Isolation and electronic structures of derivatized manganocene, ferrocene and cobaltocene anions
The discovery of ferrocene nearly 70 years ago marked the genesis of metallocene chemistry. Although the ferrocenium cation was discovered soon afterwards, a derivatized ferrocenium dication was only isolated in 2016 and the monoanion of ferrocene has only been observed in low-temperature electroche...
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Veröffentlicht in: | Nature chemistry 2021-03, Vol.13 (3), p.243-248 |
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description | The discovery of ferrocene nearly 70 years ago marked the genesis of metallocene chemistry. Although the ferrocenium cation was discovered soon afterwards, a derivatized ferrocenium dication was only isolated in 2016 and the monoanion of ferrocene has only been observed in low-temperature electrochemical studies. Here we report the isolation of a derivatized ferrocene anion in the solid state as part of an isostructural family of 3
d
metallocenates, which consist of anionic complexes of a metal centre (manganese, iron or cobalt) sandwiched between two bulky Cp
ttt
ligands (where Cp
ttt
is {1,2,4-C
5
H
2
t
Bu
3
}). These thermally and air-sensitive complexes decompose rapidly above −30 °C; however, we were able to characterize all metallocenates by a wide range of physical techniques and ab initio calculations. These data have allowed us to map the electronic structures of this metallocenate family, including an unexpected high-spin
S
= 3/2 ground state for the 19
e
−
derivatized ferrocene anion.
Unlike ferrocene and its cationic counterpart ferrocenium, the ferrocene monoanion is an unusual species that has been observed through low-temperature electrochemical studies. Now, a family of isostructural 3
d
metallocenates has been isolated that consists of a manganocene, a cobaltocene and a high-spin ferrocene anion stabilized by cyclopentadienyl ligands bearing bulky aliphatic groups. |
doi_str_mv | 10.1038/s41557-020-00595-w |
format | Article |
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d
metallocenates, which consist of anionic complexes of a metal centre (manganese, iron or cobalt) sandwiched between two bulky Cp
ttt
ligands (where Cp
ttt
is {1,2,4-C
5
H
2
t
Bu
3
}). These thermally and air-sensitive complexes decompose rapidly above −30 °C; however, we were able to characterize all metallocenates by a wide range of physical techniques and ab initio calculations. These data have allowed us to map the electronic structures of this metallocenate family, including an unexpected high-spin
S
= 3/2 ground state for the 19
e
−
derivatized ferrocene anion.
Unlike ferrocene and its cationic counterpart ferrocenium, the ferrocene monoanion is an unusual species that has been observed through low-temperature electrochemical studies. Now, a family of isostructural 3
d
metallocenates has been isolated that consists of a manganocene, a cobaltocene and a high-spin ferrocene anion stabilized by cyclopentadienyl ligands bearing bulky aliphatic groups.</description><identifier>ISSN: 1755-4330</identifier><identifier>EISSN: 1755-4349</identifier><identifier>DOI: 10.1038/s41557-020-00595-w</identifier><identifier>PMID: 33318673</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>639/638/263 ; 639/638/263/406 ; 639/638/563/606 ; 639/638/563/979 ; 639/638/911 ; Analytical Chemistry ; Anions ; Biochemistry ; Cations ; Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science ; Cobalt ; Coordination compounds ; Electrochemistry ; Inorganic and Physical Chemistry ; Inorganic Chemistry ; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY ; Ligands ; Low temperature ; Manganese ; Organic Chemistry ; Physical Chemistry</subject><ispartof>Nature chemistry, 2021-03, Vol.13 (3), p.243-248</ispartof><rights>The Author(s), under exclusive licence to Springer Nature Limited 2020</rights><rights>The Author(s), under exclusive licence to Springer Nature Limited 2020.