[2 + 3] cycloaddition of the pyrrolin N-oxide (-)O[upper bond 1 start](+)N[double bond, length as m-dash]CHCH(2)CH(2)C[upper bond 1 end]Me(2) with 2-cyanopyridine NC(5)H(4)(2-CN) in the presence of PdCl(2) at room temperature in acetone gives the ketoimine palladium(II) complex cis-[PdCl(2){N(=[upper bond 1 start]CCH(2)CH(2)C(Me)(2)N[upper bond 1 end]H)C(=O)C(5)H(4)N}] containing the (E)-N-(5,5-dimethylpyrrolidin-2-ylidene)picolinamide ligand, in good yield (85%). The reaction of with 3-cyanopyridine NC(5)H(4)(3-CN) or 4-cyanopyridine NC(5)H(4)(4-CN) under the same experimental conditions gives the simple adducts of cyanopyridines trans-[PdCl(2){NC(5)H(4)(3-CN)}(2)] or trans-[PdCl(2){NC(5)H(4)(4-CN)}(2)] , respectively. When the cyanopyridines NC(5)H(3)R(1)R(2) (R(1) = 2-CN, R(2) = H ; R(1) = 3-CN, R(2) = H ; R(1) = 4-CN, R(2) = H ; R(1) = 4-CN, R(2) = 2-Cl ; R(1) = 3-CN, R(2) = 5-Me ) are heated at 100 degrees C for 12 h with 2-butanone oxime (used as a reagent and solvent) in the presence of PdCl(2), the 2,4-dipyridyl-1,3,5-triazapentadienate (or bis-imidoylamidinate) palladium(II) complexes [Pd{HN[double bond, length as m-dash]C(NC(5)H(3)R(2))NC(NC(5)H(3)R(2))[double bond, length as m-dash]NH}(2)] (2-NC(5)H(3), R(2) = H ; 3-NC(5)H(3), R(2) = H ; 4-NC(5)H(3), R(2) = H ; 4-NC(5)H(3), R(2) = 2-Cl ; 3-NC(5)H(3), R(2) = 5-Me ) are synthesized by one-pot template transformations followed by deprotonation by a base (n-PrNH(2)). The compounds were characterized by IR, (1)H and (13)C NMR spectroscopies, FAB(+)-MS, elemental analyses and, in the cases of , , and , also by X-ray diffraction analyses. The catalytic activity of complexes and was studied under microwave irradiation for C-C coupling reactions, in the solid phase on a silica gel support, and it was found that complex is the most active one with the maximum TON of 2.0.10(5) and TOF of 1.3.10(4) min(-1) for Suzuki-Miyaura, and TON of 800 and TOF of 27 min(-1) for Heck reactions.
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Crit Rev Microbiol
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Oral Microbiology, Bristol Dental School, University of Bristol, United Kingdom.
This review discusses the chemical properties, synthesis and detection, and biological functions of a molecular group of cis-2-unsaturated fatty acids, containing fatty acid carbon chains of various lengths and cis double-bond configurations, known as the diffusible signaling factor family (DSFF). Early postulation of the conserved nature of the DSFF among Gram-negative bacteria have now been challenged by the latest evidences that unraveled their presence in a various other distinct microorganisms. Over the last decade, a significant depth and breadth of understanding has been made on the multifaceted functions of DSFFs among bacteria, and their interactions with evolutionarily divergent fungi, plants insects and small animals.
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January 2025
University of Sussex, Department of Chemistry, School of Life Sciences, BN1 9QJ, Brighton, UNITED KINGDOM OF GREAT BRITAIN AND NORTHERN IRELAND.
The synthesis, structures and magnetic properties of an η5-silole complex and an η5-stannole complex of erbium are reported. The sandwich complex anions [(η5-CpSi)Er(η8-COT)]- and [(η5-CpSn)Er(η8-COT)]-, where CpSi is [SiC4-2,5-(SiMe3)2-3,4-Ph2]2- (1Si), CpSn is [SnC4-2,5-(SiMe3)2-3,4-Me2]2- (1Sn) and COT = cyclo-octatetraenyl, were obtained as their [K(2.2.
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January 2025
State Key Laboratory of Solidification Processing, Center for Nano Energy Materials, School of Materials Science and Engineering, Northwestern Polytechnical University (NPU), Shaanxi Joint Laboratory of Graphene Xi'an 710072 China
The oxidative dehydrogenation of propane with CO (CO-ODP) is a green industrial process for producing propene. Cerium oxide-supported platinum-based (Pt/CeO) catalysts exhibit remarkable reactivity toward propane and CO due to the unique delicate balance of C-H and C[double bond, length as m-dash]O bond activation. However, the simultaneous activation and cleavage of C-H, C-C, and C-O bonds on Pt/CeO-based catalysts may substantially impede the selective activation of C-H bonds during the CO-ODP process.
View Article and Find Full Text PDFACS Omega
January 2025
Instituto de Física, Universidade Federal de Goiás, Goiânia, Goiás 74001-970, Brazil.
We investigate the energetic and structural properties of small lithium clusters doped with a carbon atom using a combination of computational methods, including density functional theory (DFT), diffusion quantum Monte Carlo (DMC), and the Hartree-Fock (HF) approximation. We calculate the lowest energy structures, total ground-state energies, electron populations, binding energies, and dissociation energies as a function of cluster size. Our results show that carbon doping significantly enhances the stability of lithium clusters, increasing the magnitude of the binding energy by 0.
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January 2025
Chulalongkorn University, Chemistry, THAILAND.
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