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Half-Sandwich Nickelacarboranes Derived from [7-(MeO(CH2)2S)-7,8-C2B9H11]
New carboranyl thioethers 1-MeO(CH2)nS-1,2-C2B10H11 (n = 2, 3) were prepared by the alkylation of the trimethylammonium salt of 1-mercapto-ortho-carborane with 1-bromo- 2-methoxyethane and 1-bromo-3-methoxypropane, respectively. Their deboronation with cesium fluoride in ethanol gave the correspondi...
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Published in: | Inorganics 2023-03, Vol.11 (3), p.127 |
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description | New carboranyl thioethers 1-MeO(CH2)nS-1,2-C2B10H11 (n = 2, 3) were prepared by the alkylation of the trimethylammonium salt of 1-mercapto-ortho-carborane with 1-bromo- 2-methoxyethane and 1-bromo-3-methoxypropane, respectively. Their deboronation with cesium fluoride in ethanol gave the corresponding nido-carboranes Cs[7-MeO(CH2)nS-7,8-C2B9H11] (n = 2, 3). The reactions of Cs[7-MeO(CH2)2S-7,8-C2B9H11] with various nickel(II) phosphine complexes [(dppe)NiCl2] and [(R’R2P)2NiCl2] (R = R’ = Ph, Bu; R = Me, R’ = Ph; R = Ph, R’ = Me, Et) were studied and a series of nickelacarboranes 3,3-dppe-1-MeO(CH2)2S-closo-3,1,2-NiC2B9H10 and 3,3- (R’R2P)2-1-MeO(CH2)2S-closo-3,1,2-NiC2B9H10 (R = R’ = Bu; R = Me, R’ = Ph; R = Ph, R’ = Me, Et) was prepared. The molecular crystal structure of 3,3-dppe-1-MeO(CH2)2S-closo-3,1,2-NiC2B9H10 was determined by single-crystal X-ray diffraction. |
doi_str_mv | 10.3390/inorganics11030127 |
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Their deboronation with cesium fluoride in ethanol gave the corresponding nido-carboranes Cs[7-MeO(CH2)nS-7,8-C2B9H11] (n = 2, 3). The reactions of Cs[7-MeO(CH2)2S-7,8-C2B9H11] with various nickel(II) phosphine complexes [(dppe)NiCl2] and [(R’R2P)2NiCl2] (R = R’ = Ph, Bu; R = Me, R’ = Ph; R = Ph, R’ = Me, Et) were studied and a series of nickelacarboranes 3,3-dppe-1-MeO(CH2)2S-closo-3,1,2-NiC2B9H10 and 3,3- (R’R2P)2-1-MeO(CH2)2S-closo-3,1,2-NiC2B9H10 (R = R’ = Bu; R = Me, R’ = Ph; R = Ph, R’ = Me, Et) was prepared. The molecular crystal structure of 3,3-dppe-1-MeO(CH2)2S-closo-3,1,2-NiC2B9H10 was determined by single-crystal X-ray diffraction.</description><identifier>ISSN: 2304-6740</identifier><identifier>EISSN: 2304-6740</identifier><identifier>DOI: 10.3390/inorganics11030127</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Alkylation ; Carbon ; Carborane ; carboranyl thioethers ; Catalysis ; Cesium ; Cesium fluorides ; Crystal structure ; Ethanol ; half-sandwich complexes ; Ligands ; Molecular structure ; Nickel chloride ; nickelacarboranes ; nido-carborane ligands ; Phosphine ; phosphine ligands ; Phosphines ; Single crystals ; Solvents ; Symmetry ; synthesis ; Thioethers ; X-ray diffraction</subject><ispartof>Inorganics, 2023-03, Vol.11 (3), p.127</ispartof><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c385t-51f88dd4539977f3313f5a39f3680c49dffcbe9df7c8306f0383f750a48f0c9d3</citedby><cites>FETCH-LOGICAL-c385t-51f88dd4539977f3313f5a39f3680c49dffcbe9df7c8306f0383f750a48f0c9d3</cites><orcidid>0000-0003-0617-0118 ; 0000-0002-5442-367X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2791651935/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2791651935?