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c604t-f837e32c788d01450aea1b278728291dd0d952387d6694e2aae0c2e6df63d0193</citedby><cites>FETCH-LOGICAL-c604t-f837e32c788d01450aea1b278728291dd0d952387d6694e2aae0c2e6df63d0193</cites><orcidid>0000-0002-4320-2548 ; 0000-0002-5916-8786 ; 0000-0002-0880-3225 ; 0000-0001-6742-3620 ; 0000-0002-2481-4063 ; 0000-0001-8225-3252 ; 0000-0003-1575-7754 ; 0000-0002-8604-0171 ; 0000000208803225 ; 0000000259168786 ; 0000000224814063 ; 0000000286040171 ; 0000000315757754 ; 0000000243202548 ; 0000000167423620 ; 0000000182253252</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33318673$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/servlets/purl/1760584$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Goodwin, Conrad A. P.</creatorcontrib><creatorcontrib>Giansiracusa, Marcus J.</creatorcontrib><creatorcontrib>Greer, Samuel M.</creatorcontrib><creatorcontrib>Nicholas, Hannah M.</creatorcontrib><creatorcontrib>Evans, Peter</creatorcontrib><creatorcontrib>Vonci, Michele</creatorcontrib><creatorcontrib>Hill, Stephen</creatorcontrib><creatorcontrib>Chilton, Nicholas F.</creatorcontrib><creatorcontrib>Mills, David P.</creatorcontrib><creatorcontrib>Los Alamos National Lab. (LANL), Los Alamos, NM (United States)</creatorcontrib><title>Isolation and electronic structures of derivatized manganocene, ferrocene and cobaltocene anions</title><title>Nature chemistry</title><addtitle>Nat. Chem</addtitle><addtitle>Nat Chem</addtitle><description>The discovery of ferrocene nearly 70 years ago marked the genesis of metallocene chemistry. Although the ferrocenium cation was discovered soon afterwards, a derivatized ferrocenium dication was only isolated in 2016 and the monoanion of ferrocene has only been observed in low-temperature electrochemical studies. Here we report the isolation of a derivatized ferrocene anion in the solid state as part of an isostructural family of 3
d
metallocenates, which consist of anionic complexes of a metal centre (manganese, iron or cobalt) sandwiched between two bulky Cp
ttt
ligands (where Cp
ttt
is {1,2,4-C
5
H
2
t
Bu
3
}). These thermally and air-sensitive complexes decompose rapidly above −30 °C; however, we were able to characterize all metallocenates by a wide range of physical techniques and ab initio calculations. These data have allowed us to map the electronic structures of this metallocenate family, including an unexpected high-spin
S
= 3/2 ground state for the 19
e
−
derivatized ferrocene anion.
Unlike ferrocene and its cationic counterpart ferrocenium, the ferrocene monoanion is an unusual species that has been observed through low-temperature electrochemical studies. Now, a family of isostructural 3
d
metallocenates has been isolated that consists of a manganocene, a cobaltocene and a high-spin ferrocene anion stabilized by cyclopentadienyl ligands bearing bulky aliphatic groups.</description><subject>639/638/263</subject><subject>639/638/263/406</subject><subject>639/638/563/606</subject><subject>639/638/563/979</subject><subject>639/638/911</subject><subject>Analytical Chemistry</subject><subject>Anions</subject><subject>Biochemistry</subject><subject>Cations</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Cobalt</subject><subject>Coordination compounds</subject><subject>Electrochemistry</subject><subject>Inorganic and Physical Chemistry</subject><subject>Inorganic Chemistry</subject><subject>INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY</subject><subject>Ligands</subject><subject>Low temperature</subject><subject>Manganese</subject><subject>Organic Chemistry</subject><subject>Physical Chemistry</subject><issn>1755-4330</issn><issn>1755-4349</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kU9v1DAQxSNERUvhC3BAEVw4EBj_dy6VUFWgUiUucDZee7JNlbWL7bRqP33Npl0KB062Nb_3ZjyvaV4R-ECA6Y-ZEyFUBxQ6ANGL7vpJc0CUEB1nvH-6uzPYb57nfAEgBSPyWbPPGCNaKnbQ_DzNcbJljKG1wbc4oSsphtG1uaTZlTlhbuPQekzjVeVu0bcbG9Y2RIcB37cDprS9bvUuruxUHt7VNb9o9gY7ZXx5fx42Pz6ffD_-2p19-3J6_OmscxJ46QbNFDLqlNYeCBdg0ZIVVVpRTXviPfheUKaVl7LnSK1FcBSlHySrgp4dNkeL7-W82qCvE5RkJ3OZxo1NNyba0fxdCeO5WccroyQBTqEavFkMYi6jyW4s6M5dDKFuxBAlQWheoXf3XVL8NWMuZjNmh9NkA8Y5G8oVUM241hV9-w96EecU6g4q1VdOSKYqRRfKpZhzwmE3MQHzO2WzpGxqymabsrmuoteP_7qTPMRaAbYAuZbCGtOf3v-xvQN0cbRO</recordid><startdate>20210301</startdate><enddate>20210301</enddate><creator>Goodwin, Conrad A. 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P.</creatorcontrib><creatorcontrib>Giansiracusa, Marcus J.</creatorcontrib><creatorcontrib>Greer, Samuel M.</creatorcontrib><creatorcontrib>Nicholas, Hannah M.