One-Pot, Single-Step, and Gram-Scale Synthesis of Mononuclear [(η6-arene)Ni(N-heterocyclic carbene)] Complexes: Useful Precursors of the Ni0–NHC Unit

2014 ◽  
Vol 33 (5) ◽  
pp. 1276-1282 ◽  
Author(s):  
Yoichi Hoshimoto ◽  
Yukari Hayashi ◽  
Haruka Suzuki ◽  
Masato Ohashi ◽  
Sensuke Ogoshi
2020 ◽  
Vol 7 (1) ◽  
pp. 23-39 ◽  
Author(s):  
Kantharaju Kamanna ◽  
Santosh Y. Khatavi

Multi-Component Reactions (MCRs) have emerged as an excellent tool in organic chemistry for the synthesis of various bioactive molecules. Among these, one-pot MCRs are included, in which organic reactants react with domino in a single-step process. This has become an alternative platform for the organic chemists, because of their simple operation, less purification methods, no side product and faster reaction time. One of the important applications of the MCRs can be drawn in carbon- carbon (C-C) and carbon-heteroatom (C-X; X = N, O, S) bond formation, which is extensively used by the organic chemists to generate bioactive or useful material synthesis. Some of the key carbon- carbon bond forming reactions are Grignard, Wittig, Enolate alkylation, Aldol, Claisen condensation, Michael and more organic reactions. Alternatively, carbon-heteroatoms containing C-N, C-O, and C-S bond are also found more important and present in various heterocyclic compounds, which are of biological, pharmaceutical, and material interest. Thus, there is a clear scope for the discovery and development of cleaner reaction, faster reaction rate, atom economy and efficient one-pot synthesis for sustainable production of diverse and structurally complex organic molecules. Reactions that required hours to run completely in a conventional method can now be carried out within minutes. Thus, the application of microwave (MW) radiation in organic synthesis has become more promising considerable amount in resource-friendly and eco-friendly processes. The technique of microwaveassisted organic synthesis (MAOS) has successfully been employed in various material syntheses, such as transition metal-catalyzed cross-coupling, dipolar cycloaddition reaction, biomolecule synthesis, polymer formation, and the nanoparticle synthesis. The application of the microwave-technique in carbon-carbon and carbon-heteroatom bond formations via MCRs with major reported literature examples are discussed in this review.


2004 ◽  
Vol 69 (5) ◽  
pp. 996-1008 ◽  
Author(s):  
Steven J. Langford ◽  
Clint P. Woodward

A strategy in preparing a family of hexameric porphyrin cubes based on the interplay of Sn(IV)-O and Ru(II)-N interactions is described. In this first iteration, we have prepared the heptamer [SnIV(TPyP)·(4)2][Ru(CO)(TPP)]6 (4 = (E)-(3-(4-pyridyl)acrylate)) constituting a 5,10,15,20-tetra(4-pyridyl)porphyrin (TPyP) core and 5,10,15,20-tetraphenylporphyrin (TPP) faces and compared its formation by stepwise and "one-pot" strategies where up to nine components are assembled in a single step in a regiospecific manner. In one example, the heptamer is formed around the template [SnIV(TPyP)·(4)2] bearing pyridine groups in which the nitrogens radiate octahedrally along each vertex. The ability to modulate the axial vertex through choice of pyridine is also demonstrated. 1H NMR measurements on [SnIV(TPyP)·(4)2][Ru(CO)(TPP)]6 indicate that the protons on the core template are extremely shielded as a result of the anisotropy of the peripheral porphyrin units. Various NMR techniques, including NOESY experiments, have been used to characterise the heptamer in solution.


Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 521
Author(s):  
Juan Carlos Rendón-Angeles ◽  
Zully Matamoros-Veloza ◽  
Jose Luis Rodríguez-Galicia ◽  
Gimyeong Seong ◽  
Kazumichi Yanagisawa ◽  
...  

