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Tuning the packing,interpenetration,and porosity of two-dimensional networks by metal ions and ligand side groups
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作者 Xiao-Yun Tian Hao-Long Zhou +4 位作者 Xue-Wen Zhang Chao Wang Dong-Dong Zhou Xiao-Ming Chen Jie-Peng Zhang 《Inorganic Chemistry Frontiers》 2020年第18期3424-3430,共7页
Solvothermal reactions of 3-(3-methylpyridin-4-yl)benzoic acid (Hmpba) with Zn(Ⅱ),Cd(Ⅱ),or Cu(Ⅱ) salts yielded crystals of coordination polymers [Zn(mpba)_(2)] (1),[Cd(mpba)_(2)] (2),and [Cu(mpba)_(2)]·vip (... Solvothermal reactions of 3-(3-methylpyridin-4-yl)benzoic acid (Hmpba) with Zn(Ⅱ),Cd(Ⅱ),or Cu(Ⅱ) salts yielded crystals of coordination polymers [Zn(mpba)_(2)] (1),[Cd(mpba)_(2)] (2),and [Cu(mpba)_(2)]·vip (3·g),respectively,possessing two-dimensional (2D) 4-connected sql coordination networks with different packing/interpenetration modes.1 and 2 both possess close-packing two-fold interpenetrated sql nets,but the ligand orientations in their single layers and the stacking manners of their double layers are quite different and have an inversed trend of complexity.The sql nets in 3 are non-interpenetrated,which loosely pack to give a porous structure with 1D channels.Interestingly,1–3 have a completely inversed trend in packing/interpenetration and porosity,compared to the coordination networks constructed by the same metal ions and the ligand without the methyl group (3-(pyridin-4-yl)benzoic acid).The porous framework of 3 can be retained after vip removal,as demonstrated by the CO_(2)adsorption isotherms and high catalytic performances for cycloaddition of epoxides and CO_(2). 展开更多
关键词 solvothermal reactions coordination polymers double layers two dimensional networks porosity single layers stacking manners crystals coordination polymers
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