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
Hexaazatrinaphthylene (HATNA) derivatives with six alkylsulfanyl chains of different length (hexyl, octyl, decyl and dodecyl) have been designed to obtain new potential electron-carrier materials. The electron-deficient nature of these compounds has been demonstrated by cyclic voltammetry. Their thermotropic behaviour has been studied by means of differential scanning calorimetry and polarised optical microscopy. The supramolecular organisation of these discotic molecules has been explored by temperature-dependent X-ray diffraction on powders and oriented samples. In addition to various liquid crystalline columnar phases (Col(hd), Col(rd)), an anisotropic plastic crystal phase is demonstrated to exist. The charge-carrier mobilities have been measured with the pulse-radiolysis time-resolved microwave-conductivity technique. They are found to be higher in the crystalline than in the liquid crystalline phases, with maximum values of approximately 0.9 and 0.3 cm(2) V(-1) s(-1), respectively, for the decylsulfanyl derivative. Mobilities strongly depend on the nature of the side chains.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1002/chem.200400586 | DOI Listing |
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