Six-Coordinate Nitrato Complexes of Iron Porphyrins with Trans S‑Donor Ligands
The reaction of dimethyl sulfide (DMS) and tetrahydrothiophene (THT) with thin, amorphous layers of the nitrato complexes Fe(Por)(η2-O2NO) (Por = meso-tetraphenylporphyrinato dianion or meso-tetra-p-tolylporphyrinato dianion) at low temperature leads to formation of the corresponding six-coordinat...
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Veröffentlicht in: | Inorganic chemistry 2018-05, Vol.57 (9), p.4795-4798 |
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creator | Kurtikyan, Tigran S Gulyan, Gurgen M Minasyan, Hayk S Hovhannisyan, Astghik A Ford, Peter C |
description | The reaction of dimethyl sulfide (DMS) and tetrahydrothiophene (THT) with thin, amorphous layers of the nitrato complexes Fe(Por)(η2-O2NO) (Por = meso-tetraphenylporphyrinato dianion or meso-tetra-p-tolylporphyrinato dianion) at low temperature leads to formation of the corresponding six-coordinate complexes Fe(Por)(L)(η1-ONO2) (L = DMS, THT) as characterized by Fourier transform infrared and optical spectroscopy measurements. Adduct formation was accompanied by bidentate-to-monodentate linkage isomerization of the nitrato ligand, with the FeIII center remaining in a high-spin electronic state. These adducts are thermally unstable; warming to room temperature restores the initial Fe(Por)(η2-O2NO) species. |
doi_str_mv | 10.1021/acs.inorgchem.8b00253 |
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Adduct formation was accompanied by bidentate-to-monodentate linkage isomerization of the nitrato ligand, with the FeIII center remaining in a high-spin electronic state. 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These adducts are thermally unstable; warming to room temperature restores the initial Fe(Por)(η2-O2NO) species.</description><issn>0020-1669</issn><issn>1520-510X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqFkMlOwzAQhi0EglJ4BJCPXFK8xFmOKGyVKqjUInGzHMdpXSVxsBPR3ngFXpEnwVVLr0gjzWj0_7N8AFxhNMKI4Fsh3Ug3xi7kUtWjJEeIMHoEBpgRFDCM3o_BwPdQgKMoPQPnzq0QQikNo1NwRtKI0iSkAzCd6XWQGWML3YhOwRfdWdEZmJm6rdRaOWhKOLamgVNj2-XG6sbBT90t4dwKX85-vr7vjb8DTvRCNIW7ACelqJy63OcheHt8mGfPweT1aZzdTQJB06QLSlYkSShzQVKUK1zEgrISs1jGaSGZYpQUoaJRkpdSRmmS5qVKipJRRZUPTOkQ3OzmttZ89Mp1vNZOqqoSjTK94wQRGhMW-jQEbCeV1jhnVclbq2thNxwjvoXJPUx-gMn3ML3ver-iz2tVHFx_9LwA7wRb_8r0tvEf_zP0F1cQhuA</recordid><startdate>20180507</startdate><enddate>20180507</enddate><creator>Kurtikyan, Tigran S</creator><creator>Gulyan, Gurgen M</creator><creator>Minasyan, Hayk S</creator><creator>Hovhannisyan, Astghik A</creator><creator>Ford, Peter C</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5509-9912</orcidid><orcidid>https://orcid.org/0000-0002-7472-5966</orcidid></search><sort><creationdate>20180507</creationdate><title>Six-Coordinate Nitrato Complexes of Iron Porphyrins with Trans S‑Donor Ligands</title><author>Kurtikyan, Tigran S ; Gulyan, Gurgen M ; Minasyan, Hayk S ; Hovhannisyan, Astghik A ; Ford, Peter C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a398t-f5d884cba290be1d7a35f157c79dc5e532d4e368bfcc6989bfe8df53e3ee3e133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kurtikyan, Tigran S</creatorcontrib><creatorcontrib>Gulyan, Gurgen M</creatorcontrib><creatorcontrib>Minasyan, Hayk S</creatorcontrib><creatorcontrib>Hovhannisyan, Astghik A</creatorcontrib><creatorcontrib>Ford, Peter C</creatorcontrib><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>Kurtikyan, Tigran S</au><au>Gulyan, Gurgen M</au><au>Minasyan, Hayk S</au><au>Hovhannisyan, Astghik A</au><au>Ford, Peter C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Six-Coordinate Nitrato Complexes of Iron Porphyrins with Trans S‑Donor Ligands</atitle><jtitle>Inorganic chemistry</jtitle><addtitle>Inorg. Chem</addtitle><date>2018-05-07</date><risdate>2018</risdate><volume>57</volume><issue>9</issue><spage>4795</spage><epage>4798</epage><pages>4795-4798</pages><issn>0020-1669</issn><eissn>1520-510X</eissn><abstract>The reaction of dimethyl sulfide (DMS) and tetrahydrothiophene (THT) with thin, amorphous layers of the nitrato complexes Fe(Por)(η2-O2NO) (Por = meso-tetraphenylporphyrinato dianion or meso-tetra-p-tolylporphyrinato dianion) at low temperature leads to formation of the corresponding six-coordinate complexes Fe(Por)(L)(η1-ONO2) (L = DMS, THT) as characterized by Fourier transform infrared and optical spectroscopy measurements. Adduct formation was accompanied by bidentate-to-monodentate linkage isomerization of the nitrato ligand, with the FeIII center remaining in a high-spin electronic state. These adducts are thermally unstable; warming to room temperature restores the initial Fe(Por)(η2-O2NO) species.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>29633843</pmid><doi>10.1021/acs.inorgchem.8b00253</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-5509-9912</orcidid><orcidid>https://orcid.org/0000-0002-7472-5966</orcidid><oa>free_for_read</oa></addata></record> |
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title | Six-Coordinate Nitrato Complexes of Iron Porphyrins with Trans S‑Donor Ligands |
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