{"title":"质子化甲烷(CH5+)中五价碳的确认:来自分子Handycam技术的见解","authors":"Moumita Dinda, Sudipta Nayak, Arijit Bag","doi":"10.1016/j.cartre.2025.100574","DOIUrl":null,"url":null,"abstract":"<div><div>The existence of pentavalent carbon has intrigued scientists since the discovery of CH<span><math><msubsup><mrow></mrow><mrow><mn>5</mn></mrow><mrow><mo>+</mo></mrow></msubsup></math></span> in 1952 but remains elusive due to the lack of definitive evidence. The present study unveils the mystery through a comprehensive investigation of the structural and bonding nature of CH<span><math><msubsup><mrow></mrow><mrow><mn>5</mn></mrow><mrow><mo>+</mo></mrow></msubsup></math></span> employing the newly developed Molecular Handycam Technique (MHT) by Bag and co-workers, focusing on its formation pathways and energetic favorability. Computational analysis at the coupled cluster theory (CCSD) level, we examine the formation of CH<span><math><msubsup><mrow></mrow><mrow><mn>5</mn></mrow><mrow><mo>+</mo></mrow></msubsup></math></span> through the association of CH<span><math><msubsup><mrow></mrow><mrow><mn>3</mn></mrow><mrow><mo>+</mo></mrow></msubsup></math></span> and H<sub>2</sub>, compared to the protonation of methane. Our findings reveal a preference for the former pathway, highlighting distinct structural configurations, including a global minimum and two alternative geometries. We demonstrate the participation of higher orbitals of carbon (3d<span><math><msub><mrow></mrow><mrow><msup><mrow><mi>z</mi></mrow><mrow><mn>2</mn></mrow></msup></mrow></msub></math></span>) and its interaction with the bond pair of the approaching H<span><math><msub><mrow></mrow><mrow><mn>2</mn></mrow></msub></math></span> molecule in the formation and stabilization of the fifth C-H bond. This analytical approach provides critical insights into the expanded valency of carbon, which could lead to a new class of carbon compounds.</div></div>","PeriodicalId":52629,"journal":{"name":"Carbon Trends","volume":"21 ","pages":"Article 100574"},"PeriodicalIF":3.9000,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Confirmation of pentavalent carbon in protonated methane (CH5+ ): Insights from Molecular Handycam Technique\",\"authors\":\"Moumita Dinda, Sudipta Nayak, Arijit Bag\",\"doi\":\"10.1016/j.cartre.2025.100574\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The existence of pentavalent carbon has intrigued scientists since the discovery of CH<span><math><msubsup><mrow></mrow><mrow><mn>5</mn></mrow><mrow><mo>+</mo></mrow></msubsup></math></span> in 1952 but remains elusive due to the lack of definitive evidence. The present study unveils the mystery through a comprehensive investigation of the structural and bonding nature of CH<span><math><msubsup><mrow></mrow><mrow><mn>5</mn></mrow><mrow><mo>+</mo></mrow></msubsup></math></span> employing the newly developed Molecular Handycam Technique (MHT) by Bag and co-workers, focusing on its formation pathways and energetic favorability. Computational analysis at the coupled cluster theory (CCSD) level, we examine the formation of CH<span><math><msubsup><mrow></mrow><mrow><mn>5</mn></mrow><mrow><mo>+</mo></mrow></msubsup></math></span> through the association of CH<span><math><msubsup><mrow></mrow><mrow><mn>3</mn></mrow><mrow><mo>+</mo></mrow></msubsup></math></span> and H<sub>2</sub>, compared to the protonation of methane. Our findings reveal a preference for the former pathway, highlighting distinct structural configurations, including a global minimum and two alternative geometries. We demonstrate the participation of higher orbitals of carbon (3d<span><math><msub><mrow></mrow><mrow><msup><mrow><mi>z</mi></mrow><mrow><mn>2</mn></mrow></msup></mrow></msub></math></span>) and its interaction with the bond pair of the approaching H<span><math><msub><mrow></mrow><mrow><mn>2</mn></mrow></msub></math></span> molecule in the formation and stabilization of the fifth C-H bond. This analytical approach provides critical insights into the expanded valency of carbon, which could lead to a new class of carbon compounds.</div></div>\",\"PeriodicalId\":52629,\"journal\":{\"name\":\"Carbon Trends\",\"volume\":\"21 \",\"pages\":\"Article 100574\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2025-09-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Carbon Trends\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2667056925001233\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Carbon Trends","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667056925001233","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Confirmation of pentavalent carbon in protonated methane (CH5+ ): Insights from Molecular Handycam Technique
The existence of pentavalent carbon has intrigued scientists since the discovery of CH in 1952 but remains elusive due to the lack of definitive evidence. The present study unveils the mystery through a comprehensive investigation of the structural and bonding nature of CH employing the newly developed Molecular Handycam Technique (MHT) by Bag and co-workers, focusing on its formation pathways and energetic favorability. Computational analysis at the coupled cluster theory (CCSD) level, we examine the formation of CH through the association of CH and H2, compared to the protonation of methane. Our findings reveal a preference for the former pathway, highlighting distinct structural configurations, including a global minimum and two alternative geometries. We demonstrate the participation of higher orbitals of carbon (3d) and its interaction with the bond pair of the approaching H molecule in the formation and stabilization of the fifth C-H bond. This analytical approach provides critical insights into the expanded valency of carbon, which could lead to a new class of carbon compounds.