic conjugation of the core organic species, to couple adjacent nanostructures (e.g., nanocrystals), or to facilitate dispersion, mixing and/or blending of nanostructures (e.g., nanocrystals) in various matrixes. In one aspect, the present invention provides conductive compositions for modification of charge transport across a nanostructure (e.g., nanocrystal)containing matrix. The conductive composition typically include (1) a conjugated organic moiety as the body structure, or core of the conductive mol.; (2) a nanostructure (e.g., nanocrystal) binding head group coupled to the body structure at a 1st position on the conjugated organic moiety; and (3) a tail group coupled to the body structure at a 2nd position on the conjugated organic moiety. After formation of an exciton in the nanostructure (e.g., nanocrystal) containing matrix, the conductive composition facilitates the injection and/or extraction of charge (electron and/or hole) with respect to the attached nanostructure, thereby modifying charge transport across a nanostructure-containing matrix. 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 charge transfer mol electronic device nanocrystal, Electric Phenomena: Conductors, Semiconductors, Resistors, Contacts and other aspects.Related Products of 146370-51-6

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Ether – Wikipedia,
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On June 30, 1999, Li, Xiao-Chang; Liu, Yunqi; Liu, Michelle S.; Jen, Alex K.-Y. published an article.Reference of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene The title of the article was Synthesis, Properties, and Application of New Luminescent Polymers with Both Hole and Electron Injection Abilities for Light-Emitting Devices. And the article contained the following:

New luminescent polymers that contain both electron-withdrawing cyano groups and electron-rich moieties, triphenylamine (TPA) or tetraphenyldiaminobiphenyl (TPD), were synthesized by Knoevenagel condensation of 1,4-bis(cyanomethyl)-2-[(2-ethylhexyl)oxy]-5-methoxybenzene with the dialdehyde of TPA or TPD, resp. The polymers were characterized by NMR, FT-IR, microanal., GPC, DSC, and TGA. Efficient orange photoluminescence was observed with an absolute quantum efficiency of 48% for the TPA incorporated polymer (TPA-CNPPV). Cyclic voltammetry investigation showed that the polymers presented reversible oxidation and reduction with relatively low potentials, which suggested that the polymers have both good electron and hole injection abilities. We demonstrated an effective approach to synthesize polymers with the triad properties of efficient photoluminescence, good hole injection and high electron-affinity properties, which are highly desirable for application in light-emitting devices. This point was supported by the demonstration of a single layer light-emitting device with a configuration of ITO/TPA-CNPPV/Al, in which good external quantum efficiency (0.1%) and bright luminance of 2100 cd/m2 was achieved. Multilayer LEDs using the polymers as the active layers and different charge injection/transporting layers were also investigated. The experimental process involved the reaction of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene(cas: 146370-51-6).Reference of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene

The Article related to luminescent polymer light emitting device, Chemistry of Synthetic High Polymers: Organic Addition Polymerization and other aspects.Reference of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene

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