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Synthesis and Characterization of 8-(Dimethylamino)-1-naphthyl Derivatives of Aluminum, Gallium, and Indium
The group 13 dichlorides of formula Ar‘MCl2 [Ar‘ = 8-(dimethylamino)-1-naphthyl (8-(Me2N)C10H6)], M = Al (1), Ga (2), and In (3), have been prepared via the salt elimination reaction of 1 equiv of Ar‘Li with MCl3 in toluene solution at −78 °C. The reaction of 1 with LiAlH4 in diethyl ether solution...
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Published in: | Inorganic chemistry 2000-01, Vol.39 (1), p.27-31 |
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description | The group 13 dichlorides of formula Ar‘MCl2 [Ar‘ = 8-(dimethylamino)-1-naphthyl (8-(Me2N)C10H6)], M = Al (1), Ga (2), and In (3), have been prepared via the salt elimination reaction of 1 equiv of Ar‘Li with MCl3 in toluene solution at −78 °C. The reaction of 1 with LiAlH4 in diethyl ether solution at −78 °C produced the dihydride [Ar‘AlH2]2 (4). The X-ray crystal structures of 1−4 have been determined and show that 1 and 2 are monomeric while 3 and 4 are dimeric in the solid state. The reaction of 1 with RLi in toluene solution at −78 °C results in ligand redistribution and formation of Ar‘2AlR (R = Me (5), t-Bu (6)). The chloride analogue of 5 and 6, Ar‘2AlCl (7), can be prepared directly from the reaction of 2 equiv of Ar‘Li with AlCl3 in toluene solution at −78 °C. The homoleptic derivative Ar‘3Al (8) was obtained when 3 equiv of Ar‘Li was employed. Crystal data for 1: monoclinic, space group P21, a = 6.534(1) Å, b = 10.801(1) Å, c = 9.631(2) Å, β = 105.57(2)°, V = 654.8(2) Å3, Z = 2, R = 0.0453. Crystal data for 2: monoclinic, space group P21, a = 6.552(2) Å, b = 10.833(2) Å, c = 9.601(2) Å, β = 106.05(2)°, V = 654.9(3) Å3, Z = 2, R = 0.0609. Crystal data for 3: monoclinic, space group P21/c, a = 7.401(2) Å, b = 15.746 Å, c = 10.801(4) Å, β = 92.37(3)°, V = 1257.6(7) Å3, Z = 2, R = 0.0712. Crystal data for 4: monoclinic, space group P21/c, a = 13.343(2) Å, b = 11.228(2) Å, c = 7.505(1) Å, β = 100.64(1)°, V = 1105.0(4) Å3, Z = 4, R = 0.0560. |
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The reaction of 1 with LiAlH4 in diethyl ether solution at −78 °C produced the dihydride [Ar‘AlH2]2 (4). The X-ray crystal structures of 1−4 have been determined and show that 1 and 2 are monomeric while 3 and 4 are dimeric in the solid state. The reaction of 1 with RLi in toluene solution at −78 °C results in ligand redistribution and formation of Ar‘2AlR (R = Me (5), t-Bu (6)). The chloride analogue of 5 and 6, Ar‘2AlCl (7), can be prepared directly from the reaction of 2 equiv of Ar‘Li with AlCl3 in toluene solution at −78 °C. The homoleptic derivative Ar‘3Al (8) was obtained when 3 equiv of Ar‘Li was employed. Crystal data for 1: monoclinic, space group P21, a = 6.534(1) Å, b = 10.801(1) Å, c = 9.631(2) Å, β = 105.57(2)°, V = 654.8(2) Å3, Z = 2, R = 0.0453. Crystal data for 2: monoclinic, space group P21, a = 6.552(2) Å, b = 10.833(2) Å, c = 9.601(2) Å, β = 106.05(2)°, V = 654.9(3) Å3, Z = 2, R = 0.0609. Crystal data for 3: monoclinic, space group P21/c, a = 7.401(2) Å, b = 15.746 Å, c = 10.801(4) Å, β = 92.37(3)°, V = 1257.6(7) Å3, Z = 2, R = 0.0712. Crystal data for 4: monoclinic, space group P21/c, a = 13.343(2) Å, b = 11.228(2) Å, c = 7.505(1) Å, β = 100.64(1)°, V = 1105.0(4) Å3, Z = 4, R = 0.0560.