Antiferromagnetic Exchange Interaction among the Three Spins Placed in an Isosceles Triangular Configuration in 2,4-Dimethoxy-1,3,5-benzenetriyltris(N-tert-butyl nitroxide)

2,4-Dimethoxy-1,3,5-benzenetriyltris(N-tert-butyl nitroxide) (3) was prepared by lithiation of 2,4-dimethoxy-1,3,5-tribromobenzene followed by the reaction with 2-methyl-2-nitrosopropane and subsequent oxidation with Ag2O. The triradical crystallizes in the orthorhombic space group Pnma (no. 62) wit...

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Veröffentlicht in:Journal of the American Chemical Society 1996-10, Vol.118 (39), p.9347-9351
Hauptverfasser: Fujita, Junpei, Tanaka, Masakazu, Suemune, Hiroshi, Koga, Noboru, Matsuda, Kenji, Iwamura, Hiizu
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container_end_page 9351
container_issue 39
container_start_page 9347
container_title Journal of the American Chemical Society
container_volume 118
creator Fujita, Junpei
Tanaka, Masakazu
Suemune, Hiroshi
Koga, Noboru
Matsuda, Kenji
Iwamura, Hiizu
description 2,4-Dimethoxy-1,3,5-benzenetriyltris(N-tert-butyl nitroxide) (3) was prepared by lithiation of 2,4-dimethoxy-1,3,5-tribromobenzene followed by the reaction with 2-methyl-2-nitrosopropane and subsequent oxidation with Ag2O. The triradical crystallizes in the orthorhombic space group Pnma (no. 62) with four molecules in the unit cell of dimensions a = 18.200(3) Å, b = 19.018(3) Å, and c = 6.659(5) Å. X-ray analysis for an orange plate single crystal of 3 revealed that the three nitroxide radicals in a molecule have large dihedral angles (90° and 79°) between N−O bonds and the benzene ring plane in the all-syn conformation and the distances between them are 5.44 and 5.28 Å. An EPR spectrum of triradical 3 in frozen toluene solution showed quartet signals (g = 2.0062, |D/hc| = 0.010, and |E/hc| = 0.0004 cm-1) in addition to the signals at g = 4.019 and 6.035 due to Δm s = 2 and 3 transitions, respectively. Temperature dependence of molar susceptibility for a microcrystalline sample obtained by SQUID measurements suggested that the antiferromagnetic interaction produces a doublet ground state in triradical 3. Experimental data were fitted in terms of the equation derived from an isosceles triangular three spin system (H = −2J(S A1 S B + S B S A2 + αS A1 S A2)) with negative J's to afford two sets of the best fitting parameters:  J/k B = −41.5 K, α = 0.31 and J/k B = −22.3 K, α = 2.29. The former J/k B value is more consistent with J/k B = −39.7 K for the reference biradical, 1-bromo-2,4-dimethoxy-3,5-benzenediylbis(N-tert-butyl nitroxide) (4). In triradical 3, therefore, the ground spin state would be a doublet with the stronger antiferromagnetic interaction between the spins at 1 and 3 positions and 3 and 5 positions polarizing the ferromagnetic alignment of the 1 and 5 spins, providing the first demonstration of an organic triradical showing competing interactions.
