C07D327/04

Process for producing sulfonic acid group-containing monomer

The present disclosure is directed to provide a process capable of producing a sulfonic acid group-containing monomer in a good yield, which can be used as a raw material of fluorine-based polymer electrolytes, such as membranes for fuel cells, catalyst binder polymers for fuel cells, and membranes for chlor-alkali electrolysis. A process for producing a sulfonic acid group-containing monomer represented by the general formula (3) includes the step of mixing and stirring a cyclic compound represented by the general formula (1) and a silanol compound represented by the general formula (2).

Process for producing sulfonic acid group-containing monomer

The present disclosure is directed to provide a process capable of producing a sulfonic acid group-containing monomer in a good yield, which can be used as a raw material of fluorine-based polymer electrolytes, such as membranes for fuel cells, catalyst binder polymers for fuel cells, and membranes for chlor-alkali electrolysis. A process for producing a sulfonic acid group-containing monomer represented by the general formula (3) includes the step of mixing and stirring a cyclic compound represented by the general formula (1) and a silanol compound represented by the general formula (2).

Process for the purification of organic sulfur compounds
11518752 · 2022-12-06 · ·

A process for the purification of organic sulfur compounds involves bringing the organic sulfur compounds, in a liquid phase, into contact with an oxide of a metal from groups VIIb or VIIIb and an oxide of a metal from groups Ia to IIIa of the periodic system, or alternatively, with a mixed-oxide thereof; for a contact period of at least 1 minute. Afterwards, the oxides and the organic sulfur compounds are separated.

Process for the purification of organic sulfur compounds
11518752 · 2022-12-06 · ·

A process for the purification of organic sulfur compounds involves bringing the organic sulfur compounds, in a liquid phase, into contact with an oxide of a metal from groups VIIb or VIIIb and an oxide of a metal from groups Ia to IIIa of the periodic system, or alternatively, with a mixed-oxide thereof; for a contact period of at least 1 minute. Afterwards, the oxides and the organic sulfur compounds are separated.

Reduction of the odor of monothiocarbonate compounds by addition of oxidants
20220289697 · 2022-09-15 · ·

A process reduces the odor of compounds with al least one five-membered cyclic monothiocarbonate group, referred to as monothiocarbonate compounds. The monothiocarbonate compounds are in are liquid phase and are brought into contact with an oxidant.

Process for the synthesis of polycarbonates from cyclic monothiocarbonates
20220220254 · 2022-07-14 · ·

A process can be used for the synthesis of compounds containing at least one non-cyclic carbonate group, wherein a compound A) containing at least one five-membered cyclic monothiocarbonate group is reacted with at least one hydroxy group of a compound B) or of compound A) itself.

Preparation of a cured polymer comprising urethane groups and silicon atoms
11384207 · 2022-07-12 · ·

A process prepares a cross-linked polymer containing urethane groups and silicon atoms. Starting materials of the process include a compound A) with a five-membered cyclic monothiocarbonate group, a compound B) with an amino group, selected from primary or secondary amino groups or blocked amino groups, and optionally, a compound C) with at least one functional group that reacts with a group —SH. One of the compounds contains a silicon-functional group. In one example of the process, compounds A) and B), and optionally C), are then reacted under exclusion of water to obtain a polymer with curable silicon-functional groups. The polymer is applied to a surface, gap, or a three-dimensional template. The silicon-functional groups are cured with ambient water. The polymer contains 0.001 to 0.3 mol of silicon per 100 g of the polymer.

Preparation of a cured polymer comprising urethane groups and silicon atoms
11384207 · 2022-07-12 · ·

A process prepares a cross-linked polymer containing urethane groups and silicon atoms. Starting materials of the process include a compound A) with a five-membered cyclic monothiocarbonate group, a compound B) with an amino group, selected from primary or secondary amino groups or blocked amino groups, and optionally, a compound C) with at least one functional group that reacts with a group —SH. One of the compounds contains a silicon-functional group. In one example of the process, compounds A) and B), and optionally C), are then reacted under exclusion of water to obtain a polymer with curable silicon-functional groups. The polymer is applied to a surface, gap, or a three-dimensional template. The silicon-functional groups are cured with ambient water. The polymer contains 0.001 to 0.3 mol of silicon per 100 g of the polymer.

ELECTROLYTE, ELECTROCHEMICAL DEVICE, AND ELECTRONIC DEVICE

An electrolyte includes a compound represented by formula I-A, where A.sup.1, A.sup.2, and A.sup.3 are each independently selected from formula I-B or formula I-C, and at least two of A.sup.1, A.sup.2, and A.sup.3 are formula I-C. In formula I-A, n is selected from integers 1 to 10, and m is selected from 0 or 1. In formula I-B and formula I-C, custom-characterrepresents a site at which two adjacent atoms are joined. The electrolyte can significantly improve high-temperature storage performance, cycle performance, and floating charge performance of the electrochemical device.

##STR00001##

ELECTROLYTE AND ELECTROCHEMICAL APPARATUS
20220216515 · 2022-07-07 ·

An electrochemical apparatus, including a positive electrode, a negative electrode, an separator, and an electrolyte, wherein the positive electrode comprises a current collector and a positive active material layer, and the positive active material layer comprises a positive active material; and the electrolyte comprises a compound of Formula I:

##STR00001## wherein R.sub.11, R.sub.12, R.sub.13, R.sub.14, R.sub.15 and R.sub.16 are each independently selected from: H, halogen, and the following substituted or unsubstituted groups: a C.sub.1-8 alkyl group, a C.sub.2-8 alkenyl group, a C.sub.2-8 alkynyl group, or a C.sub.6-12 aryl group; and an amount of the compound of Formula I required per 1 g of the positive active material is about 0.001 g to about 0.064 g. The present application can effectively improve high-temperature storage and high-temperature cycle performance of an electrochemical apparatus.