Chen Ting, Shi Zhangping, Zhang Guanghui, Chan Hang Cheong, Shu Yijin, Gao Qingsheng, Tang Yi
Department of Chemistry, College of Chemistry and Materials Science , Jinan University , Guangzhou 510632 , P. R. China.
Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Laboratory of Advanced Materials and Collaborative Innovation Center of Chemistry for Energy Materials , Fudan University , Shanghai 200433 , China.
ACS Appl Mater Interfaces. 2018 Dec 12;10(49):42475-42483. doi: 10.1021/acsami.8b16496. Epub 2018 Nov 30.
In heterogeneous catalysis, strong metal-support interactions are highly desired to improve catalytic turnover on metal catalysts. Herein, molybdenum is uniformly incorporated into mesoporous silica (KIT-6) to accomplish strong interactions with iridium catalysts, and consequently, active and selective hydrogenation of carbonyl compounds. Mo-incorporated KIT-6 (Mo-KIT-6) affords electronic interactions to improve the proportion of metallic Ir species, avoiding the easy surface oxidation of ultrafine metals in silica mesocavities. Owing to the effective H activation and subsequent hydrogenation on metallic Ir sites, optimal Ir/Mo-KIT-6 with a high Ir/Ir ratio delivers prominent performance in the hydrogenation of amides to amines and α,β-unsaturated aldehydes to unsaturated alcohols. As for N-acetylmorpholine hydrogenation, the Ir/Mo-KIT-6 catalyst achieves efficient turnover toward N-ethylmorpholine with high selectivity (>99%) and exhibits activity that relies on the engineered chemical state of Ir sites. Such promotion is further proved to be universal in cinnamaldehyde hydrogenation. This work will provide new opportunities for catalyst design through surface/interface engineering.
在多相催化中,非常希望通过强金属-载体相互作用来提高金属催化剂的催化周转率。在此,钼被均匀地掺入介孔二氧化硅(KIT-6)中,以实现与铱催化剂的强相互作用,从而实现羰基化合物的活性和选择性氢化。掺入钼的KIT-6(Mo-KIT-6)提供电子相互作用,以提高金属铱物种的比例,避免二氧化硅介孔中的超细金属易于发生表面氧化。由于在金属铱位点上有效的氢活化以及随后的氢化反应,具有高Ir/Ir比的最佳Ir/Mo-KIT-6在酰胺氢化为胺以及α,β-不饱和醛氢化为不饱和醇的反应中表现出卓越的性能。对于N-乙酰基吗啉氢化反应,Ir/Mo-KIT-6催化剂以高选择性(>99%)实现了向N-乙基吗啉的高效转化,并表现出依赖于铱位点工程化学状态的活性。这种促进作用在肉桂醛氢化反应中进一步被证明是普遍存在的。这项工作将通过表面/界面工程为催化剂设计提供新的机会。