Department of Chemistry, University of California, Berkeley, Berkeley, CA, 94720, USA.
Institut des Sciences et Ingénierie Chimiques, École Polytechnique Fédérale de Lausanne (EPFL), 1051, Sion, Switzerland.
Angew Chem Int Ed Engl. 2016 Jul 18;55(30):8605-9. doi: 10.1002/anie.201602950. Epub 2016 Jun 1.
A chromium(II)-based metal-organic framework Cr3 [(Cr4 Cl)3 (BTT)8 ]2 (Cr-BTT; BTT(3-) =1,3,5-benzenetristetrazolate), featuring coordinatively unsaturated, redox-active Cr(2+) cation sites, was synthesized and investigated for potential applications in H2 storage and O2 production. Low-pressure H2 adsorption and neutron powder diffraction experiments reveal moderately strong Cr-H2 interactions, in line with results from previously reported M-BTT frameworks. Notably, gas adsorption measurements also reveal excellent O2 /N2 selectivity with substantial O2 reversibility at room temperature, based on selective electron transfer to form Cr(III) superoxide moieties. Infrared spectroscopy and powder neutron diffraction experiments were used to confirm this mechanism of selective O2 binding.
一种基于铬(II)的金属-有机骨架 Cr3 [(Cr4 Cl)3 (BTT)8 ]2 (Cr-BTT;BTT(3-) =1,3,5-苯三氮唑),具有配位不饱和、氧化还原活性的 Cr(2+)阳离子位点,被合成并研究了其在 H2 存储和 O2 生产中的潜在应用。低压 H2 吸附和中子粉末衍射实验表明存在中等强度的 Cr-H2 相互作用,与之前报道的 M-BTT 框架的结果一致。值得注意的是,气体吸附测量还表明,在室温下具有出色的 O2/N2 选择性和大量的 O2 可逆性,这是基于选择性电子转移形成 Cr(III)过氧化物基团。红外光谱和粉末中子衍射实验用于证实这种选择性 O2 结合的机制。