Moon Hoi Ri, Kobayashi Norihito, Suh Myunghyun Paik
Department of Chemistry, Seoul National University, Seoul 151-747, Republic of Korea.
Inorg Chem. 2006 Oct 16;45(21):8672-6. doi: 10.1021/ic0611948.
A 3D porous metal-organic framework generating 1D channels, [Mn(NDC)(DEF)]n (1), has been prepared from the solvothermal reaction of Mn(II) and 2,6-naphthalenedicarboxylic acid (H2NDC) in diethylformamide (DEF). When DEF molecules coordinating Mn(II), which occupy the channels, are removed from 1 by heating the crystal of 1 at 250 degrees C under vacuum for 18 h, structural change occurs as evidenced by X-ray powder diffraction patterns. Desolvated solid [Mn(NDC)]n (2), which contains coordinatively unsaturated Mn(II) sites, reveals remarkable sorption capabilities for N2, H2, CO2, and CH4 gases and exhibits type I sorption behavior indicative of permanent microporosity.
一种生成一维通道的三维多孔金属有机框架[Mn(NDC)(DEF)]n(1),是通过Mn(II)与2,6-萘二甲酸(H2NDC)在二乙酰胺(DEF)中进行溶剂热反应制备而成。当配位Mn(II)的DEF分子(占据通道)通过在250℃真空下加热1的晶体18小时从1中去除时,X射线粉末衍射图谱证明发生了结构变化。去溶剂化的固体[Mn(NDC)]n(2)含有配位不饱和的Mn(II)位点,对N2、H2、CO2和CH4气体显示出显著的吸附能力,并表现出表明具有永久微孔性的I型吸附行为。