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Title: | Highly Porous Ionic Solids Consisting of Au<sup>I</sup><inf>3</inf>Co<sup>III</sup><inf>2</inf>Complex Anions and Aqua Metal Cations |
Authors: | Sireenart Surinwong Naoto Kuwamura Tatsuhiro Kojima Nobuto Yoshinari Apinpus Rujiwatra Takumi Konno |
Authors: | Sireenart Surinwong Naoto Kuwamura Tatsuhiro Kojima Nobuto Yoshinari Apinpus Rujiwatra Takumi Konno |
Keywords: | Chemistry |
Issue Date: | 16-Aug-2021 |
Abstract: | Treatment of Na3[Au3Co2(d-pen)6] (Na3[1]; d-H2pen = d-penicillamine) with M(OAc)2 (M = NiII, MnII) in water gave ionic crystals of [M(H2O)6]3[1]2 (2M) in which [1]3- anions are hydrogen-bonded with [M(H2O)6]2+ cations to form a 3D porous framework with a porosity of ca. 80%. Soaking crystals of 2Ni in its mother liquor afforded crystals of [Ni(H2O)6]2[{Ni(H2O)4}(1)2] (3Ni) in which [1]3- anions are connected to trans-[Ni(H2O)4]2+ and [Ni(H2O)6]2+ cations through coordination and hydrogen bonds, respectively, to form a 1D porous framework with a porosity ca. 60%. Further soaking crystals led to [{Ni(H2O)4}3(1)2] (4Ni), in which [1]3- anions are connected to cis-[Ni(H2O)4]2+ and trans-[Ni(H2O)4]2+ cations through coordination bonds in a dense framework with a porosity of ca. 30%. A similar two-step crystal-to-crystal transformation mediated by solvent proceeded when crystals of 2Mn were soaked in a mother liquor. However, the transformation of 2Mn generated [{Mn(H2O)4}(H1)] (4′Mn) as the final product, in which [H1]2- anions are connected to cis-[Mn(H2O)4]2+ cations through coordination bonds in a very dense framework with a porosity ca. 5% by way of [Mn(H2O)6]2[{Mn(H2O)4}(1)2] (3Mn), which is isostructural with 3Ni. While all the compounds adsorbed H2O and CO2 depending on the degree of their porosity, unusually large NH3 adsorption capacities were observed for 4Ni and 4′Mn, which have dense frameworks. |
URI: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85113586307&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/76099 |
ISSN: | 1520510X 00201669 |
Appears in Collections: | CMUL: Journal Articles |
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