Synthesis, Characterization, and Reactivity of [LiC(SiMe2H)3]·2THF: Formation of 1,1,3,3-Tetramethyl-2,2,4,4-tetrakis(dimethylsilyl)- 1,3-disilacyclobutane, [Me2SiC(SiMe2H)2]2
Reaction of [HC(SiMe2H)3] with [(CH3)2CH]2NLi in tetrahydrofuran afforded [LiC(SiMe2H)3]·2THF (1) in excellent yield. Reactions of 1 with Me3SiCl, MeSiHCl2, HSiCl3 and MeSiCl3 at −78 °C gave [Me3SiC(SiMe2H)3] (2), [(HMeClSi)C(SiMe2H)3] (3), [(HCl2Si)C(SiMe2H)3] (4), and [(MeCl2Si)C(SiMe2H)3] (5), re...
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Veröffentlicht in: | Organometallics 1999-04, Vol.18 (9), p.1804-1807 |
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creator | Hawrelak, Eric J Ladipo, Folami T Sata, Daisuke Braddock-Wilking, Janet |
description | Reaction of [HC(SiMe2H)3] with [(CH3)2CH]2NLi in tetrahydrofuran afforded [LiC(SiMe2H)3]·2THF (1) in excellent yield. Reactions of 1 with Me3SiCl, MeSiHCl2, HSiCl3 and MeSiCl3 at −78 °C gave [Me3SiC(SiMe2H)3] (2), [(HMeClSi)C(SiMe2H)3] (3), [(HCl2Si)C(SiMe2H)3] (4), and [(MeCl2Si)C(SiMe2H)3] (5), respectively. At room temperature, reaction between 1 and SiCl4 in toluene resulted in multiple products, including a new highly substituted 1,3-disilacyclobutane [Me2SiC(SiMe2H)2]2 (6). 6 was isolated in moderate yield from reaction of 1 with 2 equiv of SiCl4. |
doi_str_mv | 10.1021/om980863p |
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Reactions of 1 with Me3SiCl, MeSiHCl2, HSiCl3 and MeSiCl3 at −78 °C gave [Me3SiC(SiMe2H)3] (2), [(HMeClSi)C(SiMe2H)3] (3), [(HCl2Si)C(SiMe2H)3] (4), and [(MeCl2Si)C(SiMe2H)3] (5), respectively. At room temperature, reaction between 1 and SiCl4 in toluene resulted in multiple products, including a new highly substituted 1,3-disilacyclobutane [Me2SiC(SiMe2H)2]2 (6). 6 was isolated in moderate yield from reaction of 1 with 2 equiv of SiCl4.</description><identifier>ISSN: 0276-7333</identifier><identifier>EISSN: 1520-6041</identifier><identifier>DOI: 10.1021/om980863p</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Organometallics, 1999-04, Vol.18 (9), p.1804-1807</ispartof><rights>Copyright © 1999 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a210t-83f48cabfa07d538e21272ee2730705ad77bd68deb3f8a2f164c96140844d4403</citedby><cites>FETCH-LOGICAL-a210t-83f48cabfa07d538e21272ee2730705ad77bd68deb3f8a2f164c96140844d4403</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/om980863p$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/om980863p$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids></links><search><creatorcontrib>Hawrelak, Eric J</creatorcontrib><creatorcontrib>Ladipo, Folami T</creatorcontrib><creatorcontrib>Sata, Daisuke</creatorcontrib><creatorcontrib>Braddock-Wilking, Janet</creatorcontrib><title>Synthesis, Characterization, and Reactivity of [LiC(SiMe2H)3]·2THF: Formation of 1,1,3,3-Tetramethyl-2,2,4,4-tetrakis(dimethylsilyl)- 1,3-disilacyclobutane, [Me2SiC(SiMe2H)2]2</title><title>Organometallics</title><addtitle>Organometallics</addtitle><description>Reaction of [HC(SiMe2H)3] with [(CH3)2CH]2NLi in tetrahydrofuran afforded [LiC(SiMe2H)3]·2THF (1) in excellent yield. Reactions of 1 with Me3SiCl, MeSiHCl2, HSiCl3 and MeSiCl3 at −78 °C gave [Me3SiC(SiMe2H)3] (2), [(HMeClSi)C(SiMe2H)3] (3), [(HCl2Si)C(SiMe2H)3] (4), and [(MeCl2Si)C(SiMe2H)3] (5), respectively. At room temperature, reaction between 1 and SiCl4 in toluene resulted in multiple products, including a new highly substituted 1,3-disilacyclobutane [Me2SiC(SiMe2H)2]2 (6). 