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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Two lanthanide coordination polymers (CPs) {[Er(Hmtbd)(Hmtbd)(HO)]·2HO} () and [Yb(Hmtbd)(Hmtbd)(HO)] () carrying an N-heterocyclic carboxylate ligand 5-(3-methylformate-1-1,2,4-triazole-1-methyl)benzen-1,3-dicarboxylate (Hmtbd) were prepared under solvothermal conditions. The single-crystal X-ray diffraction data demonstrate that and are isostructural and display 1D chain structure. Alternating current (AC) impedance measurements illustrate that the highest proton conductivities of and can attain 5.09 × 10 and 3.09 × 10 S·cm at 100 °C and 98% relative humidity (RH), respectively. The value of exceeds those of most reported lanthanide-based crystalline materials and ranks second among the described Er-CPs under similar conditions, whereas the value for is the highest proton conductivity among the previous Yb-CPs. Coupled with the structural analyses of the two CPs and HO vapor adsorption, the calculated values help to deduce their proton conductive mechanisms. Notably, the N-heterocyclic units (triazole), carboxyl, and hydrogen-bonding network all play key roles in the proton-transfer process. The prominent proton conductive abilities of both CPs show great promise as efficient proton conductors.
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http://dx.doi.org/10.1021/acs.inorgchem.1c01616 | DOI Listing |