Shin, Jaeho et al. published their research in Koen Yoshishu – Nippon Setchaku Gakkai Nenji Taikai in 2021 | CAS: 112-49-2

2,5,8,11-Tetraoxadodecane (cas: 112-49-2) belongs to ethers. Ether is less polar than esters, alcohols or amines because of the oxygen atom that is unable to participate in hydrogen bonding due to the presence of bulky alkyl groups on both sides of the oxygen atom. But ether is more polar than alkenes. Electron-deficient reagents are also stabilized by ethers. For example, borane (BH3) is a useful reagent for making alcohols. Pure borane exists as its dimer, diborane (B2H6), a toxic gas that is inconvenient and hazardous to use. Borane forms stable complexes with ethers, however, and it is often supplied and used as its liquid complex with tetrahydrofuran (THF).Electric Literature of C8H18O4

Rapid epoxy cure and transamination behavior in vinylogous urethane epoxy using glyme-metal ions was written by Shin, Jaeho;Yi, Mobeom;Kim, Hyunjoong. And the article was included in Koen Yoshishu – Nippon Setchaku Gakkai Nenji Taikai in 2021.Electric Literature of C8H18O4 This article mentions the following:

Here we fabricated three different types of ILs containing lithium or zinc ligand with glyme mol. The unique functions of ionic liquids to intervene oxirane and carbonyl oxygen made the metal-glyme mixture a potential latent cure accelerator in epoxy cure reaction and a catalyst of transamination reaction at the same time. In the experiment, the researchers used many compounds, for example, 2,5,8,11-Tetraoxadodecane (cas: 112-49-2Electric Literature of C8H18O4).

2,5,8,11-Tetraoxadodecane (cas: 112-49-2) belongs to ethers. Ether is less polar than esters, alcohols or amines because of the oxygen atom that is unable to participate in hydrogen bonding due to the presence of bulky alkyl groups on both sides of the oxygen atom. But ether is more polar than alkenes. Electron-deficient reagents are also stabilized by ethers. For example, borane (BH3) is a useful reagent for making alcohols. Pure borane exists as its dimer, diborane (B2H6), a toxic gas that is inconvenient and hazardous to use. Borane forms stable complexes with ethers, however, and it is often supplied and used as its liquid complex with tetrahydrofuran (THF).Electric Literature of C8H18O4

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

Han, Binghong et al. published their research in ACS Applied Materials & Interfaces in 2021 | CAS: 112-49-2

2,5,8,11-Tetraoxadodecane (cas: 112-49-2) belongs to ethers. The oxygen atom in ethers are more electronegative than carbon, thus the hydrogens which are alpha to the ethers are more acidic than the simple hydrocarbons. Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3.HPLC of Formula: 112-49-2

Probing the Reactivity of the Active Material of a Li-Ion Silicon Anode with Common Battery Solvents was written by Han, Binghong;Zhang, Yunya;Liao, Chen;Trask, Stephen E.;Li, Xiang;Uppuluri, Ritesh;Vaughey, John T.;Key, Baris;Dogan, Fulya. And the article was included in ACS Applied Materials & Interfaces in 2021.HPLC of Formula: 112-49-2 This article mentions the following:

Calculations and modeling have shown that replacing the traditional graphite anode with silicon can greatly improve the energy d. of lithium-ion batteries. However, the large volume change of silicon particles and high reactivity of lithiated silicon when in contact with the electrolyte lead to rapid capacity fading during charging/discharging processes. In this report, we use specific lithium silicides (LS) as model compounds to systematically study the reaction between lithiated Si and different electrolyte solvents, which provides a powerful platform to deconvolute and evaluate the degradation of various organic solvents in contact with the active lithiated Si-electrode surface after lithiation. NMR (NMR) characterization results show that a cyclic carbonate such as ethylene carbonate is chem. less stable than a linear carbonate such as ethylmethyl carbonate, fluoroethylene carbonate, and triglyme as they are found to be more stable when mixed with LS model compounds Guided by the exptl. results, two ethylene carbonate (EC)-free electrolytes are studied, and the electrochem. results show improvements with graphite-free Si electrodes relative to the traditional ethylene-carbonate-based electrolytes. More importantly, the study contributes to our understanding of the significant fundamental chem. and electrochem. stability differences between silicon and traditional graphite lithium-ion battery (LIB) anodes and suggests a focused development of electrolytes with specific chem. stability vs lithiated silicon which can passivate the surface more effectively. In the experiment, the researchers used many compounds, for example, 2,5,8,11-Tetraoxadodecane (cas: 112-49-2HPLC of Formula: 112-49-2).