6 was isolated in moderate yield from reaction of 1 with 2 equiv of SiCl4.</description><issn>0276-7333</issn><issn>1520-6041</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNptkM-O0zAQxi3ESpTCgTfIBamV7MX_ErvcUETpSq12tQlcqspyEkd1myYr20WEE1eeh8Pe91F4EtItWi6cRvPNb77RfAC8IfiSYEredYeZxDJhd8_AiMQUowRz8hyMMBUJEoyxF-Cl9zuMcSIYHYFfWd-GrfHWwyjdaqfLYJz9roPtWhjptopuzaDZrzb0UVdH66VNJ5ldGbqYss3DPc0X8_e_f_yM5p07PG6dKAIJZJCh3ASnDyZs-wZRSCGHHIWTtrd-UtnzxNumb6ZoWGKoskOny75suuIYdGtgtB5uZf-O0g19BS5q3Xjz-m8dg8_zj3m6QMvrT1fphyXSlOCAJKu5LHVRayyqmElDCRXUGCoYFjjWlRBFlcjKFKyWmtYk4eUsIRxLzivOMRuD6dm3dJ33ztTqztmDdr0iWJ3SVk9pDyw6s9YH8-0J1G6vhqBFrPKbTH1Z5ctUzm5VNvBvz7wuvdp1R9cOn_zH9w8jmIz9</recordid><startdate>19990426</startdate><enddate>19990426</enddate><creator>Hawrelak, Eric J</creator><creator>Ladipo, Folami T</creator><creator>Sata, Daisuke</creator><creator>Braddock-Wilking, Janet</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19990426</creationdate><title>Synthesis, Characterization, and Reactivity of [LiC(SiMe2H)3]·2THF: Formation of 1,1,3,3-Tetramethyl-2,2,4,4-tetrakis(dimethylsilyl)- 1,3-disilacyclobutane, [Me2SiC(SiMe2H)2]2</title><author>Hawrelak, Eric J ; Ladipo, Folami T ; Sata, Daisuke ; Braddock-Wilking, Janet</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a210t-83f48cabfa07d538e21272ee2730705ad77bd68deb3f8a2f164c96140844d4403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hawrelak, Eric J</creatorcontrib><creatorcontrib>Ladipo, Folami T</creatorcontrib><creatorcontrib>Sata, Daisuke</creatorcontrib><creatorcontrib>Braddock-Wilking, Janet</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Organometallics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hawrelak, Eric J</au><au>Ladipo, Folami T</au><au>Sata, Daisuke</au><au>Braddock-Wilking, Janet</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis, Characterization, and Reactivity of [LiC(SiMe2H)3]·2THF: Formation of 1,1,3,3-Tetramethyl-2,2,4,4-tetrakis(dimethylsilyl)- 1,3-disilacyclobutane, [Me2SiC(SiMe2H)2]2</atitle><jtitle>Organometallics</jtitle><addtitle>Organometallics</addtitle><date>1999-04-26</date><risdate>1999</risdate><volume>18</volume><issue>9</issue><spage>1804</spage><epage>1807</epage><pages>1804-1807</pages><issn>0276-7333</issn><eissn>1520-6041</eissn><abstract>Reaction of [HC(SiMe2H)3] with [(CH3)2CH]2NLi in tetrahydrofuran afforded [LiC(SiMe2H)3]·2THF (1) in excellent yield. Reactions of 1 with Me3SiCl, MeSiHCl2, HSiCl3 and MeSiCl3 at −78 °C gave [Me3SiC(SiMe2H)3] (2), [(HMeClSi)C(SiMe2H)3] (3), [(HCl2Si)C(SiMe2H)3] (4), and [(MeCl2Si)C(SiMe2H)3] (5), respectively. At room temperature, reaction between 1 and SiCl4 in toluene resulted in multiple products, including a new highly substituted 1,3-disilacyclobutane [Me2SiC(SiMe2H)2]2 (6). 6 was isolated in moderate yield from reaction of 1 with 2 equiv of SiCl4.</abstract><pub>American Chemical Society</pub><doi>10.1021/om980863p</doi><tpages>4</tpages></addata></record> |
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title | Synthesis, Characterization, and Reactivity of [LiC(SiMe2H)3]·2THF: Formation of 1,1,3,3-Tetramethyl-2,2,4,4-tetrakis(dimethylsilyl)- 1,3-disilacyclobutane, [Me2SiC(SiMe2H)2]2 |
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