Endotracheal intubation holds significant importance in trauma point care and emergency medicine. However, laryngeal injury and subsequent chronic complications can result from the friction between the mucosa and the tube during intubation. Here we present a lubricant coating based on hyaluronic acid. Inspired by mussels, hyaluronic acid was first conjugated with dopamine to obtain HD, and then a triblock copolymer Pluronic F127 (F127) was complexed with HD to form a micelle layer. Dopamine can assist coating deposition on the tube under weak alkaline conditions, while improving the coating stability. The micelle layer formed by F127 and HD provides excellent water retention and lubrication performance. The friction coefficient of the HD-F127 coating was 56% lower than that of the control, as determined by a friction performance test.
气管插管在创伤点护理和急诊医学中具有重要意义。然而,在插管过程中,喉粘膜和插管之间的摩擦可能会导致喉损伤和随后的慢性并发症。在此,我们介绍一种基于透明质酸的润滑涂层。受贻贝的启发,我们首先将透明质酸与多巴胺共轭,得到 HD,然后将三嵌段共聚物 Pluronic F127(F127)与 HD 复配,形成胶束层。在弱碱性条件下,多巴胺可以帮助涂层在管材上沉积,同时提高涂层的稳定性。F127 和 HD 形成的胶束层具有优异的保水和润滑性能。经摩擦性能测试,HD-F127 涂层的摩擦系数比对照组低 56%。
{"title":"Coatings based on dopamine-modified hyaluronic acid and Pluronic F127 for tracheal intubation","authors":"Chenggang Wu, Xiyi Yang, Xiaofeng Tang, Shuping Zhang","doi":"10.1071/ch23218","DOIUrl":"https://doi.org/10.1071/ch23218","url":null,"abstract":"<p>Endotracheal intubation holds significant importance in trauma point care and emergency medicine. However, laryngeal injury and subsequent chronic complications can result from the friction between the mucosa and the tube during intubation. Here we present a lubricant coating based on hyaluronic acid. Inspired by mussels, hyaluronic acid was first conjugated with dopamine to obtain HD, and then a triblock copolymer Pluronic F127 (F127) was complexed with HD to form a micelle layer. Dopamine can assist coating deposition on the tube under weak alkaline conditions, while improving the coating stability. The micelle layer formed by F127 and HD provides excellent water retention and lubrication performance. The friction coefficient of the HD-F127 coating was 56% lower than that of the control, as determined by a friction performance test.</p>","PeriodicalId":8575,"journal":{"name":"Australian Journal of Chemistry","volume":"101 1","pages":""},"PeriodicalIF":1.1,"publicationDate":"2024-04-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140801365","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Surface-enhanced Raman spectroscopy (SERS) is a powerful molecular spectroscopy technique that combines Raman spectroscopy with nanostructured metallic surfaces to amplify the Raman signals of target molecules by more than 103. The high sensitivity of SERS poses a significant opportunity for pesticide detection in complex matrices at ultralow concentrations. In this study, we improved the SERS sensitivity for imidacloprid (IMD) by employing silver nanostars (AgNs) coated with gold nanostars (AuNs) as the SERS-active substrate. The SERS response towards IMD detection increased based on the combination of AuNs and AgNs on the substrate surface. The intensity of the SERS signal of IMD using the AuNs/AgNs substrate increased compared to using individual metal nanoparticle substrates. The excellent reproducibility of SERS intensity using the AuNs/AgNs substrate was achieved with a low relative standard derivative (RSD) of 4.87% for 20 different spots on the same sample and 5.19% for 20 different samples. This detection system can be used for multiple tests, which is crucial for the advancement of handheld sensors designed for field use, where minimal or no high-level technical support is accessible.
