Shoukat Hamza, Altaf Ataf Ali, Hamayun Muhammad, Ullah Shaheed, Kausar Samia, Hamza Muhammad, Muhammad Shabbir, Badshah Amin, Rasool Nasir, Imran Muhammad
Department of Chemistry, University of Gujrat, Hafiz Hayat Campus, Gujrat 50700, Pakistan.
Department of Chemistry, University of Okara, Okara 56300, Pakistan.
ACS Omega. 2021 Jul 20;6(30):19606-19615. doi: 10.1021/acsomega.1c02163. eCollection 2021 Aug 3.
Oxidation of toluene (an organic pollutant), into useful chemical products, is of great interest nowadays. However, efficient conversion of toluene under mild and sustainable conditions is a thought-provoking task. Here, we report MnMoO nanomaterials , synthesized through a very facile solvothermal approach. Catalytic efficiencies of MnMoO nanomaterials were evaluated by direct oxidation of toluene via C-H activation. Toluene was converted into benzaldehyde and benzyl alcohol in the presence of HO as an oxidant at 80 °C. The reaction parameters, that is, catalyst dose, time, and toluene concentration, were varied to obtain the optimal conditions for the oxidation process. The 40.62% maximum toluene conversion rate was obtained after 18 h of oxidation activity with 0.06 g of catalyst . A maximum of 78% benzaldehyde selectivity was obtained with 0.06 g of catalyst after 18 h of toluene oxidation activity. Also, 62.33% benzyl alcohol selectivity was achieved using 0.1 g of catalyst after 1 h of activity. Several catalytic cycles were run with to evaluate catalyst reusability. Potential % toluene conversion was obtained for up to six cycles and their turnover frequencies were found to be 1.94-1.01 s. FTIR spectra of catalyst before and after recovery indicate no significant change. The good conversion rate of toluene and efficient selectivity toward benzaldehyde and benzyl alcohol indicates the robustness and high potential of these catalysts to oxidize toluene under a milder, greener, and hazardous chlorine-free environment.
将甲苯(一种有机污染物)氧化为有用的化学产品,如今备受关注。然而,在温和且可持续的条件下实现甲苯的高效转化是一项引人深思的任务。在此,我们报道了通过一种非常简便的溶剂热法合成的锰钼氧化物纳米材料。通过甲苯经C-H活化的直接氧化来评估锰钼氧化物纳米材料的催化效率。在80℃下,以过氧化氢作为氧化剂,甲苯在该条件下被转化为苯甲醛和苯甲醇。改变反应参数,即催化剂用量、时间和甲苯浓度,以获得氧化过程的最佳条件。在使用0.06 g催化剂进行18小时氧化活性后,获得了40.62%的最大甲苯转化率。在甲苯氧化活性18小时后,使用0.06 g催化剂获得了高达78%的苯甲醛选择性。此外,在反应1小时后,使用0.1 g催化剂实现了62.33%的苯甲醇选择性。进行了几个催化循环以评估催化剂的可重复使用性。在多达六个循环中获得了潜在的甲苯转化率,并且发现它们的周转频率为1.94 - 1.01 s⁻¹。回收前后催化剂的傅里叶变换红外光谱表明没有显著变化。甲苯的良好转化率以及对苯甲醛和苯甲醇的高效选择性表明这些催化剂在更温和、更绿色且无有害氯的环境中氧化甲苯具有稳健性和高潜力。