Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
The high thermal stability and chemical durability of amide-linked covalent organic frameworks (amide COFs) make them a promising material for a range of new applications. Nevertheless, the low reversibility of the amide bond presents a significant challenge to the direct synthesis of amide-bonded COFs. In this paper, we present a simple method for synthesizing amide COFs. The synthesis of imine-linked COFs was initially achieved through the reaction of 2,4,6-tris(4-aminophenyl)-1,3,5-triazine and 2,5-dimethoxybenzene-1,4-dicarboxaldehyde. Subsequently, amide COFs were synthesized via the oxidation of the imine bond into an amide bond, utilizing ammonium persulfate as the oxidizing agent. Due to the difference of link bond, two COFs separately displayed distinct and significant fluorescence enhancement for Al and Ce, which was highly sensitive and less affected by environmental factors. The strategy offers a novel approach to the convenient and environmentally benign synthesis of amide COFs, which may facilitate their wider applications.
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Source |
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http://dx.doi.org/10.1016/j.saa.2024.125620 | DOI Listing |
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