</creatorcontrib><creatorcontrib>Evans, Peter</creatorcontrib><creatorcontrib>Vonci, Michele</creatorcontrib><creatorcontrib>Hill, Stephen</creatorcontrib><creatorcontrib>Chilton, Nicholas F.</creatorcontrib><creatorcontrib>Mills, David P.</creatorcontrib><creatorcontrib>Los Alamos National Lab. (LANL), Los Alamos, NM (United States)</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Chemoreception Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV - Hybrid</collection><collection>OSTI.GOV</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nature chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Goodwin, Conrad A. P.</au><au>Giansiracusa, Marcus J.</au><au>Greer, Samuel M.</au><au>Nicholas, Hannah M.</au><au>Evans, Peter</au><au>Vonci, Michele</au><au>Hill, Stephen</au><au>Chilton, Nicholas F.</au><au>Mills, David P.</au><aucorp>Los Alamos National Lab. (LANL), Los Alamos, NM (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Isolation and electronic structures of derivatized manganocene, ferrocene and cobaltocene anions</atitle><jtitle>Nature chemistry</jtitle><stitle>Nat. Chem</stitle><addtitle>Nat Chem</addtitle><date>2021-03-01</date><risdate>2021</risdate><volume>13</volume><issue>3</issue><spage>243</spage><epage>248</epage><pages>243-248</pages><issn>1755-4330</issn><eissn>1755-4349</eissn><abstract>The discovery of ferrocene nearly 70 years ago marked the genesis of metallocene chemistry. Although the ferrocenium cation was discovered soon afterwards, a derivatized ferrocenium dication was only isolated in 2016 and the monoanion of ferrocene has only been observed in low-temperature electrochemical studies. Here we report the isolation of a derivatized ferrocene anion in the solid state as part of an isostructural family of 3
d
metallocenates, which consist of anionic complexes of a metal centre (manganese, iron or cobalt) sandwiched between two bulky Cp
ttt
ligands (where Cp
ttt
is {1,2,4-C
5
H
2
t
Bu
3
}). These thermally and air-sensitive complexes decompose rapidly above −30 °C; however, we were able to characterize all metallocenates by a wide range of physical techniques and ab initio calculations. These data have allowed us to map the electronic structures of this metallocenate family, including an unexpected high-spin
S
= 3/2 ground state for the 19
e
−
derivatized ferrocene anion.
Unlike ferrocene and its cationic counterpart ferrocenium, the ferrocene monoanion is an unusual species that has been observed through low-temperature electrochemical studies. Now, a family of isostructural 3
d
metallocenates has been isolated that consists of a manganocene, a cobaltocene and a high-spin ferrocene anion stabilized by cyclopentadienyl ligands bearing bulky aliphatic groups.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>33318673</pmid><doi>10.1038/s41557-020-00595-w</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-4320-2548</orcidid><orcidid>https://orcid.org/0000-0002-5916-8786</orcidid><orcidid>https://orcid.org/0000-0002-0880-3225</orcidid><orcidid>https://orcid.org/0000-0001-6742-3620</orcidid><orcidid>https://orcid.org/0000-0002-2481-4063</orcidid><orcidid>https://orcid.org/0000-0001-8225-3252</orcidid><orcidid>https://orcid.org/0000-0003-1575-7754</orcidid><orcidid>https://orcid.org/0000-0002-8604-0171</orcidid><orcidid>https://orcid.org/0000000208803225</orcidid><orcidid>https://orcid.org/0000000259168786</orcidid><orcidid>https://orcid.org/0000000224814063</orcidid><orcidid>https://orcid.org/0000000286040171</orcidid><orcidid>https://orcid.org/0000000315757754</orcidid><orcidid>https://orcid.org/0000000243202548</orcidid><orcidid>https://orcid.org/0000000167423620</orcidid><orcidid>https://orcid.org/0000000182253252</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 639/638/263 639/638/263/406 639/638/563/606 639/638/563/979 639/638/911 Analytical Chemistry Anions Biochemistry Cations Chemistry Chemistry and Materials Science Chemistry/Food Science Cobalt Coordination compounds Electrochemistry Inorganic and Physical Chemistry Inorganic Chemistry INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY Ligands Low temperature Manganese Organic Chemistry Physical Chemistry |
title | Isolation and electronic structures of derivatized manganocene, ferrocene and cobaltocene anions |
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