Reactivity of [ReOCl3(PPh3)2] towards substituted anilines
The reactivity of [ReOCl3(PPh3)2] towards o‐toluidine, m‐toluidine, o‐fluoroaniline, m‐fluoroaniline, p‐bromoaniline, p‐chloroaniline and p‐anisidine was examined and novel rhenium(V) imido complexes [Re(NC6H4R)Cl3(PPh3)2] (R=o‐Me, m‐Me, o‐F, m‐F, p‐Cl, p‐Br, p‐OMe) were obtained. The resulting prod...
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creator | Cvetković, Olivera Theiner, Johannes Wolff, Mariusz J. Hultzsch, Kai C. |
description | The reactivity of [ReOCl3(PPh3)2] towards o‐toluidine, m‐toluidine, o‐fluoroaniline, m‐fluoroaniline, p‐bromoaniline, p‐chloroaniline and p‐anisidine was examined and novel rhenium(V) imido complexes [Re(NC6H4R)Cl3(PPh3)2] (R=o‐Me, m‐Me, o‐F, m‐F, p‐Cl, p‐Br, p‐OMe) were obtained. The resulting products were characterized by elemental analysis, electrospray ionization high‐resolution mass spectrometry (ESI‐HRMS), 1H, 13C{1H}, 19F and 31P{1H} NMR, FT‐IR spectroscopy, and X‐ray crystallography. For m‐toluidine, m‐fluroaniline and p‐chloroaniline, the rhenium(V) imido‐amino mononuclear [Re(NC6H4R)Cl3(H2NC6H4R)(PPh3)] (R=m‐F, p‐Cl) complexes and the binuclear [{Re(m‐NC6H4Me)Cl2(m‐H2NC6H4Me)(PPh3)}2O] complex were isolated as side products and characterized by X‐ray crystallography. All six‐coordinate rhenium(V) complexes display distorted octahedral coordination geometry. |
doi_str_mv | 10.1002/zaac.202400007 |
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The resulting products were characterized by elemental analysis, electrospray ionization high‐resolution mass spectrometry (ESI‐HRMS), 1H, 13C{1H}, 19F and 31P{1H} NMR, FT‐IR spectroscopy, and X‐ray crystallography. For m‐toluidine, m‐fluroaniline and p‐chloroaniline, the rhenium(V) imido‐amino mononuclear [Re(NC6H4R)Cl3(H2NC6H4R)(PPh3)] (R=m‐F, p‐Cl) complexes and the binuclear [{Re(m‐NC6H4Me)Cl2(m‐H2NC6H4Me)(PPh3)}2O] complex were isolated as side products and characterized by X‐ray crystallography. 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The resulting products were characterized by elemental analysis, electrospray ionization high‐resolution mass spectrometry (ESI‐HRMS), 1H, 13C{1H}, 19F and 31P{1H} NMR, FT‐IR spectroscopy, and X‐ray crystallography. For m‐toluidine, m‐fluroaniline and p‐chloroaniline, the rhenium(V) imido‐amino mononuclear [Re(NC6H4R)Cl3(H2NC6H4R)(PPh3)] (R=m‐F, p‐Cl) complexes and the binuclear [{Re(m‐NC6H4Me)Cl2(m‐H2NC6H4Me)(PPh3)}2O] complex were isolated as side products and characterized by X‐ray crystallography. All six‐coordinate rhenium(V) complexes display distorted octahedral coordination geometry.</description><subject>Aniline</subject><subject>aniline derivatives</subject><subject>Anisidine</subject><subject>Chemical analysis</subject><subject>Crystallography</subject><subject>imido complexes</subject><subject>Infrared spectroscopy</subject><subject>Mass spectrometry</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Rhenium</subject><subject>Toluidine</subject><subject>X-ray diffraction</subject><issn>0044-2313</issn><issn>1521-3749</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><recordid>eNqFkE1LAzEQQIMoWKtXzwte9LA1ySRN11tZ6gcUWopeFAlJNsGUtVuTrKX-erdU9Ohc5vLeDDyEzgkeEIzp9ZdSZkAxZbgbcYB6hFOSg2DFIephzFhOgcAxOolx2REEc95DNwurTPKfPm2zxmUvCzsra7icz9_gir5mqdmoUMUstjomn9pkq0ytfO1XNp6iI6fqaM9-dh893U4ey_t8Ort7KMfT3AChIqeCKgeVBsEtY9w54GKomQCti1ElNKOu4FYw66qR5hYMNxhbZpkyGjtDoI8u9nfXoflobUxy2bRh1b2UgIEIRodi1FGDPWVCE2OwTq6Df1dhKwmWuz5y10f-9umEYi9sfG23_9DyeTwu_9xveodoWg</recordid><startdate>20240402</startdate><enddate>20240402</enddate><creator>Cvetković, Olivera</creator><creator>Theiner, Johannes</creator><creator>Wolff, Mariusz J.