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,44590,75126</link.rule.ids></links><search><creatorcontrib>Semyonov, Dmitriy K.</creatorcontrib><creatorcontrib>Stogniy, Marina Yu</creatorcontrib><creatorcontrib>Suponitsky, Kyrill Yu</creatorcontrib><creatorcontrib>Sivaev, Igor B.</creatorcontrib><title>Half-Sandwich Nickelacarboranes Derived from [7-(MeO(CH2)2S)-7,8-C2B9H11]</title><title>Inorganics</title><description>New carboranyl thioethers 1-MeO(CH2)nS-1,2-C2B10H11 (n = 2, 3) were prepared by the alkylation of the trimethylammonium salt of 1-mercapto-ortho-carborane with 1-bromo- 2-methoxyethane and 1-bromo-3-methoxypropane, respectively. Their deboronation with cesium fluoride in ethanol gave the corresponding nido-carboranes Cs[7-MeO(CH2)nS-7,8-C2B9H11] (n = 2, 3). The reactions of Cs[7-MeO(CH2)2S-7,8-C2B9H11] with various nickel(II) phosphine complexes [(dppe)NiCl2] and [(R’R2P)2NiCl2] (R = R’ = Ph, Bu; R = Me, R’ = Ph; R = Ph, R’ = Me, Et) were studied and a series of nickelacarboranes 3,3-dppe-1-MeO(CH2)2S-closo-3,1,2-NiC2B9H10 and 3,3- (R’R2P)2-1-MeO(CH2)2S-closo-3,1,2-NiC2B9H10 (R = R’ = Bu; R = Me, R’ = Ph; R = Ph, R’ = Me, Et) was prepared. The molecular crystal structure of 3,3-dppe-1-MeO(CH2)2S-closo-3,1,2-NiC2B9H10 was determined by single-crystal X-ray diffraction.</description><subject>Alkylation</subject><subject>Carbon</subject><subject>Carborane</subject><subject>carboranyl thioethers</subject><subject>Catalysis</subject><subject>Cesium</subject><subject>Cesium fluorides</subject><subject>Crystal structure</subject><subject>Ethanol</subject><subject>half-sandwich complexes</subject><subject>Ligands</subject><subject>Molecular structure</subject><subject>Nickel chloride</subject><subject>nickelacarboranes</subject><subject>nido-carborane ligands</subject><subject>Phosphine</subject><subject>phosphine ligands</subject><subject>Phosphines</subject><subject>Single crystals</subject><subject>Solvents</subject><subject>Symmetry</subject><subject>synthesis</subject><subject>Thioethers</subject><subject>X-ray diffraction</subject><issn>2304-6740</issn><issn>2304-6740</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNplUV1LwzAUDaLgmPsDPhV82cBqkts0yaPOjw6me5g-iYQ0zdXOrp3ppvjvrU5E8L6cy-VwzuEeQg4ZPQHQ9LSsm_Bk69K1jFGgjMsd0uNAkziVCd39s--TQdsuaDeagQLVI5PMVhjPbV28l-45ui3di6-ssyFvgq19G134UL75IsLQLKMHGQ9v_Gw4zviIz0exPFbxmJ_rjLHHA7KHtmr94Af75P7q8m6cxdPZ9WR8No0dKLGOBUOliiIRoLWUCMAAhQWNkCrqEl0gutx3IJ0CmiLtcqIU1CYKqdMF9Mlkq1s0dmFWoVza8GEaW5rvQ_cKY8O6dJU3OUeXSiVcImUiHOa-sxWpRK89ZQo7raOt1io0rxvfrs2i2YS6i2-41CwVTIPoWHzLcqFp2-Dx15VR89WA-d8AfALEBncQ</recordid><startdate>20230301</startdate><enddate>20230301</enddate><creator>Semyonov, Dmitriy K.</creator><creator>Stogniy, Marina Yu</creator><creator>Suponitsky, Kyrill Yu</creator><creator>Sivaev, Igor B.</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PADUT</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-0617-0118</orcidid><orcidid>https://orcid.org/0000-0002-5442-367X</orcidid></search><sort><creationdate>20230301</creationdate><title>Half-Sandwich Nickelacarboranes Derived from [7-(MeO(CH2)2S)-7,8-C2B9H11]</title><author>Semyonov, Dmitriy K. ; Stogniy, Marina Yu ; Suponitsky, Kyrill Yu ; Sivaev, Igor B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c385t-51f88dd4539977f3313f5a39f3680c49dffcbe9df7c8306f0383f750a48f0c9d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Alkylation</topic><topic>Carbon</topic><topic>Carborane</topic><topic>carboranyl