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首页> 外文期刊>ACS Omega >New Set of Multicomponent Crystals as Efficient Heterogeneous Catalysts for the Synthesis of Cyclic Carbonates
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New Set of Multicomponent Crystals as Efficient Heterogeneous Catalysts for the Synthesis of Cyclic Carbonates

机译:新型多组分晶体作为合成环状碳酸酯的高效多相催化剂

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Three new multicomponent crystals 1a–1c of Zn(II), Mn(II), and Co(II), respectively, were synthesized by the reaction of 2,6-bis(hydroxymethyl)pyridine, the respective metal salts, and sodium benzoate in a 1:1:2 ratio. One component of these multicomponent crystals 1a–1c is the dicationic 2,6-bis(hydroxymethyl)pyridine metal complex and the other component is the dianionic tetrabenzoate complex of the same metal. The complexes were fully characterized by single-crystal X-ray structure determination. The X-ray structure of these compounds 1a–1c reveals the formation of 1D supramolecular chain parallel to the crystallographic b axis via H-bonding interactions between the dicationic and dianionic parts of the respective compound. The Mn(II) (1b) and Co(II) (1c) complexes show antiferromagnetic coupling between the two associated metal centers via the H-bonding interaction pathway. All the three compounds 1a–1c were tested as heterogeneous catalytic systems for the successful conversion of epoxides to cyclic carbonates in solvent-free condition under approximately 10 bar of pressure of CO2 and temperature ranging between 60 and 80 °C along with tetrabutyl ammonium bromide acting as a cocatalyst. All the three compounds 1a–1c were found to have turnover number more than 1000 for the respective epoxides except for the conversion of cyclohexene oxide to cyclohexene carbonate.
机译:通过2,6-双(羟甲基)吡啶,各自的金属盐和苯甲酸钠的反应分别合成了三个新的Zn(II),Mn(II)和Co(II)的多组分晶体1a-1c以1:1:2的比例。这些多组分晶体1a-1c的一个组分是2,6-双(羟甲基)吡啶金属双金属配合物,另一组分是同一金属的双阴离子四苯甲酸酯配合物。通过单晶X射线结构测定充分表征了该配合物。这些化合物1a-1c的X射线结构通过相应化合物的双键和双键部分之间的H键相互作用揭示了平行于晶体b轴的1D超分子链的形成。 Mn(II)(1b)和Co(II)(1c)配合物通过H键相互作用途径显示出两个相关金属中心之间的反铁磁耦合。所有三种化合物1a-1c均已作为非均相催化体系进行了测试,可在无溶剂条件下,在大约10 bar的CO2压力和60至80°C的温度范围内,将环氧化物成功转化为环状碳酸酯,同时使用四丁基溴化铵。作为助催化剂。发现这三种化合物1a-1c各自的环氧化物的周转数均大于1000,但环氧环己烯转化为碳酸环己烯除外。

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