An, Kang et al. published their research in Organic Electronics in 2020 |CAS: 578-58-5

The Article related to polyhexylthiophene nonfullerene polymer solar cell film morphol optical property, Electrochemical, Radiational, and Thermal Energy Technology: Energy-Conversion Devices and Their Components and other aspects.Safety of 2-Methylanisole

On July 31, 2020, An, Kang; Zhong, Wenkai; Ying, Lei published an article.Safety of 2-Methylanisole The title of the article was Enhanced performance of P3HT-based non-fullerene polymer solar cells by optimizing film morphology using non-halogenated solvent. And the article contained the following:

Increasing research interests have been paid to developing efficient polymer solar cells by using integrating non-fullerene acceptors with poly (3-hexylthiophene) (P3HT), owing to the low-cost, promising performance and excellent stability. Here we systematically studied how processing solvents influence the overall performances of polymer solar cells using P3HT as the electron donor. It is very interesting to note that the devices processed with the non-halogenated solvent, 2-methylanisole in presence of 1-methylnaphthalene as solvent additive, exhibit reduced bimol. and trap-assisted monomol. recombination, facile charge extraction and enhanced charge carrier mobilities. Careful morphol. investigation reveals that the optimizing crystallites, phase purity as well as nanofibrous structure is effective to the enhancement of charge generation and transport. It is also worth noting that these P3HT:O-IDTBR based devices processed with these non-halogenated solvents exhibitean impressive power conversion efficiency of 7.1% with a high fill factor of 75.09% on a device area of 0.05 cm2, and the efficiency remained 6.89% even in a device with large active layer area of 1 cm2, while also showing promising thermal stability. This study provides a new scope of processing P3HT based polymer solar cells by using non-halogenated solvents, which is compatible and has great promise for future applications. The experimental process involved the reaction of 2-Methylanisole(cas: 578-58-5).Safety of 2-Methylanisole

The Article related to polyhexylthiophene nonfullerene polymer solar cell film morphol optical property, Electrochemical, Radiational, and Thermal Energy Technology: Energy-Conversion Devices and Their Components and other aspects.Safety of 2-Methylanisole

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

Zhang, Lei et al. published their research in Journal of Applied Polymer Science in 2021 |CAS: 91-16-7

The Article related to pmma graphene oxide composite electrolyte surface structure elec current, Electrochemical, Radiational, and Thermal Energy Technology: Energy-Conversion Devices and Their Components and other aspects.Application In Synthesis of 1,2-Dimethoxybenzene

On April 10, 2021, Zhang, Lei; Jin, Gan; Ma, Tianlin; Wang, Shi published an article.Application In Synthesis of 1,2-Dimethoxybenzene The title of the article was Ion transport in topological all-solid-state polymer electrolyte improved via graphene-oxide. And the article contained the following:

Designing and constructing novel topol. all-solid-state polymer electrolyte (SPE) matrixes can improve the ionic conducting ability of the prepared SPEs compared with the linear ones. Here, we construct a novel topol. polymer electrolyte matrix using triphenylene as core and block poly(Me methacrylate)-poly(poly[ethylene glycol] Me ether methacrylate) as arm. Specifically, the arm is attached onto the core via sequential atom transfer radical polymerization The mol. weight of the polymers is well controlled via adjusting the inventory rating of monomers, the optimal SPE obtained via solution casting has an ambient temperature ionic conductivity of 3.69 × 10-5 S cm-1, which is higher than typical linear poly(ethylene oxide)-based SPE (usually 10-6-10-8 S cm-1). The electrochem. performance is further improved through adding given contents of graphene-oxide into the SPE. Thus, we believe, through mol. designing and the widely used composite tactics, new class of electrolytes with high-electrochem. performance for all-solid-state Li-ion batteries can be developed. The experimental process involved the reaction of 1,2-Dimethoxybenzene(cas: 91-16-7).Application In Synthesis of 1,2-Dimethoxybenzene

The Article related to pmma graphene oxide composite electrolyte surface structure elec current, Electrochemical, Radiational, and Thermal Energy Technology: Energy-Conversion Devices and Their Components and other aspects.Application In Synthesis of 1,2-Dimethoxybenzene

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

Nakashima, Kensuke et al. published their research in Chemical Science in 2020 |CAS: 91-16-7

The Article related to hexahydroxytriphenylene crystalline porous structure lithium ion battery, Electrochemical, Radiational, and Thermal Energy Technology: Energy-Conversion Devices and Their Components and other aspects.Product Details of 91-16-7

