α- and β-Bis(1,1,1-trifluoro-5,5-dimethyl-5-methoxyacetylacetonato)copper(II): Transforming the Dense Polymorph into a Versatile New Microporous Framework
Bis(1,1,1-trifluoro-5,5-dimethyl-5-methoxy-acetylacetonato)copper(II) was prepared in two polymorphic modifications. The orthorhombic α-form is stable and densely packed, with four trans and four cis square bischelate building blocks per unit cell. These are connected through additional coordination...
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Veröffentlicht in: | Journal of the American Chemical Society 1999-05, Vol.121 (17), p.4179-4188 |
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creator | Soldatov, D. V. Ripmeester, J. A. Shergina, S. I. Sokolov, I. E. Zanina, A. S. Gromilov, S. A. Dyadin, Yu. A. |
description | Bis(1,1,1-trifluoro-5,5-dimethyl-5-methoxy-acetylacetonato)copper(II) was prepared in two polymorphic modifications. The orthorhombic α-form is stable and densely packed, with four trans and four cis square bischelate building blocks per unit cell. These are connected through additional coordination bonds to form a dense polymer network. For the trigonal β-form, the square bischelate complex units are present exclusively as the trans isomers. The distinctive assembly of these units results in a lattice with an open pore volume of about 17% that is accessible to a wide range of guests. The compound has a remarkably strong affinity for the porous β-form as evident from the efficient α-to-β conversion on contact not only with liquid guests but also with organic vapors at pressures well below the saturation pressure. Although the open β-form is metastable, it has a remarkable kinetic stability, most likely because of the trans-to-cis isomerization that must accompany the β-to-α transformation. Many sorbents play a dual role as stabilizing guest and as catalyst promoting the α-to-β or β-to-α conversion. Because of its versatile sorption properties and relative robustness, the β-form of the complex can be classified as a novel organic zeolite mimic. |
doi_str_mv | 10.1021/ja981443u |
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The compound has a remarkably strong affinity for the porous β-form as evident from the efficient α-to-β conversion on contact not only with liquid guests but also with organic vapors at pressures well below the saturation pressure. Although the open β-form is metastable, it has a remarkable kinetic stability, most likely because of the trans-to-cis isomerization that must accompany the β-to-α transformation. Many sorbents play a dual role as stabilizing guest and as catalyst promoting the α-to-β or β-to-α conversion. 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For the trigonal β-form, the square bischelate complex units are present exclusively as the trans isomers. The distinctive assembly of these units results in a lattice with an open pore volume of about 17% that is accessible to a wide range of guests. The compound has a remarkably strong affinity for the porous β-form as evident from the efficient α-to-β conversion on contact not only with liquid guests but also with organic vapors at pressures well below the saturation pressure. Although the open β-form is metastable, it has a remarkable kinetic stability, most likely because of the trans-to-cis isomerization that must accompany the β-to-α transformation. Many sorbents play a dual role as stabilizing guest and as catalyst promoting the α-to-β or β-to-α conversion. 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V.</creatorcontrib><creatorcontrib>Ripmeester, J. A.</creatorcontrib><creatorcontrib>Shergina, S. I.</creatorcontrib><creatorcontrib>Sokolov, I. E.</creatorcontrib><creatorcontrib>Zanina, A. S.</creatorcontrib><creatorcontrib>Gromilov, S. A.</creatorcontrib><creatorcontrib>Dyadin, Yu. A.</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>Soldatov, D. V.</au><au>Ripmeester, J. A.</au><au>Shergina, S. I.</au><au>Sokolov, I. E.</au><au>Zanina, A. S.</au><au>Gromilov, S. A.</au><au>Dyadin, Yu. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>α- and β-Bis(1,1,1-trifluoro-5,5-dimethyl-5-methoxyacetylacetonato)copper(II): Transforming the Dense Polymorph into a Versatile New Microporous Framework</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J. Am. Chem. Soc</addtitle><date>1999-05-05</date><risdate>1999</risdate><volume>121</volume><issue>17</issue><spage>4179</spage><epage>4188</epage><pages>4179-4188</pages><issn>0002-7863</issn><eissn>1520-5126</eissn><abstract>Bis(1,1,1-trifluoro-5,5-dimethyl-5-methoxy-acetylacetonato)copper(II) was prepared in two polymorphic modifications. The orthorhombic α-form is stable and densely packed, with four trans and four cis square bischelate building blocks per unit cell. These are connected through additional coordination bonds to form a dense polymer network. For the trigonal β-form, the square bischelate complex units are present exclusively as the trans isomers. The distinctive assembly of these units results in a lattice with an open pore volume of about 17% that is accessible to a wide range of guests. The compound has a remarkably strong affinity for the porous β-form as evident from the efficient α-to-β conversion on contact not only with liquid guests but also with organic vapors at pressures well below the saturation pressure. Although the open β-form is metastable, it has a remarkable kinetic stability, most likely because of the trans-to-cis isomerization that must accompany the β-to-α transformation. Many sorbents play a dual role as stabilizing guest and as catalyst promoting the α-to-β or β-to-α conversion. Because of its versatile sorption properties and relative robustness, the β-form of the complex can be classified as a novel organic zeolite mimic.</abstract><pub>American Chemical Society</pub><doi>10.1021/ja981443u</doi><tpages>10</tpages></addata></record> |
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title | α- and β-Bis(1,1,1-trifluoro-5,5-dimethyl-5-methoxyacetylacetonato)copper(II): Transforming the Dense Polymorph into a Versatile New Microporous Framework |
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