Ino-Chloridolithates from Ionothermal Synthesis

Anionic lithium-containing species were predicted to impact ionic liquid-based electrochemical applications but have hitherto never been isolated from ionic liquid systems. Here, we report the first representatives of this class of compounds, ino-chloridolithates, comprising [LiCl2]− and [Li2Cl3]− p...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Inorganic chemistry 2021-12, Vol.60 (24), p.19145-19151
Hauptverfasser: Bekiş, Deniz F, Küllmey, Tim, Ghazanfari, Mohammad R, Burda, Robert, Voloshina, Elena, von Randow, Clara A, Fuß, Friederike, Liesegang, Moritz, Paulus, Beate, Pöppler, Ann-Christin, Thiele, Günther
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 19151
container_issue 24
container_start_page 19145
container_title Inorganic chemistry
container_volume 60
creator Bekiş, Deniz F
Küllmey, Tim
Ghazanfari, Mohammad R
Burda, Robert
Voloshina, Elena
von Randow, Clara A
Fuß, Friederike
Liesegang, Moritz
Paulus, Beate
Pöppler, Ann-Christin
Thiele, Günther
description Anionic lithium-containing species were predicted to impact ionic liquid-based electrochemical applications but have hitherto never been isolated from ionic liquid systems. Here, we report the first representatives of this class of compounds, ino-chloridolithates, comprising [LiCl2]− and [Li2Cl3]− polyanions from ionothermal reactions. Such compounds are obtained at moderate temperatures with imidazolium-based ionic liquids and LiCl. The addition of an auxiliary ammonium salt enhances the lattice energy to yield an ammonium lithate in good yields, which enables extensive investigations including solid-state nuclear magnetic resonance, infrared, and Raman spectroscopy. The structural motifs of ino-lithates are related to ino-silicates, as 1D-extended anionic substructures are formed. Despite this analogy, according to density functional theory calculations with periodic boundary conditions, no evidence of covalent bonding in the anionic moieties is found–indicating packing effects to be the main cause for the formation. Based on an in-depth analysis of the different synthetic parameters, this class of compounds is discussed as an intermediate in ionic liquid applications and could serve as a model system for electrochemical lithium-based systems.
doi_str_mv 10.1021/acs.inorgchem.1c02943
format Article
fullrecord <record><control><sourceid>proquest_webof</sourceid><recordid>TN_cdi_webofscience_primary_000730343300001</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2608109789</sourcerecordid><originalsourceid>FETCH-LOGICAL-a351t-383ef7ebe68d06bd804256895c1de5aede8275eb9d00e0508a7f16da7eab3c293</originalsourceid><addsrcrecordid>eNqNkE1Lw0AQhhdRbK3-BKVHQdLOZrvJ5ijBj0LBgwrewmYzsVuS3bqbIP33bkntVU_zHp53ZngIuaYwoxDTuVR-po11n2qN7YwqiLMFOyFjymOIOIWPUzIGCJkmSTYiF95vACBji-ScjNhCpCLmYkzmS2OjfN1Ypyvb6G4tO_TT2tl2urTGdmt0rWymrzsTotf-kpzVsvF4dZgT8v748JY_R6uXp2V-v4ok47SLmGBYp1hiIipIykrAIuaJyLiiFXKJFYo45VhmFQACByHTmiaVTFGWTMUZm5DbYe_W2a8efVe02itsGmnQ9r6IExAUslTsUT6gylnvHdbF1ulWul1Bodi7KoKr4uiqOLgKvZvDib5ssTq2fuUEQAzAN5a29kqjUXjEgs2UAQuLQgKa60522prc9qYL1bv_VwNNB3r_6Mb2zgS1f3z_A4Bemp4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2608109789</pqid></control><display><type>article</type><title>Ino-Chloridolithates from Ionothermal Synthesis</title><source>ACS Publications</source><source>Web of Science - Science Citation Index Expanded - 2021&lt;img src="https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg" /&gt;</source><creator>Bekiş, Deniz F ; Küllmey, Tim ; Ghazanfari, Mohammad R ; Burda, Robert ; Voloshina, Elena ; von Randow, Clara A ; Fuß, Friederike ; Liesegang, Moritz ; Paulus, Beate ; Pöppler, Ann-Christin ; Thiele, Günther</creator><creatorcontrib>Bekiş, Deniz F ; Küllmey, Tim ; Ghazanfari, Mohammad R ; Burda, Robert ; Voloshina, Elena ; von Randow, Clara A ; Fuß, Friederike ; Liesegang, Moritz ; Paulus, Beate ; Pöppler, Ann-Christin ; Thiele, Günther</creatorcontrib><description>Anionic lithium-containing species were predicted to impact ionic liquid-based electrochemical applications but have hitherto never been isolated from ionic liquid systems. Here, we report the first representatives of this class of compounds, ino-chloridolithates, comprising [LiCl2]− and [Li2Cl3]− polyanions from ionothermal reactions. Such compounds are obtained at moderate temperatures with imidazolium-based ionic liquids and LiCl. The addition of an auxiliary ammonium salt enhances the lattice energy to yield an ammonium lithate in good yields, which enables extensive investigations including solid-state nuclear magnetic resonance, infrared, and Raman spectroscopy. The structural motifs of ino-lithates are related to ino-silicates, as 1D-extended anionic substructures are formed. Despite this analogy, according to density functional theory calculations with periodic boundary conditions, no evidence of covalent bonding in the anionic moieties is found–indicating packing effects to be the main cause for the formation. Based on an in-depth analysis of the different synthetic parameters, this class of compounds is discussed as an intermediate in ionic liquid applications and could serve as a model system for electrochemical lithium-based systems.</description><identifier>ISSN: 0020-1669</identifier><identifier>EISSN: 1520-510X</identifier><identifier>DOI: 10.1021/acs.inorgchem.1c02943</identifier><identifier>PMID: 34878258</identifier><language>eng</language><publisher>WASHINGTON: American Chemical Society</publisher><subject>Chemistry ; Chemistry, Inorganic &amp; Nuclear ; Physical Sciences ; Science &amp; Technology</subject><ispartof>Inorganic chemistry, 2021-12, Vol.60 (24), p.19145-19151</ispartof><rights>2021 The Authors. Published by American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>0</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000730343300001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-a351t-383ef7ebe68d06bd804256895c1de5aede8275eb9d00e0508a7f16da7eab3c293</citedby><cites>FETCH-LOGICAL-a351t-383ef7ebe68d06bd804256895c1de5aede8275eb9d00e0508a7f16da7eab3c293</cites><orcidid>0000-0002-3848-3015 ; 0000-0002-5363-4248 ; 0000-0002-0624-1708 ; 0000-0003-2935-9335 ; 0000-0002-1799-1125</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.inorgchem.1c02943$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.inorgchem.1c02943$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>315,781,785,2766,27081,27929,27930,39263,56743,56793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34878258$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bekiş, Deniz F</creatorcontrib><creatorcontrib>Küllmey, Tim</creatorcontrib><creatorcontrib>Ghazanfari, Mohammad R</creatorcontrib><creatorcontrib>Burda, Robert</creatorcontrib><creatorcontrib>Voloshina, Elena</creatorcontrib><creatorcontrib>von Randow, Clara A</creatorcontrib><creatorcontrib>Fuß, Friederike</creatorcontrib><creatorcontrib>Liesegang, Moritz</creatorcontrib><creatorcontrib>Paulus, Beate</creatorcontrib><creatorcontrib>Pöppler, Ann-Christin</creatorcontrib><creatorcontrib>Thiele, Günther</creatorcontrib><title>Ino-Chloridolithates from Ionothermal Synthesis</title><title>Inorganic chemistry</title><addtitle>INORG CHEM</addtitle><addtitle>Inorg. Chem</addtitle><description>Anionic lithium-containing species were predicted to impact ionic liquid-based electrochemical applications but have hitherto never been isolated from ionic liquid systems. Here, we report the first representatives of this class of compounds, ino-chloridolithates, comprising [LiCl2]− and [Li2Cl3]− polyanions from ionothermal reactions. Such compounds are obtained at moderate temperatures with imidazolium-based ionic liquids and LiCl. The addition of an auxiliary ammonium salt enhances the lattice energy to yield an ammonium lithate in good yields, which enables extensive investigations including solid-state nuclear magnetic resonance, infrared, and Raman spectroscopy. The structural motifs of ino-lithates are related to ino-silicates, as 1D-extended anionic substructures are formed. Despite this analogy, according to density functional theory calculations with periodic boundary conditions, no evidence of covalent bonding in the anionic moieties is found–indicating packing effects to be the main cause for the formation. Based on an in-depth analysis of the different synthetic parameters, this class of compounds is discussed as an intermediate in ionic liquid applications and could serve as a model system for electrochemical lithium-based systems.</description><subject>Chemistry</subject><subject>Chemistry, Inorganic &amp; Nuclear</subject><subject>Physical Sciences</subject><subject>Science &amp; Technology</subject><issn>0020-1669</issn><issn>1520-510X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>HGBXW</sourceid><recordid>eNqNkE1Lw0AQhhdRbK3-BKVHQdLOZrvJ5ijBj0LBgwrewmYzsVuS3bqbIP33bkntVU_zHp53ZngIuaYwoxDTuVR-po11n2qN7YwqiLMFOyFjymOIOIWPUzIGCJkmSTYiF95vACBji-ScjNhCpCLmYkzmS2OjfN1Ypyvb6G4tO_TT2tl2urTGdmt0rWymrzsTotf-kpzVsvF4dZgT8v748JY_R6uXp2V-v4ok47SLmGBYp1hiIipIykrAIuaJyLiiFXKJFYo45VhmFQACByHTmiaVTFGWTMUZm5DbYe_W2a8efVe02itsGmnQ9r6IExAUslTsUT6gylnvHdbF1ulWul1Bodi7KoKr4uiqOLgKvZvDib5ssTq2fuUEQAzAN5a29kqjUXjEgs2UAQuLQgKa60522prc9qYL1bv_VwNNB3r_6Mb2zgS1f3z_A4Bemp4</recordid><startdate>20211220</startdate><enddate>20211220</enddate><creator>Bekiş, Deniz F</creator><creator>Küllmey, Tim</creator><creator>Ghazanfari, Mohammad R</creator><creator>Burda, Robert</creator><creator>Voloshina, Elena</creator><creator>von Randow, Clara A</creator><creator>Fuß, Friederike</creator><creator>Liesegang, Moritz</creator><creator>Paulus, Beate</creator><creator>Pöppler, Ann-Christin</creator><creator>Thiele, Günther</creator><general>American Chemical Society</general><general>Amer Chemical Soc</general><scope>BLEPL</scope><scope>DTL</scope><scope>HGBXW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-3848-3015</orcidid><orcidid>https://orcid.org/0000-0002-5363-4248</orcidid><orcidid>https://orcid.org/0000-0002-0624-1708</orcidid><orcidid>https://orcid.org/0000-0003-2935-9335</orcidid><orcidid>https://orcid.org/0000-0002-1799-1125</orcidid></search><sort><creationdate>20211220</creationdate><title>Ino-Chloridolithates from Ionothermal Synthesis</title><author>Bekiş, Deniz F ; Küllmey, Tim ; Ghazanfari, Mohammad R ; Burda, Robert ; Voloshina, Elena ; von Randow, Clara A ; Fuß, Friederike ; Liesegang, Moritz ; Paulus, Beate ; Pöppler, Ann-Christin ; Thiele, Günther</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a351t-383ef7ebe68d06bd804256895c1de5aede8275eb9d00e0508a7f16da7eab3c293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Chemistry</topic><topic>Chemistry, Inorganic &amp; Nuclear</topic><topic>Physical Sciences</topic><topic>Science &amp; Technology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bekiş, Deniz F</creatorcontrib><creatorcontrib>Küllmey, Tim</creatorcontrib><creatorcontrib>Ghazanfari, Mohammad R</creatorcontrib><creatorcontrib>Burda, Robert</creatorcontrib><creatorcontrib>Voloshina, Elena</creatorcontrib><creatorcontrib>von Randow, Clara A</creatorcontrib><creatorcontrib>Fuß, Friederike</creatorcontrib><creatorcontrib>Liesegang, Moritz</creatorcontrib><creatorcontrib>Paulus, Beate</creatorcontrib><creatorcontrib>Pöppler, Ann-Christin</creatorcontrib><creatorcontrib>Thiele, Günther</creatorcontrib><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Web