King Ashley M, Wingad Richard L, Pridmore Natalie E, Pringle Paul G, Wass Duncan F
Cardiff Catalysis Institute, School of Chemistry, Cardiff University, Main Building, Park Place, Cardiff CF10 3AT, United Kingdom.
School of Chemistry, University of Bristol, Cantock's Close, Bristol BS8 1TS, United Kingdom.
Organometallics. 2021 Aug 23;40(16):2844-2851. doi: 10.1021/acs.organomet.1c00313. Epub 2021 Aug 4.
We report a variety of rhenium complexes supported by bidentate and tridentate phosphinoamine ligands and their use in the formation of the advanced biofuel isobutanol from methanol and ethanol. Rhenium pincer complexes - are effective catalysts for this process, with giving isobutanol in 35% yields, with 97% selectivity in the liquid fraction, over 16 h with catalyst loadings as low as 0.07 mol %. However, these catalysts show poorer overall selectivity, with the formation of a significant amount of carboxylate salt solid byproduct also being observed. Production of the active catalyst has been followed by P NMR spectroscopy, and the importance of the presence of base and elevated temperatures to catalyst activation has been established. Complexes supported by diphosphine ligands are inactive for Guerbet chemistry; however, complexes supported by bidentate phosphinoamine ligands show greater selectivity for isobutanol formation over carboxylate salts. The novel complex was able to produce isobutanol in 28% yield over 17 h. The importance of the N-H moiety to the catalytic performance has also been established, giving further weight to the hypothesis that these catalysts operate via a cooperative mechanism.
我们报道了一系列由双齿和三齿膦胺配体支撑的铼配合物,以及它们在由甲醇和乙醇制备高级生物燃料异丁醇中的应用。铼钳形配合物是该过程的有效催化剂,在催化剂负载低至0.07 mol%的情况下,16小时内可产生35%产率的异丁醇,在液体馏分中的选择性为97%。然而,这些催化剂的整体选择性较差,还观察到有大量羧酸盐固体副产物生成。通过磷核磁共振光谱对活性催化剂的生成进行了跟踪,并确定了碱的存在和升高温度对催化剂活化的重要性。由双膦配体支撑的配合物对格尔伯特化学反应无活性;然而,由双齿膦胺配体支撑的配合物对异丁醇生成的选择性高于羧酸盐。新型配合物在17小时内能够产生28%产率的异丁醇。还确定了N-H部分对催化性能的重要性,进一步支持了这些催化剂通过协同机制起作用的假设。