Afshan Khurshid , Muhammad Nawaz Tahir , Tilo Söhnel , Ehsan Ullah Mughal , Ryan J. Trovitch , M. Naveed Zafar
{"title":"用于电催化还原二氧化碳的钯 (II) 亚吡啶磺酰胺 (PYSA)","authors":"Afshan Khurshid , Muhammad Nawaz Tahir , Tilo Söhnel , Ehsan Ullah Mughal , Ryan J. Trovitch , M. Naveed Zafar","doi":"10.1016/j.molstruc.2024.140582","DOIUrl":null,"url":null,"abstract":"<div><div>A new class of donor flexible nitrogen ligands, namely pyridylidene sulfonamides (PYSAs; <em>N</em>-(1-benzylpyridin-4(1<em>H</em>)-ylidene)benzene-sulfonamide, <em>N</em>-(1-benzylpyridin-4(1<em>H</em>)-ylidene)thiophene-2-sulfonamide, <em>N</em>-(1-benzylpyridin-4(1<em>H</em>)-ylidene)pyridine-2-sulfonamide and <em>N</em>-(1-benzylpyridin-4(1<em>H</em>)-ylidene)-8-quinoline-sulfonamide), were prepared from 4-amino-1-benzylpyridin-1-ium chloride and various aromatic sulfonyl chlorides. The treatment of PYSAs with [(CH<sub>3</sub>CN)<sub>2</sub>PdCl<sub>2</sub>] afforded the corresponding Pd(II) complexes. The newly synthesized compounds were characterized by multinuclear <sup>1</sup>H and <sup>13</sup>C 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 CO<sub>2</sub> 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.</div></div>","PeriodicalId":16414,"journal":{"name":"Journal of Molecular Structure","volume":"1322 ","pages":"Article 140582"},"PeriodicalIF":4.0000,"publicationDate":"2024-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Palladium (II) pyridylidene sulfonamides (PYSAs) for electrocatalytic reduction of CO2\",\"authors\":\"Afshan Khurshid , Muhammad Nawaz Tahir , Tilo Söhnel , Ehsan Ullah Mughal , Ryan J. Trovitch , M. Naveed Zafar\",\"doi\":\"10.1016/j.molstruc.2024.140582\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A new class of donor flexible nitrogen ligands, namely pyridylidene sulfonamides (PYSAs; <em>N</em>-(1-benzylpyridin-4(1<em>H</em>)-ylidene)benzene-sulfonamide, <em>N</em>-(1-benzylpyridin-4(1<em>H</em>)-ylidene)thiophene-2-sulfonamide, <em>N</em>-(1-benzylpyridin-4(1<em>H</em>)-ylidene)pyridine-2-sulfonamide and <em>N</em>-(1-benzylpyridin-4(1<em>H</em>)-ylidene)-8-quinoline-sulfonamide), were prepared from 4-amino-1-benzylpyridin-1-ium chloride and various aromatic sulfonyl chlorides. The treatment of PYSAs with [(CH<sub>3</sub>CN)<sub>2</sub>PdCl<sub>2</sub>] afforded the corresponding Pd(II) complexes. The newly synthesized compounds were characterized by multinuclear <sup>1</sup>H and <sup>13</sup>C 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 CO<sub>2</sub> 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.</div></div>\",\"PeriodicalId\":16414,\"journal\":{\"name\":\"Journal of Molecular Structure\",\"volume\":\"1322 \",\"pages\":\"Article 140582\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2024-11-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Molecular Structure\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0022286024030904\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Molecular Structure","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022286024030904","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
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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