用于电催化还原二氧化碳的钯 (II) 亚吡啶磺酰胺 (PYSA)

IF 4 2区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Molecular Structure Pub Date : 2024-11-13 DOI:10.1016/j.molstruc.2024.140582
Afshan Khurshid , Muhammad Nawaz Tahir , Tilo Söhnel , Ehsan Ullah Mughal , Ryan J. Trovitch , M. Naveed Zafar
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引用次数: 0

摘要

一类新的供体柔性氮配体,即吡啶亚磺酰胺(PYSAs);N-(1-苄基吡啶-4(1H)-亚基)苯磺酰胺、N-(1-苄基吡啶-4(1H)-亚基)噻吩-2-磺酰胺、N-(1-苄基吡啶-4(1H)-亚基)噻吩-2-磺酰胺、N-(1-苄基吡啶-4(1H)-亚基)吡啶-2-磺酰胺和 N-(1-苄基吡啶-4(1H)-亚基)-8-喹啉-磺酰胺)由 4-氨基-1-苄基吡啶-1-鎓氯化物和各种芳香族磺酰氯制备而成。用[(CH3CN)2PdCl2]处理PYSAs,可得到相应的钯(II)配合物。新合成的化合物通过多核 1H 和 13C NMR 光谱、红外光谱、元素分析和单晶 X 射线衍射进行了表征。然后,在氮气和二氧化碳的惰性气氛下,在质子存在和不存在的情况下,对它们的氧化还原化学性质进行了评估。通过收集循环伏安图和峰值电位下峰值电流的增强,可以推断出二氧化碳与每种钯(II)催化剂之间存在明显的相互作用。在 3600 秒的批量电解条件下,所有催化剂都很稳定。
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Palladium (II) pyridylidene sulfonamides (PYSAs) for electrocatalytic reduction of CO2
A new class of donor flexible nitrogen ligands, namely pyridylidene sulfonamides (PYSAs; N-(1-benzylpyridin-4(1H)-ylidene)benzene-sulfonamide, N-(1-benzylpyridin-4(1H)-ylidene)thiophene-2-sulfonamide, N-(1-benzylpyridin-4(1H)-ylidene)pyridine-2-sulfonamide and N-(1-benzylpyridin-4(1H)-ylidene)-8-quinoline-sulfonamide), were prepared from 4-amino-1-benzylpyridin-1-ium chloride and various aromatic sulfonyl chlorides. The treatment of PYSAs with [(CH3CN)2PdCl2] afforded the corresponding Pd(II) complexes. The newly synthesized compounds were characterized by multinuclear 1H and 13C NMR spectroscopy, IR spectroscopy, elemental analysis, and single-crystal X-ray diffraction. Their redox chemistry was then evaluated under an inert atmosphere of nitrogen and carbon dioxide, both in the presence and absence of protons. An apparent interaction of CO2 with each Pd(II) catalyst was inferred by the collection of cyclic voltammograms and the enhancement of peak currents at respective peak potentials. All catalysts were robust under bulk electrolysis conditions over 3600 s.
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来源期刊
Journal of Molecular Structure
Journal of Molecular Structure 化学-物理化学
CiteScore
7.10
自引率
15.80%
发文量
2384
审稿时长
45 days
期刊介绍: The Journal of Molecular Structure is dedicated to the publication of full-length articles and review papers, providing important new structural information on all types of chemical species including: • Stable and unstable molecules in all types of environments (vapour, molecular beam, liquid, solution, liquid crystal, solid state, matrix-isolated, surface-absorbed etc.) • Chemical intermediates • Molecules in excited states • Biological molecules • Polymers. The methods used may include any combination of spectroscopic and non-spectroscopic techniques, for example: • Infrared spectroscopy (mid, far, near) • Raman spectroscopy and non-linear Raman methods (CARS, etc.) • Electronic absorption spectroscopy • Optical rotatory dispersion and circular dichroism • Fluorescence and phosphorescence techniques • Electron spectroscopies (PES, XPS), EXAFS, etc. • Microwave spectroscopy • Electron diffraction • NMR and ESR spectroscopies • Mössbauer spectroscopy • X-ray crystallography • Charge Density Analyses • Computational Studies (supplementing experimental methods) We encourage publications combining theoretical and experimental approaches. The structural insights gained by the studies should be correlated with the properties, activity and/ or reactivity of the molecule under investigation and the relevance of this molecule and its implications should be discussed.
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