{"title":"Surface-enhanced Raman spectroscopy (SERS) substrate based on gold nanostars–silver nanostars for imidacloprid detection","authors":"Norhayati Abu Bakar, Joseph George Shapter","doi":"10.1071/ch23189","DOIUrl":"https://doi.org/10.1071/ch23189","url":null,"abstract":"<p>Surface-enhanced Raman spectroscopy (SERS) is a powerful molecular spectroscopy technique that combines Raman spectroscopy with nanostructured metallic surfaces to amplify the Raman signals of target molecules by more than 10<sup>3</sup>. The high sensitivity of SERS poses a significant opportunity for pesticide detection in complex matrices at ultralow concentrations. In this study, we improved the SERS sensitivity for imidacloprid (IMD) by employing silver nanostars (AgNs) coated with gold nanostars (AuNs) as the SERS-active substrate. The SERS response towards IMD detection increased based on the combination of AuNs and AgNs on the substrate surface. The intensity of the SERS signal of IMD using the AuNs/AgNs substrate increased compared to using individual metal nanoparticle substrates. The excellent reproducibility of SERS intensity using the AuNs/AgNs substrate was achieved with a low relative standard derivative (RSD) of 4.87% for 20 different spots on the same sample and 5.19% for 20 different samples. This detection system can be used for multiple tests, which is crucial for the advancement of handheld sensors designed for field use, where minimal or no high-level technical support is accessible.</p>","PeriodicalId":8575,"journal":{"name":"Australian Journal of Chemistry","volume":"298 1","pages":""},"PeriodicalIF":1.1,"publicationDate":"2024-04-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140591736","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Antibiotic concentrations in wastewater generated by industries such as sewage treatment plants, medical pharmaceuticals and aquaculture has exceeded acceptable levels. It is particularly urgent to seek a method that can efficiently remove antibiotics. The removal potential of three quinolone antibiotics, pefloxacin (PF), levofloxacin (LF) and norfloxacin (NF), in simulated contaminated water was studied using a biochar-based nanomaterial prepared by a hydrothermal method. The data were fitted with adsorption kinetics, isotherms and thermodynamics. The results showed that ZnS–MoS2 activated biochar (ZMMBC) acheived maximum adsorption amounts of 199.42, 125.00 and 142.58 mg g–1 for PF, LF and NF, suggesting that ZMMBC has excellent adsorption performance. The adsorption mechanisms of PF, LF and NF molecules on ZMMBC include complexation, pore filling, π–π interactions, electrostatic interactions and hydrogen bond interactions.
{"title":"Research on the sustainable effect of ZnS and MoS 2 decorated biochar nanocomposites for removing quinolones from antibiotic-polluted aqueous solutions","authors":"Ying-Jie Gan, Yue-hui Wang, Ya-ru Dang, Wen-jie Hao, Zheng-rong Hu, Zhi-wei Zhang, Yu-min Luo, Yan-bo Wu, Ai-jun Song, Zhong-bao Zhao","doi":"10.1071/ch23170","DOIUrl":"https://doi.org/10.1071/ch23170","url":null,"abstract":"<p>Antibiotic concentrations in wastewater generated by industries such as sewage treatment plants, medical pharmaceuticals and aquaculture has exceeded acceptable levels. It is particularly urgent to seek a method that can efficiently remove antibiotics. The removal potential of three quinolone antibiotics, pefloxacin (PF), levofloxacin (LF) and norfloxacin (NF), in simulated contaminated water was studied using a biochar-based nanomaterial prepared by a hydrothermal method. The data were fitted with adsorption kinetics, isotherms and thermodynamics. The results showed that ZnS–MoS<sub>2</sub> activated biochar (ZMMBC) acheived maximum adsorption amounts of 199.42, 125.00 and 142.58 mg g<sup>–1</sup> for PF, LF and NF, suggesting that ZMMBC has excellent adsorption performance. The adsorption mechanisms of PF, LF and NF molecules on ZMMBC include complexation, pore filling, π–π interactions, electrostatic interactions and hydrogen bond interactions.</p>","PeriodicalId":8575,"journal":{"name":"Australian Journal of Chemistry","volume":"52 1","pages":""},"PeriodicalIF":1.1,"publicationDate":"2024-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140591637","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Oliver E. Hutt, Jamie A. Freemont, Stella Kyi, Stuart W. Littler, Ross P. McGeary, Peter J. Duggan, John Tsanaktsidis, Helen F. Cole, Maurice G. Kerr, Elizabeth H. Krenske, John H. Ryan
The reactions of pyrethrin I, cinerin I and jasmolin I with sodium hydroxide in ethanol afforded an approximately 1:1 ratio of two respective cyclopentadienone dimers, isolated in good yield. A combination of one-dimensional and two-dimensional NMR spectroscopic studies allowed determination of the structure and stereochemistry of the dimers. The dimers are formed by cycloaddition reactions of the less substituted alkene of the cyclopentadienone, and by regioisomeric endo transition states. Density functional theory calculations were in accord with the experimental findings showing the products formed by ambimodal transition states. One such transition state led to two initial products with the less stable product undergoing facile conversion to the other more stable, experimentally observed product. These studies clarify the structures of the altered pyrethrolone reported by Staudinger and Ruzicka in 1924.
