Category: 103-50-4

An article Guest induced transition from beta to alpha nanoporous crystalline forms of PPO WOS:000509481800006 published article about SYNDIOTACTIC POLYSTYRENE; GAS SORPTION; POLY(2,6-DIMETHYL-1,4-PHENYLENE OXIDE); AMORPHOUS PHASES; SINGLE-CRYSTALS; X-RAY; TRANSPORT; FILMS; MEMBRANES; DELTA in [Guerra, Gaetano] Univ Salerno, Dipartimento Chim & Biol, Via Giovanni Paolo II 132, I-84084 Fisciano, Italy; Univ Salerno, INSTM Res Unit, Via Giovanni Paolo II 132, I-84084 Fisciano, Italy in 2020, Cited 49. The Name is Benzyl ether. Through research, I have a further understanding and discovery of 103-50-4. COA of Formula: C14H14O

The stability of a and beta nanoporous-crystalline (NC) forms of Poly(2,6-dimethyl-1,4-phenylene) oxide (PPO), in the presence of guest molecules leading to crystallization in a and beta-form (alpha and beta-guests), is explored. Sorption of liquid guests at 30 degrees C and 60 degrees C is studied both for NC films and NC aerogels. WAXD and FTIR characterizations show that, for all considered conditions, NC alpha-phases after guest sorption/desorption remain unaltered. NC beta-phases, on the contrary, after alpha-guest sorption can be transformed in co-crystalline (CC) alpha-phases that after guest desorption are transformed in NC alpha-phases. All conducted experiments also show that possible planar orientations of NC films (c//or c perpendicular to orientations) remain essentially unaltered, after sorption of all considered guest molecules. The presently discovered beta ->alpha transition constitutes a route to obtain unoriented alpha-form films, which till now were not available by known preparation procedures.

Welcome to talk about 103-50-4, If you have any questions, you can contact Nagendra, B; Cozzolino, A; Golla, M; Daniel, C; Rizzo, P; Guerra, G or send Email.. COA of Formula: C14H14O

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Category: ethers-buliding-blocks. In 2020 CATAL SCI TECHNOL published article about MEDIUM-RANGE STRUCTURE; HYDROTHERMAL CONVERSION; NANOSIZED ZEOLITES; CATALYTIC-ACTIVITY; EXTERNAL SURFACE; BETA; NANOZEOLITES; MECHANISM; EFFICIENT; INSIGHT in [Xu, Lanjian; Yuan, Yangyang; Han, Qiao; Dong, Lei; Chen, Lei; Zhang, Xiaomin; Xu, Lei] Chinese Acad Sci, Dalian Inst Chem Phys, Natl Lab Clean Energy, Dalian 116023, Peoples R China; [Xu, Lanjian; Han, Qiao; Dong, Lei; Chen, Lei] Univ Chinese Acad Sci, Beijing 100049, Peoples R China in 2020, Cited 51. The Name is Benzyl ether. Through research, I have a further understanding and discovery of 103-50-4.

A novel interzeolite transformation strategy using internally confined organic structure directing agents (OSDAs), called the OSDA-confined strategy, is proposed for highly crystalline nanosized high-silica ZSM-5 zeolite synthesis, by which high yield and fast synthesis of ZSM-5 is achieved using BEA zeolite as a raw material. The transformation process was investigated by XRD, SEM, ICP, FTIR and UV Raman spectroscopy, which revealed that the decomposition of a parent zeolite and the crystallization process of products were well modulated by the confined OSDA. The transformation process could be divided into three stages consisting of raw material deconstruction, small size product formation and product growth. The strong etching power of NaOH contributes to the fast decomposition of BEA zeolites. In addition, tetrapropylammonium hydroxide (TPAOH) as an OSDA was confined in the parent zeolite instead of being added into the mother liquid, achieving a high local concentration of TPAOH, which could reduce the decomposition rate of the parent BEA zeolite and promote the efficient organization of the building units generated by the decomposition of the BEA zeolite. Thereof, a high yield was achieved by the synergistic effect of NaOH and occluded TPAOH. During the interzeolite transformation process, the six-membered rings (6Rs), five-membered rings (5Rs) and four-membered rings (4Rs) in the BEA zeolite framework were disassembled and combined with the help of 5Rs to produce the ZSM-5 zeolite structure. Moreover, due to the nanoscale and large surface area, the obtained ZSM-5 zeolite catalyst showed extremely high catalytic activity in the self-etherification reaction of benzyl alcohol (BA) to dibenzyl ether (DE). This study provides insights into the interzeolite transformation process, which would be helpful for achieving size control and high-efficiency synthesis.

