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
The construction of the unsymmetrical 1,2-bis(silylene) pentacarbonyl chromium(0) complex was achieved through the reaction of chlorosilylene with half an equivalent of KCr(CO). X-ray diffraction analysis of confirms the formation of the Si-Si bond and the coordination of one of the silicon atoms to the Cr center. Density functional theory (DFT) calculations disclose that highest occupied molecular orbital (HOMO) mainly corresponds to the lone pair of electrons on the silicon atom and the σ-bonding interaction between two Si atoms. Based on its unique electronic structure, its diverse reactivity toward the transition metal compounds and small molecules was investigated in detail. The reactions of with Fe(CO) or CuCl yielded the 1,2-bis(silylene)-stabilized heterobimetallic complex or oxidized product , respectively. Additionally, treatments of with selenium, CO, or MeSiN led to the formation of the corresponding selenium-, oxo-, and nitrogen-bridged complexes . All compounds were characterized by multinuclear NMR spectroscopy and X-ray crystallography.
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Source |
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http://dx.doi.org/10.1021/acs.inorgchem.4c01803 | DOI Listing |
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