除虫菊素 I、西尼林 I 和茉莉素 I 与氢氧化钠在乙醇中的反应生成了两种各自比例约为 1:1 的环戊二烯酮二聚体,并以良好的收率分离出来。结合一维和二维核磁共振光谱研究,可以确定二聚体的结构和立体化学性质。二聚物是通过环戊二烯酮中取代程度较低的烯烃的环加成反应以及通过区域异构内生过渡态形成的。密度泛函理论的计算结果与实验结果一致,显示了由非模态过渡态形成的产物。其中一种转变态产生了两种初始产物,稳定性较差的产物很容易转化为另一种更稳定的实验观察到的产物。这些研究澄清了 Staudinger 和 Ruzicka 于 1924 年报告的改变后的除虫菊酯酮的结构。
{"title":"Revisiting Staudinger and Ruzicka’s altered pyrethrolone: the cyclopentadienone dimers derived from pyrethrin I, cinerin I and jasmolin I","authors":"Oliver E. Hutt, Jamie A. Freemont, Stella Kyi, Stuart W. Littler, Ross P. McGeary, Peter J. Duggan, John Tsanaktsidis, Helen F. Cole, Maurice G. Kerr, Elizabeth H. Krenske, John H. Ryan","doi":"10.1071/ch23197","DOIUrl":"https://doi.org/10.1071/ch23197","url":null,"abstract":"<p>The reactions of pyrethrin I, cinerin I and jasmolin I with sodium hydroxide in ethanol afforded an approximately 1:1 ratio of two respective cyclopentadienone dimers, isolated in good yield. A combination of one-dimensional and two-dimensional NMR spectroscopic studies allowed determination of the structure and stereochemistry of the dimers. The dimers are formed by cycloaddition reactions of the less substituted alkene of the cyclopentadienone, and by regioisomeric <i>endo</i> transition states. Density functional theory calculations were in accord with the experimental findings showing the products formed by ambimodal transition states. One such transition state led to two initial products with the less stable product undergoing facile conversion to the other more stable, experimentally observed product. These studies clarify the structures of the altered pyrethrolone reported by Staudinger and Ruzicka in 1924.</p>","PeriodicalId":8575,"journal":{"name":"Australian Journal of Chemistry","volume":"41 1","pages":""},"PeriodicalIF":1.1,"publicationDate":"2024-03-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140107859","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Yiwen Wang, Aijun Gong, Lina Qiu, Yuzhen Bai, Yang Liu, Ge Gao, Weiyu Zhao
Diglycolamide (DGA) extractant is a kind of rare-earth extractant with promising applications that has the advantages of high extraction capacity, ease of synthesis, good thermal stability and good radiation stability. It is a green extractant that contains only four elements, C, H, O and N, and produces no residue after incineration. The properties of DGAs containing branched N,N′-alkyl substituents have been much studied in recent years, and it has been shown that branched side chains lead to better separation. The introduction of structurally rigid elements in DGA provides new possibilities for separation of rare earth elements (REEs). Owing to the tiny differences in the chemical properties of adjacent REES, the simple use of DGA extractant cannot meet all separation requirements, and a masking agent is added to the aqueous phase to improve the separation by coextraction to meet the requirements of different processes. This review presents the structural analysis of the complexes and crystals of diglycolamide extractants with rare-earth ions through different characterization means, and the effects of different structural extractants, solvents, nitric acid and phase modifiers on extraction behavior are reviewed. This review pays special attention to the effect of the side chain structure of diglycolamide on extraction behavior, which provides a theoretical basis and guiding direction for the field of separation of the REEs by diglycolamide extractants.