Category: ethers-buliding-blocks. Welcome to talk about 103-50-4, If you have any questions, you can contact Xu, LJ; Yuan, YY; Han, Q; Dong, L; Chen, L; Zhang, XM; Xu, L or send Email.

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Category: ethers-buliding-blocks. Gambe, J; Jouin, J; Remondiere, F; Thomas, P; Masson, O in [Gambe, Jess; Jouin, Jenny; Remondiere, Fabien; Thomas, Philippe; Masson, Olivier] Ctr Europeen Ceram, IRCER UMR 7315, 12 Rue Atlantis, F-87068 Limoges, France published Solvent effect in the nonaqueous synthesis of ZrO2 nanoparticles under alkaline conditions in 2020, Cited 37. The Name is Benzyl ether. Through research, I have a further understanding and discovery of 103-50-4.

This work deals with the synthesis of zirconium dioxide (ZrO2) nanoparticles (NPs) in different solvents and their structural characterization for better understanding the oxygen donor solvent/zirconium precursor/NPs structure relationships. By selecting solvents over their capacity to produce different crystalline states from alkalinized zirconium alkoxide, spherical nanoparticles with a size of about 1.3-3 nm and a narrow size distribution were elaborated using a nonaqueous solvothermal sol-gel route. Conventional X-ray diffraction (XRD) was used to determine the average structure and crystallite size of the nanoparticles. Well-crystallized and single-phased nanoparticles with average monoclinic and tetragonal structure were obtained with benzaldehyde and benzyl alcohol, respectively, and a much distorted structure was observed for the synthesis in anisole. The atomic pair distribution functions (PDF) of the samples were also analyzed to access the local structure of the nanoparticles. The PDF of the benzaldehyde-prepared sample is consistent with the monoclinic structure. However, the local structure of nanoparticles synthesized with benzyl alcohol does not fully conform to the tetragonal structure observed by XRD, but exhibits monoclinic-like distortions. Lastly, the anisole-prepared nanoparticles present large structural distortions at the medium range and monoclinic local structural features. The restructuring of this last sample was studied by post-treatments in different solvents and leads to the expression of the tetragonal polymorph. Moreover, it seems that the main structural features are obtained in the early stages of the nanoparticles’ formation.

Category: ethers-buliding-blocks. Welcome to talk about 103-50-4, If you have any questions, you can contact Gambe, J; Jouin, J; Remondiere, F; Thomas, P; Masson, O or send Email.

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An article Simultaneous acquisition of Fe3O4 monocrystals: Tunable magnetic properties with various morphologies WOS:000522647100006 published article about IRON-OXIDE NANOPARTICLES; FACILE SYNTHESIS; STABILIZER in [Zheng, Zemin; Li, Huiyong; Hu, Dafeng; Jiang, Hao; Geng, Xuemin; Lu, Jiangwei; Zhang, Xudong; Yang, Peng; Wan, Yanfen] Yunnan Univ, Sch Mat Sci & Engn, Yunnan Key Lab Micro Nano Mat & Technol, Kunming 650091, Yunnan, Peoples R China; [Cao, Yiming; Li, Zhe] Qujing Normal Univ, Ctr Magnet Mat & Devices, Qujing 655011, Yunnan, Peoples R China; [Cao, Yiming; Li, Zhe] Qujing Normal Univ, Key Lab Adv Funct & Low Dimens Mat, Yunnan Higher Educ Inst, Qujing 655011, Yunnan, Peoples R China in 2020, Cited 26. The Name is Benzyl ether. Through research, I have a further understanding and discovery of 103-50-4. Recommanded Product: Benzyl ether