Nakashima, Kensuke; Shimizu, Takeshi; Kamakura, Yoshinobu; Hinokimoto, Akira; Kitagawa, Yasutaka; Yoshikawa, Hirofumi; Tanaka, Daisuke published an article in 2020, the title of the article was A new design strategy for redox-active molecular assemblies with crystalline porous structures for lithium-ion batteries.Product Details of 91-16-7 And the article contains the following content:

A new design strategy for high-performance organic cathode active materials for lithium-ion batteries is presented, which involves the assembly of redox-active organic mols. with a crystalline porous structure using mixed-stacked charge-transfer (CT) complexes. Hexahydroxytriphenylene was used as a donor mol. and 1,4,5,8,9,12-hexaazatriphenylene-2,3,6,7,10,11-hexacarbonitrile as an acceptor mol. to give a new porous CT complex (PCT-1) with a pseudo-hexagonal mixed columnar structure. X-ray diffraction measurements and sorption experiments demonstrated that the intercolumnar spaces in PCT-1 can incorporate various mols. accompanied by lattice expansion. A lithium metal battery containing PCT-1 as a cathode active material exhibited a high capacity of 288 mA h g-1 at 500 mA g-1, and this performance was attributed to a combination of the redox-active units and the porous structure of PCT-1. The experimental process involved the reaction of 1,2-Dimethoxybenzene(cas: 91-16-7).Product Details of 91-16-7

The Article related to hexahydroxytriphenylene crystalline porous structure lithium ion battery, Electrochemical, Radiational, and Thermal Energy Technology: Energy-Conversion Devices and Their Components and other aspects.Product Details of 91-16-7

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

Lee, Junwoo et al. published their research in Advanced Energy Materials in 2020 |CAS: 578-58-5

The Article related to lead capturable hole transport dopant solar cell electronic property, Electrochemical, Radiational, and Thermal Energy Technology: Energy-Conversion Devices and Their Components and other aspects.Application In Synthesis of 2-Methylanisole

On February 28, 2020, Lee, Junwoo; Kim, Guan-Woo; Kim, Minjun; Park, Sang Ah; Park, Taiho published an article.Application In Synthesis of 2-Methylanisole The title of the article was Nonaromatic Green-Solvent-Processable, Dopant-Free, and Lead-Capturable Hole Transport Polymers in Perovskite Solar Cells with High Efficiency. And the article contained the following:

With the recent developments in the efficiency of perovskite solar cells (PSCs), diverse functionalities are necessary for next-generation charge-transport layers. Specifically, the hole-transport layer (HTL) in the various synthesized materials modified with functional groups is explored. A novel donor-acceptor type polymer, alkoxy-PTEG, composed of benzo[1,2-b:4,5:b’]dithiophene and tetraethylene glycol (TEG)-substituted 2,1,3-benzothiadiazole is reported. The alkoxy-PTEG exhibits high solubility even in nonaromatic solvents, such as 3-methylcyclohexanone (3-MC), and can prevent possible lead leakage via chelation. The optical and electronic properties of alkoxy-PTEG are thoroughly analyzed. Finally, a dopant-free alkoxy-PTEG device processed with 3-MC exhibits 19.9% efficiency and a device with 2-Me anisole, which is a reported aromatic food additive, exhibits 21.2% efficiency in a tin oxide planar structure. The PSC device shows 88% stability after 30 d at ambient conditions (40-50% relative humidity and room temperature). In addition, NMR reveals that TEG groups can chelate lead ions with moderate strength (Kbinding = 2.76), and this strength is considered to be nondestructive to the perovskite lattice to prevent lead leakage. This is the first report to consider lead leakage and provide solutions to reduce this problem. The experimental process involved the reaction of 2-Methylanisole(cas: 578-58-5).Application In Synthesis of 2-Methylanisole

The Article related to lead capturable hole transport dopant solar cell electronic property, Electrochemical, Radiational, and Thermal Energy Technology: Energy-Conversion Devices and Their Components and other aspects.Application In Synthesis of 2-Methylanisole

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

Waddell, Lachlan J. N. et al. published their research in Synthesis in 2022 |CAS: 578-58-5

The Article related to diaryl sulfonamide one pot preparation, arene primary sulfonamide amidation iron copper catalyst, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Sulfenic, Sulfinic, and Sulfonic Acids and Derivatives and other aspects.Synthetic Route of 578-58-5

