Fluoroalkane derivative, gelling agent and gel composition
A technology of derivatives and fluoroalkanes, applied in the field of carbon dioxide absorbing compositions, which can solve the problems of few examples and the like
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preparation example Construction
[0078] The preparation method of the gel composition of the present embodiment is not particularly limited, and can be mixed while heating a non-aqueous solvent, a gelling agent (that is, compound (1) or compound (2)), and other additives, After obtaining a uniform mixed solution, the temperature of the mixed solution is lowered to prepare the gel composition of the present embodiment. There is no particular requirement on the mixing order of the components. It is preferable to mix the gelling agent after preparing a solution consisting of a non-aqueous solvent and additives in advance, since it is easier to obtain a uniform mixed solution.
[0079] The electrode of this embodiment is an electrode for an electrochemical device containing one or more compounds (1) or compounds (2). In the method of adding the compound (1) or compound (2) to the electrode, for example, it may be introduced at the same time when preparing the electrode active material mixture, or it may be coated...
Embodiment 1~8、 comparative example 1~3
[0107] Gelation ability was evaluated by adding any one of various non-aqueous solvents shown in Tables 1 to 3 to compounds represented by the following formulas (3) to (12). The results are shown in Tables 1-3.
[0108] Stability evaluation was performed by adding any one of various non-aqueous solvents shown in Table 4 to compounds represented by the following formulas (4) to (12). The results are shown in Table 4.
Embodiment 9~11
[0110] Gelation ability was evaluated by adding any one of various ionic liquids shown in Table 5 to compounds represented by the following formulas (3), (4) and (13). The results are shown in Table 5.
[0111]
[0112]
[0113] In addition, the compound represented by said Formula (3) (it is called compound (3). The same applies hereinafter) was synthesize|combined by the following method.
[0114] First, compound (a) is obtained by the following route. Specifically, in a 200mL eggplant-shaped bottle, 2-(perfluorohexyl)-1-iodoethane 15.04g (3.17×10 -2 mol) and p-bromothiophenol 5.97g (3.16×10 -2 mol) and dry tetrahydrofuran (dry THF) 10mL solution, add triethylamine 4.88g (4.82×10 -2 mol), using an oil bath at 84°C to reflux for 20 hours. After returning to room temperature, a solid was confirmed in the solution, and the solid was removed by suction filtration.
[0115] After transferring the filtrate to a 300 mL separating funnel, cyclopentyl methyl ether was adde...
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