Fe3O4 nanoparticles (NPs) with a face-centered cubic (fcc) structure and two different morphologies (nanospheres and nanoprisms) were synthesized by a facile one-step method. The synthesized Fe3O4 nanospheres and nanoprisms were monocrystalline and separable in a magnetic field. In different volume ratios of oleylamine (OAm) to dibenzyl ether, the sizes of the prepared Fe3O4 NPs ranged from 5 to 21 nm. The OAm amount in the synthesis can significantly control the morphology of Fe3O4 NPs. As the OAm content increased from 10 ml to 30 ml, the faceted nanoprisms shrank while the nanospheres enlarged. At an OAm content of 25 ml, the nanoprisms diminished while more hexagonal and sphere-like particles appeared, implying a critical point of morphology transition from triangle to hexagon. The magnetic properties also depended on the NP morphology and size. The prepared Fe3O4 NPs are promising candidates in medical applications such as magnetic resonance imaging, targeted drug delivery, blood purification, and tumor hyperthermia.

Welcome to talk about 103-50-4, If you have any questions, you can contact Zheng, ZM; Cao, YM; Li, Z; Li, HY; Hu, DF; Jiang, H; Geng, XM; Lu, JW; Zhang, XD; Yang, P; Wan, YF or send Email.. Recommanded Product: Benzyl ether

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Category: ethers-buliding-blocks. Recently I am researching about ASYMMETRIC TRANSFER HYDROGENATION; METAL-COMPLEXES; ENANTIOSELECTIVE HYDROSILYLATION; SELECTIVE REDUCTION; MANGANESE COMPLEXES; IRON COMPLEXES; KETONES; ALDEHYDES; EFFICIENT; HYDROSILATION, Saw an article supported by the Max Planck SocietyMax Planck SocietyFoundation CELLEX; RWTH Aachen University; Bundesministerium fur Bildung und Forschung as part of the project MANGANFederal Ministry of Education & Research (BMBF) [03SF0508]; Cluster of Excellence The Fuel Science Center. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Martinez-Ferrate, O; Chatterjee, B; Werle, C; Leitner, W. The CAS is 103-50-4. Through research, I have a further understanding and discovery of Benzyl ether

Manganese(i) complexes bearing triazole ligands are reported as catalysts for the hydrosilylation of carbonyl and carboxyl compounds. The desired reaction proceeds readily at 80 degrees C within 3 hours at catalyst loadings as low as 0.25 to 1 mol%. Hence, good to excellent yields of alcohols could be obtained for a wide range of substrates including ketones, esters, and carboxylic acids illustrating the versatility of the metal/ligand combination.

Category: ethers-buliding-blocks. Welcome to talk about 103-50-4, If you have any questions, you can contact Martinez-Ferrate, O; Chatterjee, B; Werle, C; Leitner, W or send Email.

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Authors Nagendra, B; Rizzo, P; Daniel, C; Guerra, G in AMER CHEMICAL SOC published article about STRESS-INDUCED CRYSTALLIZATION; STRAIN-INDUCED CRYSTALLIZATION; SYNDIOTACTIC POLYSTYRENE; ISOTACTIC POLYPROPYLENE; UNIPLANAR ORIENTATIONS; INDUCED NUCLEATION; OPTICAL-PROPERTIES; RANDOM COPOLYMERS; PHASE; CLATHRATE in [Nagendra, Baku; Rizzo, Paola; Daniel, Christophe; Guerra, Gaetano] Univ Salerno, Dipartimento Chim & Biol, INSTM Res Unit, I-84084 Fisciano, SA, Italy in 2021, Cited 51. Computed Properties of C14H14O. The Name is Benzyl ether. Through research, I have a further understanding and discovery of 103-50-4