On October 31, 2022, Waddell, Lachlan J. N.; Henry, Martyn C.; Mostafa, Mohamed A. B.; Sutherland, Andrew published an article.Synthetic Route of 578-58-5 The title of the article was One-Pot Synthesis of Diaryl Sulfonamides using an Iron- and Copper-Catalyzed Aryl C-H Amidation Process. And the article contained the following:

A one-pot, two-stage synthesis of diaryl sulfonamides using sequential iron and copper catalysis is developed. Regioselective para-iodination of activated arenes by the super Lewis acid, iron triflimide and N-iodosuccinimide (NIS), is followed by a copper(I)-catalyzed N-arylation reaction. The process is found to be applicable for the coupling of a range of anisoles, anilines and acetanilides with primary sulfonamides and is used for the one-pot synthesis of biol. important compounds The experimental process involved the reaction of 2-Methylanisole(cas: 578-58-5).Synthetic Route of 578-58-5

The Article related to diaryl sulfonamide one pot preparation, arene primary sulfonamide amidation iron copper catalyst, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Sulfenic, Sulfinic, and Sulfonic Acids and Derivatives and other aspects.Synthetic Route of 578-58-5

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

Yuan, Shuqing et al. published their research in Synthesis in 2021 |CAS: 93-04-9

The Article related to pyridinylphenyl ether chromium catalyst reductive deoxygenation, methoxymethylnaphthalene chromium catalyst reductive deoxygenation, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Hydrocarbons (Saturated and Unsaturated Side Chains) and other aspects.Application of 93-04-9

On September 30, 2021, Yuan, Shuqing; Ling, Liang; Tang, Jinghua; Luo, Meiming; Zeng, Xiaoming published an article.Application of 93-04-9 The title of the article was Chromium-Catalyzed Reductive Cleavage of Unactivated Aromatic and Benzylic C-O Bonds. And the article contained the following:

Reductive cleavage of aromatic and benzylic C-O bonds by chromium catalysis was reported. This deoxygenative reaction was promoted by low-cost CrCl2 precatalyst combined with poly(Me hydrogen siloxane) as the mild reducing agent, providing a strategy in forming reduced motifs by cleavage of unactivated C-O bonds. A range of functional groups such as bromide, chloride, fluoride, hydroxyl, amino and alkoxycarbonyl was retained in the reduction The experimental process involved the reaction of 2-Methoxynaphthalene(cas: 93-04-9).Application of 93-04-9

The Article related to pyridinylphenyl ether chromium catalyst reductive deoxygenation, methoxymethylnaphthalene chromium catalyst reductive deoxygenation, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Hydrocarbons (Saturated and Unsaturated Side Chains) and other aspects.Application of 93-04-9

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

Panja, Subir et al. published their research in Chemical Science in 2022 |CAS: 91-16-7

The Article related to arene alpha beta unsaturated ester regioselective olefination, non directed palladium catalyst electrooxidative fujiwara moritani, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Hydrocarbons (Saturated and Unsaturated Side Chains) and other aspects.Synthetic Route of 91-16-7

Panja, Subir; Ahsan, Salman; Pal, Tanay; Kolb, Simon; Ali, Wajid; Sharma, Sulekha; Das, Chandan; Grover, Jagrit; Dutta, Arnab; Werz, Daniel B.; Paul, Amit; Maiti, Debabrata published an article in 2022, the title of the article was Non-directed Pd-catalysed electrooxidative olefination of arenes.Synthetic Route of 91-16-7 And the article contains the following content:

The Fujiwara-Moritani reaction is a powerful tool for the olefination of arenes by Pd-catalyzed C-H activation. However, the need for superstoichiometric amounts of toxic chem. oxidants makes the reaction unattractive from an environmental and atom-economical view. Herein, authors report the first non-directed and regioselective olefination of simple arenes via an electrooxidative Fujiwara-Moritani reaction. The versatility of this operator-friendly approach was demonstrated by a broad substrate scope which includes arenes, heteroarenes and a variety of olefins. Electroanal. studies suggest the involvement of a Pd(II)/Pd(IV) catalytic cycle via a Pd(III) intermediate. The experimental process involved the reaction of 1,2-Dimethoxybenzene(cas: 91-16-7).Synthetic Route of 91-16-7

The Article related to arene alpha beta unsaturated ester regioselective olefination, non directed palladium catalyst electrooxidative fujiwara moritani, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Hydrocarbons (Saturated and Unsaturated Side Chains) and other aspects.Synthetic Route of 91-16-7

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

Tang, Ren-Jin et al. published their research in Journal of Organic Chemistry in 2018 |CAS: 321-28-8

