一價銠金屬催化肉桂胺衍生物進行不對稱氫芳基化反應
Rhodium(I)-Catalyzed Asymmetric Hydroarylation of Cinnamylamine Derivatives
一價銠金屬催化反應已經被廣泛應用於有機化學合成領域中。而本研究以具保護基之肉桂胺衍生物1與四芳基硼鈉試劑2a作為起始物進行銠金屬不對稱氫芳基化催化反應，得到具有保護基的掌性2,3-雙芳基丙胺衍生物3，並探討此反應的掌性雙烯配基對於反應的影響。本研究已完成使用Ts（對甲苯磺醯基）保護基之肉桂胺衍生物1a作為起始物進行反應，並改變與銠金屬錯合的配基，發現當配基使用2,5號位為芳基取代之配基L（掌性雙環[2,2,1]雙烯配基）時，反應有較好的位置選擇性，其中最佳的是芳基取代為苯基之配基L1，其位置選擇性比例為1:0:0.09。目前將進行改變起始物1之氮上的保護基，以L1作為配基進行反應，並與1a比較，優化反應性及產率。
Greenhouse Gases Reduction: Conversion of Methane and Carbon Dioxide into Clean Energy
In the upcoming years, both population and energy consumption are expected to increase dramatically [1]. Industrialization has led to a dramatic shift in the energy environment [2], with predictions of a 57% increase in demand for energy between 2002 and 2025 [3]. In addition to organic materials like trees and solid waste, fossil fuels like coal, natural gas, and oil provide more than 90% of the world's energy needs. Their overuse has resulted in the release of climate-altering greenhouse gases like carbon dioxide (CO2) and methane (CH4) into the atmosphere [4]. Scientists and other stakeholders are putting more emphasis on finding solutions to global warming, increasing energy production in order to meet increasing demands, and decreasing emissions of greenhouse gases. Using greenhouse gasses to make useful chemicals or fuels is one solution to both problems [5]. This motivated researchers to investigate the potential of CO2 and CH4 as clean energy sources. The process of dry reforming of methane (DRM) has been identified as a potentially successful strategy for transforming CO2 into marketable syngas with a balanced H2/CO composition [6], [7], [8], [9]. The economic viability of DRM, the reactor type, the availability of raw materials, and the intended use of the produced syngas are all-important considerations. Though DRM is gaining popularity, maintaining its long-term stability is difficult due to carbon accumulation from CO disproportionation and methane degradation [10], [11]. The catalyst used, as well as other parameters like as pressure, temperature, feed concentration, and reactor size, are critical to the process's effectiveness. In this scenario, a nickel catalyst on a La2O3/SiO2 substrate with microspheres and a core-shell structure will be developed to improve the conversion of greenhouse gases into profitable syngas. This catalyst is projected to improve the efficiency and performance of the DRM process significantly.
Utilization of Nano cellulose from date palm waste for improvement of thermal stability in epoxy composite
Nano additives is becoming popular trends nowadays due to its nanosize (1-100 nm). Incorporating nano additives in polymer could increase different properties such as mechanical, physical, electrical and thermal stability (1, 2). Different nano additives has been used such as nano copper oxide, nano silica, nano zinc oxide, nano titanium dioxide but most of these come from synthetic or metal oxides that considered as non-environmentally friendly and harmful to human when exposed or inhaled (3). One of the green materials that become attention by researchers is nano cellulose. Nano cellulose can be extracted in different methods and sources such as from wood, and non-woody resources such as kenaf, jute, bamboo as well as from bacteria such as Acetobacter species(4). This making nano cellulose abundantly available in resources. Nano cellulose can be in the form of nano crystalline cellulose (CNC) or NCC or can be in form of nano fibrillated cellulose (NFC) and bacterial nanocellulose (BNC)(5). This nanocellulose has many advantages that can give improvement in different applications such as mechanical, physical, thermal and improving the biodegradation when added together in different matrices (6, 7). Polymers have a problem in thermal stability while processing. It hard to control and maintain the thermal stability of polymer during processing and most polymers considered to have low in thermal stability except for thermosetting polymers such as epoxy. Epoxy has been widely used in many fields such as coating, adhesive, laminates, castings and many more (8). But the drawbacks of epoxy while using is hard to maintain and controll the thermal properties when processing of this materials and used for long period due to aging and attack by free radicals causing by UV radiation (9, 10). In this study we are incorporating nano additives into epoxy as polymer matrix to enhance and improve the thermal stability of composite by crosslinking the polymer chains with the nano additives. Furthermore, the nano additive used is come from nano cellulose extracted from date palm waste and thus to create an environmentally friendly and sustainable nano additives products.
Glass Coloring by the production of Colloidal Hydroxide
When doing an experiment to produce colloidal ferric hydroxide, the bottom of the beaker used was colored in yellow-brown with thin film interference. This phenomenon is well-known, but the cause has not been clearly studied. As a result of the research, the coloration on the bottom of the beaker is caused by β-FeOOH forming a thin film which is chemically bonded with Si-OH on the glass surface. Also, the amount of β-FeOOH depends on the number of experiments, the area of the bottom of the beaker, and the concentration of FeCl3 aq. We found that it can be possible to determine the amount of β-FeOOH from the formula m=knsc and the adhesion constant was found to be 6.8✕10-3 (L/m2). In addition, from machine learning we predicted that the thin film thickness becomes thicker as it moves away from the center.
一價銠金屬催化肉桂胺衍生物進行不對稱氫芳基化反應
Rhodium(I)-Catalyzed Asymmetric Hydroarylation of Cinnamylamine Derivatives
一價銠金屬催化反應已經被廣泛應用於有機化學合成領域中。而本研究以具保護基之肉桂胺衍生物1與四芳基硼鈉試劑2a作為起始物進行銠金屬不對稱氫芳基化催化反應，得到具有保護基的掌性2,3-雙芳基丙胺衍生物3，並探討此反應的掌性雙烯配基對於反應的影響。本研究已完成使用Ts（對甲苯磺醯基）保護基之肉桂胺衍生物1a作為起始物進行反應，並改變與銠金屬錯合的配基，發現當配基使用2,5號位為芳基取代之配基L（掌性雙環[2,2,1]雙烯配基）時，反應有較好的位置選擇性，其中最佳的是芳基取代為苯基之配基L1，其位置選擇性比例為1:0:0.09。目前將進行改變起始物1之氮上的保護基，以L1作為配基進行反應，並與1a比較，優化反應性及產率。