</creator><creator>Hultzsch, Kai C.</creator><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>WIN</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-1739-6684</orcidid><orcidid>https://orcid.org/0000-0002-9265-7557</orcidid><orcidid>https://orcid.org/0000-0002-5298-035X</orcidid><orcidid>https://orcid.org/0009-0007-8171-3457</orcidid></search><sort><creationdate>20240402</creationdate><title>Reactivity of [ReOCl3(PPh3)2] towards substituted anilines</title><author>Cvetković, Olivera ; Theiner, Johannes ; Wolff, Mariusz J. ; Hultzsch, Kai C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3127-272af3db375e445ff3576b473bb98d7b42f95e74efd8b5e3c5c00e4e4acb0fc13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Aniline</topic><topic>aniline derivatives</topic><topic>Anisidine</topic><topic>Chemical analysis</topic><topic>Crystallography</topic><topic>imido complexes</topic><topic>Infrared spectroscopy</topic><topic>Mass spectrometry</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Rhenium</topic><topic>Toluidine</topic><topic>X-ray diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cvetković, Olivera</creatorcontrib><creatorcontrib>Theiner, Johannes</creatorcontrib><creatorcontrib>Wolff, Mariusz J.</creatorcontrib><creatorcontrib>Hultzsch, Kai C.</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Online Library Free Content</collection><collection>CrossRef</collection><jtitle>Zeitschrift für anorganische und allgemeine Chemie (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cvetković, Olivera</au><au>Theiner, Johannes</au><au>Wolff, Mariusz J.</au><au>Hultzsch, Kai C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reactivity of [ReOCl3(PPh3)2] towards substituted anilines</atitle><jtitle>Zeitschrift für anorganische und allgemeine Chemie (1950)</jtitle><date>2024-04-02</date><risdate>2024</risdate><volume>650</volume><issue>7</issue><epage>n/a</epage><issn>0044-2313</issn><eissn>1521-3749</eissn><abstract>The reactivity of [ReOCl3(PPh3)2] towards o‐toluidine, m‐toluidine, o‐fluoroaniline, m‐fluoroaniline, p‐bromoaniline, p‐chloroaniline and p‐anisidine was examined and novel rhenium(V) imido complexes [Re(NC6H4R)Cl3(PPh3)2] (R=o‐Me, m‐Me, o‐F, m‐F, p‐Cl, p‐Br, p‐OMe) were obtained. The resulting products were characterized by elemental analysis, electrospray ionization high‐resolution mass spectrometry (ESI‐HRMS), 1H, 13C{1H}, 19F and 31P{1H} NMR, FT‐IR spectroscopy, and X‐ray crystallography. For m‐toluidine, m‐fluroaniline and p‐chloroaniline, the rhenium(V) imido‐amino mononuclear [Re(NC6H4R)Cl3(H2NC6H4R)(PPh3)] (R=m‐F, p‐Cl) complexes and the binuclear [{Re(m‐NC6H4Me)Cl2(m‐H2NC6H4Me)(PPh3)}2O] complex were isolated as side products and characterized by X‐ray crystallography. All six‐coordinate rhenium(V) complexes display distorted octahedral coordination geometry.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/zaac.202400007</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-1739-6684</orcidid><orcidid>https://orcid.org/0000-0002-9265-7557</orcidid><orcidid>https://orcid.org/0000-0002-5298-035X</orcidid><orcidid>https://orcid.org/0009-0007-8171-3457</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aniline aniline derivatives Anisidine Chemical analysis Crystallography imido complexes Infrared spectroscopy Mass spectrometry NMR Nuclear magnetic resonance Rhenium Toluidine X-ray diffraction |
title | Reactivity of [ReOCl3(PPh3)2] towards substituted anilines |
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