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
Electrodics of CCl4 reduction in 1-butyl-3-methylimmidazolium tetrafluoroborate [BMIM][BF4] room temperature ionic liquid (RTIL) is reported. A convolutive analysis of the cyclic voltammograms suggests that CCl4 electroreduction follows stepwise (outer sphere) dissociative electron transfer pathway, rather than the sticky dissociative (inner sphere) electron transfer, as in the case of conventional organic solvents. This difference in the mechanism of electron transfer initiated bond cleavage is attributed to the solvent specific effects, namely, stabilization of CCl4*- intermediate radical anion in RTIL, which in turn decreases the electron transfer rate and thus the carbon-halogen bond cleavage rates. Electroreduction of CCl4 in RTIL through outer sphere electron transfer would be a promising pathway for its direct conversion to methane.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/jp809749k | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!