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Impact of Linker Engineering on the Catalytic Activity of Metal–Organic Frameworks Containing Pd(II)–Bipyridine Complexes
ACS Catalysis ( IF 11.3 ) Pub Date : 2016-08-23 00:00:00 , DOI: 10.1021/acscatal.6b01753
Xinle Li 1, 2 , Ryan Van Zeeland 1 , Raghu V. Maligal-Ganesh 1, 2 , Yuchen Pei 1, 2 , Gregory Power 1 , Levi Stanley 1 , Wenyu Huang 1, 2
Affiliation  

A series of mixed-linker bipyridyl metal–organic framework (MOF)-supported palladium(II) catalysts were used to elucidate the electronic and steric effects of linker substitution on the activity of these catalysts in the context of Suzuki–Miyaura cross-coupling reactions. m-6,6′-Me2bpy-MOF-PdCl2 exhibited 110- and 496-fold enhancements in activity compared to nonfunctionalized m-bpy-MOF-PdCl2 and m-4,4′-Me2bpy-MOF-PdCl2, respectively. This result clearly demonstrates that the stereoelectronic properties of metal-binding linker units are critical to the activity of single-site organometallic catalysts in MOFs and highlights the importance of linker engineering in the design and development of efficient MOF catalysts.

中文翻译:

接头工程对含Pd(II)-联吡啶配合物的金属有机骨架的催化活性的影响

在铃木-宫浦交叉偶联反应的背景下,使用了一系列混合连接的联吡啶金属-有机骨架(MOF)负载的钯(II)催化剂,阐明了连接基取代对这些催化剂活性的电子和空间影响。 。与未官能化的m-bpy-MOF-PdCl 2和m-4,4'-Me 2 bpy-MOF-相比,m-6,6'-Me 2 bpy-MOF-PdCl 2的活性提高了110倍和496倍氯化钯2, 分别。该结果清楚地表明,金属结合连接单元的立体电子性质对于MOF中单中心有机金属催化剂的活性至关重要,并突出了连接器工程在高效MOF催化剂的设计和开发中的重要性。
更新日期:2016-08-23
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