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Self-Assembled Bio-Organometallic Nanocatalysts for Highly Enantioselective Direct Aldol Reactions
Langmuir ( IF 3.7 ) Pub Date : 2020-11-11 , DOI: 10.1021/acs.langmuir.0c01485
Xuejiao Yang 1 , Liwei Zhang 1 , Yaoyu Liang 1 , Yuefei Wang 1, 2 , Yuhe Shen 1 , Qiguo Xing 1 , Wei Qi 1, 2, 3 , Pengfei Wang 4 , Xiao Liu 1 , Mengyao Yang 1 , Rongxin Su 1, 2, 3 , Mingxia He 4 , Zhimin He 1
Affiliation  

Supramolecular nanocatalysts were designed for asymmetric reactions through the self-assembly process of a bio-organometallic molecule, ferrocene-l-prolinamide (Fc-CO-NH-P). Fc-CO-NH-P could self-assemble into versatile nanostructures in water, including nanospheres, nanosheets, nanoflowers, and pieces. In particular, the self-assembled nanoflowers exhibited a superior specific surface area, high stability, and delicate three-dimensional (3D) chiral catalytic active sites. The nanoflowers could serve as heterogeneous catalysts with an excellent catalytic performance toward direct aldol reactions in aqueous solution, achieving both high yield (>99%) and stereoselectivity (anti/syn = 97:3, ee% >99%). This study proposed a significant strategy to fabricate supramolecular chiral catalysts, serving as a favorable template for designing new asymmetric catalysts.

中文翻译:

自组装的生物有机金属纳米催化剂的高度对映选择性直接羟醛反应。

超分子纳米催化剂被设计用于通过生物有机金属分子的自组装过程,二茂铁-不对称反应-脯氨酰胺(Fc-CO-NH-P)。Fc-CO-NH-P可以在水中自组装成通用的纳米结构,包括纳米球,纳米片,纳米花和碎片。特别地,自组装的纳米花表现出优异的比表面积,高稳定性和精细的三维(3D)手性催化活性位点。纳米花可以用作非均相催化剂,对水溶液中的直接羟醛反应具有优异的催化性能,既可实现高收率(> 99%)又可实现立体选择性(反/ syn = 97:3,ee%> 99%)。这项研究提出了一种重要的策略来制备超分子手性催化剂,作为设计新型不对称催化剂的有利模板。
更新日期:2020-11-25
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