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Photoionization of stable mesoionic compounds
Photoelectron spectra, electronic structure, reactivity. [Display omitted] •Electronic structures of three mesoionic compounds.•Simulated UV photoelectron spectra of mesoionics in the gas phase.•Relationship between the electronic structures and reactivity of mesoionics. The electronic structures an...
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Published in: | Journal of molecular liquids 2022-10, Vol.363, p.119807, Article 119807 |
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container_title | Journal of molecular liquids |
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creator | Novak, Igor |
description | Photoelectron spectra, electronic structure, reactivity.
[Display omitted]
•Electronic structures of three mesoionic compounds.•Simulated UV photoelectron spectra of mesoionics in the gas phase.•Relationship between the electronic structures and reactivity of mesoionics.
The electronic structures and valence ionizations of three mesoionic compounds: 3-methylsydnone, 3-phenylsydnone and 3-methyl-2-phenyl-1,3,4-thiadiazole-5-thione have been studied using high-level ab initio methods: electron-propagator theory (EPT) and coupled cluster method (IP-EOM-CCSD). We discuss the influence of valence electronic structure on chemical reactivity using global and local electrophilicity indices. We also discuss (non)aromatic character of the studied molecules using information pertaining to photoelectron spectra. |
doi_str_mv | 10.1016/j.molliq.2022.119807 |
format | article |
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[Display omitted]
•Electronic structures of three mesoionic compounds.•Simulated UV photoelectron spectra of mesoionics in the gas phase.•Relationship between the electronic structures and reactivity of mesoionics.
The electronic structures and valence ionizations of three mesoionic compounds: 3-methylsydnone, 3-phenylsydnone and 3-methyl-2-phenyl-1,3,4-thiadiazole-5-thione have been studied using high-level ab initio methods: electron-propagator theory (EPT) and coupled cluster method (IP-EOM-CCSD). We discuss the influence of valence electronic structure on chemical reactivity using global and local electrophilicity indices. We also discuss (non)aromatic character of the studied molecules using information pertaining to photoelectron spectra.</description><identifier>ISSN: 0167-7322</identifier><identifier>EISSN: 1873-3166</identifier><identifier>DOI: 10.1016/j.molliq.2022.119807</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Electronic structure ; Electrophilicities ; Mesoionics ; Photoelectron spectra</subject><ispartof>Journal of molecular liquids, 2022-10, Vol.363, p.119807, Article 119807</ispartof><rights>2022 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c255t-eb5ed1ce17363296b3b49da6b7d68d517ddb299bcec6ff5c80dcc3cc6e1e4f63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Novak, Igor</creatorcontrib><title>Photoionization of stable mesoionic compounds</title><title>Journal of molecular liquids</title><description>Photoelectron spectra, electronic structure, reactivity.
[Display omitted]
•Electronic structures of three mesoionic compounds.•Simulated UV photoelectron spectra of mesoionics in the gas phase.•Relationship between the electronic structures and reactivity of mesoionics.
The electronic structures and valence ionizations of three mesoionic compounds: 3-methylsydnone, 3-phenylsydnone and 3-methyl-2-phenyl-1,3,4-thiadiazole-5-thione have been studied using high-level ab initio methods: electron-propagator theory (EPT) and coupled cluster method (IP-EOM-CCSD). We discuss the influence of valence electronic structure on chemical reactivity using global and local electrophilicity indices. We also discuss (non)aromatic character of the studied molecules using information pertaining to photoelectron spectra.</description><subject>Electronic structure</subject><subject>Electrophilicities</subject><subject>Mesoionics</subject><subject>Photoelectron spectra</subject><issn>0167-7322</issn><issn>1873-3166</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9j8tKxDAYhYMoWEffwEVfoDWXJmk3ggzeYEAXsw_Nn7-Y0jZjUgV9ejvWtauzOBfOR8g1oyWjTN305RiGwb-XnHJeMtbUVJ-QjNVaFIIpdUqyJaYLLTg_Jxcp9ZRSKWuakeL1LczBh8l_t_MieejyNLd2wHzE9GtADmE8hI_JpUty1rVDwqs_3ZD9w_1--1TsXh6ft3e7AriUc4FWomOATAsleKOssFXjWmW1U7WTTDtnedNYQFBdJ6GmDkAAKGRYdUpsSLXOQgwpRezMIfqxjV-GUXMkNr1Zic2R2KzES-12reFy7dNjNAk8ToDOR4TZuOD_H_gBw1Zirw</recordid><startdate>20221001</startdate><enddate>20221001</enddate><creator>Novak, Igor</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20221001</creationdate><title>Photoionization of stable mesoionic compounds</title><author>Novak, Igor</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c255t-eb5ed1ce17363296b3b49da6b7d68d517ddb299bcec6ff5c80dcc3cc6e1e4f63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Electronic structure</topic><topic>Electrophilicities</topic><topic>Mesoionics</topic><topic>Photoelectron spectra</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Novak, Igor</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of molecular liquids</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Novak, Igor</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photoionization of stable mesoionic compounds</atitle><jtitle>Journal of molecular liquids</jtitle><date>2022-10-01</date><risdate>2022</risdate><volume>363</volume><spage>119807</spage><pages>119807-</pages><artnum>119807</artnum><issn>0167-7322</issn><eissn>1873-3166</eissn><abstract>Photoelectron spectra, electronic structure, reactivity.
[Display omitted]
•Electronic structures of three mesoionic compounds.•Simulated UV photoelectron spectra of mesoionics in the gas phase.•Relationship between the electronic structures and reactivity of mesoionics.
The electronic structures and valence ionizations of three mesoionic compounds: 3-methylsydnone, 3-phenylsydnone and 3-methyl-2-phenyl-1,3,4-thiadiazole-5-thione have been studied using high-level ab initio methods: electron-propagator theory (EPT) and coupled cluster method (IP-EOM-CCSD). We discuss the influence of valence electronic structure on chemical reactivity using global and local electrophilicity indices. We also discuss (non)aromatic character of the studied molecules using information pertaining to photoelectron spectra.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.molliq.2022.119807</doi></addata></record> |
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ispartof | Journal of molecular liquids, 2022-10, Vol.363, p.119807, Article 119807 |
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source | ScienceDirect Journals |
subjects | Electronic structure Electrophilicities Mesoionics Photoelectron spectra |
title | Photoionization of stable mesoionic compounds |
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