doi_str_mv 10.1021/ja961849b
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The triradical crystallizes in the orthorhombic space group Pnma (no. 62) with four molecules in the unit cell of dimensions a = 18.200(3) Å, b = 19.018(3) Å, and c = 6.659(5) Å. X-ray analysis for an orange plate single crystal of 3 revealed that the three nitroxide radicals in a molecule have large dihedral angles (90° and 79°) between N−O bonds and the benzene ring plane in the all-syn conformation and the distances between them are 5.44 and 5.28 Å. An EPR spectrum of triradical 3 in frozen toluene solution showed quartet signals (g = 2.0062, |D/hc| = 0.010, and |E/hc| = 0.0004 cm-1) in addition to the signals at g = 4.019 and 6.035 due to Δm s = 2 and 3 transitions, respectively. Temperature dependence of molar susceptibility for a microcrystalline sample obtained by SQUID measurements suggested that the antiferromagnetic interaction produces a doublet ground state in triradical 3. Experimental data were fitted in terms of the equation derived from an isosceles triangular three spin system (H = −2J(S A1 S B + S B S A2 + αS A1 S A2)) with negative J's to afford two sets of the best fitting parameters:  J/k B = −41.5 K, α = 0.31 and J/k B = −22.3 K, α = 2.29. The former J/k B value is more consistent with J/k B = −39.7 K for the reference biradical, 1-bromo-2,4-dimethoxy-3,5-benzenediylbis(N-tert-butyl nitroxide) (4). In triradical 3, therefore, the ground spin state would be a doublet with the stronger antiferromagnetic interaction between the spins at 1 and 3 positions and 3 and 5 positions polarizing the ferromagnetic alignment of the 1 and 5 spins, providing the first demonstration of an organic triradical showing competing interactions.</description><identifier>ISSN: 0002-7863</identifier><identifier>EISSN: 1520-5126</identifier><identifier>DOI: 10.1021/ja961849b</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Journal of the American Chemical Society, 1996-10, Vol.118 (39), p.9347-9351</ispartof><rights>Copyright © 1996 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a361t-7e68efedc7836c5650e04f110125e58a1d767593038e11acf1805d2df5d5103b3</citedby><cites>FETCH-LOGICAL-a361t-7e68efedc7836c5650e04f110125e58a1d767593038e11acf1805d2df5d5103b3</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/ja961849b$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ja961849b$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids></links><search><creatorcontrib>Fujita, Junpei</creatorcontrib><creatorcontrib>Tanaka, Masakazu</creatorcontrib><creatorcontrib>Suemune, Hiroshi</creatorcontrib><creatorcontrib>Koga, Noboru</creatorcontrib><creatorcontrib>Matsuda, Kenji</creatorcontrib><creatorcontrib>Iwamura, Hiizu</creatorcontrib><title>Antiferromagnetic Exchange Interaction among the Three Spins Placed in an Isosceles Triangular Configuration in 2,4-Dimethoxy-1,3,5-benzenetriyltris(N-tert-butyl nitroxide)</title><title>Journal of the American Chemical Society</title><addtitle>J. Am. Chem. Soc</addtitle><description>2,4-Dimethoxy-1,3,5-benzenetriyltris(N-tert-butyl nitroxide) (3) was prepared by lithiation of 2,4-dimethoxy-1,3,5-tribromobenzene followed by the reaction with 2-methyl-2-nitrosopropane and subsequent oxidation with Ag2O. The triradical crystallizes in the orthorhombic space group Pnma (no. 62) with four molecules in the unit cell of dimensions a = 18.200(3) Å, b = 19.018(3) Å, and c = 6.659(5) Å. X-ray analysis for an orange plate single crystal of 3 revealed that the three nitroxide radicals in a molecule have large dihedral angles (90° and 79°) between N−O bonds and the benzene ring plane in the all-syn conformation and the distances between them are 5.44 and 5.28 Å. An EPR spectrum of triradical 3 in frozen toluene solution showed quartet signals (g = 2.0062, |D/hc| = 0.010, and |E/hc| = 0.0004 cm-1) in addition to the signals at g = 4.019 and 6.035 due to Δm s = 2 and 3 transitions, respectively. Temperature dependence of molar susceptibility for a microcrystalline sample obtained by SQUID measurements suggested that the antiferromagnetic interaction produces a doublet ground state in triradical 3. Experimental data were fitted in terms of the equation derived from an isosceles triangular three spin system (H = −2J(S A1 S B + S B S A2 + αS A1 S A2)) with negative J's to afford two sets of the best fitting parameters:  J/k B = −41.5 K, α = 0.31 and J/k B = −22.3 K, α = 2.29. The former J/k B value is more consistent with J/k B = −39.7 K for the reference biradical, 1-bromo-2,4-dimethoxy-3,5-benzenediylbis(N-tert-butyl nitroxide) (4). In triradical 3, therefore, the ground spin state would be a doublet with the stronger antiferromagnetic interaction between the spins at 1 and 3 positions and 3 and 5 positions polarizing the ferromagnetic alignment of the 1 and 5 spins, providing the first demonstration of an organic triradical showing competing interactions.