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
Electron spin relaxation times T and T of Tb and Tm in 1:1 water:ethanol and of Tb doped (2%) in crystalline La(oxalate) decahydrate were measured between about 4.2 and 10 K. Both cations are non-Kramers ions and have J = 6 ground states. Echo-detected spectra are compared with CW spectra and with field-stepped direct-detected EPR spectra. Due to the strong temperature dependence of T, measurements were not made above 10 K. Between about 4.2 and 6 K T is strongly concentration dependent between 1 and ~50 mM. T values at 4.2 K are in the μs range which is orders of magnitude faster than for 3d transition metals. Phase memory times, T, are less than 500 ns, which is short relative to values observed for 3d transition metals and organic radicals at 4 K. T is longer in the oxalate lattice which is attributed to the lower proton concentration in oxalate than in the organic solvent, which decreases nuclear spin diffusion. The rigidity of the crystalline lattice also may contribute to longer T.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8224541 | PMC |
http://dx.doi.org/10.1007/s00723-020-01262-6 | DOI Listing |
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