二甘醇酰胺(DGA)萃取剂是一种应用前景广阔的稀土萃取剂,具有萃取能力强、易于合成、热稳定性好、辐射稳定性好等优点。它是一种绿色萃取剂,只含有 C、H、O 和 N 四种元素,焚烧后不产生残渣。近年来,人们对含有支化 N,N′-烷基取代基的 DGA 的特性进行了大量研究,结果表明支化侧链能带来更好的分离效果。在 DGA 中引入结构刚性元素为稀土元素(REE)的分离提供了新的可能性。由于相邻稀土元素的化学性质存在微小差异,单纯使用DGA萃取剂无法满足所有分离要求,因此需要在水相中加入掩蔽剂,通过共萃取提高分离效果,以满足不同工艺的要求。本综述通过不同的表征手段,对二甘醇酰胺萃取剂与稀土离子的络合物和晶体进行了结构分析,并综述了不同结构的萃取剂、溶剂、硝酸和相改性剂对萃取行为的影响。本综述特别关注了二甘醇酰胺侧链结构对萃取行为的影响,为二甘醇酰胺萃取剂分离稀土元素领域提供了理论依据和指导方向。
{"title":"Application of diglycolamide extractant in rare-earth extraction","authors":"Yiwen Wang, Aijun Gong, Lina Qiu, Yuzhen Bai, Yang Liu, Ge Gao, Weiyu Zhao","doi":"10.1071/ch23188","DOIUrl":"https://doi.org/10.1071/ch23188","url":null,"abstract":"<p>Diglycolamide (DGA) extractant is a kind of rare-earth extractant with promising applications that has the advantages of high extraction capacity, ease of synthesis, good thermal stability and good radiation stability. It is a green extractant that contains only four elements, C, H, O and N, and produces no residue after incineration. The properties of DGAs containing branched <i>N</i>,<i>N</i>′-alkyl substituents have been much studied in recent years, and it has been shown that branched side chains lead to better separation. The introduction of structurally rigid elements in DGA provides new possibilities for separation of rare earth elements (REEs). Owing to the tiny differences in the chemical properties of adjacent REES, the simple use of DGA extractant cannot meet all separation requirements, and a masking agent is added to the aqueous phase to improve the separation by coextraction to meet the requirements of different processes. This review presents the structural analysis of the complexes and crystals of diglycolamide extractants with rare-earth ions through different characterization means, and the effects of different structural extractants, solvents, nitric acid and phase modifiers on extraction behavior are reviewed. This review pays special attention to the effect of the side chain structure of diglycolamide on extraction behavior, which provides a theoretical basis and guiding direction for the field of separation of the REEs by diglycolamide extractants.</p>","PeriodicalId":8575,"journal":{"name":"Australian Journal of Chemistry","volume":"22 1","pages":""},"PeriodicalIF":1.1,"publicationDate":"2024-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140037476","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Rare-earth perovskite oxides have become a research hotspot in the fields of environment and energy owing to their structural tunability, excellent redox properties, high stability and high catalytic activity. Researchers have designed and developed different rare-earth perovskite catalysts for tackling environmental pollutants in recent years. This review summarizes recent research progress on rare-earth perovskite catalysts in the catalytic oxidation and photocatalytic degradation of pollutants, gas sensing of volatile organic compounds and photocatalytic water splitting for hydrogen production and carbon dioxide reduction and conversion, and summarizes the mechanism of these reactions. It also discusses in detail the relationship between structural modification, synthesis process and the physical–chemical properties of the catalysts. Finally, the challenges with rare-earth chalcocite catalysts in the field of environment and energy are discussed.
