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
Scopoletin is highly fluorescent in water and acts as a photoacid exhibiting excited-state proton transfer, ESPT, competitive with fluorescence. Its absorbance and emission spectral characteristics yield ground-state and excited-state pK values of 7.4 ± 0.1 and 1.4 ± 0.1, respectively. The pK implies an ESPT rate constant an order of magnitude smaller than that for umbelliferone. This report provides quantum yield measurements in water that are comparable to quinine sulfate, and fluorescence lifetime values that are on a par with other similar coumarins yet provide insight into the ESPT process. The scopoletin anion is observed in tetrahydrofuran by reaction with a strong base. The Stokes shift of aqueous scopoletin is >100 nm in the pH range 3 to 7 due in part to its action as a photoacid. Modeling by density functional theory methods provides reasonable support for the experimental results.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1007/s10895-019-02471-4 | DOI Listing |
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