山东大学学报(理学版) ›› 2015, Vol. 50 ›› Issue (01): 76-80.doi: 10.6040/j.issn.1671-9352.0.2014.233
王梅, 郭海玲, 刘晨光, 蔡大妮
WANG Mei, GUO Hai-ling, LIU Chen-guang, CAI Da-ni
摘要: 开发了一种绿色调制协同法合成分层结构的稀土金属有机骨架材料Eu(BTC)(H2O)6,解决了传统合成方法中使用大量的、有毒有机溶剂的难题,用乙醇和碱性添加剂代替传统的有毒溶剂DMF。首先用乙醇将有机配体溶解,然后加入碱性添加剂使有机配体去质子化,从而使其与金属中心Eu3+成功配位,通过添加剂的-COO-与BTC配体的-COO-竞争与Eu3+的配位合成形貌各异的Eu(BTC)(H2O)6晶体。绿色调制协同法,利用碱性物质乙酸钠和甲酸钠作为调制剂成功制备了多种形貌的Eu(BTC)(H2O)6,包括十字花状晶体、小麦状晶体、麻花状晶体、花状晶体、稻草捆状晶体和杂乱的稻草捆状晶体。这些多形貌的晶体利用粉末X射线衍射、扫描电子显微镜、红外光谱和热重等表征确定了晶体的结构、形貌及化学组成。
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[1] MA L, ABNEY C, LIN W. Enantioselective catalysis with homochiral metal-organic frameworks[J]. Chem Soc Rev, 2009, 38:1248-1256. [2] KESKIN S, SHOLL D S. Assessment of a metal-organic framework membrane for gas separations using atomically detailed calculations:CO2, CH4, N2, H2 mixtures in MOF-5[J]. Ind Eng Chem Res, 2009, 48(2):914-922. [3] MILLWARD A R, YAGHI O M. Metal-organic frameworks with exceptionally high capacity for storage of carbon dioxide at room temperature[J]. J Am Chem Soc, 2005, 127:17998-17999. [4] CHEN B, WANG L, XIAO Y, et al. A luminescent metal-organic framework with lewis basic pyridyl sites for the sensing of metal ions[J]. Angew Chem Int Ed, 2009, 48: 500-503. [5] KESKIN S, KIZILEL S. Biomedical applications of metal organic frameworks[J]. Ind Eng Chem Res, 2011, 50:1799-1812. [6] BLANCO-BRIEVA G, CAMPOS-MARTIN J M, AL-ZAHRANI S M, et al. Effectiveness of metal-organic frameworks for removal of refractory organo-sulfur compound present in liquid fuels[J]. Fuel, 2011, 90:90-197. [7] GUO H, ZHU Y, QIU S, et al. Coordination modulation induced synthesis of nanoscale Eu1-xTbx-metal-organic frameworks for luminescent thin films[J]. Adv Mater, 2010, 22:4190-4192. [8] WU P, WANG J, LI Y, et al. Luminescent sensing and catalytic performances of a multifunctional lanthanide-organic framework comprising a triphenylamine moiety[J]. Adv Funct Mater, 2011, 21:2788-2794. [9] LUO J, XU H, LIU Y, et al. Hydrogen adsorption in a highly stable porous rare-earth metal-organic framework: sorption properties and neutron diffraction studies[J]. J Am Chem Soc, 2008, 130:9626-9627. [10] LIU K, YOU H, JIA G, et al. Hierarchically Nanostructured coordination polymer: facile and rapid fabrication and tunable morphologies[J]. Cryst Growth Des, 2010, 10: 790-797. [11] LIU K, YOU H, JIA G, et al. Coordination-induced formation of one-dimensional nanostructures of europium benzene-1,3,5-tricarboxylate and its solid-state thermal transformation[J]. Crystal Growth Design, 2009, 9(8): 3519-3524. [12] RIETER W J, TAYLOR K M L, LIN W. Surface modification and functionalization of nanoscale metal-organic frameworks for controlled release and luminescence sensing[J]. J Am Chem Soc, 2007, 129(32): 9852-9853. [13] RIETER W J, TAYLOR K M L, AN H, et al. Nanoscale metal-organic frameworks as potential multimodal contrast enhancing agents[J] J Am Chem Soc, 2006, 128: 9024-9025. [14] TAYLOR K M L, RIETER W J, LIN W. Manganese-based nanoscale metal-organic frameworks for magnetic resonance imaging[J]. J Am Chem Soc, 2008, 130(44): 14358-14359. [15] LI Z, QIU L, XU T, et al. Ultrasonic synthesis of the microporous metal-organic framework Cu3(BTC)2 at ambient temperature and pressure: An efficient and environmentally friendly method[J]. Mater Lett, 2009, 63:78-80. [16] ROWSELL J L C, YAGHI O M. Metal-organic frameworks: a new class of porous materials[J]. Microporous Mesoporous Mater, 2004, 73:3-14. [17] HERMES S, WITTE T, HIKOV T, et al. Trapping metal-organic framework nanocrystals:an in-situ time-resolved light scattering study on the crystal growth of MOF-5 in solution[J] J Am Chem Soc, 2007, 129(17):5324-5325. [18] GASSENSMITH J J, FURUKAWA H, SMALDONE R A et al. Strong and reversible binding of carbon dioxide in a green metal-organic framework[J]. J Am Chem Soc, 2011, 133(39):15312-15315. [19] TSURUOKA T, FURUKAWA S, TAKASHIMA Y, et al. Nanoporous nanorods fabricated by coordination modulation and oriented attachment growth[J]. Angew Chem Int Ed, 2009, 48(26): 4739-4743. |
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