Russian Journal of General Chemistry, Journal Year: 2024, Volume and Issue: 94(11), P. 3090 - 3098
Published: Nov. 1, 2024
Language: Английский
Russian Journal of General Chemistry, Journal Year: 2024, Volume and Issue: 94(11), P. 3090 - 3098
Published: Nov. 1, 2024
Language: Английский
Journal of Molecular Structure, Journal Year: 2025, Volume and Issue: unknown, P. 141679 - 141679
Published: Feb. 1, 2025
Language: Английский
Citations
31Journal of Molecular Structure, Journal Year: 2025, Volume and Issue: unknown, P. 142176 - 142176
Published: March 1, 2025
Language: Английский
Citations
3Inorganic Chemistry, Journal Year: 2025, Volume and Issue: 64(1), P. 443 - 451
Published: Jan. 2, 2025
Proton exchange membrane fuel cells (PEMFCs) are developing into very meaningful clean energy to fundamentally address environmental pollution. Among which the most studied Nafion series membranes limited under large-scale use, and some strong oxidizing groups such as hydrogen peroxide will attack structure of Nafion, shortening lifespan PEMFCs. Therefore, it is crucial develop a proton-conductive material with stability broad application. In this study, novel hourglass-type P4Mo6-based POMOFs denoted (H2timb)2[Mn3(H3P4Mo6O31)2]·4H2O was synthesized using 1,3,5-tri(1H-imidazole-1-yl)benzene (timb) ligand. It found that CUST-577 exhibited an excellent proton conductivity 8.9 × 10–3 S cm–1 at 80 °C 98% RH (relative humidity), proving conducted by protons. addition, also had greater H2O2 decomposition ability, thereby improving longevity cells. three-electrode system, displayed specific capacitance (Cs) value 308 F g–1 current density 0.15 A g–1, retention 88.3% after 2000 cycles. Since electrolyte can deliver protons for redox reaction various pseudocapacitor (PC) electrode materials, may be promising polyacid-based conductor PC material.
Language: Английский
Citations
1Inorganic Chemistry Communications, Journal Year: 2025, Volume and Issue: unknown, P. 114134 - 114134
Published: Feb. 1, 2025
Language: Английский
Citations
1Crystal Growth & Design, Journal Year: 2025, Volume and Issue: 25(5), P. 1636 - 1643
Published: Feb. 19, 2025
Developing a mechanochemical, solvent-free approach for forming C–C bonds in place of traditional solvent-based synthesis is significant green chemistry. Herein, novel Cu-complex-functionalized polyoxoniobate-based hybrid material [Cu(tpy)2]{[Cu(tpy)(H2O)]2[Nb10O28]}·5.5H2O (1, tpy = 2,2′:6′,2″-terpyridine) successfully synthesized and thoroughly characterized. 1 displays excellent thermal solvent stability highly mechanical force tolerant. Catalytic studies reveal that can catalyze the Knoevenagel condensations series aromatic aldehydes with malononitrile to build bond compounds under mechanochemical ball milling conditions. The catalytic system conducted no additional heating, lower oscillating frequency, without solvent. remarkable performance catalyst be attributed two factors: one sufficient contact between reagents facilitated by force, as well preactivated it; other synergistic effect Lewis acid–base sites (Cu2+ [Nb10O28]6–) within catalyst. exhibits outstanding recyclability applied gram-scale reactions. To best our knowledge, this work represents first example mechanochemically driven organic transformation using polyoxometalate-based
Language: Английский
Citations
0Journal of Catalysis, Journal Year: 2025, Volume and Issue: unknown, P. 116088 - 116088
Published: March 1, 2025
Language: Английский
Citations
0Inorganic Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: March 19, 2025
The oxidation of C-H bonds holds paramount importance in the realms organic synthesis and industrial chemistry. However, conventional methods are fraught with environmental concerns economic drawbacks. Consequently, heterogeneous catalysis solvent-free reactions have emerged as focal points research. This work reports two polyoxometalates-based complexes incorporating [P2Mo5O23]6- ({P2Mo5}) unit catalysts for bond oxidation: (CuIL2)4[H2(P2Mo5O23)]·H2O (1) (HL)6(P2Mo5O23)·H2O (2) (L = benzimidazole), which exhibit similar stacking modes but obvious structural differences: ligands L coordinated Cu ions to form {CuIL2} subunits complex 1, while 2 has fully protonated L. Notably, 1 demonstrated exceptional catalytic activity compared 2, efficiently oxidizing diphenylmethane (DPM) absence solvent achieving conversion rates high 99.5% selectivity benzophenone (BP) 100% within 6 h. reasons their different performances were unveiled. More importantly, even when reaction was scaled up by 10-fold (with amount substrate DMP reaching 10 mmol), still maintained activity, highlighting its substantial potential applications.
Language: Английский
Citations
0Inorganic Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: May 3, 2025
It is of great research value to develop an efficient and stable catalyst that can achieve the oxidation alkenes obtain epoxides, which serve as a multifunctional intermediate with important commercial value. Based on this, three-dimensional (3D) supramolecular framework H[CuI(H3bdcbpy)2(Mo12O38)(H2O)] (1, H4bdcbpy·2Cl = N,N'-bis(3,5-dicarboxybenzyl-4,4'-bipyridine·dichloride) was obtained from carboxylate-functionalized 1D coordination polymers, were derived unusual in situ [Mo12O38]4- cluster Cu-electron-deficient carboxylate complex units. The catalytic performance 1 epoxidation using TBHP examined, revealing its remarkable efficiency conversion cis-cyclooctene, high rate 99% outstanding selectivity 100%. Complex exhibited higher activity than unmodified H4bdcbpy·2Cl, CuCl2·2H2O, Na2MoO4·2H2O, well most previously reported polyoxometalate (POM)-based metal-organic complexes (POMOCs). Moreover, reaction kinetics mechanism explored free radical trapping experiments control experiments. stability also investigated.
Language: Английский
Citations
0European Journal of Inorganic Chemistry, Journal Year: 2024, Volume and Issue: unknown
Published: Oct. 31, 2024
Abstract The development of new catalytic materials for the fast and efficient photocatalytic reduction toxic Cr(VI) to less Cr(III) across a wide pH range water environment has become one most challenging topics. Herein, two isopolymolybdate‐based Ni(II)‐complexes [Ni II (bcbpy) 2 (β‐Mo 8 O 26 ) 0.5 (H O)] ⋅ 4H ( BHU‐5 [θ‐Mo ] BHU‐6 , Hbcbpy=1‐(4‐carboxybenzyl)‐4,4′‐bipyridinium) were synthesized via hydrothermal reaction with mixture Na MoO 4 2H O, NiCl 6H HbcbpyCl ligands. Single‐crystal X‐ray diffraction analysis displays that contain binuclear nickel‐bcbpy units, which in association different isopolymolybdates, forming distinct 1D chain 2D layer network structures, respectively. When used as photocatalysts Cr(VI), exhibited activities, achieving removal efficiencies 92 % 98 under visible light irradiation within 45 min. These surpass those pristine HbcbpyCl, reported polymolybdate‐based catalysts. Moreover, demonstrated high removing maintained structural stability 3.5–11.5. influence structures on efficiency was further studied. mechanism kinetics investigated detail.
Language: Английский
Citations
1Russian Journal of General Chemistry, Journal Year: 2024, Volume and Issue: 94(11), P. 3090 - 3098
Published: Nov. 1, 2024
Language: Английский
Citations
0