One-pot hydrothermal preparation of Ca3Cr2Si3O12 uvarovite nanoparticles under alkaline conditions was investigated for the first time. The experimental parameters selected for the study considered the concentration of the KOH solvent solution (0.01 to 5.0 M), the agitation of the autoclave (50 rpm), and the nominal content of Si4+ (2.2–3.0 mole). Fine uvarovite particles were synthesised at 200 °C after a 3 h interval in a highly concentrated 5.0 M KOH solution. The crystallisation of single-phase Ca3Cr2Si3O12 particles proceeded free of by-products via a one-pot process involving a single-step reaction. KOH solutions below 2.5 M and water hindered the crystallisation of the Ca3Cr2Si3O12 particles. The hydrothermal treatments carried out with stirring (50 rpm) and non-stirring triggered the crystallisation of irregular anhedral particles with average sizes of 8.05 and 12.25 nm, respectively. These particles spontaneously assembled into popcorn-shaped agglomerates with sizes varying from 66 to 156 nm. All the powders prepared by the present method exhibited CIE-L*a*b* values that correspond to the Victoria green colour spectral space and have a high near infrared reflectance property. The particle size and structural crystallinity are factors affecting the Victoria pigment optical properties, such as CIE-L*a*b* values, green tonality, and near-infrared reflectance.


Author(s):  
Priyabrata Roy ◽  
Binay Krishna Ghorai

One-pot three-component coupling ofo-alkynylheteroaryl carbonyl derivatives with Fischer carbene complexes and dienophiles leading to the synthesis of quinoxaline and phenazine ring systems has been investigated. This involves the generation of furo[3,4-b]pyrazine and furo[3,4-b]quinoxaline as transient intermediates, which were trapped with Diels–Alder dienophiles. This is the first report on furo[3,4-b]pyrazine intermediates.


2016 ◽  
Vol 18 (3) ◽  
pp. 742-752 ◽  
Author(s):  
Zhong Sun ◽  
Lifang Xue ◽  
Shengtian Wang ◽  
Xiaohong Wang ◽  
Junyou Shi

A new series of heteropolyacids [(CH3)3NCH2CH2OH]nH5−nAlW12O40 are used to catalyse the single step conversion of cellulose into levulinic acid (LA). The highest reported yield of LA directly from cellulose was achieved with 74.8% yield and 98.9% conversion in one pot.


2009 ◽  
Vol 15 (39) ◽  
pp. 9981-9986 ◽  
Author(s):  
Morgane A. N. Virboul ◽  
Martin Lutz ◽  
Maxime A. Siegler ◽  
Anthony L. Spek ◽  
Gerard van Koten ◽  
...  

2016 ◽  
Vol 12 ◽  
pp. 1772-1777 ◽  
Author(s):  
Lena Huck ◽  
Juan F González ◽  
Elena de la Cuesta ◽  
J Carlos Menéndez

A sequential three-component process is described, starting from 3-arylmethylene-2,5-piperazinediones and involving a one-pot sequence of reactions achieving regioselective opening of the 2,5-diketopiperazine ring and diastereoselective generation of an aziridine ring. This method allows the preparation of N-unprotected, trisubstituted aziridines bearing a peptide side chain under mild conditions. Their transformation into β-trifluoroacetamido-α-ketoamide and α,β-diketoamide frameworks was also achieved in a single step.


e-Polymers ◽  
2006 ◽  
Vol 6 (1) ◽  
Author(s):  
Adam Kiersnowski ◽  
Maria Trelinska-Wlazlak ◽  
Justyna Dolega ◽  
Jacek Piglowski

AbstractThis article describes simple preparation methods of poly(methyl methacrylate) (PMMA)/synthetic montmorillonite nanocomposites by single-step insitu polymerizations. Compatibility between PMMA and the silicate was ensured by an addition of (3-acrylamidepropyl) trimethylammonium chloride (AAPTMA). The work also compares how different synthetic routes, namely emulsion and solution polymerization, affect the structure as well as thermal and mechanical properties of obtained nanocomposites. The results of structural investigations clearly show, that both the techniques lead to intercalated nanocomposites, but emulsion polymerization allows more effective deflocculating and intercalating of the clay with acrylic copolymers. The addition of small amounts of layered silicates causes an increase in thermal stability and stiffness of the materials. It is demonstrated that at 5 wt. % of the filler, the temperature of 10 % weight loss was shifted up by nearly 50 K in comparison to the neat PMMA. In the same sample, the Young’s modulus of the material was found to be increased by 26 %.


2018 ◽  
Vol 5 (15) ◽  
pp. 2345-2348 ◽  
Author(s):  
Deng-Jie Zhu ◽  
Wen Ding ◽  
Dong-Hui Wang ◽  
Min Xue ◽  
Yong Yang

A new type of carbazole-based sulfonamide macrocycle was synthesized efficiently in one single step.


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