Fluoro Nitrenoid Complexes FN=MF 2 (M=Co, Rh, Ir): Electronic Structure Dichotomy and Formation of Nitrido Fluorides N≡MF 3
The fluoronitrenoid metal complexes FNCoF and FNRhF as well as the first ternary Rh and Ir complexes NIrF and NRhF are described. They were obtained by the reaction of excited Group-9 metal atoms with NF and their IR spectra, isolated in solid rare gases (neon and argon), were recorded. Aided by the...
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creator | Stüker, Tony Hohmann, Thomas Beckers, Helmut Riedel, Sebastian |
description | The fluoronitrenoid metal complexes FNCoF
and FNRhF
as well as the first ternary Rh
and Ir
complexes NIrF
and NRhF
are described. They were obtained by the reaction of excited Group-9 metal atoms with NF
and their IR spectra, isolated in solid rare gases (neon and argon), were recorded. Aided by the observed
N isotope shifts and quantum-chemical predictions, all four stretching fundamentals of the novel complexes were safely assigned. The F-N stretching frequencies of the fluoronitrenoid complexes FNCoF
(1056.8 cm
) and FNRhF
(872.6 cm
) are very different and their N-M bonds vary greatly. In FNCoF
, the FN ligand is singly bonded to Co and bears considerable iminyl/nitrene radical character, while the N-Rh bond in FNRhF
is a strong double bond with comparatively strong σ- and π-bonds. The anticipated rearrangement of FNCoF
to the nitrido Co
complex is predicted to be endothermic and was not observed. |
doi_str_mv | 10.1002/anie.202010950 |
format | Article |
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and FNRhF
as well as the first ternary Rh
and Ir
complexes NIrF
and NRhF
are described. They were obtained by the reaction of excited Group-9 metal atoms with NF
and their IR spectra, isolated in solid rare gases (neon and argon), were recorded. Aided by the observed
N isotope shifts and quantum-chemical predictions, all four stretching fundamentals of the novel complexes were safely assigned. The F-N stretching frequencies of the fluoronitrenoid complexes FNCoF
(1056.8 cm
) and FNRhF
(872.6 cm
) are very different and their N-M bonds vary greatly. In FNCoF
, the FN ligand is singly bonded to Co and bears considerable iminyl/nitrene radical character, while the N-Rh bond in FNRhF
is a strong double bond with comparatively strong σ- and π-bonds. The anticipated rearrangement of FNCoF
to the nitrido Co
complex is predicted to be endothermic and was not observed.</description><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.202010950</identifier><identifier>PMID: 32886443</identifier><language>eng</language><publisher>Germany</publisher><ispartof>Angewandte Chemie International Edition, 2020-12, Vol.59 (51), p.23174-23179</ispartof><rights>2020 The Authors. Published by Wiley-VCH GmbH.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1073-3679a09023dfd34ec5d768d66f10352c5896820266d9f1997dcc75f9d6cd55d63</citedby><cites>FETCH-LOGICAL-c1073-3679a09023dfd34ec5d768d66f10352c5896820266d9f1997dcc75f9d6cd55d63</cites><orcidid>0000-0003-4552-5719 ; 0000-0002-6161-3586</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32886443$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stüker, Tony</creatorcontrib><creatorcontrib>Hohmann, Thomas</creatorcontrib><creatorcontrib>Beckers, Helmut</creatorcontrib><creatorcontrib>Riedel, Sebastian</creatorcontrib><title>Fluoro Nitrenoid Complexes FN=MF 2 (M=Co, Rh, Ir): Electronic Structure Dichotomy and Formation of Nitrido Fluorides N≡MF 3</title><title>Angewandte Chemie International Edition</title><addtitle>Angew Chem Int Ed Engl</addtitle><description>The fluoronitrenoid metal complexes FNCoF
and FNRhF
as well as the first ternary Rh
and Ir
complexes NIrF
and NRhF
are described. They were obtained by the reaction of excited Group-9 metal atoms with NF
and their IR spectra, isolated in solid rare gases (neon and argon), were recorded. Aided by the observed
