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Histidine-Controlled Homochiral and Ferroelectric Metal–Organic Frameworks
A new multifunctional enantiopure ligand, (S)-2-(1,8-naphthalimido)-3-(4-imidazole)propanoate (s-nip), containing a homochiral center derived from l-histidine and a strong π···π stacking 1,8-naphthalimide synthon, has been used to prepare three novel metal–organic frameworks. The frameworks of [Zn(s...
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Published in: | Crystal growth & design 2015-02, Vol.15 (2), p.687-694 |
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container_issue | 2 |
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container_title | Crystal growth & design |
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creator | Yu, Lei Hua, Xiu-Ni Jiang, Xi-Jie Qin, Lan Yan, Xiao-Zhi Luo, Lai-Hui Han, Lei |
description | A new multifunctional enantiopure ligand, (S)-2-(1,8-naphthalimido)-3-(4-imidazole)propanoate (s-nip), containing a homochiral center derived from l-histidine and a strong π···π stacking 1,8-naphthalimide synthon, has been used to prepare three novel metal–organic frameworks. The frameworks of [Zn(s-nip)2] n (1) and {[Co(s-nip)2]·(H2O)0.5} n (2) are isostructural three-dimensional (3D) homochiral supramolecular structures organized one-dimensional (1D) ribbons by strong hydrogen bonds and π···π interactions, which display ferroelectric behavior at room temperature. The complex [Cu(nia)2·(H2O)5] n (3) was constructed under a hydrothermal in situ ligand synthesis reaction, in which the new ligand 2-(1,8-naphthalimido)-3-(4-imidazole)acrylate (nia) was formed from the s-nip ligand via a dehydrogenation reaction. The two-dimensional network of 3 stacks into a 3D structure via π···π interactions resulting in 1D hydrophilic channels. |
doi_str_mv | 10.1021/cg5013796 |
format | article |
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The frameworks of [Zn(s-nip)2] n (1) and {[Co(s-nip)2]·(H2O)0.5} n (2) are isostructural three-dimensional (3D) homochiral supramolecular structures organized one-dimensional (1D) ribbons by strong hydrogen bonds and π···π interactions, which display ferroelectric behavior at room temperature. The complex [Cu(nia)2·(H2O)5] n (3) was constructed under a hydrothermal in situ ligand synthesis reaction, in which the new ligand 2-(1,8-naphthalimido)-3-(4-imidazole)acrylate (nia) was formed from the s-nip ligand via a dehydrogenation reaction. 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Growth Des</addtitle><date>2015-02-04</date><risdate>2015</risdate><volume>15</volume><issue>2</issue><spage>687</spage><epage>694</epage><pages>687-694</pages><issn>1528-7483</issn><eissn>1528-7505</eissn><abstract>A new multifunctional enantiopure ligand, (S)-2-(1,8-naphthalimido)-3-(4-imidazole)propanoate (s-nip), containing a homochiral center derived from l-histidine and a strong π···π stacking 1,8-naphthalimide synthon, has been used to prepare three novel metal–organic frameworks. The frameworks of [Zn(s-nip)2] n (1) and {[Co(s-nip)2]·(H2O)0.5} n (2) are isostructural three-dimensional (3D) homochiral supramolecular structures organized one-dimensional (1D) ribbons by strong hydrogen bonds and π···π interactions, which display ferroelectric behavior at room temperature. The complex [Cu(nia)2·(H2O)5] n (3) was constructed under a hydrothermal in situ ligand synthesis reaction, in which the new ligand 2-(1,8-naphthalimido)-3-(4-imidazole)acrylate (nia) was formed from the s-nip ligand via a dehydrogenation reaction. The two-dimensional network of 3 stacks into a 3D structure via π···π interactions resulting in 1D hydrophilic channels.</abstract><pub>American Chemical Society</pub><doi>10.1021/cg5013796</doi><tpages>8</tpages></addata></record> |
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title | Histidine-Controlled Homochiral and Ferroelectric Metal–Organic Frameworks |
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