<?xml version="1.0" encoding="UTF-8"?>
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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1021/acs.inorgchem.8b03366</dc:identifier><dc:language>eng</dc:language><dc:creator>Esteruelas, M.A.</dc:creator><dc:creator>Fernández, I.</dc:creator><dc:creator>García-Yebra, C.</dc:creator><dc:creator>Martín, J.</dc:creator><dc:creator>Oñate, E.</dc:creator><dc:title>Cycloosmathioborane Compounds: Other Manifestations of the Hückel Aromaticity</dc:title><dc:identifier>ART-2019-110659</dc:identifier><dc:description>The discovery of cycloosmathioborane compounds is reported. These species, which are prepared by the simultaneous dehydrogenation of a trihydride hydrogensulfide osmium(IV) complex and a BH 3 NHR 2 amine-borane, bear an Os-S-B three-membered ring, being a manifestation of the 4n + 2 Hückel aromaticity in which n = 0 and where the two p electrons of the ring are provided by the S atom.</dc:description><dc:date>2019</dc:date><dc:source>http://zaguan.unizar.es/record/87530</dc:source><dc:doi>10.1021/acs.inorgchem.8b03366</dc:doi><dc:identifier>http://zaguan.unizar.es/record/87530</dc:identifier><dc:identifier>oai:zaguan.unizar.es:87530</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/E06-17R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/CTQ2016-78205-P</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/CTQ2016-81797-REDC</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/CTQ2017-82935-P</dc:relation><dc:identifier.citation>Inorganic Chemistry 58, 4 (2019), 2265-2269</dc:identifier.citation><dc:rights>All rights reserved</dc:rights><dc:rights>http://www.europeana.eu/rights/rr-f/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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