The dependence of polymer film transparency on different kinds of planar orientations of nanoporous-crystalline (NC) phases of syndiotactic polystyrene (sPS) and poly(2,6-dimethyl-1,4-phenylene)oxide (PPO) is described. The two polymers exhibit opposite behavior: film transparency is improved for sPS and PPO by orientations of the chain axes of the NC phases being parallel (c(parallel to)) and perpendicular (c(perpendicular to)) to the film plane, respectively. This behavior can be rationalized by the negative and positive birefringence of sPS and PPO chains, respectively. In fact, to maximize transparency, the refractive index of the NC phase along the perpendicular to the film plane has to be increased to come closer to that of the corresponding amorphous phase. This can be pursued by controlling the orientation of the NC phases and hence of the associated refractive index ellipsoids.

Computed Properties of C14H14O. Welcome to talk about 103-50-4, If you have any questions, you can contact Nagendra, B; Rizzo, P; Daniel, C; Guerra, G or send Email.

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Wu, XY; Qiao, K; Qin, H; Zhang, D; Gao, D; Yang, Z; Fang, Z; Guo, K in [Wu, Xiaoyu; Qiao, Kai; Qin, Hong; Zhang, Dong; Gao, Di; Fang, Zheng; Guo, Kai] Nanjing Tech Univ, Coll Biotechnol & Pharmaceut Engn, Nanjing 211816, Jiangsu, Peoples R China; [Yang, Zhao] China Pharmaceut Univ, Sch Engn, 639 Longmian Ave, Nanjing 211198, Jiangsu, Peoples R China; [Fang, Zheng; Guo, Kai] Nanjing Tech Univ, State Key Lab Mat Oriented Chem Engn, Nanjing 210009, Peoples R China published Silver(i)-mediated oxidative C(sp(3))-H amination of ethers with azole derivatives under mild conditions in 2019, Cited 68. COA of Formula: C14H14O. The Name is Benzyl ether. Through research, I have a further understanding and discovery of 103-50-4.

A silver(i)-mediated oxidative N-H/C(sp(3))-H coupling of NH-azoles with ethers has been developed. Various substrates were well N-alkylated in this methodology and the corresponding desired products were given in moderate to good yields. Moreover, the late-stage alkylation of bioactive molecules was achieved. This protocol involved C(sp(3))-N bond formation via a radical pathway generated in the presence of low cost and readily available heptafluoroisopropyl iodide (i-C3F7I). Generally, this reaction features excellent functional group compatibility, broad substrate scope, good regioselectivity, and fast access to pharmaceuticals such as SQ 22536.

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Product Details of 103-50-4. Zhang, S; Han, F; Yan, SR; He, MY; Miao, CX; He, LN in [Zhang, Shuai; He, Liang-Nian] Nankai Univ, Coll Chem, State Key Lab, Tianjin 300071, Peoples R China; [Zhang, Shuai; He, Liang-Nian] Nankai Univ, Coll Chem, Inst Elementoorgan Chem, Tianjin 300071, Peoples R China; [Zhang, Shuai; Han, Feng; Yan, Shaorui; He, Mingyue; Miao, Chengxia] Inst Shandong Agr Univ, Coll Chem & Mat Sci, Tai An 271018, Shandong, Peoples R China published Efficient Catalysts In situ Generated from Zinc, Amide and Benzyl Bromide for Epoxide/CO2 Coupling Reaction at Atmospheric Pressure in 2019, Cited 58. The Name is Benzyl ether. Through research, I have a further understanding and discovery of 103-50-4.

Herein, in situ generated efficient catalysts were designed for fixation of CO2 to cyclic carbonates under mild conditions. Zinc bromide and N,N-dibenzyl-N,N-dimethylammonium bromide, being proved as active catalyst species, were in situ generated from cheap Zn powder, dimethyl formamide and benzyl bromide, and catalyzed the cycloaddition reaction of CO2 and various terminal epoxides in moderate to excellent yields at 80 degrees C and atmospheric pressure of CO2. The protocol circumvents the preparation of active catalysts, simultaneously possesses good catalytic activity under mild conditions.