thioethers</topic><topic>Catalysis</topic><topic>Cesium</topic><topic>Cesium fluorides</topic><topic>Crystal structure</topic><topic>Ethanol</topic><topic>half-sandwich complexes</topic><topic>Ligands</topic><topic>Molecular structure</topic><topic>Nickel chloride</topic><topic>nickelacarboranes</topic><topic>nido-carborane ligands</topic><topic>Phosphine</topic><topic>phosphine ligands</topic><topic>Phosphines</topic><topic>Single crystals</topic><topic>Solvents</topic><topic>Symmetry</topic><topic>synthesis</topic><topic>Thioethers</topic><topic>X-ray diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Semyonov, Dmitriy K.</creatorcontrib><creatorcontrib>Stogniy, Marina Yu</creatorcontrib><creatorcontrib>Suponitsky, Kyrill Yu</creatorcontrib><creatorcontrib>Sivaev, Igor B.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: 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>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>Materials Science Database</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library (ProQuest Database)</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Research Library China</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Inorganics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Semyonov, Dmitriy K.</au><au>Stogniy, Marina Yu</au><au>Suponitsky, Kyrill Yu</au><au>Sivaev, Igor B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Half-Sandwich Nickelacarboranes Derived from [7-(MeO(CH2)2S)-7,8-C2B9H11]</atitle><jtitle>Inorganics</jtitle><date>2023-03-01</date><risdate>2023</risdate><volume>11</volume><issue>3</issue><spage>127</spage><pages>127-</pages><issn>2304-6740</issn><eissn>2304-6740</eissn><abstract>New carboranyl thioethers 1-MeO(CH2)nS-1,2-C2B10H11 (n = 2, 3) were prepared by the alkylation of the trimethylammonium salt of 1-mercapto-ortho-carborane with 1-bromo- 2-methoxyethane and 1-bromo-3-methoxypropane, respectively. Their deboronation with cesium fluoride in ethanol gave the corresponding nido-carboranes Cs[7-MeO(CH2)nS-7,8-C2B9H11] (n = 2, 3). The reactions of Cs[7-MeO(CH2)2S-7,8-C2B9H11] with various nickel(II) phosphine complexes [(dppe)NiCl2] and [(R’R2P)2NiCl2] (R = R’ = Ph, Bu; R = Me, R’ = Ph; R = Ph, R’ = Me, Et) were studied and a series of nickelacarboranes 3,3-dppe-1-MeO(CH2)2S-closo-3,1,2-NiC2B9H10 and 3,3- (R’R2P)2-1-MeO(CH2)2S-closo-3,1,2-NiC2B9H10 (R = R’ = Bu; R = Me, R’ = Ph; R = Ph, R’ = Me, Et) was prepared. The molecular crystal structure of 3,3-dppe-1-MeO(CH2)2S-closo-3,1,2-NiC2B9H10 was determined by single-crystal X-ray diffraction.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/inorganics11030127</doi><orcidid>https://orcid.org/0000-0003-0617-0118</orcidid><orcidid>https://orcid.org/0000-0002-5442-367X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alkylation Carbon Carborane carboranyl thioethers Catalysis Cesium Cesium fluorides Crystal structure Ethanol half-sandwich complexes Ligands Molecular structure Nickel chloride nickelacarboranes nido-carborane ligands Phosphine phosphine ligands Phosphines Single crystals Solvents Symmetry synthesis Thioethers X-ray diffraction |
title | Half-Sandwich Nickelacarboranes Derived from [7-(MeO(CH2)2S)-7,8-C2B9H11] |
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