{"title":"Status of rare-earth perovskite catalysts in environmental applications","authors":"Pengyun Li, Aijun Gong, Jiandi Li, Lina Qiu, Xianghai Wang, Yue Chen, Jiayi Yin, Xinyu Huang, Yifan Chen","doi":"10.1071/ch23148","DOIUrl":"https://doi.org/10.1071/ch23148","url":null,"abstract":"<p>Rare-earth perovskite oxides have become a research hotspot in the fields of environment and energy owing to their structural tunability, excellent redox properties, high stability and high catalytic activity. Researchers have designed and developed different rare-earth perovskite catalysts for tackling environmental pollutants in recent years. This review summarizes recent research progress on rare-earth perovskite catalysts in the catalytic oxidation and photocatalytic degradation of pollutants, gas sensing of volatile organic compounds and photocatalytic water splitting for hydrogen production and carbon dioxide reduction and conversion, and summarizes the mechanism of these reactions. It also discusses in detail the relationship between structural modification, synthesis process and the physical–chemical properties of the catalysts. Finally, the challenges with rare-earth chalcocite catalysts in the field of environment and energy are discussed.</p>","PeriodicalId":8575,"journal":{"name":"Australian Journal of Chemistry","volume":"26 1","pages":""},"PeriodicalIF":1.1,"publicationDate":"2024-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140037269","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A facile oxidative cyclization of β-ketothioamides for the simultaneous formation of a compound library similar to natural product benzothiazole derivatives has been developed. The oxidative cyclization of β-ketothioamides resulted in the simultaneous formation of four classes of previously unknown benzothiazole derivatives. This chemistry’s versatility adds a valuable component to the methodology for obtaining benzothiazole derivatives.
{"title":"Simultaneous diversity-oriented synthesis of benzothiazoles and related diverse analogues by iodine-catalyzed intramolecular cyclization from identical substrates","authors":"Meng Cui, Xue-Lin Wang, Mengzhou Wang, Jian-Wu Xie","doi":"10.1071/ch23144","DOIUrl":"https://doi.org/10.1071/ch23144","url":null,"abstract":"<p>A facile oxidative cyclization of <i>β</i>-ketothioamides for the simultaneous formation of a compound library similar to natural product benzothiazole derivatives has been developed. The oxidative cyclization of <i>β</i>-ketothioamides resulted in the simultaneous formation of four classes of previously unknown benzothiazole derivatives. This chemistry’s versatility adds a valuable component to the methodology for obtaining benzothiazole derivatives.</p>","PeriodicalId":8575,"journal":{"name":"Australian Journal of Chemistry","volume":"22 1","pages":""},"PeriodicalIF":1.1,"publicationDate":"2024-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140037181","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
In this study, the corrosion inhibition behavior of N,N′-(1,4-phenylene)bis(1,1-di(pyridin-2-yl)methanimine) (PBDPM) on mild steel in 1 M HCl at 30°C was evaluated under steady conditions. The corrosion inhibitor was synthesized by a one-step method. Electrochemical, energy dispersion spectrum (EDS) and water contact angle results revealed the adsorption behavior of the inhibitor at the metal–solution interface. The adsorption of PBDPM obeys the Langmuir adsorption isotherm. It is obvious that PBDPM exhibits good inhibition performance presumably due to its high surface coverage, as it forms a dense protective film on the surface of mild steel. The adsorption configuration and structure–activity relationships of the inhibitor were also explored theoretically by density functional theory (DFT) and molecular dynamics (MD), and the thermodynamic parameters and molecular active sites (the values of electrophilic attack and nucleophilic attack) were calculated.
