José da Silva Márcio, Vergara Torres Jonh Alexander, Vilanculo Castelo Bandane
Marcio Jose da Silva, Chemistry Department, Federal University of Vicosa, University Campus Avenue P.H. Rolfs, Vicosa 36570-000 Minas Gerais State Brazil
Castelo Bandane Vilanculo, Chemistry Department, Pedagogic University of Mozambique, FCNM, Campus of Lhanguene Av. de Moçambique, Km 1 Maputo Mozambique 4040
RSC Adv. 2022 Apr 19;12(19):11796-11806. doi: 10.1039/d2ra01258h. eCollection 2022 Apr 13.
In this work, vanadium-doped phosphomolybdic acids were evaluated as catalysts in green oxidation routes of terpene alcohols with hydrogen peroxide. A series of phosphomolybdic acids containing a variable load of vanadium cations (, V ions) were synthesized, and tested as catalysts in geraniol oxidation, the model molecule selected. All the catalysts were characterized by powder X-ray diffraction, attenuated diffuse reflectance infrared spectroscopy, UV-Vis spectroscopy, thermogravimetric analysis, N adsorption-desorption isotherms, scanning electronic microscopy, X-ray dispersive spectroscopy, and -butylamine potentiometric titration. Various catalysts were evaluated; phosphomolybdic acids with general formulae H PMo V O ( = 0, 1, 2 and 3), and common Brønsted acids (, HSO, HPO, and -toluene sulfonic acid). Among them, vanadium monosubstituted phosphomolybdic acid was the most active catalyst and selective toward epoxide. The effect of main reaction variables, such as temperature, load catalyst, and reactant stoichiometry was assessed. Evaluating the effect of substrate, it was verified that only allylic alcohols such as geraniol and nerol were successfully epoxidized, demonstrating that this is a hydroxy group-assisted reaction. The effect of vanadium doping on the physicochemical properties of the phosphomolybdic acid catalysts was evaluated and used to explain their catalytic performance.
在本研究中,评估了钒掺杂磷钼酸在萜烯醇与过氧化氢的绿色氧化反应路径中作为催化剂的性能。合成了一系列含有可变负载钒阳离子(V离子)的磷钼酸,并将其作为催化剂用于香叶醇氧化反应,香叶醇为选定的模型分子。所有催化剂均通过粉末X射线衍射、衰减全反射红外光谱、紫外可见光谱、热重分析、N吸附-脱附等温线、扫描电子显微镜、X射线色散光谱和丁胺电位滴定进行了表征。评估了多种催化剂;通式为H₃PMo₁₂ - xVₓO₄₀(x = 0、1、2和3)的磷钼酸以及常见的布朗斯特酸(H₂SO₄、H₃PO₄和对甲苯磺酸)。其中,单钒取代的磷钼酸是最具活性且对环氧化物具有选择性的催化剂。评估了主要反应变量的影响,如温度、催化剂负载量和反应物化学计量比。通过评估底物的影响,证实只有烯丙醇如香叶醇和橙花醇能够成功环氧化,表明这是一个羟基辅助的反应。评估了钒掺杂对磷钼酸催化剂物理化学性质的影响,并用于解释它们的催化性能。