Article
Chemistry, Multidisciplinary
Shuoyan Xiong, Alexandria Hong, Brad C. Bailey, Heather A. Spinney, Todd D. Senecal, Hannah Bailey, Theodor Agapie
Summary: We address the challenge of insertion copolymerization of polar olefins and ethylene by designing ligands. The neutral nickel phosphine enolate catalysts with large phosphine substituents at the axial positions of Ni exhibit high activity and result in highly linear copolymers. The study reveals a strong correlation between axial steric hindrance and catalyst performance.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
(2022)
Article
Chemistry, Multidisciplinary
Krzysztof Kacprzak, Adam Lewera
Summary: The Pd/Al2O3, Pd/TiO2, and Pt/Al2O3 catalysts were used for selective hydrogenation of MeC CH and CH2=C=CH2 in the C-3 fraction stream. Pd-containing catalysts showed higher activity and selectivity than Pt/Al2O3, but excessive H-2 reduced their selectivity. Pd/TiO2 catalyst showed higher activity and a slight decrease in selectivity compared to Pd/Al2O3, making it a potential alternative.
PRZEMYSL CHEMICZNY
(2023)
Article
Chemistry, Multidisciplinary
Hae Sol Lee, Nam Sun Kim, Dong-il Kwon, Su-Kyung Lee, Muhammad Numan, Taesung Jung, Kanghee Cho, Michal Mazur, Hae Sung Cho, Changbum Jo
Summary: Organic functionalization of zeolites can adjust their effective pore diameters, allowing for challenging separations. Post-functionalized zeolites demonstrate ideal selectivity in separating light olefins and paraffins.
ADVANCED MATERIALS
(2021)
Article
Chemistry, Applied
Zinan Dai, Zehao Yu, Ying Bai, Jiayun Li, Jiajian Peng
Summary: A simple method for hydrosilylation of olefins using air-stable cobalt catalysts has been developed. The catalyst system consists of cobalt(II) salts and terpyridine derivatives, allowing for smooth processing under mild conditions without the need for Grignard reagents or NaHBEt(3) as an activator.
APPLIED ORGANOMETALLIC CHEMISTRY
(2021)
Review
Chemistry, Physical
Shepherd Siangwata, Cody Williams, Nikechukwu Omosun, Siyabonga Ngubane, Gregory S. Smith
Summary: Metallodendrimers have shown great potential as catalysts in hydroformylation reactions involving olefins, with their dendritic scaffolds influencing both the activity and selectivity of the catalyst. The recyclability of rhodium-bearing metallodendrimers through heterogenization of homogeneous catalysts presents an attractive option for sustainable use of mineral resources, especially in the case of rare, expensive, and fast-depleting metals like rhodium.
APPLIED CATALYSIS A-GENERAL
(2021)
Article
Chemistry, Multidisciplinary
Florian Puls, Philipp Linke, Olga Kataeva, Hans-Joachim Knoelker
Summary: This paper describes a convenient method for the oxidation of olefins to ketones using Fe(dbm)(3) or a combination of iron(II) chloride and neocuproine as catalysts and phenylsilane as an additive. The reactions are efficient and have a high yield and selectivity.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
(2021)
Article
Multidisciplinary Sciences
Yantao Li, Qianzhen Shao, Hengchi He, Chengjian Zhu, Xiao-Song Xue, Jin Xie
Summary: The authors present a method to synthesize tetrasubstituted olefins via dual photo- and nickel catalysis under an air atmosphere, without the need for an inert atmosphere. The synthesis of these compounds under mild conditions is challenging, but the authors were able to achieve it by using readily available carboxylic acids and alkenyl triflates. The method shows promise for applications in complex molecule modification and gram-scale synthesis.
NATURE COMMUNICATIONS
(2022)
Article
Chemistry, Organic
Fuyang Yue, Jianyang Dong, Yuxiu Liu, Qingmin Wang
Summary: The protocol allows for the direct visible-light-mediated alkenylation of alkyl boronic acids at room temperature without an external Lewis base, and proposes a mechanism involving benzenesulfinate activation of alkyl boronic acids. It has been demonstrated to be efficient for functionalizing a broad range of cyclic and acyclic primary and secondary alkyl boronic acids with various alkenyl sulfones.