{"title":"Experimental and computational study of a multi-active-site Schiff base as corrosion inhibitor of mild steel in 1M HCl","authors":"Xiaolong Li, Ting Long, Qian Wu, Chuan Lai, Yue Li, Junlan Li, Boyan Ren, Keqian Deng, Chaozheng Long, Shuting Zhao","doi":"10.1071/ch23196","DOIUrl":"https://doi.org/10.1071/ch23196","url":null,"abstract":"<p>In this study, the corrosion inhibition behavior of <i>N</i>,<i>N</i>′-(1,4-phenylene)bis(1,1-di(pyridin-2-yl)methanimine) (PBDPM) on mild steel in 1 M HCl at 30°C was evaluated under steady conditions. The corrosion inhibitor was synthesized by a one-step method. Electrochemical, energy dispersion spectrum (EDS) and water contact angle results revealed the adsorption behavior of the inhibitor at the metal–solution interface. The adsorption of PBDPM obeys the Langmuir adsorption isotherm. It is obvious that PBDPM exhibits good inhibition performance presumably due to its high surface coverage, as it forms a dense protective film on the surface of mild steel. The adsorption configuration and structure–activity relationships of the inhibitor were also explored theoretically by density functional theory (DFT) and molecular dynamics (MD), and the thermodynamic parameters and molecular active sites (the values of electrophilic attack and nucleophilic attack) were calculated.</p>","PeriodicalId":8575,"journal":{"name":"Australian Journal of Chemistry","volume":"7 1","pages":""},"PeriodicalIF":1.1,"publicationDate":"2024-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139557150","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Alex C. Bissember, Reyne Pullen, Gwendolyn A. Lawrie
This Highlight article considers key contributions made by Professor Brian Yates to the Australian chemistry academic community in recognition of his seminal leadership that led to the establishment of the Chemistry Threshold Learning Outcomes (CTLOs) as national assessment standards. These CTLOs currently underpin the Royal Australian Chemical Institute (RACI) process of the professional accreditation of chemistry majors in Australian tertiary institutions and, hence, provide benchmarks of learning in our discipline. Examples of contemporary assessment approaches in chemistry are presented to inform academics who are seeking to assess learning outcomes beyond threshold standards and to inspire future innovative assessment approaches.
{"title":"Recognising a beacon of teaching and learning leadership in Australian chemistry","authors":"Alex C. Bissember, Reyne Pullen, Gwendolyn A. Lawrie","doi":"10.1071/ch23146","DOIUrl":"https://doi.org/10.1071/ch23146","url":null,"abstract":"<p>This Highlight article considers key contributions made by Professor Brian Yates to the Australian chemistry academic community in recognition of his seminal leadership that led to the establishment of the Chemistry Threshold Learning Outcomes (CTLOs) as national assessment standards. These CTLOs currently underpin the Royal Australian Chemical Institute (RACI) process of the professional accreditation of chemistry majors in Australian tertiary institutions and, hence, provide benchmarks of learning in our discipline. Examples of contemporary assessment approaches in chemistry are presented to inform academics who are seeking to assess learning outcomes beyond threshold standards and to inspire future innovative assessment approaches.</p>","PeriodicalId":8575,"journal":{"name":"Australian Journal of Chemistry","volume":"8 1","pages":""},"PeriodicalIF":1.1,"publicationDate":"2024-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139410663","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A novel Co(OAc)2/N-hydroxyphthalimide (NHPI)-catalyzed oxidation of 3-arylmethyl sulfonyl imines to prepare 3-arylcarbonyl analogues has been realized. 3-Arylcarbonyl sulfonyl imines were comprehensively synthesized from benzyl substrates for the first time. The reactions proceeded in moderate to excellent yields. Mechanistic investigation suggests that 3-(hydroperoxy(phenyl)methyl)benzo[d]isothiazole 1,1-dioxide A is the key intermediate for the formation of products 2.
{"title":"Cobalt(II) catalytic oxidation of arylmethyl sulfonyl imines to arylcarbonyl analogues","authors":"Zetao Ma, Peipei Ma, Hongli Wu, Haifeng Gan","doi":"10.1071/ch23190","DOIUrl":"https://doi.org/10.1071/ch23190","url":null,"abstract":"<p>A novel Co(OAc)<sub>2</sub>/<i>N</i>-hydroxyphthalimide (NHPI)-catalyzed oxidation of 3-arylmethyl sulfonyl imines to prepare 3-arylcarbonyl analogues has been realized. 3-Arylcarbonyl sulfonyl imines were comprehensively synthesized from benzyl substrates for the first time. The reactions proceeded in moderate to excellent yields. Mechanistic investigation suggests that 3-(hydroperoxy(phenyl)methyl)benzo[<i>d</i>]isothiazole 1,1-dioxide <b>A</b> is the key intermediate for the formation of products <b>2</b>.</p>","PeriodicalId":8575,"journal":{"name":"Australian Journal of Chemistry","volume":"4 1","pages":""},"PeriodicalIF":1.1,"publicationDate":"2024-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139410667","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}