N isotope shifts and quantum-chemical predictions, all four stretching fundamentals of the novel complexes were safely assigned. The F-N stretching frequencies of the fluoronitrenoid complexes FNCoF
(1056.8 cm
) and FNRhF
(872.6 cm
) are very different and their N-M bonds vary greatly. In FNCoF
, the FN ligand is singly bonded to Co and bears considerable iminyl/nitrene radical character, while the N-Rh bond in FNRhF
is a strong double bond with comparatively strong σ- and π-bonds. The anticipated rearrangement of FNCoF
to the nitrido Co
complex is predicted to be endothermic and was not observed.</description><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNo9kE9LwzAYxoMobk6vHiVHhXUmTZM0wg5SVx1sE_xzLjVJWaRtRtqCO_gB_Bh-NT-J2aY7vc_heX4v_AA4x2iEEQqv89roUYhChJGg6AD0MQ1xQDgnhz5HhAQ8prgHTprm3ffjGLFj0CM-sCgiffCZlp11Fi5M63RtjYKJrVal_tANTBfjeQpDeDkfJ3YIn5ZDOHVXN3BSatk6WxsJn1vXybZzGt4ZubStrdYwrxVMravy1tga2mLLNsrC7SujPHnx8_Xt0eQUHBV52eizvzsAr-nkJXkIZo_30-R2FkiMOAkI4yJHAoVEFYpEWlLFWawYKzAiNJQ0Fiz2EhhTosBCcCUlp4VQTCpKFSMDMNpxpbNN43SRrZypcrfOMMo2HrONx2zv0Q8udoNV91Zpta__iyO_e3ZtWg</recordid><startdate>20201214</startdate><enddate>20201214</enddate><creator>Stüker, Tony</creator><creator>Hohmann, Thomas</creator><creator>Beckers, Helmut</creator><creator>Riedel, Sebastian</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0003-4552-5719</orcidid><orcidid>https://orcid.org/0000-0002-6161-3586</orcidid></search><sort><creationdate>20201214</creationdate><title>Fluoro Nitrenoid Complexes FN=MF 2 (M=Co, Rh, Ir): Electronic Structure Dichotomy and Formation of Nitrido Fluorides N≡MF 3</title><author>Stüker, Tony ; Hohmann, Thomas ; Beckers, Helmut ; Riedel, Sebastian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1073-3679a09023dfd34ec5d768d66f10352c5896820266d9f1997dcc75f9d6cd55d63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stüker, Tony</creatorcontrib><creatorcontrib>Hohmann, Thomas</creatorcontrib><creatorcontrib>Beckers, Helmut</creatorcontrib><creatorcontrib>Riedel, Sebastian</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stüker, Tony</au><au>Hohmann, Thomas</au><au>Beckers, Helmut</au><au>Riedel, Sebastian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fluoro Nitrenoid Complexes FN=MF 2 (M=Co, Rh, Ir): Electronic Structure Dichotomy and Formation of Nitrido Fluorides N≡MF 3</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew Chem Int Ed Engl</addtitle><date>2020-12-14</date><risdate>2020</risdate><volume>59</volume><issue>51</issue><spage>23174</spage><epage>23179</epage><pages>23174-23179</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><abstract>The fluoronitrenoid metal complexes FNCoF
and FNRhF
as well as the first ternary Rh
and Ir
complexes NIrF
and NRhF
are described. They were obtained by the reaction of excited Group-9 metal atoms with NF
and their IR spectra, isolated in solid rare gases (neon and argon), were recorded. Aided by the observed
N isotope shifts and quantum-chemical predictions, all four stretching fundamentals of the novel complexes were safely assigned. The F-N stretching frequencies of the fluoronitrenoid complexes FNCoF
(1056.8 cm
) and FNRhF
(872.6 cm
) are very different and their N-M bonds vary greatly. In FNCoF
, the FN ligand is singly bonded to Co and bears considerable iminyl/nitrene radical character, while the N-Rh bond in FNRhF
is a strong double bond with comparatively strong σ- and π-bonds. The anticipated rearrangement of FNCoF
to the nitrido Co
complex is predicted to be endothermic and was not observed.</abstract><cop>Germany</cop><pmid>32886443</pmid><doi>10.1002/anie.202010950</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0003-4552-5719</orcidid><orcidid>https://orcid.org/0000-0002-6161-3586</orcidid></addata></record> |
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language | eng |
recordid | cdi_crossref_primary_10_1002_anie_202010950 |
source | Wiley Online Library All Journals |
title | Fluoro Nitrenoid Complexes FN=MF 2 (M=Co, Rh, Ir): Electronic Structure Dichotomy and Formation of Nitrido Fluorides N≡MF 3 |
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