</description><identifier>ISSN: 0020-1669</identifier><identifier>EISSN: 1520-510X</identifier><identifier>DOI: 10.1021/ic990707q</identifier><identifier>PMID: 11229027</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>Inorganic chemistry, 2000-01, Vol.39 (1), p.27-31</ispartof><rights>Copyright © 2000 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a415t-9c64b077b306193adc6f0e2dbbbce70a6e15ad40fbb2d3c56832f3a7acce4d9e3</citedby><cites>FETCH-LOGICAL-a415t-9c64b077b306193adc6f0e2dbbbce70a6e15ad40fbb2d3c56832f3a7acce4d9e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11229027$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hair, Gregory S</creatorcontrib><creatorcontrib>Battle, Scott L</creatorcontrib><creatorcontrib>Decken, Andreas</creatorcontrib><creatorcontrib>Cowley, Alan H</creatorcontrib><creatorcontrib>Jones, Richard A</creatorcontrib><title>Synthesis and Characterization of 8-(Dimethylamino)-1-naphthyl Derivatives of Aluminum, Gallium, and Indium</title><title>Inorganic chemistry</title><addtitle>Inorg. Chem</addtitle><description>The group 13 dichlorides of formula Ar‘MCl2 [Ar‘ = 8-(dimethylamino)-1-naphthyl (8-(Me2N)C10H6)], M = Al (1), Ga (2), and In (3), have been prepared via the salt elimination reaction of 1 equiv of Ar‘Li with MCl3 in toluene solution at −78 °C. The reaction of 1 with LiAlH4 in diethyl ether solution at −78 °C produced the dihydride [Ar‘AlH2]2 (4). The X-ray crystal structures of 1−4 have been determined and show that 1 and 2 are monomeric while 3 and 4 are dimeric in the solid state. The reaction of 1 with RLi in toluene solution at −78 °C results in ligand redistribution and formation of Ar‘2AlR (R = Me (5), t-Bu (6)). The chloride analogue of 5 and 6, Ar‘2AlCl (7), can be prepared directly from the reaction of 2 equiv of Ar‘Li with AlCl3 in toluene solution at −78 °C. The homoleptic derivative Ar‘3Al (8) was obtained when 3 equiv of Ar‘Li was employed. Crystal data for 1: monoclinic, space group P21, a = 6.534(1) Å, b = 10.801(1) Å, c = 9.631(2) Å, β = 105.57(2)°, V = 654.8(2) Å3, Z = 2, R = 0.0453. Crystal data for 2: monoclinic, space group P21, a = 6.552(2) Å, b = 10.833(2) Å, c = 9.601(2) Å, β = 106.05(2)°, V = 654.9(3) Å3, Z = 2, R = 0.0609. Crystal data for 3: monoclinic, space group P21/c, a = 7.401(2) Å, b = 15.746 Å, c = 10.801(4) Å, β = 92.37(3)°, V = 1257.6(7) Å3, Z = 2, R = 0.0712. Crystal data for 4: monoclinic, space group P21/c, a = 13.343(2) Å, b = 11.228(2) Å, c = 7.505(1) Å, β = 100.64(1)°, V = 1105.0(4) Å3, Z = 4, R = 0.0560.</description><issn>0020-1669</issn><issn>1520-510X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNpt0F1LHDEYBeBQWupWe9E_UOampULHvkkmyebS7lq1CC34gXfhnUyGjc7HmsyI6683wy72plc5JA8ncAj5ROGIAqM_vNUaFKiHN2RGBYNcULh9S2YAKVMp9R75EOMdAGheyPdkj1LGNDA1I_eXm25Yuehjhl2VLVYY0A4u-GccfN9lfZ3N829L37phtWmw9V1_mNO8w_VqusiWiT4m-ujiZI-bMZGx_Z6dYtP4KUy1512V8gF5V2MT3cfduU-uf51cLc7yiz-n54vjixwLKoZcW1mUoFTJQVLNsbKyBseqsiytU4DSUYFVAXVZsopbIeec1RwVWuuKSju-T75ue9ehfxhdHEzro3VNg53rx2gUE2KuNE_wcAtt6GMMrjbr4FsMG0PBTMua12WT_bwrHcvWVf_kbsoE8i3wcXBPr-8Y7o1UXAlz9ffS3Ijl4ufv26U5S_7L1qON5q4fQ5c2-c_HL_ozkC4</recordid><startdate>20000110</startdate><enddate>20000110</enddate><creator>Hair, Gregory