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
Following the recent preparation of infinitene ( , , 862-871), a computational (ωB97XD/6-311G(d)) exploration of 42 isomeric compounds with 12 fused phenyl rings identified structures with linking number of zero (ring, saddle, and ribbon shapes), two (infinitene-like shape), and one (Möbius infinitene shape) is reported. An infinitene isomer composed of two [5]helicene fragments connected to two stacked phenyl rings and a Möbius infinitene isomer are identified that are more stable than the known infinitene. The energies of the structures are examined by assessing their macrocyclization (strain) energies, π-stacking, and possible aromaticity. Examples of fused phenyl molecules with linking numbers of 3, 4, 5, and 6 are shown, indicating the potential topological range that these molecules can possess.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1021/acs.joc.2c02975 | DOI Listing |
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