Heidar Darmandeh, Thorsten Scherpf, Kai-Stephan Feichtner, Christopher Schwarz, Viktoria H Gessner
{"title":"金属化Ylides [cy3c - so2tol]M (M = Li, Na, K)的合成、分离和晶体结构","authors":"Heidar Darmandeh, Thorsten Scherpf, Kai-Stephan Feichtner, Christopher Schwarz, Viktoria H Gessner","doi":"10.1002/zaac.201900333","DOIUrl":null,"url":null,"abstract":"<p><p>The preparation and isolation of the metalated ylides [Cy<sub>3</sub>PCSO<sub>2</sub>Tol]M ( <b><sup>Cy</sup>1-M</b>) (with M = Li, Na, K) are reported. In contrast to its triphenylphosphonium analogue the synthesis of <b><sup>Cy</sup>1-M</b> revealed to be less straight forward. Synthetic routes to the phosphonium salt precursor <b><sup>Cy</sup>1</b>-<b>H<sub>2</sub></b> via different methods revealed to be unsuccessful or low-yielding. However, nucleophilic attack of the ylide Cy<sub>3</sub>P = CH<sub>2</sub> at toluenesulfonyl fluoride under basic conditions proved to be a high-yielding method directly leading to the ylide <b><sup>Cy</sup>1-H</b>. Metalation to the yldiides was finally achieved with strong bases such as <i>n</i>BuLi, NaNH<sub>2</sub>, or BnK. In the solid state, the lithium compound forms a tetrameric structure consisting of a (C-S-O-Li)<sub>4</sub> macrocycle, which incorporates an additional molecule of lithium iodide. The potassium compound forms a <i>C</i> <sub>4</sub>-symmetric structure with a (K<sub>4</sub>O<sub>4</sub>)<sub>2</sub> octahedral prism as central structural motif. Upon deprotonation the P-C-S linkage undergoes a remarkable contraction typical for metalated ylides.</p>","PeriodicalId":54398,"journal":{"name":"Zeitschrift fur Anorganische und Allgemeine Chemie","volume":"646 13","pages":"835-841"},"PeriodicalIF":1.1000,"publicationDate":"2020-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/zaac.201900333","citationCount":"5","resultStr":"{\"title\":\"Synthesis, Isolation and Crystal Structures of the Metalated Ylides [Cy<sub>3</sub>P-C-SO<sub>2</sub>Tol]M (M = Li, Na, K).\",\"authors\":\"Heidar Darmandeh, Thorsten Scherpf, Kai-Stephan Feichtner, Christopher Schwarz, Viktoria H Gessner\",\"doi\":\"10.1002/zaac.201900333\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The preparation and isolation of the metalated ylides [Cy<sub>3</sub>PCSO<sub>2</sub>Tol]M ( <b><sup>Cy</sup>1-M</b>) (with M = Li, Na, K) are reported. In contrast to its triphenylphosphonium analogue the synthesis of <b><sup>Cy</sup>1-M</b> revealed to be less straight forward. Synthetic routes to the phosphonium salt precursor <b><sup>Cy</sup>1</b>-<b>H<sub>2</sub></b> via different methods revealed to be unsuccessful or low-yielding. However, nucleophilic attack of the ylide Cy<sub>3</sub>P = CH<sub>2</sub> at toluenesulfonyl fluoride under basic conditions proved to be a high-yielding method directly leading to the ylide <b><sup>Cy</sup>1-H</b>. Metalation to the yldiides was finally achieved with strong bases such as <i>n</i>BuLi, NaNH<sub>2</sub>, or BnK. In the solid state, the lithium compound forms a tetrameric structure consisting of a (C-S-O-Li)<sub>4</sub> macrocycle, which incorporates an additional molecule of lithium iodide. The potassium compound forms a <i>C</i> <sub>4</sub>-symmetric structure with a (K<sub>4</sub>O<sub>4</sub>)<sub>2</sub> octahedral prism as central structural motif. Upon deprotonation the P-C-S linkage undergoes a remarkable contraction typical for metalated ylides.</p>\",\"PeriodicalId\":54398,\"journal\":{\"name\":\"Zeitschrift fur Anorganische und Allgemeine Chemie\",\"volume\":\"646 13\",\"pages\":\"835-841\"},\"PeriodicalIF\":1.1000,\"publicationDate\":\"2020-07-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1002/zaac.201900333\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Zeitschrift fur Anorganische und Allgemeine Chemie\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/zaac.201900333\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2020/4/22 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zeitschrift fur Anorganische und Allgemeine Chemie","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/zaac.201900333","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2020/4/22 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Synthesis, Isolation and Crystal Structures of the Metalated Ylides [Cy3P-C-SO2Tol]M (M = Li, Na, K).
The preparation and isolation of the metalated ylides [Cy3PCSO2Tol]M ( Cy1-M) (with M = Li, Na, K) are reported. In contrast to its triphenylphosphonium analogue the synthesis of Cy1-M revealed to be less straight forward. Synthetic routes to the phosphonium salt precursor Cy1-H2 via different methods revealed to be unsuccessful or low-yielding. However, nucleophilic attack of the ylide Cy3P = CH2 at toluenesulfonyl fluoride under basic conditions proved to be a high-yielding method directly leading to the ylide Cy1-H. Metalation to the yldiides was finally achieved with strong bases such as nBuLi, NaNH2, or BnK. In the solid state, the lithium compound forms a tetrameric structure consisting of a (C-S-O-Li)4 macrocycle, which incorporates an additional molecule of lithium iodide. The potassium compound forms a C4-symmetric structure with a (K4O4)2 octahedral prism as central structural motif. Upon deprotonation the P-C-S linkage undergoes a remarkable contraction typical for metalated ylides.
期刊介绍:
ZAAC is an international scientific journal which publishes original papers on new relevant research results from all areas of inorganic chemistry, solid state chemistry, and co-ordination chemistry.
The contributions reflect the latest findings in these research areas and serve the development of new materials, such as super-hard materials, electrical superconductors, or intermetallic compounds. Up-to-date physical methods for the characterization of new chemical compounds and materials are also described.