Article
Chemistry, Multidisciplinary
Yangzhong Qin, Qilei Zhu, Rui Sun, Jacob M. Ganley, Robert R. Knowles, Daniel G. Nocera
Summary: The selectivity and reaction mechanism for the photocatalytic anti-Markovnikov hydroamination of unactivated alkenes with primary amines to produce secondary amines has been revealed through time-resolved laser kinetics measurements of key reaction intermediates. The absence of back-electron transfer between the photogenerated aminium radical cation and reduced photocatalyst complex leads to the selectivity for primary amine alkylation. The turnover of the photocatalyst occurs through a reaction between Ir(II) and a thiyl radical, with the in situ formation of an off-cycle disulfide suppressing this turnover and reducing reaction efficiency.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
(2021)
Article
Multidisciplinary Sciences
Muliang Zhang, Jinghui Zhang, Qingyao Li, Yumeng Shi
Summary: Given the importance of vicinal diamine units in various fields, a strategy that avoids the use of stoichiometric strong oxidants is highly desirable. This study presents the application of ligand-to-metal charge transfer (LMCT) excitation to achieve 1,2-diazidation reactions using iron salt as the catalyst. The LMCT-homolysis mode enables the generation of electrophilic azidyl radical intermediate and subsequent carbon-nitrogen bond formation, providing a versatile and eco-friendly approach for the synthesis of structurally diverse diazides from alkenes.
NATURE COMMUNICATIONS
(2022)
Article
Chemistry, Multidisciplinary
Dongcheng He, Teng Li, Xingchao Dai, Shujuan Liu, Xinjiang Cui, Feng Shi
Summary: This study successfully prepared a series of MICs and found that due to the interaction of imprinting molecules and imprinting ligands, the MICs not only improved catalytic selectivity but also enhanced catalytic activity.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
(2023)
Review
Chemistry, Physical
Yuming Li, Shuting Fu, Qiyang Zhang, Hongyu Liu, Yajun Wang
Summary: This article summarizes the preparation and application of gallium-based catalysts in the catalytic conversion of light alkanes. It describes different conversion routes, discusses preparation methods, and explores current limitations and future perspectives.
Article
Chemistry, Applied
C. Coffano, A. Porta, C. G. Visconti, F. Rabino, G. Franzoni, B. Picutti, L. Lietti
Summary: This study investigates the one-pot conversion of CO2 into lower olefins using a physical mixture of a methanol synthesis catalyst and a methanol-to-olefins (MTO) zeolite. The individual reactions are tested under CO2 to olefins conditions, providing insights on the reaction mechanism and catalyst stability. The operating conditions and the effects of different catalyst samples are analyzed. The study also compares the methanol-mediated and modified Fischer-Tropsch (MFT) routes, highlighting the strengths and weaknesses of each reaction pathway.
Article
Chemistry, Multidisciplinary
Saikat Maiti, Joon Ho Rhlee
Summary: Stereoselective dicarbofunctionalization of terminal aryl alkynes has been achieved through reductive Ni-catalysis, utilizing alkyl iodide and aryl iodide as electrophilic coupling partners to accomplish exclusive regioselective and anti-addition selective alkylarylation.
CHEMICAL COMMUNICATIONS
(2021)
Article
Chemistry, Organic
Su Chen, Luc Van Meervelt, Erik V. Van der Eycken, Upendra K. Sharma
Summary: A mild visible-light-driven palladium-catalyzed radical tandem dearomatization reaction of indoles with unactivated alkenes is described. This reaction exhibited moderate to good yields and good to excellent diastereoselectivities. Under visible-light irradiation, a photo-excited state of the palladium complex was formed, which enabled the transfer of a single electron to N-(2-bromobenzoyl)indoles, leading to a hybrid palladium radical chemistry. This approach provides efficient and atom-economical access to diverse 2,3-disubstituted indoline derivatives.