of Science - Science Citation Index Expanded - 2021</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Inorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bekiş, Deniz F</au><au>Küllmey, Tim</au><au>Ghazanfari, Mohammad R</au><au>Burda, Robert</au><au>Voloshina, Elena</au><au>von Randow, Clara A</au><au>Fuß, Friederike</au><au>Liesegang, Moritz</au><au>Paulus, Beate</au><au>Pöppler, Ann-Christin</au><au>Thiele, Günther</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ino-Chloridolithates from Ionothermal Synthesis</atitle><jtitle>Inorganic chemistry</jtitle><stitle>INORG CHEM</stitle><addtitle>Inorg. Chem</addtitle><date>2021-12-20</date><risdate>2021</risdate><volume>60</volume><issue>24</issue><spage>19145</spage><epage>19151</epage><pages>19145-19151</pages><issn>0020-1669</issn><eissn>1520-510X</eissn><abstract>Anionic lithium-containing species were predicted to impact ionic liquid-based electrochemical applications but have hitherto never been isolated from ionic liquid systems. Here, we report the first representatives of this class of compounds, ino-chloridolithates, comprising [LiCl2]− and [Li2Cl3]− polyanions from ionothermal reactions. Such compounds are obtained at moderate temperatures with imidazolium-based ionic liquids and LiCl. The addition of an auxiliary ammonium salt enhances the lattice energy to yield an ammonium lithate in good yields, which enables extensive investigations including solid-state nuclear magnetic resonance, infrared, and Raman spectroscopy. The structural motifs of ino-lithates are related to ino-silicates, as 1D-extended anionic substructures are formed. Despite this analogy, according to density functional theory calculations with periodic boundary conditions, no evidence of covalent bonding in the anionic moieties is found–indicating packing effects to be the main cause for the formation. Based on an in-depth analysis of the different synthetic parameters, this class of compounds is discussed as an intermediate in ionic liquid applications and could serve as a model system for electrochemical lithium-based systems.</abstract><cop>WASHINGTON</cop><pub>American Chemical Society</pub><pmid>34878258</pmid><doi>10.1021/acs.inorgchem.1c02943</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-3848-3015</orcidid><orcidid>https://orcid.org/0000-0002-5363-4248</orcidid><orcidid>https://orcid.org/0000-0002-0624-1708</orcidid><orcidid>https://orcid.org/0000-0003-2935-9335</orcidid><orcidid>https://orcid.org/0000-0002-1799-1125</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0020-1669
ispartof Inorganic chemistry, 2021-12, Vol.60 (24), p.19145-19151
issn 0020-1669
1520-510X
language eng
recordid cdi_webofscience_primary_000730343300001
source ACS Publications; Web of Science - Science Citation Index Expanded - 2021<img src="https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg" />
subjects Chemistry
Chemistry, Inorganic & Nuclear
Physical Sciences
Science & Technology
title Ino-Chloridolithates from Ionothermal Synthesis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-12T02%3A51%3A53IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_webof&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ino-Chloridolithates%20from%20Ionothermal%20Synthesis&rft.jtitle=Inorganic%20chemistry&rft.au=Bekis%CC%A7,%20Deniz%20F&rft.date=2021-12-20&rft.volume=60&rft.issue=24&rft.spage=19145&rft.epage=19151&rft.pages=19145-19151&rft.issn=0020-1669&rft.eissn=1520-510X&rft_id=info:doi/10.1021/acs.inorgchem.1c02943&rft_dat=%3Cproquest_webof%3E2608109789%3C/proquest_webof%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2608109789&rft_id=info:pmid/34878258&rfr_iscdi=true