Welcome to talk about 103-50-4, If you have any questions, you can contact Zhang, S; Han, F; Yan, SR; He, MY; Miao, CX; He, LN or send Email.. Product Details of 103-50-4

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HPLC of Formula: C14H14O. Authors Tekale, DP; Yadav, GD; Dalai, AK in MDPI published article about in [Tekale, Devendra P.; Yadav, Ganapati D.] Inst Chem Technol, Dept Chem Engn, Nathalal Parekh Marg, Mumbai 400019, Maharashtra, India; [Dalai, Ajay K.] Univ Saskatchewan, Catalysis & Chem React Engn Lab, Dept Chem & Biol Engn, Saskatoon, SK S7N 5A9, Canada in 2021, Cited 41. The Name is Benzyl ether. Through research, I have a further understanding and discovery of 103-50-4

Value addition to glycerol, the sole co-product in biodiesel production, will lead to reform of the overall biodiesel economy. Different valuable chemicals can be produced from glycerol using heterogeneous catalysis and these valuable chemicals are useful in industries such as cosmetics, pharmaceuticals, fuels, soap, paints, and fine chemicals. Therefore, the conversion of glycerol to valuable chemicals using heterogeneous catalysis is a noteworthy area of research. Etherification of glycerol with alkenes or alcohols is an important reaction in converting glycerol to various value-added chemicals. This article describes reaction of glycerol with benzyl alcohol in solvent-free medium by using a clay supported modified heteropolyacid (HPA), Cs2.5H0.5PW12O40/K-10 (Cs-DTP/K-10) as solid catalyst and its comparison with other catalysts in a batch reactor. Mono-Benzyl glycerol ether (MBGE) was the major product formed in the reaction along with formation of di-benzyl glycerol ether (DBGE). The effects of different parameters were studied to optimize the reaction parameters. This work provides an insight into characterization of Cs2.5H0.5PW12O40/K-10 catalyst by advanced techniques such as surface area measurement, X-ray analysis, ICP-MS, FT-IR, and SEM. Reaction products were characterized and confirmed by using the GCMS method. The kinetic model was developed from an insight into the reaction mechanism. The apparent energy of activation was found to be 18.84 kcal/mol.

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An article Selective catalytic oxidation over Au-Pd/titanate nanotubes and the influence of the catalyst preparation method on the activity WOS:000472188100015 published article about LIQUID-PHASE OXIDATION; TITANATE NANOTUBES; BIMETALLIC CATALYSTS; GOLD; NANOPARTICLES; STABILITY; CHEMISTRY; PALLADIUM; TIO2; SIO2 in [Khawaji, Motaz; Chadwick, David] Imperial Coll London, Dept Chem Engn, London SW7 2AZ, England in 2019, Cited 41. Computed Properties of C14H14O. The Name is Benzyl ether. Through research, I have a further understanding and discovery of 103-50-4

The dependence of the selective oxidation catalytic activity of Au-Pd supported on titanate nanotubes on the catalyst preparation method has been investigated. The most active Au-Pd/Ti-NT catalyst for the selective oxidation of benzyl alcohol is shown to be that prepared using colloidal synthesis and immobilization with PVA as a stabilizer, which has markedly superior catalytic activity compared to catalysts prepared by deposition-precipitation, adsorption, and dry impregnation methods. Au-Pd NPs stabilized by graphene oxide sheets and immobilized on Ti-NT has also been studied and while not optimum shows promising catalytic activity. The superior catalytic activity of the catalysts prepared by colloidal synthesis is attributed to the high metal dispersion on the external surfaces of Ti-NT, the narrow particle size distribution, and the high degree of Au-Pd alloying. This work also demonstrates that in the adsorption method of preparation using HAuCl4.3H(2)O and PdCl2 precursors, the uptake of Pd ions in solution by Ti-NT is proportional to the sodium content in Ti-NT, which implies that Na is involved in an ion-exchange reaction with Pd ions.

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Ether – Wikipedia,
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