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
Here, we demonstrate the use of Pt(0) nanoparticles immobilised on a polymeric monolithic support as a ligand-free heterogeneous catalytic system for the reduction of (13) CO2 at room temperature and atmospheric pressure. The described system effectively reduces (13) CO2 with dihydrosilanes as the hydrogen source to yield a mixture of silylformates, silylacetals and methoxysilanes, which upon further hydrolysis with D2 O, produces their respective C1-type products, that is H(13) COOD, (13) CH2 (OD)2 and (13) CH3 OD. If a monohydrosilane was used as the hydrogen source, a selective reduction of (13) CO2 to a product mixture of only silylformates was observed. Addition of diethylamine to this reaction mixture results in the formation of H(13) COOH and Et2 N(13) CHO. This robust catalytic system is not only maintenance-free and simple to handle, as compared with organometallic and organocatalyst systems, but also shows 3- to 11-fold better catalytic activity and exhibits higher turnover numbers (TONs) up to 21 900 (activity=6.22 kg CO 2 gPt (-1) bar(-1) ).
Download full-text PDF |
Source |
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http://dx.doi.org/10.1002/chem.201304845 | DOI Listing |
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