氢解
催化作用
化学
偏磷酸盐
选择性
路易斯酸
苯酚
铝
磷酸铝
有机化学
无机化学
酚类
磷酸盐
磷酸钠
柠檬酸
相(物质)
多相催化
催化剂载体
化学合成
酸催化
作者
Kento Oshida,Akito Ai,Shinji Tanaka,Yuichiro Okuzumi,Yuga Ezoe,Takeyuki Nogami,Rin Seki,Hiroki Miura,Tetsuya Shishido,Akira Nakayama,Xiongjie Jin,Kyoko Nozaki
摘要
ABSTRACT Understanding the active structure of phosphate‐based supports is essential for designing catalysts for selective C─O bond hydrogenolysis. Herein, 31 P solid‐state NMR analysis revealed that the support in our previously reported Pt/Al(PO 3 ) 3 catalyst was actually an aluminum condensed phosphate mixture (ACPM), rather than a single aluminum metaphosphate (AMP) phase, consisting of aluminum metaphosphate (AMP), aluminum cyclohexaphosphate (ACP), and aluminum tripolyphosphate (ATPP), with the ATPP phase located on the catalyst surface. Guided by these findings, a Pt/ATPP catalyst was developed, showing high selectivity for the hydrogenolysis of 4‐heptylphenol to heptylbenzene. Mechanistic studies suggested that the Lewis acid sites on ATPP contribute to the enhanced selectivity by facilitating C─O bond activation, a key step in phenol hydrogenolysis.
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