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: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
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
A supramolecular assembly was constructed based on the tetraphenylethylene derivatives (TPEs) and --cucurbit[10]uril (-Q[10]). Upon introduction of the dye Rhodamine B (RB) into the TPEs@-Q[10] assembly, an energy transfer process can occur from the TPEs@-Q[10] assembly to RB. Moreover, after the addition of Nile Red (NiR), a two-step sequential energy transfer process from the TPEs@-Q[10] assembly to RB and then to NiR can occur. Additionally, the dye Eosin Y (ESY) was introduced into the TPEs@-Q[10] assembly and an energy transfer process can take place from the TPEs@-Q[10] assembly to ESY. To utilize the harvested energy from the TPEs@-Q[10]-RB-NiR and TPEs@-Q[10]-ESY system, we applied the TPEs@-Q[10] assembly-based light-harvesting systems (LHSs) as a catalyst for the advancement of the photocatalytic dehalogenation reaction in aqueous solution. When promoted with 0.5 mol % catalyst, the reaction yield reached 78 and 68%, demonstrating the promising potential of TPEs@-Q[10] assembly-based LHSs in the promotion of the photocatalytic dehalogenation reaction.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1021/acsami.3c19359 | DOI Listing |
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