Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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A series of chalcone-based compounds with varied functional groups were designed and synthesized through green chemistry. Polarity-tuned solvatochromic photophysical studies were thoroughly performed using steady-state absorption and emission spectroscopic techniques. These donor-acceptor structured chalcones were capable of exhibiting excitation dependent fluorescence (EDF), which is widely known as the red edge effect, with a large Stokes shift above 140 nm, making them capable of accessing the yellow to blue region of the spectrum. Furthermore, the ease of tuning the fluorescence property was utilized in the field of biosensors to obtain tunable brilliant blue to green colors for the first time. Computational studies indicated the presence of relatively compact states, which might be one of the key factors responsible for the red edge effect.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12035810 | PMC |
http://dx.doi.org/10.1039/d4ra06978a | DOI Listing |