S</creator><creator>Battle, Scott L</creator><creator>Decken, Andreas</creator><creator>Cowley, Alan H</creator><creator>Jones, Richard A</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20000110</creationdate><title>Synthesis and Characterization of 8-(Dimethylamino)-1-naphthyl Derivatives of Aluminum, Gallium, and Indium</title><author>Hair, Gregory S ; Battle, Scott L ; Decken, Andreas ; Cowley, Alan H ; Jones, Richard A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a415t-9c64b077b306193adc6f0e2dbbbce70a6e15ad40fbb2d3c56832f3a7acce4d9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hair, Gregory S</creatorcontrib><creatorcontrib>Battle, Scott L</creatorcontrib><creatorcontrib>Decken, Andreas</creatorcontrib><creatorcontrib>Cowley, Alan H</creatorcontrib><creatorcontrib>Jones, Richard A</creatorcontrib><collection>Istex</collection><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>Hair, Gregory S</au><au>Battle, Scott L</au><au>Decken, Andreas</au><au>Cowley, Alan H</au><au>Jones, Richard A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Characterization of 8-(Dimethylamino)-1-naphthyl Derivatives of Aluminum, Gallium, and Indium</atitle><jtitle>Inorganic chemistry</jtitle><addtitle>Inorg. Chem</addtitle><date>2000-01-10</date><risdate>2000</risdate><volume>39</volume><issue>1</issue><spage>27</spage><epage>31</epage><pages>27-31</pages><issn>0020-1669</issn><eissn>1520-510X</eissn><abstract>The group 13 dichlorides of formula Ar‘MCl2 [Ar‘ = 8-(dimethylamino)-1-naphthyl (8-(Me2N)C10H6)], M = Al (1), Ga (2), and In (3), have been prepared via the salt elimination reaction of 1 equiv of Ar‘Li with MCl3 in toluene solution at −78 °C. The reaction of 1 with LiAlH4 in diethyl ether solution at −78 °C produced the dihydride [Ar‘AlH2]2 (4). The X-ray crystal structures of 1−4 have been determined and show that 1 and 2 are monomeric while 3 and 4 are dimeric in the solid state. The reaction of 1 with RLi in toluene solution at −78 °C results in ligand redistribution and formation of Ar‘2AlR (R = Me (5), t-Bu (6)). The chloride analogue of 5 and 6, Ar‘2AlCl (7), can be prepared directly from the reaction of 2 equiv of Ar‘Li with AlCl3 in toluene solution at −78 °C. The homoleptic derivative Ar‘3Al (8) was obtained when 3 equiv of Ar‘Li was employed. Crystal data for 1: monoclinic, space group P21, a = 6.534(1) Å, b = 10.801(1) Å, c = 9.631(2) Å, β = 105.57(2)°, V = 654.8(2) Å3, Z = 2, R = 0.0453. Crystal data for 2: monoclinic, space group P21, a = 6.552(2) Å, b = 10.833(2) Å, c = 9.601(2) Å, β = 106.05(2)°, V = 654.9(3) Å3, Z = 2, R = 0.0609. Crystal data for 3: monoclinic, space group P21/c, a = 7.401(2) Å, b = 15.746 Å, c = 10.801(4) Å, β = 92.37(3)°, V = 1257.6(7) Å3, Z = 2, R = 0.0712. Crystal data for 4: monoclinic, space group P21/c, a = 13.343(2) Å, b = 11.228(2) Å, c = 7.505(1) Å, β = 100.64(1)°, V = 1105.0(4) Å3, Z = 4, R = 0.0560.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>11229027</pmid><doi>10.1021/ic990707q</doi><tpages>5</tpages></addata></record> |
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title | Synthesis and Characterization of 8-(Dimethylamino)-1-naphthyl Derivatives of Aluminum, Gallium, and Indium |
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