http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114316171-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d890ad239375a780e6827d3407f15ef3
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G12-08
filingDate 2022-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5d24054f71fdf927a22d6e49b39f7b2c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b53c6720132f6fad524186c5a363365e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_369af72fc961d9400ae489ca0daf2ba4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4680854ee7668f024d91e7b2edf8d77b
publicationDate 2022-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-114316171-A
titleOfInvention Preparation method of novel acylhydrazone bond gel through one-step crosslinking polymerization
abstract The invention provides a preparation method of novel acylhydrazone bond gel by one-step crosslinking polymerization. The method is characterized in that 1,3, 5-benzene trimethyl acyl chloride is used as a starting material and reacts with absolute ethyl alcohol to generate triethyl trimesate, and then the triethyl trimesate reacts with hydrazine hydrate to generate trimesoyl hydrazide. And finally, adopting trimesoyl hydrazine and aldehyde as organic monomers to construct a module, taking dimethyl sulfoxide as a solvent medium according to the Schiff base reaction principle and acylhydrazone covalent bonds as cross-linking points, and rapidly and directly synthesizing a series of novel acylhydrazone bond polymer gels at room temperature in one step. Compared with the existing preparation method of the acylhydrazone bond gel material, the novel acylhydrazone bond gel is completed through one-step crosslinking polymerization of organic monomers of hydrazide and aldehyde, the process that the prior acylhydrazone bond gel material is firstly designed and synthesized into a gel factor and then a crosslinking group is searched is omitted, and the design concept is more advanced and novel. The synthesis method is simple, low in cost, mild in condition, high in reaction rate and yield, and has good development and application potential in the aspect of intelligent materials.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114907278-B
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114907278-A
priorityDate 2022-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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