2,5,8,11-Tetraoxadodecane (cas: 112-49-2) belongs to ethers. The oxygen atom in ethers are more electronegative than carbon, thus the hydrogens which are alpha to the ethers are more acidic than the simple hydrocarbons. Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3.HPLC of Formula: 112-49-2

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

Nguyen, Manh Tien et al. published their research in Fluid Phase Equilibria in 2020 | CAS: 112-49-2

2,5,8,11-Tetraoxadodecane (cas: 112-49-2) belongs to ethers. Ether is less polar than esters, alcohols or amines because of the oxygen atom that is unable to participate in hydrogen bonding due to the presence of bulky alkyl groups on both sides of the oxygen atom. Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3.Reference of 112-49-2

Effects of zwitterionic molecules on ionic association in ethylene oxide-based electrolytes was written by Nguyen, Manh Tien;Shao, Qing. And the article was included in Fluid Phase Equilibria in 2020.Reference of 112-49-2 This article mentions the following:

This work investigates the effect of zwitterionic mols. on ionic association in ethylene oxide (EO)-based electrolytes using mol. dynamics simulations. Zwitterionic mols. can associate with cations and anions because they possess both pos. and neg. charged groups. This unique feature can be leveraged to develop electrolytes with high ionic conductivity if we understand how zwitterionic mols. influence ionic associations We investigate the ionic associations in the electrolytes composed of oligo(ethylene oxide) (EO) (EOx, x = 2, 3, 4, and 5), LiTFSI and zwitterionic mols. containing cationic imidazole group and anionic sulfonate group using mol. dynamics simulations. The analyzed properties include the radial distribution functions between Li+, [TFSI], EOx and zwitterionic mols., the structures and dynamics of Li+-[TFSI], Li+– EOx and Li+-zwitterion associations, and the diffusion coefficients of Li+, [TFSI], EOx and zwitterionic mols. The simulation results show two distinct effects of zwitterionic mols. on ionic associations in the electrolytes. First, they could release Li+ from the trapping effect of EOx chains and accelerate Li+ transport. Second, they can associate with Li+ themselves and slow down the Li+ transport. The competition between these two effects relates to the length of the EOx chains. Our simulations suggest that zwitterionic mols. could help manipulate the ionic conductivity of polyethylene oxide electrolytes. In the experiment, the researchers used many compounds, for example, 2,5,8,11-Tetraoxadodecane (cas: 112-49-2Reference of 112-49-2).

2,5,8,11-Tetraoxadodecane (cas: 112-49-2) belongs to ethers. Ether is less polar than esters, alcohols or amines because of the oxygen atom that is unable to participate in hydrogen bonding due to the presence of bulky alkyl groups on both sides of the oxygen atom. Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3.Reference of 112-49-2

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

Nguyen, Manh Tien et al. published their research in Fluid Phase Equilibria in 2020 | CAS: 112-49-2

2,5,8,11-Tetraoxadodecane (cas: 112-49-2) belongs to ethers. Ether is less polar than esters, alcohols or amines because of the oxygen atom that is unable to participate in hydrogen bonding due to the presence of bulky alkyl groups on both sides of the oxygen atom. Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3.Reference of 112-49-2

Effects of zwitterionic molecules on ionic association in ethylene oxide-based electrolytes was written by Nguyen, Manh Tien;Shao, Qing. And the article was included in Fluid Phase Equilibria in 2020.Reference of 112-49-2 This article mentions the following:

This work investigates the effect of zwitterionic mols. on ionic association in ethylene oxide (EO)-based electrolytes using mol. dynamics simulations. Zwitterionic mols. can associate with cations and anions because they possess both pos. and neg. charged groups. This unique feature can be leveraged to develop electrolytes with high ionic conductivity if we understand how zwitterionic mols. influence ionic associations We investigate the ionic associations in the electrolytes composed of oligo(ethylene oxide) (EO) (EOx, x = 2, 3, 4, and 5), LiTFSI and zwitterionic mols. containing cationic imidazole group and anionic sulfonate group using mol. dynamics simulations. The analyzed properties include the radial distribution functions between Li+, [TFSI], EOx and zwitterionic mols., the structures and dynamics of Li+-[TFSI], Li+– EOx and Li+-zwitterion associations, and the diffusion coefficients of Li+, [TFSI], EOx and zwitterionic mols. The simulation results show two distinct effects of zwitterionic mols. on ionic associations in the electrolytes. First, they could release Li+ from the trapping effect of EOx chains and accelerate Li+ transport. Second, they can associate with Li+ themselves and slow down the Li+ transport. The competition between these two effects relates to the length of the EOx chains. Our simulations suggest that zwitterionic mols. could help manipulate the ionic conductivity of polyethylene oxide electrolytes. In the experiment, the researchers used many compounds, for example, 2,5,8,11-Tetraoxadodecane (cas: 112-49-2Reference of 112-49-2).

2,5,8,11-Tetraoxadodecane (cas: 112-49-2) belongs to ethers. Ether is less polar than esters, alcohols or amines because of the oxygen atom that is unable to participate in hydrogen bonding due to the presence of bulky alkyl groups on both sides of the oxygen atom. Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3.Reference of 112-49-2

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