</description><issn>0002-7863</issn><issn>1520-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNptkM9qGzEQh0VpoG7SQ99Al0IDVqORVtr1MTh_aghpwFt6FLJ21pa71gZJBrvP1IeMWpeceplhmI9vmB8hH4F_AS7gamtnGppqtnpDJqAEZwqEfksmnHPB6kbLd-R9StsyVqKBCfl9HbLvMcZxZ9cBs3f09uA2NqyRLkLGaF32Y6B2N4Y1zRuk7SYi0uWzD4k-DdZhR33ZB7pIY3I4YKJt9EWwH2yk8zH0fr2P9q-lgGJasRu_w7wZD0cGUzlVbIXhF5bj0R-HUtLnR1YuZ7ba5-NAg89xPPgOLy_IWW-HhB_-9XPy_e62nX9lD9_uF_PrB2alhsxq1A322Lm6kdoprTjyqgfgIBSqxkJX61rNJJcNAljXQ8NVJ7pedQq4XMlzcnnyujimFLE3z9HvbDwa4OZPzOY15sKyE-tTxsMraONPo2tZK9M-LY2Au0r9WNamLfynE29dMttxH0P55D_eF5edjWY</recordid><startdate>19961002</startdate><enddate>19961002</enddate><creator>Fujita, Junpei</creator><creator>Tanaka, Masakazu</creator><creator>Suemune, Hiroshi</creator><creator>Koga, Noboru</creator><creator>Matsuda, Kenji</creator><creator>Iwamura, Hiizu</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19961002</creationdate><title>Antiferromagnetic Exchange Interaction among the Three Spins Placed in an Isosceles Triangular Configuration in 2,4-Dimethoxy-1,3,5-benzenetriyltris(N-tert-butyl nitroxide)</title><author>Fujita, Junpei ; Tanaka, Masakazu ; Suemune, Hiroshi ; Koga, Noboru ; Matsuda, Kenji ; Iwamura, Hiizu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a361t-7e68efedc7836c5650e04f110125e58a1d767593038e11acf1805d2df5d5103b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fujita, Junpei</creatorcontrib><creatorcontrib>Tanaka, Masakazu</creatorcontrib><creatorcontrib>Suemune, Hiroshi</creatorcontrib><creatorcontrib>Koga, Noboru</creatorcontrib><creatorcontrib>Matsuda, Kenji</creatorcontrib><creatorcontrib>Iwamura, Hiizu</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Journal of the American Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fujita, Junpei</au><au>Tanaka, Masakazu</au><au>Suemune, Hiroshi</au><au>Koga, Noboru</au><au>Matsuda, Kenji</au><au>Iwamura, Hiizu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antiferromagnetic Exchange Interaction among the Three Spins Placed in an Isosceles Triangular Configuration in 2,4-Dimethoxy-1,3,5-benzenetriyltris(N-tert-butyl nitroxide)</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J. Am. Chem. Soc</addtitle><date>1996-10-02</date><risdate>1996</risdate><volume>118</volume><issue>39</issue><spage>9347</spage><epage>9351</epage><pages>9347-9351</pages><issn>0002-7863</issn><eissn>1520-5126</eissn><abstract>2,4-Dimethoxy-1,3,5-benzenetriyltris(N-tert-butyl nitroxide) (3) was prepared by lithiation of 2,4-dimethoxy-1,3,5-tribromobenzene followed by the reaction with 2-methyl-2-nitrosopropane and subsequent oxidation with Ag2O. The triradical crystallizes in the orthorhombic space group Pnma (no. 62) with four molecules in the unit cell of dimensions a = 18.200(3) Å, b = 19.018(3) Å, and c = 6.659(5) Å. X-ray analysis for an orange plate single crystal of 3 revealed that the three nitroxide radicals in a molecule have large dihedral angles (90° and 79°) between N−O bonds and the benzene ring plane in the all-syn conformation and the distances between them are 5.44 and 5.28 Å. An EPR spectrum of triradical 3 in frozen toluene solution showed quartet signals (g = 2.0062, |D/hc| = 0.010, and |E/hc| = 0.0004 cm-1) in addition to the signals at g = 4.019 and 6.035 due to Δm s = 2 and 3 transitions, respectively. Temperature dependence of molar susceptibility for a microcrystalline sample obtained by SQUID measurements suggested that the antiferromagnetic interaction produces a doublet ground state in triradical 3. Experimental data were fitted in terms of the equation derived from an isosceles triangular three spin system (H = −2J(S A1 S B + S B S A2 + αS A1 S A2)) with negative J's to afford two sets of the best fitting parameters:  J/k B = −41.5 K, α = 0.31 and J/k B = −22.3 K, α = 2.29. The former J/k B value is more consistent with J/k B = −39.7 K for the reference biradical, 1-bromo-2,4-dimethoxy-3,5-benzenediylbis(N-tert-butyl nitroxide) (4). In triradical 3, therefore, the ground spin state would be a doublet with the stronger antiferromagnetic interaction between the spins at 1 and 3 positions and 3 and 5 positions polarizing the ferromagnetic alignment of the 1 and 5 spins, providing the first demonstration of an organic triradical showing competing interactions.</abstract><pub>American Chemical Society</pub><doi>10.1021/ja961849b</doi><tpages>5</tpages></addata></record>
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