The Article related to arene benzylic alc friedel crafts benzylation bisulfate, diarylmethane preparation, bisulfate friedel crafts benzylation catalyst, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Hydrocarbons (Saturated and Unsaturated Side Chains) and other aspects.Application of 321-28-8

On November 16, 2018, Tang, Ren-Jin; Milcent, Thierry; Crousse, Benoit published an article.Application of 321-28-8 The title of the article was Bisulfate Salt-Catalyzed Friedel-Crafts Benzylation of Arenes with Benzylic Alcohols. And the article contained the following:

A method of direct Friedel-Crafts benzylation of arenes with benzylic alcs. using cheap and readily available bisulfate salt as the catalyst in hexafluoroisopropanol, is reported. The catalytic system is powerful with a quite diverse group of functionalized arenes and benzylic alcs. These mild conditions provide a straightforward synthesis of a variety of unsym. diarylmethanes in high yield with good to high regioselectivity. An SN1 mechanism involving activation of the hydroxy group through a hydrogen bond is proposed. The experimental process involved the reaction of 1-Fluoro-2-methoxybenzene(cas: 321-28-8).Application of 321-28-8

The Article related to arene benzylic alc friedel crafts benzylation bisulfate, diarylmethane preparation, bisulfate friedel crafts benzylation catalyst, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Hydrocarbons (Saturated and Unsaturated Side Chains) and other aspects.Application of 321-28-8

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

Lamola, Jairus L. et al. published their research in RSC Advances in 2021 |CAS: 93-04-9

The Article related to phosphacyclic ligand preparation, biaryl preparation, aryl halide phenylboronic acid suzuki miyaura coupling palladium catalyst, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Hydrocarbons (Saturated and Unsaturated Side Chains) and other aspects.Category: ethers-buliding-blocks

Lamola, Jairus L.; Moshapo, Paseka T.; Holzapfel, Cedric W.; Maumela, Munaka Christopher published an article in 2021, the title of the article was Evaluation of P-bridged biaryl phosphine ligands in palladium-catalyzed Suzuki-Miyaura cross-coupling reactions.Category: ethers-buliding-blocks And the article contains the following content:

A family of biaryl phosphacyclic ligands derived from phobane and phosphatrioxa-adamantane frameworks was described. The rigid biaryl phosphacycles were efficient for synthesis of biaryls ArAr1 [Ar = 3-MeC6H4, 2-naphthyl, 2-thienyl, etc.; Ar1 = Ph, 2-MeC6H4, 2,6-di-MeC6H3] via palladium-catalyzed Suzuki-Miyaura cross-coupling of aryl bromides/chlorides with phenylboronic acids. In particular, coupling reactions of the challenging sterically hindered and heterocyclic substrates were viable at room temperature The experimental process involved the reaction of 2-Methoxynaphthalene(cas: 93-04-9).Category: ethers-buliding-blocks

The Article related to phosphacyclic ligand preparation, biaryl preparation, aryl halide phenylboronic acid suzuki miyaura coupling palladium catalyst, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Hydrocarbons (Saturated and Unsaturated Side Chains) and other aspects.Category: ethers-buliding-blocks

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

Zhang, Wenxuan et al. published their research in Journal of Organic Chemistry in 2022 |CAS: 150-78-7

The Article related to axially chiral styrene preparation enantioselective strong bronsted acid catalyst, alkynyphenol aromatic ether friedel crafts, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Hydrocarbons (Saturated and Unsaturated Side Chains) and other aspects.Synthetic Route of 150-78-7

On July 15, 2022, Zhang, Wenxuan; Sun, Jiaying; Lian, Zhendong; Song, Ran; Yang, Daoshan; Lv, Jian published an article.Synthetic Route of 150-78-7 The title of the article was Enantioselective Friedel-Crafts Reaction of 2-Alkynyphenols with Aromatic Ethers by Chiral Bronsted Acid Catalysis. And the article contained the following:

Herein, authors report chiral strong Bronsted acid-catalyzed enantioselective Friedel-Crafts reaction of 2-alkynyphenols with aromatic ethers. The reaction affords the corresponding axially chiral styrenes in up to 91% yield and 97% ee. The experimental process involved the reaction of 1,4-Dimethoxybenzene(cas: 150-78-7).Synthetic Route of 150-78-7

The Article related to axially chiral styrene preparation enantioselective strong bronsted acid catalyst, alkynyphenol aromatic ether friedel crafts, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Hydrocarbons (Saturated and Unsaturated Side Chains) and other aspects.Synthetic Route of 150-78-7

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