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File: /var/www/html/index.php
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Function: require_once
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Filename: Session/Session.php
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File: /var/www/html/index.php
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Function: require_once
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Filename: helpers/my_audit_helper.php
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File: /var/www/html/application/helpers/my_audit_helper.php
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Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
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Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
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Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
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Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
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Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
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Function: require_once
The non-π-conjugated sulfate system has long been overlooked as potential deep-UV nonlinear optical (NLO) materials. Here we report two asymmetric anhydrous sulfates, namely, NHNaLi(SO) (Ι) and (NH)NaLi(SO) (Π), which consist of non-π-conjugated [SO] anions. Their single crystals can be readily grown by a facile evaporation method from water solution. Both sulfates are transparent down to the deep-UV region. Interestingly, there is a large NLO gap between I and Π, with phase-matching NLO responses of 1.1 and 0.5 times that of the benchmark KHPO, respectively. The first-principles studies reveal that the non-π-conjugated [SO] anions are the dominate NLO-active groups, and the large NLO gap between I and Π can be ascribed to the nonbonding O 2 p orbitals of different orientations in the crystallographically independent S1O groups. This work provides an innovative non-π-conjugated source that is distinct from the traditional π-conjugated ones for deep-UV NLO materials.
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Source |
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http://dx.doi.org/10.1021/jacs.9b00138 | DOI Listing |
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